The lncSIL molecule exerts a negative regulatory effect on the alveolar epithelial-mesenchymal transition induced by TGF-β1 through modulation of the EZH2/P21/CDK6 signaling pathway
10.19405/j.cnki.issn1000-1492.2024.04.007
- Author:
Wanfang Zhang
1
;
Lin Wang
2
;
Pengtao Pan
3
;
Wenxin Li
2
;
Ruili Kang
1
;
Ziren Zhu
1
;
Haoqin Chen
2
;
Xinyu Fang
2
;
Xingcan Zhang
2
;
Yuxin Zhang
2
;
Yiwen Jiang
2
;
Xinyan Li
2
;
Benqi Yuan
2
Author Information
1. School of Biological Engineering , Xinxiang University , Xinxiang 453003
2. School of International Education , Xinxiang University , Xinxiang 453003
3. Medical College of Xinxiang University , Xinxiang 453003
- Publication Type:Journal Article
- Keywords:
lncSIL;
long noncoding RNA;
idiopathic pulmonary fibrosis;
epithelial-mesenchymal transition;
transforming growth factor-β1;
enhancer of zeste homolog 2;
cell marker proteins
- From:
Acta Universitatis Medicinalis Anhui
2024;59(4):600-604
- CountryChina
- Language:Chinese
-
Abstract:
Objective :To investigate the role of lncSIL in transforming growth factor-β1(TGF-β1)-induced alveo- lar epithelial interstitial transformation (EMT) and its related signaling pathways .
Methods :Western blot was used to detect the effect of lncSIL silencing on the expression of E-cadherin ( E-cad) , alpha-smooth muscle actin ( α- SMA) and Collagen I (Col I) in the process of EMT induced by TGF-β1 . LncSIL interacting proteins were ana- lyzed by RNA pulldown . Western blot was used to detect the effect of overexpression or silencing of lncSIL on the expression of its target gene enhancer of zeste homolog 2 (EZH2) and its downstream factors P21 and cyclin-de- pendent kinase 6 (CDK6) . Flow cytometry was used to analyze the effect of lncSIL on cell cycle progression .
Results:After lncSIL silencing , the expression of α-SMA and Col I increased , the expression of E-cad decreased . RNA pulldown assay showed that EZH2 was the target protein that interacted with lncSIL , and the expression of EZH2 increased after silencing lncSIL , the expression of EZH2 downstream gene P21 decreased , CDK6 increased . Flow cytometry showed that the number of cells in S phase significantly increased . When lncSIL was overexpressed , the expression of EZH2 and CDK6 was down-regulated , the expression of P21 was up-regulated , and the number of S phase cells significantly decreased .
Conclusion :LncSIL inhibits TGF-β1-induced alveolar epithelial cell mesen- chymal transition by negatively regulating EZH2/P21 /CDK6 signaling pathway to inhibit cell cycle progression .
- Full text:2024070222104481959lncSIL通过EZH2_...诱导的肺泡上皮细胞间质转化_张万方.pdf