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Fas抗原/Fas配体相互作用参与小鼠小肠上皮内淋巴细胞诱导上皮细胞凋亡的可能性。

Potential for involvement of Fas antigen/Fas ligand interaction in apoptosis of epithelial cells by intraepithelial lymphocytes in murine small intestine.

作者信息

Inagaki-Ohara K, Nishimura H, Sakai T, Lynch D H, Yoshikai Y

机构信息

Laboratory of Host Defense and Germfree Life, Nagoya University School of Medicine, Japan.

出版信息

Lab Invest. 1997 Nov;77(5):421-9.

PMID:9389785
Abstract

Intestinal epithelial cells (i-EC), which move to the villus tips from the crypts, rapidly die by apoptosis at the villus tips and are perpetually renewed at the crypts. To determine whether the Fas antigen (Fas)/Fas ligand (FasL) system is involved in the mechanism leading to apoptosis of i-EC, we examined the expression of Fas and FasL on the i-EC and intestinal intraepithelial lymphocytes (i-IEL) in normal mice. A high level of Fas was expressed on both the i-EC and i-IEL, whereas FasL was expressed in the i-IEL, especially in high-density fraction upon separation (high-density i-IEL), but not in the i-EC. The high-density i-IEL exhibited cytotoxicity against not only Fas transfectant but also the i-EC, and the cytotoxicity was inhibited by addition of Fas-Fragment c chimeric fusion protein. Thus, a significant fraction of i-IEL, such as high-density i-IEL, may partly contribute to induction of apoptosis in the effete i-EC via Fas/FasL interaction.

摘要

肠上皮细胞(i-EC)从隐窝迁移至绒毛顶端,在绒毛顶端通过凋亡迅速死亡,并在隐窝处不断更新。为了确定Fas抗原(Fas)/Fas配体(FasL)系统是否参与导致i-EC凋亡的机制,我们检测了正常小鼠i-EC和肠上皮内淋巴细胞(i-IEL)上Fas和FasL的表达。i-EC和i-IEL上均表达高水平的Fas,而FasL在i-IEL中表达,尤其是在分离后的高密度组分(高密度i-IEL)中表达,但在i-EC中不表达。高密度i-IEL不仅对Fas转染细胞具有细胞毒性,对i-EC也具有细胞毒性,并且通过添加Fas片段c嵌合融合蛋白可抑制这种细胞毒性。因此,很大一部分i-IEL,如高密度i-IEL,可能通过Fas/FasL相互作用部分地促成衰老i-EC的凋亡诱导。

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