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Fas 配体在体外椎间盘细胞凋亡中的双重作用。

Double role of Fas ligand in the apoptosis of intervertebral disc cells in vitro.

机构信息

Department of Orthopaedic Surgery, The Second Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510120, China.

出版信息

Acta Biochim Biophys Sin (Shanghai). 2009 Nov;41(11):938-47. doi: 10.1093/abbs/gmp087.

Abstract

Fas ligand (FasL) may play an important role in maintaining the immune privilege of intervertebral disc (IVD). Besides, it is closely related to the apoptosis of degenerative disc cells. Nowadays, lots of reports have described about the paradoxical effects of FasL, although the effect of FasL on IVD cells is still under debate. In this study, we tried to investigate the effects of FasL on Fas expression and on the apoptosis of nucleus pulposus (NP) cells in Sprague-Dawley rats. The results showed that the expression of Fas in NP cells was significantly increased by the recombinant FasL. Meanwhile, the apoptosis of NP cells increased markedly in a FasL dose-dependent manner. Interestingly, RNA interference results indicated that the increase of Fas expression and the NP cell apoptosis described previously were inhibited by Fas siRNA, suggesting that RNA interference might be one of novel strategies to prevent IVD cells from apoptosis.

摘要

Fas 配体 (FasL) 可能在维持椎间盘 (IVD) 的免疫特权中发挥重要作用。此外,它与退变椎间盘细胞的凋亡密切相关。如今,大量报道描述了 FasL 的矛盾作用,尽管 FasL 对 IVD 细胞的作用仍存在争议。在这项研究中,我们试图研究 FasL 对 Fas 表达和 Sprague-Dawley 大鼠髓核 (NP) 细胞凋亡的影响。结果表明,重组 FasL 显著增加了 NP 细胞中 Fas 的表达。同时,NP 细胞的凋亡呈 FasL 剂量依赖性显著增加。有趣的是,RNA 干扰结果表明,先前描述的 Fas 表达增加和 NP 细胞凋亡被 Fas siRNA 抑制,这表明 RNA 干扰可能是防止 IVD 细胞凋亡的新策略之一。

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