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PPM1A as a key target of the application of Jiawei‑Maxing‑Shigan decoction for the attenuation of radiation‑induced epithelial‑mesenchymal transition in type II alveolar epithelial cells

  • Authors:
    • Jinhua Lu
    • Shengyou Lin
    • Zechen Lin
    • Xianlei Lin
    • Yuezhong Shen
    • Jingyang Su
  • View Affiliations

  • Published online on: September 24, 2021     https://doi.org/10.3892/mmr.2021.12465
  • Article Number: 825
  • Copyright: © Lu et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

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Abstract

Radiation‑induced lung tissue injury is an important reason for the limited application of radiotherapy on thoracic malignancies. Previously, we reported that administration of Jiawei‑Maxing‑Shigan decoction (JMSD) attenuated the radiation‑induced epithelial‑mesenchymal transition (EMT) in alveolar epithelial cells (AECs) via TGF‑β/Smad signaling. The present study aimed to examine the role of protein phosphatase Mg2+/Mn2+‑dependent 1A (PPM1A) in the anti‑EMT activity of JMSD on AECs. The components in the aqueous extract of JMSD were identified by high‑performance liquid chromatography coupled with electrospray mass spectrometry. Primary rat type II AECs were treated with radiation (60Co γ‑ray at 8 Gy) and JMSD‑medicated serum. PPM1A was overexpressed and knocked down in the AECs via lentivirus transduction and the effects of JMSD administration on the key proteins related to TGF‑β1/Smad signaling were measured by western blotting. It was found that radiation decreased the PPM1A expression in the AECs and JMSD‑medicated serum upregulated the PPM1A expressions in the radiation‑induced AECs. PPM1A overexpression increased the E‑cadherin level but decreased the phosphorylated (p‑)Smad2/3, vimentin and α‑smooth muscle actin (α‑SMA) levels in the AECs. By contrast, the PPM1A knockdown decreased the E‑cadherin level and increased the p‑Smad2/3, vimentin and α‑SMA levels in the AECs and these effects could be blocked by SB431542 (TGF‑β1/Smad signaling inhibitor). JMSD administration increased the E‑cadherin level and decreased the p‑Smad2/3, vimentin and α‑SMA levels in the AECs; however, these effects could be blocked by siPPM1A‑2. In conclusion, PPM1A is a key target of JMSD administration for the attenuation of the radiation‑induced EMT in primary type II AECs via the TGF‑β1/Smad pathway.

Introduction

Currently, besides surgery and chemotherapy, radiotherapy remains one of the most commonly used treatment methods for thoracic malignant tumors such as lung cancer, breast cancer, neck cancer and lymphoma (1,2). Radiation-induced normal lung tissue injury is a common complication of chest radiotherapy and is an important reason for the limited application of radiotherapy in patients with thoracic malignancies (3,4). Main radiation-induced injury is reported to result in acute pneumonitis and, later, fibrosis in lung tissue (4). In addition, studies have indicated that radiation could result in injury of alveolar epithelial cells (AECs) and subsequently induce epithelial-mesenchymal transition (EMT) of AECs. This is one of the possible pathological mechanisms of pulmonary fibrosis after radiotherapy (5,6). Therefore, suppression of the EMT process in AECs would be beneficial for controlling or preventing the development of pulmonary fibrosis under radiotherapy.

Jiawei-Maxing-Shigan decoction (JMSD), is composed of Roasted ephedra (Herba Ephedrae), Gypsum (Gypsum Fibrosum), Paeoniae radix (Radix Paeoniae Rubra), Apricot seed (Semen Armeniacae Amarum), Mulberry (Cortex mori Radicis), Honeysuckle (Flos Lonicerae Japonicae) and Licorice (Radix Et Rhizoma Glycyrrhizae) (7) and is a clinically proven recipe for treating pediatric asthma (8), bronchitis (9), infantile mycoplasma pneumonia (10) and radioactive lung injury (7,11). Our previous study found that the main constituents of JMSD are farnesene, dihydrotanshinone I, paeonol, emodin, schisanhenol, tanshinone IIA, cryptotanshinone, columbianadin, uridine and liquiritigenin (7). Furthermore, JMSD administration can attenuate radiation-induced EMT in AECs by regulating the expression of TGF-β/Smad signaling (7). Protein phosphatase Mg2+/Mn2+-dependent 1A (PPM1A) serves an important role in the signal transduction of TGF-β/Smad signaling and can inactivate TGF-β/Smad signaling by dephosphorylating Smad2/3. PPM1A functions as a tumor suppressor in bladder and breast cancer via regulating cell invasion, EMT and cell cycle progression (1214). As part of a continuing study on the molecular mechanisms of JMSD, the present study further examined the role of PPM1A in the anti-EMT activity of JMSD on AECs.

Materials and methods

Herbal medicines

The seven herbal medicines were supplied and the JMSD water extract was prepared by the School of Pharmacy, Zhejiang Chinese Medicine University. The composition of JMSD is presented in Table I. The seven herbs were decocted by boiling in distilled water for 1 h twice as described in our previous paper (7). Then, the water extract was filtered and concentrated to 32 ml. As JMSD was a mixture, its purity could not be determined.

Table I.

Composition of Jiawei-Maxing-Shigan decoction.

Table I.

Composition of Jiawei-Maxing-Shigan decoction.

Herbal medicinesWeight (g)
Roasted ephedra (Herba Ephedrae)  9
Gypsum (Gypsum Fibrosum)18
Paeoniae radix (Radix Paeoniae Rubra)12
Apricot seed (Semen Armeniacae Amarum)12
Mulberry (Cortex mori Radicis)12
Honeysuckle (Flos Lonicerae Japonicae)  9
Licorice (Radix Et Rhizoma Glycyrrhizae)  6
Liquid chromatography coupled with electrospray mass spectrometry (HPLC/ESI-MS) analysis of JMSD

The aqueous extract of JMSD was analyzed with an Agilent 1100 HPLC system (Agilent Technologies, Inc.) coupled with electrospray mass spectrometry as previously described (7). The separation was performed on a GS-120-5-C18-BIO chromatographic column (5 µm; 250×4.6 mm i.d.; Global Chromatography Co., Ltd.) with the column temperature set at 35°C. A linear gradient elution of A (0.1% formic acid water) and B (acetonitrile) was used with the gradient procedure as follows: B 5% at 0 min, B 40% at 60 min (v/v). The flow rate was 1.0 ml/min and the injection volume was 10 µl. DAD was on and the target wavelength was simultaneously set at 210 nm. The split ratio to the mass spectrometer was 1:3. The acquisition parameters for negative ion mode were: collision gas, ultra high-purity helium (He), nebulizer gas (N2), 35 psi, drying gas (N2), 10 l/min, drying temperature, 350°C, HV, 3500 V, mass scan range, m/z 100–2200, target mass, 500 m/z, compound stability, 100%, trap drive level, 100%. All the data were analyzed using the Chemstation software (version B.04.03; Agilent Technologies, Inc.).

Animals

Male Sprague-Dawley (SD) rats (6–8 weeks; 200±20 g; n=3) and Wistar rats (6–8 weeks; 200 ± 20 g; n=6) were acquired from the Shanghai Experimental Animal Center (Shanghai, China). Rats were maintained at 25°C with 60% humidity and a 12-h light/dark cycle, and free access to food and water. The experimental protocols were approved by the animal ethics committee of Zhejiang Chinese Medicine University (Hangzhou, China; approval no. 2019485).

Chemicals

The TRIzol® kit, BCA protein quantitative kit, SYBR Green PCR kit and reverse transcription kit used in the study were bought from the Thermo Fisher Scientific, Inc. The ECL kit (cat. no. WBKLS0100) was purchased from EDM Millipore. The primary antibodies for PPM1A and phosphorylated (p-)Smad2/3 were purchased from Abcam. The primary antibodies for Smad2/3, p-Smad2/3, E-cadherin, vimentin, α-SMA and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) were purchased from Cell Signaling Technology, Inc. PLKO.1, psPAX2 and pMD2G were acquired from Addgene, Inc. DH5α competent cells were purchased from Beijing Transgen Biotech Co., Ltd.; 293T cells, from ATCC and pLVX-Puro from Clontech Laboratories, Inc.

Preparation of the JMSD-medicated serum and control serum

Wistar rats were randomly divided into the JMSD and control groups (n=3 per group). In the rats in the control and JMSD groups, 4 ml of 0.9% sodium chloride and JMSD were intragastrically administered twice per day for 3 days, respectively. At 2 h after the last administration, the rats were euthanized with intraperitoneal injections of pentobarbital sodium (100 mg/kg) and a blood sample (~6 ml) was drawn from the abdominal aorta, pooled and clotted for 2 h at room temperature. Serum was isolated carefully by centrifuging the clotted blood at 2,000 x g for 20 min at 4°C and stored at −70°C until use. In accordance with previous literature, the dose for preparation of medicated serum can be calculated as: Dose=clinical dose x animal equivalent dose x dilution (15). In the present study, the animals were given 15 x adult dose to prepare the JMSD-medicated serum. Primary type II AECs were treated the JMSD-medicated serum at doses of ~2-10%, which was diluted to ~2/100-10/100. Therefore, the dose used in this present study was not a very high dose. During the experiments, animal health and behavior were monitored daily to minimize suffering and distress. Greater than 20% weight loss, dehydration, or loss of ability to ambulate, were the signs we used to determine the time at which the animals should be euthanized. Confirmation of death was evaluated with vital signs including heart beats, pupillary response and respiratory pattern. No animals showed signs of humane endpoints and no rats were dead prior to the end of the experiments.

Preparation of type II AECs and cell culture

Primary type II AECs were prepared from SD rats as previously described (10); after the rats were euthanized with intraperitoneal injections of pentobarbital sodium (100 mg/kg). Dispase was instilled into the lung via a tracheal catheter for 15 min at 37°C. The lungs were removed, carefully teased apart and treated with DNase I for 5 min at 37°C. The cell suspension was passed through 150, 15 and 7.5 µm metal strainers and then centrifuged at 100 x g at 4°C for 8 min. The cell pellet was resuspended in Dulbecco's modified Eagle's medium (DMEM) and plated to a culture dish precoated with rat IgG. After 1 h of culture, the non-adherent cells were collected and plated to another culture dish. After culturing for another 20 min, the non-adherent cells were centrifuged at 100 x g at 4°C for 8 min. The cell pellet was resuspended in DMEM containing 20% fetal bovine serum (HyClone; Cytiva) and cultured at 37°C in a 5% CO2 incubator. The purity of the isolated cells was >90% as determined with nitroblue tetrazolium/5-bromo-4-chloro-3-indolyl phosphate staining.

Constructions of the overexpression and low expression level of lentivirus

A lentivirus was constructed commercially by Genewiz, Inc. Briefly, the plasmid vectors were extracted and subsequently co-transfected into 293T cells with the packaging plasmids using Lipofectamine® 2000 (Invitrogen; Thermo Fisher Scientific, Inc.). After 72 h of culture at 37°C, supernatant of 293T cells was collected and filtered using a 0.45-µm filter. The short interfering (si)RNA sequences used are as follows: siPPM1A-1: 5′-CCAAGUGGACUUGAGACAUUU-3′; siPPM1A-2: 5′-GCCUGAAGUCCAUGAUAUUUU-3′; siPPM1A-3′: 5′-CCUUGAGAAAGUUUGCAAUUU-3′; and siNC: 5′-CAGUACUUUUGUGUAGUACAA-3′.

Cell treatment

Primary type II AECs were divided into four groups. Groups 1 and 2 were cultured with 10% serum collected from control rats. The cells in group 3 were incubated with 2% JMSD-medicated serum (J) and 8% normal control rat serum (N). Those in group 4 were incubated with 6% J serum and 4% N serum, whereas those in group 5 were incubated with 10% J serum. Groups 2–5 were stimulated with 8 Gy of 60Co γ-rays (Hangzhou Cancer Hospital) at 3.64 Gy/min. After 24 h of culture, reverse transcription-quantitative (RT-q) PCR assay and western blotting analyses were performed.

RT-qPCR

Total RNA was isolated from cells with TRIzol® and subsequently reversed transcribed into cDNA with RevertAid First Strand cDNA Synthesis Kit (Thermo Fisher Scientific, Inc.) according to the manufacturer's protocol. Then, a real-time PCR analysis was performed using an ABI 7300 instrument (Applied Biosystems; Thermo Fisher Scientific, Inc.) at the following parameters: 95°C for 10 min, followed by 40 cycles of annealing at 95°C for 15 sec and amplification at 60°C for 45 sec. GAPDH was used as an internal control. The primers used were: PPM1A: 5′-TGCCAAATACTGCTGTGAG-3′ (forward), 5′-CTGTTGACCCACTTCTATCTG-3′ (reverse); and GAPDH: 5′-GGAGTCTACTGGCGTCTTCAC-3′ (forward), 5′-ATGAGCCCTTCCACGATGC-3′ (reverse). The mRNA level in each sample was evaluated using the ΔΔCT method (16). The experiments were repeated three times.

Western blotting assay

The proteins in the cells were prepared using a radioimmunoprecipitation assay lysis buffer (Beyotime Institute of Biotechnology) and the protein concentrations were measured using the bicinchoninic acid method. Equal amounts of protein (30 µg) were loaded on 10% sodium dodecyl sulfate-polyacrylamide gel and then transferred onto a nitrocellulose membrane and blocked with 5% skimmed milk at room temperature for 1 h. The membranes were then incubated with primary antibodies and subsequently incubated with HRP-conjugated secondary antibodies at room temperature for 1 h. Lastly, the targeting bands were detected using ECL reagents. The primary antibodies were anti-PPM1A (cat. no. ab154489, 1:1,000) and anti-p-Smad2/3 (cat. no. ab63399, 1:1,000), purchased from Abcam. Anti-Smad2/3 (cat. no. 5678, 1:1,000), anti-E-cadherin (cat. no. 14472, 1:1,000), anti-vimentin (cat. no. 5741, 1:1,000), anti-α-SMA (cat. no. 19245, 1:5,000) and anti-GAPDH (cat. no. 5174, 1:1,000) were obtained from Cell Signaling Technology, Inc. Densitometry was performed using ImageJ software (version 1.48; National Institutes of Health) with GAPDH as the loading control.

Statistical analysis

All experimental data are shown in mean ± standard deviation. One-way ANOVA followed by Sidak's post hoc test was performed to analyze statistical comparisons. P<0.05 was considered to indicate a statistically significant difference.

Results

Identification of 10 compounds

The aqueous extract from the JMSD was measured with high-performance liquid chromatography coupled with electrospray mass spectrometry (HPLC/ESI-MS) in positive- and negative-ion modes (Fig. 1, Table II). The following 10 compounds were identified: ephedrine hydrochloride (1), levistilide A (2), liquiritigenin (3), pseudoephedrine hydrochloride (4), paeoniflorin (5), astilbin (6), cycloastragenol (7), diosgenin (8), rosmarinic acid (9) and paeonol (10), by comparing the retention times and MS data with the reference standards.

Table II.

Identification of constituents from Jiawei-Maxing-Shigan decoction.

Table II.

Identification of constituents from Jiawei-Maxing-Shigan decoction.

CompoundRT/minHerbal medicines
1. Ephedrine hydrochloride0.56Honey-fried Herba Ephedrae
2. Levistilide A0.68Gypsum Fibrosum
3. Liquiritigenin1.01Radix Et Rhizoma Glycyrrhizae
4. Pseudoephedrine hydrochloride3.18Honey-fried Herba Ephedrae
5. Paeoniflorin5.09Radix Paeoniae Rubra
6. Astilbin5.70Cortex mori from Morus alba L.
7. Cycloastragenol5.10Radix Et Rhizoma Glycyrrhizae
8. Diosgenin5.74Stir-baked Semen Armeniacae Amarum
9. Rosmarinic acid6.32Flos Lonicerae Japonicae
10. Paeonol7.54Radix Paeoniae Rubra
Decreased PPM1A expression level in type II AECs following radiation treatment

Following radiation treatment (60Co γ-ray at 8 Gy), the PPM1A expression level in type II AECs was determined using RT-PCR and western blotting assays. As shown in Fig. 2, the results indicated that the radiation treatment could decrease the PPMIA expression levels in AECs both in terms of mRNA and protein expression levels (P<0.05) in an obvious time-dependent manner.

Attenuation of radiation-mediated decreased PPM1A expression level in type II AECs by JMSD-medicated serum

Furthermore, the effects of the JMSD-medicated serum on the PPM1A expressions in radiation-induced type II AECs were determined using RT-PCR and western blotting assays. The results shown in Fig. 3 suggested that JMSD-medicated sera (2, 6 and 10%) could upregulate the PPM1A expressions as compared with the vehicle (P<0.05, P<0.001 and P<0.001, respectively) in a concentration-dependent manner.

Attenuation of radiation-induced Smad activation and epithelial-mesenchymal transition by PPM1A overexpression

Consequently, PPM1A overexpressed AECs (Fig. 4A and B) were constructed to investigate the role of PPM1A. The results showed that compared with vector expression, the PPM1A and E-cadherin expressions were upregulated, whereas the p-Smad2/3, vimentin and α-SMA expressions were downregulated in the PPM1A-overexpressed AECs (Fig. 4C). Morphology analysis showed that elongated spindle-like type cells were increased in radiation-treated cells, and such morphological alteration was decreased when PPM1A was overexpressed (Fig. 4D).

Attenuation of radiation-induced Smad activation and epithelial-mesenchymal transition by JMSD-medicated serum via the regulation of PPM1A expression

Subsequently, the role of PPM1A was further studied using the siRNA interference of PPM1A. The present study designed three siRNA sequences for the PPM1A and siNC, a scrambled sequence, was used as a negative control. siPPM1A-2 was selected as the siRNA sequence for the following studies (Fig. 5A and B).

Furthermore, the results suggested that compared with the cells in the vehicle group, the PPM1A siRNA-interfered AECs showed downregulated PPM1A and E-cadherin expressions but upregulated p-Smad2/3, vimentin and α-SMA expressions (Fig. 5C). In addition, after treatment with SB431542, a TGF-β1/Smad signaling inhibitor, the p-Smad2/3, vimentin and α-SMA expression levels were decreased, whereas the E-cadherin expression level was increased in the PPM1A knockdown AECs as compared with the vehicle group. Combined with the above-mentioned results, it was hypothesized that PPM1A might be a crucial target for EMT in AECs in TGF-β1/Smad signaling.

Finally, the role of PPM1A in the attenuating effects of JMSD against radiation-induced EMT was studied in primary type II VECs. The image depicted in Fig. 6 suggested that JMSD-medicated serum could increase the E-cadherin expression level and decrease the p-Smad2/3, vimentin and α-SMA expression levels. However, these effects could be blocked by siPPM1A-2. Consequently, it is hypothesized that PPM1A-2 is a crucial target for the anti-EMT effect of JMSD in VECs.

Discussion

Herbal medicines are important alternative and complementary remedies for the treatment of various diseases, particularly those that cannot be treated with western drugs. Radiation-induced pulmonary fibrosis is an intractable disease in clinical practice and an increasing number of researchers have attempted to search for treatments for pulmonary fibrosis from herbal medicines (17). Some extracts/compounds from natural herbal medicines are feasible for treating lung pulmonary diseases, such as polydatin from Polygonum cuspidatum (18,19) and astragaloside IV from Astragalus membranaceus (20,21). JMSD administration can attenuate the radiation-induced EMT in AECs via the TGF-β/Smad signaling (7). The present study on JMSD against radiation-induced EMT found that PPM1A exhibits a crucial role in its anti-EMT activity.

TGF-β/Smad signaling serves a key effect in the EMT process of AECs and further induction of pulmonary fibrosis (22). Under radiation, the TGF-β1 expression level in bronchoalveolar lavage fluids can be increased and then, TGF-β/Smad signaling is activated (23). First, TGF-β expression can promote the phosphorylation of Smad2/3 by binding to the TGF-β receptor in the cell membrane and then the transcription of p-Smad2/3 to the cell nucleus, resulting in some transcriptional regulation of a number of genes (24). Consequently, some of the responding productions such as Snail, connective tissue growth factor and matrix metalloproteinases would be released and further result in EMT (25). PPM1A is a phosphatase of the serine/threonine PPM family and the main substrates of PPM1A include MAPK, Smad2 and Smad3 and MKKs (1214). PPM1A serves an important role in the signal transduction of TGF-β/Smad signaling and can inactivate TGF-β/Smad signaling by dephosphorylating Smad2/3 (26,27) (Fig. 7). The present study found that PPM1A expression level was reduced in type II AECs following radiation treatment. PPM1A overexpression attenuated EMT, while PPM1A knockdown showed reverse effects on EMT. Furthermore, treatment with a TGF-β1/Smad signaling inhibitor blocked PPM1A knockdown-induced EMT. Therefore, PPM1A upregulation is a potential strategy for treating EMT and pulmonary fibrosis through inhibiting TGF-β1/Smad signaling.

Previously, we have reported that JMSD attenuated radiation-induced EMT in AECs by regulating TGF-β/Smad signaling (7). The present study found that JMSD-medicated serum attenuated the radiation-mediated inhibition of PPM1A expression in type II AECs. The role of PPM1A in the anti-EMT effects of JMSD in AECs was then examined and it was found that JMSD treatment could increase the PPM1A and E-cadherin expression levels. JMSD also decreased the p-Smad2/3, vimentin and α-SMA expressions in VECs. After knockdown of the PPM1A, the regulating effects of JMSD on these proteins were blocked. The data indicated that JMSD acted against radiation-induced EMT through upregulating PPM1A.

However, the present study has some limitations. It did not investigate the biological effects of the detailed components identified using HPLC/ESI-MS owing to the limited time. In addition, upstream targets of PPM1A should also be investigated in succeeding works. The research regarding JMSD is continuing and it is hoped to investigate the detail mechanisms by which JMSD increase the PPMIA expression and the biological effects of detail components of JMSD and present the related results in the future.

Together, the present study suggested that PPM1A is a key target of JMSD administration for the attenuation of the radiation-induced EMT in primary type II alveolar epithelial cells via TGF-β1/Smad signaling.

Acknowledgements

Not applicable.

Funding

The present study was supported by Science Technology Department of Zhejiang Province (grant no. 2018C03025), Zhejiang Provincial Natural Science Foundation of China (grant no. LY15H290002) and Zhejiang Province Traditional Chinese Medicine Science and Technology Planning Project (grant no. 2021ZA099).

Availability of data and materials

The data used to support the findings of this study are available from the corresponding author upon request.

Authors' contributions

SL and JL conceived and designed the study, JL, ZL, XL, YS and JS collected and analyzed the data and SL and JL wrote the manuscript. All authors read and approved the final manuscript. SL and JL confirm the authenticity of all the raw data.

Ethics approval and consent to participate

The experimental protocols were approved by the Animal ethics committee of Zhejiang Chinese Medicine University (Hangzhou, China; approval no. 2019485).

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

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Lu J, Lin S, Lin Z, Lin X, Shen Y and Su J: PPM1A as a key target of the application of <em>Jiawei‑Maxing‑Shigan</em> decoction for the attenuation of radiation‑induced epithelial‑mesenchymal transition in type II alveolar epithelial cells. Mol Med Rep 24: 825, 2021
APA
Lu, J., Lin, S., Lin, Z., Lin, X., Shen, Y., & Su, J. (2021). PPM1A as a key target of the application of <em>Jiawei‑Maxing‑Shigan</em> decoction for the attenuation of radiation‑induced epithelial‑mesenchymal transition in type II alveolar epithelial cells. Molecular Medicine Reports, 24, 825. https://doi.org/10.3892/mmr.2021.12465
MLA
Lu, J., Lin, S., Lin, Z., Lin, X., Shen, Y., Su, J."PPM1A as a key target of the application of <em>Jiawei‑Maxing‑Shigan</em> decoction for the attenuation of radiation‑induced epithelial‑mesenchymal transition in type II alveolar epithelial cells". Molecular Medicine Reports 24.5 (2021): 825.
Chicago
Lu, J., Lin, S., Lin, Z., Lin, X., Shen, Y., Su, J."PPM1A as a key target of the application of <em>Jiawei‑Maxing‑Shigan</em> decoction for the attenuation of radiation‑induced epithelial‑mesenchymal transition in type II alveolar epithelial cells". Molecular Medicine Reports 24, no. 5 (2021): 825. https://doi.org/10.3892/mmr.2021.12465