Abstract
Key regulatory decisions during cleavage divisions in mammalian embryogenesis determine the fate of preimplantation embryonic cells. Single-cell RNA sequencing of early-stage—2-cell, 4-cell, and 8-cell—blastomeres show that the aryl hydrocarbon receptor (AHR), traditionally considered as an environmental sensor, directs blastomere differentiation. Disruption of AHR functions in Ahr knockout embryos or in embryos from dams exposed to dioxin, the prototypic xenobiotic AHR agonist, significantly impairs blastocyst formation, causing repression and loss of transcriptional heterogeneity of OCT4 and CDX2 and incidence of nonspecific downregulation of pluripotency. Trajectory—the path of differentiation—and gene variability analyses further confirm that deregulation of OCT4 functions and changes of transcriptional heterogeneity resulting from disruption of AHR functions restrict the emergence of differentiating blastomeres in 4-cell embryos. It appears that AHR directs the differentiation of progenitor blastomeres and that disruption of preimplantation AHR functions may significantly perturb embryogenesis leading to long-lasting conditions at the heart of disease in offspring’s adulthood.
Similar content being viewed by others
Introduction
Barker’s Theory of the Developmental Origins of Health and Disease (DOHaD) proposes that the environment encountered during fetal life and infancy permanently changes the body’s structure, function, and metabolism and shapes the long-term control of tissue physiology and homeostasis (Fleming et al. 2021). Accordingly, damage resulting from maternal stress, poor nutrition, or exposure to environmental pollutants during fetal life or infancy may be at the heart of adult-onset disease. Preimplantation development is a period of embryogenesis when the embryo is sensitive to environmental conditions; disturbance of this early embryonic environment may induce compensative metabolism in embryos and offspring that could be the cause of later-onset pathological conditions such as large offspring syndrome and cardiovascular disease (Fleming et al. 2004; Velazquez et al. 2016). Consistent with the DOHaD Theory concept, the adverse preimplantation environment may cause developmental alterations in the embryo, triggering a sustained state of insufficiency to increase the risk of disease in the adult.
We have recently found that the AHR, a transcription factor activated by environmental as well as by endogenous agonists, regulates stem cell pluripotency. Untimely AHR activation in pluripotent mouse embryonic stem (ES) cells lengthens mitotic progression, causing pluripotency loss and differentiation failure (Ko et al. 2016). Deletion or inhibition of the AHR accelerates hematopoietic stem cell proliferation, a condition that is useful to generate a stem cell pool for transplant therapy and tissue repair after injury (Angelos et al. 2017; Morales-Hernandez et al. 2017). Yet, however beneficial in that respect, Ahr knockout causes premature exhaustion of hematopoietic stem cells, development of a myeloproliferative disorder, and reduction of cardiomyocyte differentiation from ES cells (Wang et al. 2013; Singh et al. 2014). Considering the physiological role of pluripotency factors in stem cells, it is not surprising that AHR and OCT4—one of the three core pluripotency factors—antagonize each other’s expression. Indeed, in mouse ES cells, the pluripotency factors bind to the Ahr promoter and repress its expression (Ko et al. 2014). Conversely, in both mouse ES cells and human embryonic carcinoma cells, the AHR triggers differentiation and downregulates the expression of OCT4 and NANOG (Ko et al. 2014, 2016; Morales-Hernandez et al. 2016). Furthermore, in many stem-progenitor cell types, exposure to dioxin downregulates the expression of lineage-specific transcription factors and alters differentiation (Chen et al. 2019; Heo et al. 2019; Watson et al. 2019). Integration of these results suggests that the long-lasting effects resulting from disruption of AHR functions may be due to the dysfunctional regulation of pluripotency.
In vivo pluripotency is a transient state in inner cell mass (ICM) cells surrounded by trophoblasts, the first differentiated lineage resulting from preimplantation development. Individual preimplantation embryonic cells—blastomeres—remain loosely attached to each other until late 8-cell stage, a time when they undergo compaction. During this morphological event, blastomeres acquire not only cell-to-cell adhesion but also a geometric position and polarity within the embryo (White et al. 2016). It has been proposed that the inside-outside position and the polarization along the apicobasal axis of each blastomere define the cell fate (Suwinska et al. 2008). Indeed, the precursor cells of trophoblasts are the polarized outer blastomeres expressing trophoblast markers CDX2 and GATA3, whereas the precursors of pluripotent ICM cells are the inner blastomeres expressing pluripotency factors OCT4, SOX2, and NANOG (Sasaki 2015). Consistent with the observation that totipotency is lost in 4-cell blastomeres, precursors of ICM and trophoblasts can be identified at the 4-cell stage based on their high or low level of OCT4 expression and the mono-methylation of arginine-26 of histone H3 (H3R26me) (Torres-Padilla et al. 2007; Goolam et al. 2016). The concurrence between the emergence of differential cell fates among blastomeres and the upregulation of zygotic OCT4 at this stage suggest that OCT4 initiates blastomere differentiation (Wu and Scholer 2014; Goolam et al. 2016). Although OCT4-low and H3R26me-low 4-cell blastomeres subsequently form trophoblasts, the corresponding trophoblast differentiation only starts at later stages and seems to go along with concerted polarization and compaction (Zenker et al. 2018). Hence, while HIPPO signaling–mediated maintenance of CDX2 expression is responsible for trophoblast differentiation starting at the 16-cell stage, OCT4 seems to control the segregation of early differentiating blastomeres and act to coordinate the cellular events organizing blastomere differentiation (Anani et al. 2014; Wu and Scholer 2014; Hirate et al. 2015; Fukuda et al. 2016). Accordingly, trigger(s) of preimplantation embryonic differentiation may initiate the process by regulating Oct4 expression and the population of OCT4-expressing cells. In consideration of the AHR expression in embryos up to 8-cell stage and its role in regulation of Oct4 expression (Peters and Wiley 1995; Dey and Nebert 1998; Jain et al. 1998; Goolam et al. 2016), we hypothesize that a functional AHR is necessary to govern preimplantation development by interacting with OCT4 expression and functions for proper formation of the blastocyst.
We have compared Ahr−/− and dioxin-exposed Ahr+/+ with Ahr+/+ embryos to examine the involvement of the AHR in preimplantation embryogenesis. Both Ahr deletion and its xenobiotic activation by dioxin curtail blastocyst formation, weaken the pluripotent state of ICM, reduce the number of pluripotency factor–expressing ICM cells, and cause the abnormal expression of pluripotency factors in trophoblasts. The absence of 4-cell differentiating blastomeres concurs with the deregulation of OCT4 expression in both Ahr knockout and dioxin-exposed embryos, a condition that persists in 8-cell embryos, along with the impaired upregulation of CDX2. Trajectory analyses further indicate that the absence of differentiating blastomeres in these 4-cell embryos is due to the deregulation of OCT4 function and the changes of transcriptional heterogeneity. We conclude that AHR regulates the expression of genes involved in pluripotency control and trophoblast differentiation, notably OCT4 and CDX2, during the commitment of blastomere cell fates. Considering the importance of the cellular states in ICM and trophoblasts to subsequent embryogenesis, disruption of preimplantation AHR functions is likely to cause damage to developmental programs determining the health and disease consequences later in life.
Results
AHR regulates the reproductive outcome
The C57Bl/6 Ahr−/− mice suffer from multiple developmental lesions including patent ductus venosus that has been associated with long-lasting risk of cardiovascular disease (Lahvis et al. 2000; Lund et al. 2003; Haugen et al. 2005; Tchirikov et al. 2006; Poeppelman and Tobias 2018). Albeit not clear whether the incidence of cardiac disease correlates with patent ductus venosus–related dysfunction, developmental lesions present in Ahr−/− and dioxin-exposed mice suggest that they might be suitable models to test the DOHaD theory. Considering the role of AHR in pluripotency control, we examined whether Ahr deletion or its xenobiotic activation by dioxin during preimplantation development led to abnormal reproductive outcomes. Neonates from wild-type mice exposed to 1 μg/kg dioxin (2,3,7,8-tetrachlorodibenzo-p-dioxin; TCDD), the prototypic xenobiotic AHR agonist (hereafter referred to as Ahr+/+-TCDD mice), during preimplantation development and from Ahr knockout mice were compared to control Ahr+/+ counterparts for litter size and body weight. Relative to Ahr+/+ mice, we found an increase in Ahr−/− and a trend to increase in Ahr+/+-TCDD missing and dead pups per litter, respectively (Fig. 1A). Furthermore, we found a significant increase of body weight in Ahr+/+-TCDD neonates, and a decrease in Ahr−/− neonates relative to Ahr+/+ (Fig. 1B). These observations suggest that the poor reproductive outcomes observed in Ahr−/− and Ahr+/+-TCDD mice may result from disruption of AHR functions during embryonic development.
AHR regulates blastocyst formation and the pluripotent state of the ICM
We previously showed that untimely derepression of AHR in ES cells downregulates expression of OCT4 and SOX2 and causes premature loss of pluripotency (Ko et al. 2016). Given the role of OCT4 in organization of cellular events during differentiation of blastomeres (Wu and Scholer 2014; Goolam et al. 2016; Zenker et al. 2018), we hypothesized that interfered AHR functions may alter blastocyst formation and the in vivo pluripotent state of the ICM. To explore the consequences of disrupting AHR functions in blastocysts, Ahr−/− and Ahr+/+-TCDD embryos were compared to control embryos for possible quantitative and/or morphological differences. While comparable numbers of 2-cell embryos were found in all conditions (Fig. 2A), considerably fewer than control Ahr−/− and Ahr+/+-TCDD blastocysts were observed with many embryos showing sign of degradation without blastocele (Fig. 2B and 2C). Results consistent with these were obtained when Ahr+/+ and Ahr−/− embryos were cultured in vitro and exposed to AHR ligands. The number of blastocysts in vehicle-treated Ahr−/− cultures was significantly decreased relative to Ahr+/+ cultures exposed to control vehicle, as were the numbers in Ahr+/+ cultures treated with the AHR antagonist CH223191 and with TCDD after 4 and 4.5 days (Fig. 2D). As expected, we found no difference between vehicle and TCDD-exposed Ahr−/− groups, suggesting that effect of TCDD exposure on blastocyst formation is AHR-dependent.
To assess the differentiated state of ICM and trophoblasts in Ahr−/− and Ahr+/+-TCDD blastocysts, we examined the expression of the pluripotency factors OCT4, SOX2, and NANOG and the trophoblast marker CDX2 by immunofluorescence analyses. Ahr+/+ blastocysts showed nuclear expression of pluripotency factors in ICM and CDX2 in trophoblasts, while abnormal expression of pluripotency factors was observed in Ahr−/− and Ahr+/+-TCDD trophoblasts (Fig. 3A). Compared to the low number of Ahr+/+ embryonic cells expressing simultaneously OCT4 and CDX2, we found a significantly larger number of OCT4-CDX2 double-positive cells in both Ahr−/− and Ahr+/+-TCDD blastocysts, and no difference among Ahr+/+, Ahr−/−, and Ahr+/+-TCDD embryonic cells in the number of cells showing SOX2-CDX2 double staining (Fig. 3B). In contrast, the number of NANOG-CDX2 double-positive cells was significantly higher in Ahr+/+ than in Ahr−/− and Ahr+/+-TCDD blastocysts. When we scored the number of pluripotency factor–expressing embryonic cells and assigned them to either the ICM or the trophoblast lineage based on their position within immunostained blastocysts, we found that changes of OCT4-CDX2 and NANOG-CDX2 double-positive cell numbers in Ahr−/− and Ahr+/+-TCDD blastocysts followed the same trends observed for the bulk and the trophoblast fraction of OCT4- and NANOG-expressing cells (Fig. 3C and 3D). In addition, we found significantly fewer SOX2-expressing embryonic and ICM cells in Ahr−/− and Ahr+/+-TCDD than in Ahr+/+ blastocysts, and no difference in the SOX2-expressing trophoblasts (Fig. 3E). Relative to the numbers in Ahr+/+ blastocysts, only OCT4- and SOX2-expressing Ahr−/− and Ahr+/+-TCDD ICM cells showed a significant decrease, which corresponded to an increase in the numbers of OCT4- and SOX2-expressing trophoblasts (Fig. 3F). We found no difference in the number of CDX2-expressing trophoblasts in all immunostained blastocysts (Fig. 3G). Collectively, disruption of AHR functions seemed to specifically deregulate the level and cell-type specificity of OCT4 and SOX2 expression, suggesting that differentiation was derailed in the Ahr−/− and Ahr+/+-TCDD embryos.
AHR directs the segregation of 4-cell blastomeres
Increasing evidence supports the concept that gene expression heterogeneity is the origin of cell fate decisions (Torres-Padilla and Chambers 2014; Kalkan et al. 2017; Simon et al. 2018). During preimplantation development, the earliest signs of differentiation are observed in 4-cell embryos, where high-vs-low levels of OCT4 expression prelude ICM-vs-trophoblast cell fates (Torres-Padilla et al. 2007; Goolam et al. 2016). The Ahr gene has been identified as one of a group of genes that show significant 4-cell inter-blastomere transcriptional variability (Goolam et al. 2016), suggesting a role for the AHR in the initiation of blastomere differentiation. Accordingly, dysfunctional AHR may disrupt early blastomere differentiation and cause the impaired formation of Ahr−/− and Ahr+/+-TCDD blastocysts. Since mutual regulation between OCT4 and CDX2 is in place by the 16-cell stage, at a time when Ahr expression is undetectable (Peters and Wiley 1995; Jain et al. 1998; Hirate et al. 2015; Fukuda et al. 2016), we aimed specifically at the early 2- to 8-cell stages to explore the potential role of the AHR in regulation of the transcriptome of progenitor blastomeres. We isolated 336 single blastomeres obtained from eight embryos of each of the nine groups: Ahr+/+, Ahr−/−, and Ahr+/+-TCDD each at 2-cell, 4-cell, and 8-cell stages individually, and subjected them to Single-Cell RNA-sequencing (scRNA-seq) allowing the identification of cellular heterogeneity. Three-dimensional t-distributed stochastic neighbor embedding (3D-tSNE) using all variable genes across all cells revealed that blastomeres belonging to 8-cell embryos were distinct from blastomeres of the cluster containing both 2-cell and 4-cell blastomeres (hereafter referred to as the 2-and-4-cell cluster, Fig. 4A). We obtained a similar classification with additional analyses using hierarchical clustering of all expressed genes with expression levels ≥ 1 transcripts-per-million and by clustering cell–cell Pearson’s correlation matrix across all blastomeres analyzed (Supplementary Fig. 1B and 1C). This finding is in agreement with data previously shown by others (Hamatani et al. 2004), attesting to the reliability of our scRNA-seq approach.
To investigate if disrupted AHR function interferes with cellular heterogeneity, we performed cell–cell Pearson’s correlation analyses followed by hierarchical clustering using cells of all three or only of 2-cell and 4-cell stages for Ahr+/+, Ahr−/−, and Ahr+/+-TCDD conditions separately. Similar to the segregation obtained from analyses using all cells, Ahr+/+ 8-cell blastomeres were distinctly grouped when compared to cells belonging to the 2-and-4-cell cluster (Fig. 4B top-left panel). Ahr+/+ blastomeres that belonged to the 2-and-4-cell cluster were subsequently segregated into 2 subclusters based on their developmental stage (Fig. 4B bottom-left panel). After the segregation of Ahr−/− 8-cell blastomeres from the 2-and-4-cell cluster, no segregation of individual Ahr−/− 2-cell subcluster was observed (Fig. 4B middle panels). A few Ahr+/+-TCDD 4-cell blastomeres were grouped in the cluster containing 8-cell blastomeres followed by a clear separation of Ahr+/+-TCDD 2-cell and 4-cell subclusters (Fig. 4B right panels). To examine how different the Ahr−/− and Ahr+/+-TCDD transcriptomes are relative to wild type, we determined the correlation coefficient of 8-cell and 4-cell blastomeres relative to cells belonging to the 2-and-4-cell cluster and the 2-cell subcluster. The correlation coefficient between cells in 8-cell and 2-and-4-cell clusters was significantly increased, i.e., was evidence of higher similarity, in Ahr−/− relative to Ahr+/+ and the opposite was the case for Ahr+/+-TCDD relative to Ahr+/+ (Fig. 4C). Additionally, both Ahr−/− and Ahr+/+-TCDD 4-cell blastomeres showed higher correlation than Ahr+/+ cells when compared to the corresponding 2-cell blastomeres (Fig. 4C), indicative of a lower level of cellular heterogeneity in Ahr−/− and Ahr+/+-TCDD 2-cell and 4-cell blastomeres than in their Ahr+/+counterparts.
To identify possible subpopulation(s) in each of the nine groups, we compared the relative location of each blastomere obtained from hierarchical clustering on the correlation matrices to its relative position on the 3D-tSNE plot. Blastomeres were referred to as either “Embryonic” or “Differentiating” depending on their spatial location denoted by the arrows indicating the advancement in development on the 3D-tSNE coordinates; blastomeres with mismatching location and position were not included in the subpopulational gene expression analyses. We found that only 2 Ahr+/+ but as many as 11 Ahr−/− and 7 Ahr+/+-TCDD cells were classified as differentiating blastomeres at the 2-cell stage (Fig. 4D and Supplementary Fig. 1D–F, 1 M). At the 4-cell stage, we identified 16 Ahr+/+ and only 4 Ahr+/+-TCDD and no Ahr−/− differentiating blastomeres (Fig. 4E and Supplementary Fig. 1G–I, 1 M). At the 8-cell stage, 49 Ahr+/+, 31 Ahr−/−, and 52 Ahr+/+-TCDD blastomeres were considered as differentiating (Fig. 4F and Supplementary Fig. 1 J–L, 1 M). Statistical analysis of the difference in the numbers of differentiating blastomeres in each group showed significant reduction of differentiating cells in both 4-cell Ahr−/− and Ahr+/+-TCDD embryos and only in 8-cell Ahr−/− embryos relative to their wild-type counterparts, respectively (Fig. 4G, Supplementary Table 1 and Supplementary Fig. 1 N). Taken together, these results point at the conclusion that the AHR is required in the appearance of early cellular heterogeneity and that its deregulation specifically disrupts the initiation of blastomere differentiation at the 4-cell stage.
AHR promotes pluripotency downregulation in the 4-cell blastomeres that initiate differentiation
To identify which AHR functions were involved in initiating blastomere differentiation, we used comprehensive transcriptomic analyses via the Ingenuity Pathway Analysis (IPA) platform to explore the biological functions of genes differentially expressed between different groups and subpopulations. We identified, notably those dealing with the downregulation of Pluripotency Control and Metabolism of Inositol Phosphate Compounds in 4-cell blastomeres undergoing differentiation, suggesting that the AHR has a mechanistic role in the emergence of progenitor blastomeres.
A higher number of differentially expressed genes and many more canonical pathways were differentially enriched in the Ahr+/+ 2-cell to 4-cell transition than in the 4-cell to 8-cell transition (Supplementary Fig. 2A–F and Supplementary Data 1 and 2), suggestive of a higher degree of transcriptomic changes in 4-cell than in 8-cell blastomeres. Specifically, pathways related to pluripotency control and metabolism of inositol phosphate compounds, identified in the Ahr+/+ transition from 2-cell to 4-cell differentiating subpopulations, were not enriched when we compared either Ahr−/− or Ahr+/+-TCDD 4-cell blastomeres to their 2-cell population (Supplementary Fig. 2G–I and Supplementary Data 2). Therefore, downregulation of pluripotency and metabolism of inositol phosphate may be crucial functions of the AHR in the subpopulation of 4-cell blastomeres undergoing differentiation. Indeed, Mouse Embryonic Stem Cell Pluripotency, Role of NANOG in Mammalian Embryonic Stem Cell Pluripotency, and Metabolism of Inositol Phosphate Compounds were upregulated in the comparison of Ahr−/− and Ahr+/+-TCDD 4-cell embryonic blastomeres to Ahr+/+ 4-cell differentiating subpopulation (Fig. 5A and Supplementary Data 3).
HIPPO and mTOR signaling pathways were downregulated in the transition of Ahr+/+ 4-cell differentiating subpopulation to the 8-cell blastomeres (Supplementary Fig. 2E, 2F and Supplementary Data 2), suggesting that the initiation of trophoblast differentiation follows promptly the downregulation of pluripotency. Remarkably, signaling pathways involved in pluripotency control and metabolism of inositol phosphate compounds were non-specifically downregulated in the transition of Ahr−/− 4-cell blastomeres to both 8-cell embryonic and differentiating subpopulations (Supplementary Fig. 2 J, 2 K and Supplementary Data 2). Similar nonspecific downregulation of mTOR signaling was found when comparing Ahr+/+-TCDD 8-cell both subpopulations to 4-cell embryonic blastomeres (Supplementary Fig. 2L–O and Supplementary Data 2). Only HIPPO signaling was found upregulated in the comparison of Ahr−/− 8-cell embryonic blastomeres to Ahr+/+ 8-cell differentiating subpopulation (Fig. 5B and Supplementary Data 3). Collectively, these results suggest that disruption of AHR functions leads to delayed and non-specific regulation of pathways responsible for fate specification of progenitor blastomeres.
AHR sustains the expression and the transcriptional heterogeneity of OCT4 and CDX2 in progenitor blastomeres
To characterize how AHR regulates the emergence of progenitor blastomeres, we used the data obtained by scRNA-seq to analyze the expression of AHR, OCT4, and CDX2. Consistent with evidence shown by others (Peters and Wiley 1995; Jain et al. 1998; Goolam et al. 2016), we found the highest level of Ahr mRNA in the bulk of the Ahr+/+ 2-cell population, followed by successive decreases in the 4-cell and 8-cell embryos (Fig. 5C). No difference was observed in the bulk of the Ahr+/+-TCDD population at all stages analyzed. At the subpopulation level, a significant decrease of Ahr mRNA was detected in the transition from the Ahr+/+ 2-cell to the 4-cell differentiating subpopulation; from the Ahr+/+ 4-cell embryonic blastomeres to the 8-cell both embryonic and differentiating subpopulations; and from the Ahr+/+-TCDD 4-cell embryonic blastomeres to the 8-cell differentiating subpopulation (Fig. 5D).
High levels of Oct4 mRNA were found in the 2-cell blastomere population in all conditions, followed by a decrease at the 4-cell stage and a strong increase in 8-cell blastomeres (Fig. 5E), an expression pattern reflecting the transition of maternal-to-zygotic Oct4 transcripts at the 4-cell stage (Wu and Scholer 2014). There was a decrease of Oct4 expression in the bulk of both Ahr−/− and Ahr+/+-TCDD groups relative to Ahr+/+ at the 8-cell stage and in Ahr−/− than in Ahr+/+ 2-cell blastomeres. Similarly, we found a significant decrease of Oct4 expression in both Ahr−/− and Ahr+/+-TCDD, notably in both embryonic and differentiating blastomeres relative to the corresponding Ahr+/+ 8-cell subpopulations; in all conditions, differentiating blastomeres at 8-cell stage had higher expression levels than their embryonic counterparts (Fig. 5F). Furthermore, the levels of Oct4 transcription in Ahr−/− and Ahr+/+-TCDD 4-cell embryonic blastomeres decreased or had a trend to decrease, respectively, relative to the corresponding Ahr+/+ blastomeres. The levels of Cdx2 mRNA were high in all 8-cell blastomeres analyzed and were significantly decreased or trended to decrease in the bulk of Ahr−/− and Ahr+/+-TCDD relative to the Ahr+/+ 8-cell population (Fig. 5G). The Cdx2 mRNA levels were higher in Ahr+/+ and Ahr−/− 8-cell differentiating blastomeres than in their embryonic counterparts, with the Ahr−/− 8-cell differentiating blastomeres showing lower expression than the corresponding Ahr+/+ subpopulation (Fig. 5H). Additionally, some Ahr+/+-TCDD 8-cell embryonic blastomeres showed unusually high levels of Cdx2 mRNA causing the indistinguishable difference between embryonic and differentiating subpopulations.
In agreement to the Ahr expression at mRNA level, we found high levels and heterogenous AHR expression in Ahr+/+ 2-cell and 4-cell embryos respectively (Fig. 5I). Similar to the observation in Ahr−/− condition, we did not detect AHR expression in Ahr+/+-TCDD embryos, indicating degradation of the AHR after TCDD exposure. As expected, OCT4 and AHR protein expression was stronger in Ahr+/+ 2-cell than in 4-cell embryos (Fig. 5I). In two of the Ahr−/− 2-cell blastomeres, we found differential OCT4 expression, which was in agreement with the transcriptional heterogeneity observed. We detected AHRhigh-OCT4high and AHRlow-OCT4low inter-blastomere gene expression heterogeneity in Ahr+/+ 4-cell embryos, and the corresponding expression levels were lower in Ahr−/− and Ahr+/+-TCDD than in Ahr+/+ 4-cell embryos and no heterogeneity could be detected. At the 8-cell stage, expression of OCT4 was strong and AHR was undetectable in Ahr+/+ embryos while Ahr−/− and Ahr+/+-TCDD embryos had lowered OCT4 than wild-type. Strong and inter-blastomere heterogeneous CDX2 expression was identified in Ahr+/+ 8-cell embryos, being lower in the Ahr−/− and Ahr+/+-TCDD counterparts (Fig. 5J and supplementary Fig. 3). A higher degree of OCT4 and CDX2 inter-blastomere heterogeneity was observed in Ahr+/+ morula, which was not the case in both Ahr−/− and Ahr+/+-TCDD counterparts despite of increased expression levels. These results suggest that the crucial function of the AHR is to maintain the expression level and heterogeneity of OCT4 and subsequently CDX2 in progenitor blastomeres.
AHR regulates the transcriptional heterogeneity and the differentiation trajectory of progenitor blastomeres
We previously showed that fluctuating AHR expression in mouse ES cells regulates the heterogeneous expression of OCT4, leading to an alternative switch between the maintenance and the exit of pluripotency (Ko et al. 2016). As a consequence, AHR may control the variability of gene expression in early embryos and trigger the differentiation of progenitor blastomeres. To address this possibility, we examined genes that showed a higher level of expression variability than expected by chance—the variable genes—in the blastomere population of all 9 groups. We identified no change in Ahr−/− and Ahr+/+-TCDD 2-cell populations relative to the corresponding Ahr+/+ blastomeres (Fig. 6A, Supplementary Fig. 4A, and Supplementary Data 4). Significantly greater number of variable genes were found in both Ahr−/− and Ahr+/+-TCDD 4-cell blastomeres relative to the Ahr+/+ counterparts and in Ahr+/+-TCDD 8-cell blastomeres relative to the corresponding Ahr+/+ 8-cell population. This finding suggests that AHR governs the emergence of progenitor blastomeres by regulating the degree of transcriptional variability starting at the 4-cell stage. If it were true that the gene expression variability initiates differentiation of blastomeres, the variable genes would likely share the same identities and biological functions with genes showing differential expression levels between subpopulations. Supporting this assumption, we found a significant number of variable genes that were also differentially expressed between the paired subpopulations in each of the 5 groups in which differentiating blastomeres were identified (Fig. 6B). Comprehensive transcriptomic analysis via IPA revealed that these overlapping genes identified in Ahr+/+ 4-cell blastomeres may be involved in Mouse ES Cell Pluripotency and Xenobiotic Metabolism AHR Signaling Pathway (Fig. 6C and Supplementary Data 5). AHR Signaling, NRF2-mediated Oxidative Stress Response, and Aldosterone Signaling in Epithelial Cells were identified as the potential function of Ahr+/+, Ahr−/−, and Ahr+/+-TCDD 8-cell overlapping genes respectively (Fig. 6D and Supplementary Data 5). These findings suggest that AHR controls gene expression heterogeneity to differentially regulate pluripotency control among 4-cell blastomeres and promote the segregation of progenitor blastomeres.
In the pathway-related investigation, we found that a significant number of genes involved in the AHR signaling showed heterogeneous expression only among Ahr+/+ 4-cell blastomeres (Supplementary Fig. 4B), suggesting a role of the AHR on regulation of transcriptional heterogeneity at this stage. A few genes of the HIPPO signaling pathway showed variable levels of expression but the corresponding number did not reach significance (Supplementary Fig. 4C). Significant numbers were found for genes involved in the role of OCT4 in pluripotency control in Ahr+/+ and Ahr+/+-TCDD, but not Ahr−/− 4-cell embryos, followed by a greater number observed at 8-cell stage in all conditions (Supplementary Fig. 4D). Furthermore, significant number of the mTOR signaling genes showing heterogenous expression was only observed among Ahr+/+ 8-cell blastomeres (Supplementary Fig. 4E). Of all scored genes, we found that AHR downregulated expression of Foxa1 and Jarid2 in both Ahr−/− and Ahr+/+-TCDD 4-cell and in 8-cell embryonic subpopulations, respectively, altering the transcriptional variability of OCT4 signaling in the bulk of corresponding blastomere population (Fig. 6E and 6F). Reduced variability of HIPPO signaling in the bulk of Ahr−/− 4-cell and 8-cell blastomere populations seemed to relate to an upregulated expression of Smad4 and Ajuba in Ahr−/− 4-cell embryonic and in 8-cell both embryonic and differentiating subpopulations respectively (Fig. 6G and 6H). On the other hand, we found that AHR downregulated expression of Dgkz and Ulk1 in both Ahr−/− and Ahr+/+-TCDD 8-cell differentiating subpopulations to increase the transcriptional heterogeneity of mTOR signaling in the bulk of Ahr−/− and Ahr+/+-TCDD 8-cell blastomere populations (Fig. 6I and 6J). Taken together, these results suggest that the AHR promotes segregation of progenitor blastomeres through regulating the transcriptional heterogeneity of OCT4, HIPPO, and mTOR signaling in a stage-dependent manner.
To explore the consequence in progenitor blastomeres resulting from disruption of AHR functions, we compared the differentiation trajectory of Ahr−/− and Ahr+/+-TCDD to Ahr+/+. If our finding of the segregation of progenitor blastomeres at the 4-cell stage was true, the structure of the Ahr+/+ trajectory may contain at least one branch indicating the 4-cell differentiating subpopulation. We found that the segregation of Ahr+/+ 4-cell differentiating subpopulation was only projected by genes involved in OCT4 and mTOR signaling and by the collection of genes involved in OCT4, mTOR, and HIPPO pathways, suggesting a role of these pathways and the possible regulatory role of the OCT4 on mTOR and HIPPO signaling in the initiation of progenitor blastomere differentiation (Supplementary Fig. 5A). On the other hand, no stage- and/or subpopulation-wide separation of Ahr+/+ blastomeres could be identified in trajectories projected using neither AHR nor HIPPO signaling genes alone. As expected, we did not observe the branch indicating 4-cell differentiating subpopulation in any of the Ahr−/− and Ahr+/+-TCDD trajectories projected using genes involved in only one pathway (Supplementary Fig. 5B and 5C). Using the combination of genes of all four pathways and all variable genes, we obtained an Ahr+/+ differentiation trajectory containing the 4-cell differentiation branch, the cluster composed of 8-cell embryonic blastomeres, and the cluster including the majority of 8-cell differentiating blastomeres (Fig. 7A). Consistently, the Ahr−/− 4-cell blastomeres were not separated from their 2-cell counterparts, and the earliest differentiation of Ahr−/− embryonic cells was shown at the 8-cell stage (Fig. 7B). On the other hand, we identified neither 4-cell branch nor 8-cell segregation in the Ahr+/+-TCDD differentiation trajectory (Fig. 7C). These results indicate that the AHR regulates the transcriptional heterogeneity and pathways playing essential roles in preimplantation development to direct the differentiation of progenitor blastomeres.
Discussion
In this article, we show that the AHR, an environmental sensor and transcription factor that regulates the pluripotency in ES cells, directs the differentiation of progenitor blastomeres that determine the pluripotent state of ICM cells in blastocysts. As illustrated in the summary Fig. 8, AHR functions to promote the downregulation of pluripotency in 4-cell blastomeres that initiate differentiation. Disruption of this function by Ahr ablation, or its xenobiotic activation, leads to repression of inter-blastomere transcriptional heterogeneity of OCT4 in 4-cell embryos and of CDX2 in 8-cell and morula stage embryos. As a consequence, Ahr−/− and Ahr+/+-TCDD blastomeres follow derailed differentiation trajectories and form impaired blastocysts with low pluripotent state in the ICM and abnormal expression of pluripotency factors in trophoblasts, which may cause a poor reproductive outcome due to defective embryogenesis.
Previously, we have shown that AHR regulates the maintenance of pluripotency and interferes with the differentiation outcome of mouse ES cells (Ko et al. 2016). Unlike the association between AHR expression and the differentiated state of pluripotent stem cells shown by in vitro studies (Ko et al. 2014; Morales-Hernandez et al. 2016), expression of the AHR remains higher in the embryonic subpopulation than in the differentiating one, leading to AHRhigh-OCT4high and AHRlow-OCT4low heterogeneity in 4-cell embryos. By sustaining heterogenous expression of OCT4, the AHR may upregulate CDX2 expression and direct the differentiation of 8-cell OCT4high-CDX2high blastomeres. The AHR may also prevent the downregulation of pluripotency in embryonic blastomeres by maintaining a homogenous expression of Foxa1 and Jarid2 that have been shown to be involved in the sustenance of accessible promoters and WNT signaling in preimplantation embryos (Landeira et al. 2015; Jung et al. 2019). As a consequence, lack of AHR in Ahr−/− and Ahr+/+-TCDD (plausibly due to the proteasomal degradation of the AHR protein after activation by TCDD) embryos results in repression of OCT4 and CDX2 in all blastomeres, causing lack of 4-cell and derail of 8-cell blastomere differentiation, and reduction of ICM pluripotency. Alongside the OCT4-mediated pluripotency control, the AHR differentially regulates HIPPO and mTOR signaling to establish a distinct regulatory profile between embryonic and differentiating blastomeres. HIPPO and mTOR signaling pathways have been shown to control the self-renewal of stem-like cells and the reprogramming to pluripotency (Bora-Singhal et al. 2015; Lee et al. 2020). Yet, the interaction between these two signalings was considered a response to stress stimuli arising from energy metabolism, hypoxia, reactive oxygen species, and mechanical forces in stem cells (Zeybek et al. 2021). Accordingly, upregulated expression and variability of genes involved in HIPPO signaling such as Smad4 and Ajuba in Ahr−/− blastomeres suggest that the coordinating function of the AHR is required to support the specification of trophoblast differentiation in corresponding precursor cells (Anani et al. 2014; Hirate et al. 2015). Similarly, the AHR may also sustain mTOR signaling-mediated metabolism and embryonic physiology to ensure the segregation of differentiating blastomeres at the 8-cell stage (O'Neill 2008).
Concurrently, the AHR may downregulate the metabolism of inositol phosphate compounds to initiate blastomere differentiation. The derivatives of inositol phosphate metabolism are involved in intracellular calcium signaling and mTOR signaling essential to the maintenance of preimplantation embryonic physiology (O'Neill 2008; Armant 2015). Furthermore, inositol phosphate compounds may be one of the critical energy sources of preimplantation embryos due to the low mitochondrial activities in embryos at these stages and the hypoxic environment in the female reproductive tract (Kumar et al. 2018). Therefore, AHR may regulate the energy supply requirements that are closely related to the outcome of epigenetic reprogramming in blastomeres undergoing fate commitment (Chason et al. 2011; Harvey 2019). Induction of compensative metabolism in developing embryos under stress has been suggested to cause the later-onset pathological conditions, notably metabolic and cardiovascular diseases (Watkins et al. 2008; Chason et al. 2011; Fleming et al. 2017). In line with this hypothesis, AHR is known to mediate metabolism-related syndromes including obesity, insulin resistance, and liver fibrosis, and cardiovascular conditions such as cardiac hypertrophy (Kerley-Hamilton et al. 2012; Carreira et al. 2015; Brulport et al. 2017; Duval et al. 2017; Girer et al. 2020; Bock 2021). In conclusion, results of the present study suggest that a functional AHR is necessary to maintain the pluripotency in ICM and the proper differentiation of preimplantation embryos. Due to the importance of the preimplantation embryonic cells to the subsequent developmental program, disruption of preimplantation AHR functions may contribute to long-lasting pathological conditions to increase disease susceptibility.
Materials and methods
Preimplantation exposure, embryo collection, and in vitro embryo culture
Mice
All experiments were conducted using the highest standards of human care in accordance with the NIH Guide for the Care and Use of Laboratory Animals and were approved by the University of Cincinnati Institutional Animal Care and Use Committee. Mice were housed in a pathogen-free animal facility under a standard 12-h light/12-h dark cycle with ad libitum water and chow. Eight-week-old mice were used for all experiments, and all Ahr−/− mice used for experiments were the F1 generation obtained from the breeding between Ahr+/- female and Ahr−/− male.
Superovulation and dioxin exposure
Female mice were superovulated by intraperitoneal injection of 7.5-I.U. pregnant mare serum gonadotropin (PMSG, Calbiochem, Burlington, MA), followed by 7.5-I.U. human urine chorionic gonadotropin (hCG, Sigma, Saint Louis, MO) before overnight mating with individually housed stud males of the same genotype. Preimplantation exposure to 1 μg/kg TCDD (Cambridge Isotope Laboratory, Tewkesbury, MA) and equivalent volume of corn oil for vehicle control were performed via oral gavage at gestational days E-0.5 and E2.5 (Supplementary Fig. 6).
Litter size and neonatal body weight determination
At E19.5, the numbers of newborns and the numbers of implantation sites in uteri of the same dam were scored no later than 10 h after delivery. The numbers of missing and dead pups were determined by subtracting the number of newborns from that of implantation sites. The body weight of each of the postnatal day 1 pups were scaled and recorded individually.
Embryo collection
Details of experimental scheme regarding embryo collection can be found in Supplementary Fig. 6. Two-cell, 4-cell, 8-cell, and blastocyst stage embryos were collected from superovulated naïve Ahr+/+and Ahr−/− females that were mated at E-0.5 with males of the corresponding genotype and exposed to control oil vehicle or TCDD at 46-, 55-, 70-, and 97-h post-hCG time into M2 media (Millipore, Burlington, MA), respectively. Litter sizes and morphology of 2-cell embryos and blastocysts were observed using a binocular stereomicroscope (AmScope, Irvine, CA).
In vitro embryo culture
Naïve Ahr+/+ and Ahr−/− zygotes were recovered from plugged Ahr+/+ and Ahr−/− females, respectively, into M2 medium at 21-h post-hCG time (Supplementary Fig. 6). After removing granulosa cells by a short incubation in M2 medium containing hyaluronidase (Millipore) at 37 °C, embryos were cultured in KSOM media (Millipore and CytoSpring, Mountain View, CA) in a humidified incubator at 37 °C 5% CO2 for 5 days. In vitro exposure to 1-nM TCDD or to 10-μM AHR antagonist CH223191 (Cambridge Chemical Technologies, Cambridge, MA) was initiated before both male and female pronuclei could be clearly visualized, using DMSO dissolved in KSOM at ≤ 0.05% of the final volume as vehicle control. More than 4 replicates were performed for each experimental condition; the numbers of embryos that had reached the 2-cell stage and of embryos that formed blastocyst were scored. Efficiency of blastocyst formation was calculated as percent embryo relative to the number of embryos observed at the 2-cell stage.
Immunofluorescence and scoring of labeled embryonic cells
Immunofluorescence
Embryos were fixed in 2% paraformaldehyde (Sigma) for 10 min at room temperature and washed in 3 µg/ml polyvinylpyrrolidone dissolved in 1X PBS (Gibco, Waltham, MA, hereafter referred to as PVP-PBS). Primary antibodies against CDX2 (MA5-14,494, Thermo Fisher Scientific, Waltham, MA), OCT4 (AF-1759, R&D Systems, Minneapolis, MN), SOX2 (AF2018, R&D Systems), and NANOG (PA5-47,376, Invitrogen-Thermo Fisher Scientific), the conjugated antibody against AHR (12–5925-82, eBiosciences-Thermo Fisher Scientific) as well as Alexa-488 and Alexa-594 conjugated secondary antibodies (Invitrogen-Thermo Fisher Scientific) were used. After permeabilized in 0.25% Triton X-100 (Sigma) prepared in PVP-PBS at room temperature for 10 min, embryos were incubated with blocking buffer containing 5% donkey serum (D9663, Sigma), 2% BSA (4,022,052, Bio-World, Irving, TX), and 0.01% Tween-20 (Sigma) in PVP-PBS at room temperature for 1 h before applying primary antibody at 4 °C overnight. The next day, embryos were washed in series of PVP-PBS drops before applying secondary antibodies diluted in blocking buffer at room temperature for an hour. After washes, embryos were mounted in cavity slides (71,883–79, Globe Scientific Inc, Mahwah, NJ) with 45 μl of fluorescent mounting medium containing DAPI (H1200, Vector Laboratories, Burlingame, CA) and settled down in the dark overnight before visualization using confocal microscopy (LSM700 Carl Zeiss Microscopy, Dublin, CA).
Scoring of fluorescent embryonic cell
The number of OCT4- (green channel), SOX2- (green channel), NANOG- (green channel), and CDX2-expressing (red channel) embryonic cells were scored by manual counting throughout the z-stacks of each of the immunostained blastocysts; one example using OCT4 and CDX2-immunostained blastocyst was illustrated in Supplementary Fig. 7. The number of DAPI-stained embryonic cells was recorded as the reference number of embryonic cells in each of the blastocysts analyzed. For each of the immunostained blastocysts, the numbers of OCT4/SOX2/NANOG-CDX2 double-stained, OCT4/SOX2/NANOG-expressing, and CDX2-expressing cells were scored individually. The number of OCT4/SOX2/NANOG-expressing embryonic cells was further subdivided into either ICM or trophoblast fractions based on the relative location of each cell within blastocysts.
Isolation of single blastomeres and single-cell RNA sequencing
Isolation of single blastomeres
Embryos were incubated in Tyrode’s solution (Sigma) at room temperature to remove the zona pellucida before manual isolation of healthy single blastomeres using Femtotip II (Eppendorf, Hauppauge, NY) and carefully pipetted into cell lysis buffer containing RNase inhibitor.
Single-cell RNA-sequencing
Messenger RNAs obtained from lysed single blastomeres were converted into full-length cDNA by directly following the manufacture’s protocol of SMART-seq v4 ultra-low input RNA kit with some modifications (Takara Bio, Mountain View, CA). A 1.5-μl volume of 1X PBS containing 0.4% of BSA and one single blastomere was transferred into PCR tubes containing the lysis buffer and 10X RNase inhibitor provided by the kit. cDNA of each single blastomere was prepared by first-strand-cDNA conversion from polyA-RNA followed by 18 cycles of full-length amplification. After quality control using a Bioanalyzer High Sensitivity DNA kit (Agilent, Santa Clara, CA) and concentration measurement using Qubit dsDNA HS assay (Thermo Fisher Scientific), 150 pg of amplified cDNA were subjected to library preparation using a Nextera XT DNA library preparation kit (Illumina, San Diego, CA). After quantification using NEBNext Library Quant kit (NEB, Ipswich, MA), libraries were pooled and sequenced on the next-generation sequencer HiSeq 1000 (Illumina) under setting of 2 × 101-bp pair-ends base pairs.
Data Analysis of scRNA-seq
Data processing and quality control
Three hundred thirty-six single blastomeres were isolated and submitted to scRNA-seq, and 322 single-cell transcriptomes were generated. Fastq files with sequence reads were generated with bcl2fastq version 2.18 (Illumina). RNA-seq pair-end fastq were validated with fast-QC and summarized with multi-QC, and low quality cells, outliers were removed from further consideration in appropriate stages of analyses. The transcriptomes of 322 single blastomeres were sequenced at an averaged depth of ~ 2,600,000 reads/cell, of which an average of 86.52% was mapped to single or multiple gene loci. Count and transcript per million (TPM) data for reads were generated based on output of STAR aligner.
Cluster analysis
Three-dimensional t-distributed stochastic neighbor embedding (3D-tSNE) visualization of the all variable genes across all cells were generated using the tSNE plotly R packages. Hierarchical clustering of cells based on log2 transformed TPM for all genes with expression level ≥ 1 was performed with the Morpheus platform (https://software.broadinstitute.org/morpheus) using 1-Pearson’s correlation as the distance measurement. The cluster analysis of cell–cell correlation matrix was performed by first calculating all vectors of pairwise correlations between a single cell and all other cells followed by hierarchical clustering of rows and columns of the resulting correlation matrix using 1-Pearson’s correlation as the distance measurement.
Comprehensive transcriptomic analysis
Lists of differentially expressed genes between groups and subpopulations were submitted to comprehensive transcriptomic analysis via Ingenuity Pathway Analysis (IPA, Qiagen, Germantown, MD). Canonical pathways that were commonly identified in analyses of comparisons using six statistical cutoff levels were considered to be differentially enriched.
Identification of variable genes
The expression variability of each gene was estimated by following the parametric equation CV2 = a1/μ + a0, where the square of coefficient of variation CV2 was a function of the mean after normalization with the count number μ. Genes with an adjusted p-value (FDR) < 0.1 were considered as significantly variable.
Trajectory analysis
Projection of blastomere differentiation trajectories was performed with count data of selected genes using Monocle-2 algorithm. Analytic steps included the estimation of size factors, the estimation of dispersion and normalization, the selection of subspace for analysis, the reduction of dimension, and the visualization of trajectories.
Statistical analysis
Statistical analyses were performed via R and/or Prism. Details of all statistical analyses carried out throughout this study are provided in the file entitled Statistical Information; a p-value < 0.05 was considered significant.
Availability of supporting data
Supporting data will be available from the corresponding author upon reasonable request.
References
Anani S, Bhat S, Honma-Yamanaka N, Krawchuk D, Yamanaka Y. Initiation of Hippo signaling is linked to polarity rather than to cell position in the pre-implantation mouse embryo. Development. 2014;141:2813–24.
Angelos MG, Ruh PN, Webber BR, Blum RH, Ryan CD, Bendzick L, Shim S, Yingst AM, Tufa DM, Verneris MR, et al. Aryl hydrocarbon receptor inhibition promotes hematolymphoid development from human pluripotent stem cells. Blood. 2017;129:3428–39.
Armant DR. Intracellular Ca2+ signaling and preimplantation development. Adv Exp Med Biol. 2015;843:151–71.
Bock KW. Aryl hydrocarbon receptor (AHR), integrating energy metabolism and microbial or obesity-mediated inflammation. Biochem Pharmacol. 2021;184:114346.
Bora-Singhal N, Nguyen J, Schaal C, Perumal D, Singh S, Coppola D, Chellappan S. YAP1 regulates OCT4 activity and SOX2 expression to facilitate self-renewal and vascular mimicry of stem-like cells. Stem Cells. 2015;33:1705–18.
Brulport A, Le Corre L, Chagnon MC. Chronic exposure of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) induces an obesogenic effect in C57BL/6J mice fed a high fat diet. Toxicology. 2017;390:43–52.
Carreira VS, Fan Y, Kurita H, Wang Q, Ko CI, Naticchioni M, Jiang M, Koch S, Zhang X, Biesiada J, et al. Disruption of Ah receptor signaling during mouse development leads to abnormal cardiac structure and function in the adult. PLoS One. 2015;10:e0142440.
Chason RJ, Csokmay J, Segars JH, DeCherney AH, Armant DR. Environmental and epigenetic effects upon preimplantation embryo metabolism and development. Trends Endocrinol Metab. 2011;22:412–20.
Chen T, Jin H, Wang H, Yao Y, Aniagu S, Tong J, Jiang Y. Aryl hydrocarbon receptor mediates the cardiac developmental toxicity of EOM from PM2.5 in P19 embryonic carcinoma cells. Chemosphere. 2019;216:372–8.
Dey A, Nebert DW. Markedly increased constitutive CYP1A1 mRNA levels in the fertilized ovum of the mouse. Biochem Biophys Res Commun. 1998;251:657–61.
Duval C, Teixeira-Clerc F, Leblanc AF, Touch S, Emond C, Guerre-Millo M, Lotersztajn S, Barouki R, Aggerbeck M, Coumoul X. Chronic exposure to low doses of dioxin promotes liver fibrosis development in the C57BL/6J diet-induced obesity mouse model. Environ Health Perspect. 2017;125:428–36.
Fleming TP, Kwong WY, Porter R, Ursell E, Fesenko I, Wilkins A, Miller DJ, Watkins AJ, Eckert JJ. The embryo and its future. Biol Reprod. 2004;71:1046–54.
Fleming TP, Eckert JJ, Denisenko O. The role of maternal nutrition during the periconceptional period and its effect on offspring phenotype. Adv Exp Med Biol. 2017;1014:87–105.
Fleming TP, Sun C, Denisenko O, Caetano L, Aljahdali A, Gould JM, Khurana P. Environmental exposures around conception: developmental pathways leading to lifetime disease risk. Int J Environ Res Public Health. 2021;18.
Fukuda A, Mitani A, Miyashita T, Kobayashi H, Umezawa A, Akutsu H. Spatiotemporal dynamics of OCT4 protein localization during preimplantation development in mice. Reproduction. 2016;152:417–30.
Girer NG, Tomlinson CR, Elferink CJ. The aryl hydrocarbon receptor in energy balance: the road from dioxin-induced wasting syndrome to combating obesity with ahr ligands. Int j mol sci. 2020; 22.
Goolam M, Scialdone A, Graham SJ, Macaulay IC, Jedrusik A, Hupalowska A, Voet T, Marioni JC, Zernicka-Goetz M. Heterogeneity in Oct4 and Sox2 targets biases cell fate in 4-cell mouse embryos. Cell. 2016;165:61–74.
Hamatani T, Carter MG, Sharov AA, Ko MS. Dynamics of global gene expression changes during mouse preimplantation development. Dev Cell. 2004;6:117–31.
Harvey AJ. Mitochondria in early development: linking the microenvironment, metabolism and the epigenome. Reproduction. 2019;157:R159–79.
Haugen G, Hanson M, Kiserud T, Crozier S, Inskip H, Godfrey KM. Fetal liver-sparing cardiovascular adaptations linked to mother’s slimness and diet. Circ Res. 2005;96:12–4.
Heo JS, Lim JY, Pyo S, Yoon DW, Lee D, Ren WX, Lee SG, Kim GJ, Kim J. Environmental benzopyrene attenuates stemness of placenta-derived mesenchymal stem cells via aryl hydrocarbon receptor. Stem Cells Int. 2019;2019:7414015.
Hirate Y, Hirahara S, Inoue K, Kiyonari H, Niwa H, Sasaki H. Par-aPKC-dependent and -independent mechanisms cooperatively control cell polarity, Hippo signaling, and cell positioning in 16-cell stage mouse embryos. Dev Growth Differ. 2015;57:544–56.
Jain S, Maltepe E, Lu MM, Simon C, Bradfield CA. Expression of ARNT, ARNT2, HIF1 alpha, HIF2 alpha and Ah receptor mRNAs in the developing mouse. Mech Dev. 1998;73:117–23.
Jung YH, Kremsky I, Gold HB, Rowley MJ, Punyawai K, Buonanotte A, Lyu X, Bixler BJ, Chan AWS, Corces VG. Maintenance of CTCF- and transcription factor-mediated interactions from the gametes to the early mouse embryo. Mol Cell. 2019;75(154–171):e155.
Kalkan T, Olova N, Roode M, Mulas C, Lee HJ, Nett I, Marks H, Walker R, Stunnenberg HG, Lilley KS, et al. Tracking the embryonic stem cell transition from ground state pluripotency. Development. 2017;144:1221–34.
Kerley-Hamilton JS, Trask HW, Ridley CJ, Dufour E, Ringelberg CS, Nurinova N, Wong D, Moodie KL, Shipman SL, Moore JH, et al. Obesity is mediated by differential aryl hydrocarbon receptor signaling in mice fed a Western diet. Environ Health Perspect. 2012;120:1252–9.
Ko CI, Wang Q, Fan Y, Xia Y, Puga A. Pluripotency factors and Polycomb Group proteins repress aryl hydrocarbon receptor expression in murine embryonic stem cells. Stem Cell Res. 2014;12:296–308.
Ko CI, Fan Y, de Gannes M, Wang Q, Xia Y, Puga A. Repression of the aryl hydrocarbon receptor is required to maintain mitotic progression and prevent loss of pluripotency of embryonic stem cells. Stem cells. 2016.
Kumar RP, Ray S, Home P, Saha B, Bhattacharya B, Wilkins HM, Chavan H, Ganguly A, Milano-Foster J, Paul A et al. Regulation of energy metabolism during early mammalian development: TEAD4 controls mitochondrial transcription. Development. 2018; 145.
Lahvis GP, Lindell SL, Thomas RS, McCuskey RS, Murphy C, Glover E, Bentz M, Southard J, Bradfield CA. Portosystemic shunting and persistent fetal vascular structures in aryl hydrocarbon receptor-deficient mice. Proc Natl Acad Sci USA. 2000;97:10442–7.
Landeira D, Bagci H, Malinowski AR, Brown KE, Soza-Ried J, Feytout A, Webster Z, Ndjetehe E, Cantone I, Asenjo HG, et al. Jarid2 coordinates Nanog expression and PCP/Wnt signaling required for efficient ESC differentiation and early embryo development. Cell Rep. 2015;12:573–86.
Lee SJ, Kang KW, Kim JH, Lee BH, Jung JH, Park Y, Hong SC, Kim BS. CXCR2 Ligands and mTOR activation enhance reprogramming of human somatic cells to pluripotent stem cells. Stem Cells Dev. 2020;29:119–32.
Lund AK, Goens MB, Kanagy NL, Walker MK. Cardiac hypertrophy in aryl hydrocarbon receptor null mice is correlated with elevated angiotensin II, endothelin-1, and mean arterial blood pressure. Toxicol Appl Pharmacol. 2003;193:177–87.
Morales-Hernandez A, Gonzalez-Rico FJ, Roman AC, Rico-Leo E, Alvarez-Barrientos A, Sanchez L, Macia A, Heras SR, Garcia-Perez JL, Merino JM, et al. Alu retrotransposons promote differentiation of human carcinoma cells through the aryl hydrocarbon receptor. Nucleic Acids Res. 2016;44:4665–83.
Morales-Hernandez A, Nacarino-Palma A, Moreno-Marin N, Barrasa E, Paniagua-Quinones B, Catalina-Fernandez I, Alvarez-Barrientos A, Bustelo XR, Merino JM, Fernandez-Salguero PM. Lung regeneration after toxic injury is improved in absence of dioxin receptor. Stem Cell Research. 2017;25:61–71.
O’Neill C. Phosphatidylinositol 3-kinase signaling in mammalian preimplantation embryo development. Reprod. 2008;136:147–56.
Peters JM, Wiley LM. Evidence that murine preimplantation embryos express aryl hydrocarbon receptor. Toxicol Appl Pharmacol. 1995;134:214–21.
Poeppelman RS, Tobias JD. Patent Ductus venosus and congenital heart disease: a case report and review. Cardiol Res. 2018;9:330–3.
Sasaki H. Position- and polarity-dependent Hippo signaling regulates cell fates in preimplantation mouse embryos. Semin Cell Dev Biol. 2015;47–48:80–7.
Simon CS, Hadjantonakis AK, Schroter C. Making lineage decisions with biological noise: lessons from the early mouse embryo. Wiley Interdiscip Rev Dev Biol. 2018;7:e319.
Singh KP, Bennett JA, Casado FL, Walrath JL, Welle SL, Gasiewicz TA. Loss of aryl hydrocarbon receptor promotes gene changes associated with premature hematopoietic stem cell exhaustion and development of a myeloproliferative disorder in aging mice. Stem Cells Dev. 2014;23:95–106.
Suwinska A, Czolowska R, Ozdzenski W, Tarkowski AK. Blastomeres of the mouse embryo lose totipotency after the fifth cleavage division: expression of Cdx2 and Oct4 and developmental potential of inner and outer blastomeres of 16- and 32-cell embryos. Dev Biol. 2008;322:133–44.
Tchirikov M, Schroder HJ, Hecher K. Ductus venosus shunting in the fetal venous circulation: regulatory mechanisms, diagnostic methods and medical importance. Ultrasound Obstet Gynecol. 2006;27:452–61.
Torres-Padilla ME, Chambers I. Transcription factor heterogeneity in pluripotent stem cells: a stochastic advantage. Dev. 2014;141:2173–81.
Torres-Padilla ME, Parfitt DE, Kouzarides T, Zernicka-Goetz M. Histone arginine methylation regulates pluripotency in the early mouse embryo. Nature. 2007;445:214–8.
Velazquez MA, Smith CG, Smyth NR, Osmond C, Fleming TP. Advanced maternal age causes adverse programming of mouse blastocysts leading to altered growth and impaired cardiometabolic health in post-natal life. Hum Reprod. 2016;31:1970–80.
Wang Q, Chen J, Ko CI, Fan Y, Carreira V, Chen Y, Xia Y, Medvedovic M, Puga A. Disruption of aryl hydrocarbon receptor homeostatic levels during embryonic stem cell differentiation alters expression of homeobox transcription factors that control cardiomyogenesis. Environ Health Perspect. 2013;121:1334–43.
Watkins AJ, Ursell E, Panton R, Papenbrock T, Hollis L, Cunningham C, Wilkins A, Perry VH, Sheth B, Kwong WY, et al. Adaptive responses by mouse early embryos to maternal diet protect fetal growth but predispose to adult onset disease. Biol Reprod. 2008;78:299–306.
Watson ATD, Nordberg RC, Loboa EG, Kullman SW. Evidence for Aryl hydrocarbon receptor-mediated inhibition of osteoblast differentiation in human mesenchymal stem cells. Toxicol Sci : Off J Soc Toxicol. 2019;167:145–56.
White MD, Bissiere S, Alvarez YD, Plachta N. Mouse Embryo Compaction. Curr Top Dev Biol. 2016;120:235–58.
Wu G, Scholer HR. Role of Oct4 in the early embryo development. Cell Regen. 2014;3:7.
Zenker J, White MD, Gasnier M, Alvarez YD, Lim HYG, Bissiere S, Biro M, Plachta N. Expanding actin rings zipper the mouse embryo for blastocyst formation. Cell. 2018;173(776–791):e717.
Zeybek ND, Baysal E, Bozdemir O, Buber E. Hippo signaling: a stress response pathway in stem cells. Curr Stem Cell Res Ther. 2021;16:824–39.
Acknowledgements
We thank Dr. Ying Xia and Dr. Katherine Burns for a critical reading of the manuscript.
Funding
This work was supported by the National Institute of Environmental Health Science grants R21ES031190, R01ES010807, R01ES024744 and P30ES06096.
Author information
Authors and Affiliations
Contributions
C. K. conceived and performed experiments, data analyses, and computational analyses coordinated and interacted with all co-authors, and wrote the manuscript; J. B. performed computational analyses; H. A. Z. performed immunofluorescence experiments and data analyses; X. Z. performed single-cell RNA-sequencing; M. M. supervised the computational analyses; and A. P. conceived and supervised the work.
Corresponding author
Ethics declarations
Ethical approval and consent to participate
All animal experiments and procedures were approved by the University of Cincinnati Institutional Animal Care and Use Committee.
Consent to participate
Not applicable.
Consent for publication
The authors declare consent for publication.
Competing interests
The authors declare no competing interests.
Human ethics
Not applicable.
Additional information
Publisher's note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Ko, CI., Biesiada, J., Zablon, H.A. et al. The aryl hydrocarbon receptor directs the differentiation of murine progenitor blastomeres. Cell Biol Toxicol 39, 1657–1676 (2023). https://doi.org/10.1007/s10565-022-09755-9
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10565-022-09755-9