Analysis on differentially expressed microRNAs for TGF-β1-induced trans-differentiation in MRC-5 cells
10.11763/j.issn.2095-2619.2019.05.006
- Author:
Peiyan YANG
1
;
Ahui ZHAO
1
;
Luheng JIN
1
;
Youliang ZHAO
1
;
Xinghao YU
1
;
Jianhui ZHANG
1
;
Ruonan ZHAI
1
;
Changfu HAO
1
;
Wu YAO
1
Author Information
1. School of Public Health, Zhengzhou University Zhengzhou, Henan 450001, China
- Publication Type:Journal Article
- Keywords:
Fibroblast;
Transforming growth factor-β1;
MRC-5 cell;
Trans-differentiation;
Bioinformatics;
Pulmonary fibrosis;
Pneumoconiosis
- From:
China Occupational Medicine
2019;46(05):551-558
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE: To investigate the differentially expressed microRNAs(miRNAs) in human embryonic lung fibroblast MRC-5 cells stimulated by transforming growth factor-β1(TGF-β1) using microarray chip, and screen for key genes and signaling pathways of fibroblast trans-differentiation. METHODS: The miRNA expression gene chip dataset GSE43992 on TGF-β1 stimulated MRC-5 cells were downloaded from high-throughput Gene Expression Omnibus(GEO) database of National Center for Biotechnology Information of the United States. The R language Limma package was used to screen the differentially expressed miRNAs. Corresponding target genes were predicted by miRWalk database performed by Gene Ontology(GO) functional enrichment analysis and Kyoto Encyclopedia of Genes and Genomes(KEGG) signaling pathway enrichment analysis. The protein-protein interaction(PPI) network was constructed by the search tool for the Retrieval of Interacting Genes database. RESULTS: A total of five differentially expressed miRNAs were identified, including four up-regulated miRNAs and one down-regulated miRNA; and 42 corresponding differentially expressed target genes were predicted. GO analysis indicated that the target genes were significantly enriched in collagen catabolic process, extracellular matrix organization, membrane organization, collagen fibril organization, and cellular response to amino acid stimulus. The results of KEGG pathway analysis showed that the signaling pathways corresponding to miRNAs and target genes were mainly concentrated in 18 signaling pathways, that were mainly related to the age-ethnic signaling pathways and protein digestion and absorption miRNAs in tumors and diabetic complications. The core genes transfected into the myofibroblasts by the three fibroblasts screened by the PPI network were threonine kinase 1, estrogen receptor 1 and β-catenin. CONCLUSION: Five differentially expressed miRNAs, 42 target genes, 18 signaling pathways, and 3 core genes related to TGF-β1-induced MRC-5 cell trans-differentiation were screened. It can provide new reference for the treatment and research of many diseases including pneumoconiosis and pulmonary fibrosis.
