Screening and analysis for autophagy
10.11817/j.issn.1672-7347.2021.210374
- Author:
Hua SHANG
1
;
Qing PENG
2
;
Jiajun LIU
2
;
Yan LIU
2
;
Li LONG
3
Author Information
1. Zunyi Medical University, Zunyi Guizhou 563000. 31757450@qq.com.
2. Zunyi Medical University, Zunyi Guizhou 563000.
3. Zunyi Medical University, Zunyi Guizhou 563000. llllyyyy2012@sina.com.
- Publication Type:Journal Article
- Keywords:
autophagy;
fibroblast-like synoviocytes;
long non-coding RNA;
microarray;
rheumatoid arthritis
- MeSH:
Arthritis, Rheumatoid/genetics*;
Autophagy/genetics*;
Cell Proliferation;
Cells, Cultured;
Fibroblasts;
Humans;
RNA, Long Noncoding/genetics*;
Reproducibility of Results;
Synoviocytes
- From:
Journal of Central South University(Medical Sciences)
2021;46(10):1071-1079
- CountryChina
- Language:English
-
Abstract:
OBJECTIVES:Long non-coding RNA (lncRNA) has become a key epigenetic regulator that regulates gene expression and affects a variety of biological processes. LncRNA plays an important role in the occurrence and development of rheumatoid arthritis (RA). The study on lncRNA in peripheral blood cells of RA patients has been reported. However, there is no study on autophagy regulation by lncRNA in RA patients. This study aims to provide a new direction for the diagnosis and treatment of RA via screening the changes of lncRNAs in RA fibroblast-like synoviocytes (RA-FLSs) before and after autophagy and finding the key lncRNAs targeting RA-FLSs autophagy.
METHODS:Synovial tissues of 6 RA patients after knee and hip joint surgery were obtained, and RA-FLSs were cultured to the 5th generation for further experiments (tissue culture method). After treatment with mTOR inhibitor PP242, the expression of LC3-II was detected by Western blotting. Total RNAs of 3 cases of RA-FLSs before and after treatment with mTOR inhibitor PP242 were extracted by TRIzol and screened by Agilent Human ceRNA Microarray 2019 (4×180 K, design ID: 086188) chip. The lncRNAs with significantly changed expression levels were selected (difference multiple≥2.0,
RESULTS:RA-FLSs were successfully isolated and cultured from the synovial tissues of the patient's knee or hip joint. After 6 RA-FLSs were treated with PP242, the expression level of autophagy marker protein LC3-II was increased (
CONCLUSIONS:Differentially expressed lncRNAs in RA-FLSs have been identified with microarray analysis. In RA, differential expression of lncRNAs is involved in the autophagy of RA-FLSs. The underlying mechanisms based on bioinformatics analysis include regulating the secretion of cytokines, such as IL-6, TGF-β, TNF-α and IL-17, participating in the immune cell differentiation, such as Th17, Th1, Th2 cells and osteoclasts, as well as regulating the autophagy pathway, MAPK, FoxO, and other signaling pathways. It has been verified that the expression of ENST0000584721.1 is up-regulated and ENST0000615939.1 is down-regulated after autophagy of RA FLSs, which provides a good experimental basis for further study on the mechanism of lncRNA in RA-FLSs autophagy.
