期刊
ACTA MEDICA MEDITERRANEA
卷 38, 期 2, 页码 861-865出版社
CARBONE EDITORE
DOI: 10.19193/0393-6384_2022_2_131
关键词
T-bet; GATA-3; Th1; Th2; rheumatoid arthritis; inflammatory injury
资金
- Science and technology fund of Tianjin Hospital [TJYY1510]
This study analyzed the role of the transcriptional regulatory factor T-bet and GATA connexin 3 in the inflammatory response and related mechanisms of rheumatoid arthritis. The results showed that interference with T-bet expression can reduce inflammatory damage to rheumatoid arthritis cells and may be related to the regulation of the Th1/Th2 ratio by T-bet.
Objective: To analyse the role of the transcriptional regulatory factor (T-bet) and GATA connexin 3 (GATA-3) in inflammatory response and related mechanisms of rheumatoid arthritis (RA). Methods: Synovial tissue was obtained from RA patients and fibroblast-like synoviocytes (FLS) from patients in a control group. The synovial tissue from RA patients was divided into the RA model group and the T-bet interference group. The T-bet interference group was transfected with shRNA eukaryotic plasmids that inhibited T-bet expression. Enzyme-linked immunosorbent assay (ELISA) was used to detect Th1/Th2-related indexes in each group. Western blot analysis and immunohistochemistry showed that T cell-mediated T-bet, GATA-3, retinoic acid-related nuclear orphan receptor-??t (ROR??t) and forkhead box protein 3 (FOXP3) levels were detected in each group. Results: The levels of INF-??, TNF-?? and IL-2 in the model group and the T-bet interference group were significantly higher than in the control group, while the levels of IL-4 were significantly lower than the control group. The levels of INF-??, TNF-?? and IL-2 in the T-bet interference group were significantly lower than the model group, and the levels of IL-4 were significantly higher than the model group (P<0.05). The level of ROR??t protein in the model group and the T-bet interference group was significantly lower than the control group, the level of FOXP3 protein in the T-bet interference group was significantly higher than the model group, and the level of FOXP3 protein in the T-bet interference group was significantly lower than the model group (P<0.05). The level of GATA-3 protein in the model and the T-bet interference groups was significantly lower than the control group, the level of T-bet protein in model group was significantly higher than the control group, the level of GATA-3 protein in the T-bet interference group was significantly higher than the model group, and the level of T-bet protein was significantly lower in the model and control groups (P<0.05). Conclusion: Regulation of the T-bet/GATA-3 ratio can reduce inflammatory damage to RA cells, a mechanism that may be related to the regulation of the Th1/Th2 ratio of RA cells by T-bet.
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