decoction induces apoptosis by activating Fas/caspase-8 pathway in rheumatoid arthritis fibroblast-like synoviocytes.
10.12122/j.issn.1673-4254.2020.08.08
- Author:
Fan ZHAO
1
;
Jiayu LI
1
;
Qijin LU
1
;
Ensheng CHEN
2
;
Lixia YUAN
1
Author Information
1. School of Traditional Chinese Medicine, Southern Medical University, Guangzhou 510515, China.
2. Department of Rheumatology and Immunology, Integrated Hospital of Traditional Chinese Medicine, Southern Medical University, Guangzhou 510315, China.
- Publication Type:Journal Article
- Keywords:
Danggui Niantong decoction;
Fas/caspase-8 signal pathway;
apoptosis;
fibroblast-like synoviocytes;
rheumatoid arthritis
- MeSH:
Apoptosis;
Arthritis, Rheumatoid;
Caspase 8;
Cell Proliferation;
Cells, Cultured;
Fibroblasts;
Synovial Membrane;
Synoviocytes
- From:
Journal of Southern Medical University
2020;40(8):1119-1126
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the effect of decoction (DGNTD) on cell apoptosis and TNF receptor super family 6 (Fas)/caspase-8 pathway in rheumatoid arthritis (RA) fibroblast-like synoviocytes (FLS).
METHODS:FLS isolated from the synovial tissue of RA patients were cultured and identified using immunofluorescence staining. The cells were treated with 10% blank serum (blank control group), 10% sera containing low, moderate or high doses of DGNTD, or 20 μmol/mL KR-33493 (a Fas inhibitor) combined with 10% serum containing high-dose DGNTD. MTT assay was used to detect the proliferation of the cells after the treatments. Apoptosis of the cells was detected at 48 h in each group using Hoechst 33342 staining and flow cytometry with annexin V-FITC/PI staining. The mRNA and protein expressions of Fas, FADD, caspase-8 and caspase-3 in the cells at 48 h were detected using qPCR and Western blotting.
RESULTS:Immunofluorescence staining identified the cultured cells as FLS. Treatment with DGNTD-containing sera significantly inhibited the proliferation of FLS, and the inhibitory effects were enhanced as the dose and intervention time increased ( < 0.05). Hoechst 33342 staining and flow cytometry showed that the sera containing different doses of DGNTD significantly promoted apoptosis of FLS ( < 0.05). The expression levels of Fas, FADD, caspase-8, and caspase-3 at both mRNA and protein levels were significantly increased in the cells after treatment with different doses of DGNTD-containing sera ( < 0.05). The application of KR-33493 obviously reversed the effects of DGNTD on the FLS ( < 0.05).
CONCLUSIONS:DGNTD can induce apoptosis of the FLS by activating Fas/caspase-8 signaling pathway.
