| International Journal of Clinical and Experimental Pathology | |
| Deoxycytidine kinase promotes the migration and invasion of fibroblast-like synoviocytes from rheumatoid arthritis patients | |
| Wei Fan1  Xin-Fang Huang1  Chun-De Bao1  Fang Du1  Zhen-Yuan Zhou1  | |
| 关键词: Rheumatoid arthritis; deoxycytidine kinase; fibroblast-like synoviocyte; v-akt murine thymoma viral oncogene homolog 1; focal adhesion kinase; | |
| DOI : | |
| 学科分类:生理学与病理学 | |
| 来源: e-Century Publishing Corporation | |
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【 摘 要 】
Rheumatoid arthritis (RA) is a complex, multi-system disease whose primary site of inflammatory tissue damage is the joint. The increasing evidences indicate that activated RA fibroblast-like synoviocytes (FLS) play a critical role in the development of pannus by migrating into cartilage and bone. Furthermore FLS and T cells can activate each other in vitro and in vivo, which is crucial for the progress of RA. Deoxycytidine kinase (DCK) has been linked to peripheral T cell homeostatic proliferation and survival, which is very important for RA. Yet, the function of DCK in FLS is still unknown. Here, we present a story that DCK could regulate the migration and invasion of FLS through AKT pathway in RA patients. Moreover, DCK seems to be the upstream of AKT and FAK, and AKT inhibitor exerted the similar effect on FLS motility. In summary, our study characterized the new role of DCK in human primary FLS cells, and figured out the possible pathway DCK involved in, and these findings might propose DCK as a novel target for controlling joint destruction of RA.
【 授权许可】
Unknown
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| RO201912140866525ZK.pdf | 1243KB |
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