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细胞毒性T淋巴细胞的Fas和穿孔素非依赖机制

Fas- and perforin-independent mechanism of cytotoxic T lymphocyte.

作者信息

Kajino K, Kajino Y, Greene M I

机构信息

Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, USA.

出版信息

Immunol Res. 1998;17(1-2):89-93. doi: 10.1007/BF02786434.

Abstract

Cytotoxic T lymphocytes (CTLs) play an important role in elimination of virus-infected cells (1). Recent studies revealed at least two distinct mechanisms that CTLs utilize to destroy their target cells. Both mechanisms induce target cell apoptosis specifically and directionally, but these processes are totally different. One is pore formation on target cell membrane by perforin secreted from CTLs (perforin-granzyme pathway), and the other is ligation of Fas, which is expressed on the surface of target cells and Fas ligand, on the surface of CTLs (Fas-FasL pathway) (2). Here we review our work and describe CTL clones that have novel lytic mechanisms derived from CD4-CD8- lymph node cells of gld mice.

摘要

细胞毒性T淋巴细胞(CTLs)在清除病毒感染细胞方面发挥着重要作用(1)。最近的研究揭示了CTLs用于破坏其靶细胞的至少两种不同机制。这两种机制均特异性且定向地诱导靶细胞凋亡,但这些过程完全不同。一种是CTLs分泌的穿孔素在靶细胞膜上形成孔道(穿孔素-颗粒酶途径),另一种是靶细胞表面表达的Fas与CTLs表面的Fas配体结合(Fas-FasL途径)(2)。在此,我们回顾我们的工作,并描述从gld小鼠的CD4-CD8-淋巴结细胞衍生出的具有新型裂解机制的CTL克隆。

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