Upregulation of <i>FOXO3</i> in New-Onset Type 1 Diabetes Mellitus

Zurawek, Magdalena; Fichna, Marta; Fichna, Piotr; Czainska, Maria; Rozwadowska, Natalia

doi:https://doi.org/10.1155/2020/9484015

Journal of Immunology Research

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Abstract Introduction Methods Results and Discussion Conclusion Data Availability Ethical Approval Consent Conflicts of Interest Authors’ Contributions Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2020 | Article ID 9484015 | https://doi.org/10.1155/2020/9484015

Upregulation of FOXO3 in New-Onset Type 1 Diabetes Mellitus

Magdalena Zurawek,¹Marta Fichna,²Piotr Fichna,³Maria Czainska,⁴and Natalia Rozwadowska¹

Academic Editor: Cinzia Ciccacci

Received10 Mar 2020

Accepted22 Jul 2020

Published12 Aug 2020

Abstract

Forkhead box O (FOXO) transcription factors have been implicated in the development and differentiation of the immune cells. FOXO3 plays a crucial role in physiologic and pathologic immune response. FOXO3, cooperatively with FOXO1, control the development and function of Foxp3⁺ regulatory T cells (T_reg). Since the lack of T_reg-mediated control has fundamental impact on type 1 diabetes mellitus (T1DM) development, we investigated FOXO3 expression in patients with T1DM. FOXO3 expression was estimated in peripheral blood mononuclear cells (PBMCs) from newly diagnosed T1DM pediatric patients () and age-matched healthy donors () by reahavel-time PCR and TaqMan gene expression assays. Expression analysis revealed significant upregulation of FOXO3 in T1DM (). Stratification of the T1DM group according to the presence of initial diabetic ketoacidosis (DKA) did not indicate differences in FOXO3 expression in patients with DKA compared to a mild T1DM onset (). In conclusion, overexpression of FOXO3 is correlated with the ongoing islet autoimmune destruction and might suggest a potential role for this gene in the pathogenesis of type 1 diabetes mellitus.

1. Introduction

FOXO3 (forkhead box O3) protein belongs to the family of transcription factors included withal FOXO1, FOXO4, and FOXO6. FOXO3 is regulated via the phosphoinositide 3-kinase (PI3K)/serine/threonine-specific kinase (Akt) signaling pathway [1]. The active, nonphosphorylated FOXO3 form is localized in the nucleus and regulates gene transcription. Phosphorylation of FOXO3 in the PI3K/Akt pathway results in its exclusion from the nucleus and termination of transcriptional activity [2]. FOXO3 has been implicated in the regulation of diverse biological processes, including cell survival, proliferation, and apoptosis [3]. FOXO3 is expressed in immune cells, and recently, there has been a surge in interest to investigate the importance of FOXO3 in lymphoid homeostasis [4–6]. Upregulation of FOXO3 was observed in polymorphonuclear cells and peripheral blood mononuclear cells from patients with rheumatoid arthritis [7]. Overexpression of FOXO3 is mediated by T cell receptor stimulation [8]. In consequence, FOXO3 promotes polarization of CD4⁺ T cells towards the pathogenic T helper cells producing interferon γ and granulocyte monocyte colony-stimulating factor. FOXO3^-/^- mice exhibit reduced susceptibility to experimental autoimmune encephalomyelitis [8].

In this study, we investigate the expression level of FOXO3 in PBMCs from newly diagnosed type 1 diabetes mellitus pediatric patients. Upregulation of FOXO3 was observed in the T1DM group compared to the age-matched healthy controls—a finding that might suggest a potential role of this gene in autoimmunity.

2. Study Groups

The qRT-PCR of FOXO3 gene was conducted in 28 newly diagnosed T1DM subjects ( years, 4 females (14%), 24 males (86%)) and 27 age-matched healthy donors ( years, 13 (48%) females, 14 (52%) males). Patients were recruited at the Department of Paediatric Diabetes and Obesity, Poznan University of Medical Sciences. The diagnosis of diabetes was based upon the WHO criteria. Autoimmune origin of the disease was confirmed by positive serum autoantibodies to insulin (IAA) and/or glutamic acid decarboxylase (GADA) and/or islet antigen-2 (IA-2A). Clinical characterization of patients is summarized in Table 1. Pediatric control individuals with negative personal and family history of autoimmunity and no clinical signs of the autoimmune disorders were obtained from an outpatient pediatric practice in the course of routine screening. Only subjects with no clinical symptoms of hyperglycemia and fasting blood glucose within the reference range (≤5.5 mmol/l) were included in the control group.

3. Methods

3.1. FOXO3 Expression Analysis

FOXO3 expression was assessed in PBMCs isolated from the peripheral blood (4 ml for each subject) by density gradient centrifugation in Histopaque-1077 (Sigma Aldrich, Germany). Total RNA was extracted with a TRI Reagent (Sigma Aldrich, Germany) following the manufacturer’s protocol. The equal amount of RNA (500 ng per sample) was converted to cDNA using a QuantiTect Reverse Transcription Kit (QIAGEN, Germany). A quantitative real-time PCR using an aliquot of cDNA equivalent of 5 ng total RNA, TaqMan gene expression assay (Applied Biosystems, Thermo Fisher Scientific, USA), and HOT FIREPol Probe Universal qPCR Mix (Solis BioDyne, Estonia) was performed in a total volume of 15 μl on a BioRad CFX96 Real-Time PCR instrument (BioRad Laboratories, CA, USA). All reactions were run in triplicate. The expression level of FOXO3 (assay ID Hs00818121_m1) was normalized to beta-2 microglobulin housekeeping gene (assay ID Hs00984230_m1). Mean cycle threshold (Ct) values were estimated with BioRad CFX Manager 3.1 software. Relative expression levels were calculated using the 2^−ΔCt formula. Statistical analysis was performed using GraphPad Prism 5 (GraphPad Software Inc., CA, USA). Statistical significance of the differences between relative expression levels was determined with an unpaired -test. values < 0.05 were considered statistically significant.

4. Results and Discussion

Type 1 diabetes mellitus is an autoimmune disorder that results from the lack of endogenous insulin secretion from the pancreatic beta cells. Although T-mediated destruction of beta cells is observed, the precise etiology and pathological mechanisms are still poorly understood. Genetic predisposition and environmental factors contribute to the development of type 1 diabetes mellitus [9]. HLA locus, specifically the haplotypes DRB103-DQA105-DQB102 (DR3-DQ2) and DRB104-DQA103-DQB103:02 (DR4-DQ8) are major genetic risk factors [10]. To date, around 60 non-HLA T1DM susceptibility loci have been identified, mostly related to immune response, for instance, genes encoding lymphocyte protein tyrosine phosphatase (PTPN22), cytotoxic T-lymphocyte protein 4 (CTLA4), subunit alpha of the interleukin-2 receptor (IL2RA), and interferon-induced helicase C domain-containing protein 1 (IFIH1) [11–13].

Our previous study indicated FOXO3 as a potential target for miR-487a-3p, which is upregulated in T1DM [14]. These results prompted us to investigate the FOXO3 expression in type 1 diabetes mellitus patients. In order to reduce the interference of the initial metabolic status, PBMCs were collected from patients with normalized ketonaemia and glycemia and fully rehydrated. In addition, T1DM patients and control subjects included in the study did not present infection symptoms, confirmed by negative inflammatory tests (complete blood count, C-reactive protein tests). The type 1 diabetes mellitus group was further stratified according to the presence or absence of diabetic ketoacidosis (DKA) at initial presentation, which reflects severe and moderate disease onsets, respectively. Expression analysis revealed significant upregulation of FOXO3 in the new-onset T1DM group compared to the age-matched healthy controls (Figure 1). However, we did not observe statistically significant differences in FOXO3 expression in patients with DKA compared to the mild T1DM onset group (Figure 1). Consequently, FOXO3 expression is correlated with the ongoing autoimmune islet destruction, although not with the severity of the autoimmune process. A current study failed to confirm the previous global expression analysis of PBMCs from children with newly diagnosed type 1 diabetes mellitus (GEO DataSets, Accession GDS3875) [15]. The microarray analysis did not reveal dysregulation of FOXO3 in the group of T1DM patients at one month and at four months after diagnosis [15].

Figure 1

FOXO3 expression analysis in type 1 diabetes. (a) FOXO3 is overexpressed in the type 1 diabetes group compared to healthy controls (, mean fold change 1.54). (b) Expression level of FOXO3 gene in the T1D group stratified according to the presence of initial diabetic ketoacidosis (DKA). The patients with diabetic ketoacidosis did not present statistically significant differences in FOXO3 expression compared to the patients without DKA (). Horizontal lines indicate median with range; asterisks indicate significance, with values estimated by unpaired -test; T1D: type 1 diabetes patients; C: controls; DKA(+): cohort of patients with initial diabetic ketoacidosis; DKA(-): cohort of patients without initial diabetic ketoacidosis.

Based on our previous study, we hypothesized that overexpression of miR-487a-3p in T1DM might result in downregulation of FOXO3 and hence affect the immune function. Current results imply that FOXO3 is apparently not regulated via miR-487a-3p; however, additional in vitro study is needed to explore the manner of FOXO3 regulation. Yang et al. have demonstrated the mechanisms protecting FOXO3 from being targeted by certain miRNAs [16]. The Foxo3 pseudogene (Foxo3P) and the Foxo3 circular RNA (circ-Foxo3) act as a sponge and bind several miRNAs, including miR-22, miR-136, miR-138, miR-149, miR-433, miR-762, miR-3614-5p, and miR-3622b-5p. Subsequently, Foxo3P and circ-Foxo3 ensure FOXO3 gene expression and protein activity.

5. Conclusion

Overexpression of FOXO3 in type 1 diabetes mellitus might suggest a potential role of this gene in the development of autoimmune disease. Further in vitro and ex vivo functional studies will address the issue of FOXO3 contribution to immune tolerance dysregulation.

Data Availability

Data presented in the manuscript are available upon request from corresponding author Magdalena Zurawek, [email protected].

Ethical Approval

The study was approved by the local Ethics Committee at the Poznan University of Medical Sciences (decision No. 656/15), and all procedures were in accordance with the Declaration of Helsinki.

Informed consent was obtained from the parents/legal representatives of the minor patients.

Conflicts of Interest

The authors declare that they have no conflict of interests.

Authors’ Contributions

MZ designed the study, performed experiments, analyzed data, and wrote the manuscript, MF and PF collected T1DM patients’ samples and clinical data, MC collected control subjects’ samples, and NR revised the manuscript.

Acknowledgments

The study was supported by the Polish Diabetes Association, Artur Czyzyk Research Grant 2015.

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Copyright

Copyright © 2020 Magdalena Zurawek et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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