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General Physiology and Biophysics Vol.41, No.6, p. 559–567, 2022 |
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Title: Wnt7b/β-catenin signaling pathway mediated by retinoid acid involved in the transdifferentiation of primary fetal alveolar epithelial type II cells | ||
Author: Jinshuai Ma, Dianpu Zhang, Meng Lv, Qiqi Pan, Xiuxiang Liu | ||
Abstract: This study was designed to investigate the roles of retinoic acid (RA) in transdifferentiation of primary fetal alveolar epithelial type II cells (AECIIs) into alveolar epithelial type I cells (AECIs). Primary fetal AECIIs isolated from rats at a gestational of 19 days were divided into: (i) DMSO group treated using 0.1% DMSO; (ii) RA group, treated with 1 µM RA; and (iii) RA+BMS493 group treated with 1 µM RA and 10–8 M BMS493 (served as a pan-RA receptor antagonist). Then we determined the roles of AQP5 (a specific marker of AECIs), SP-C (a specific marker for AECIIs) and Wnt7b/β-catenin signaling pathway in the transdifferentiation of AECIIs to AECIs. SP-C mRNA and protein expression was significantly down-regulated in AECIIs exposure to RA for 24 h and 48 h, however, significant up-regulation was noticed after exposure for 72 h. AQP5 mRNA and protein expression showed significant increase in RA group, but showed significant decline in the RA+BMS493 group. Wnt7b mRNA, nucleus β-catenin and cyclin D1 were significantly up-regulated in RA group compared with DMSO group. RA may promote fetal AECIIs transdifferentiation into AECIs through activating Wnt7b/β-catenin signaling pathway. Our study contributed to the understanding on the pulmonary regeneration in cases of pulmonary injuries, together with the prevention and treatment of neonatal respiratory distress syndrome. |
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Keywords: Alveolar epithelial type II cells — Retinoic acid — Wnt7b — β-catenin — Cyclin D1 | ||
Published online: 23-Nov-2022 | ||
Year: 2022, Volume: 41, Issue: 6 | Page From: 559, Page To: 567 | |
doi:10.4149/gpb_2022037 |
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