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穿孔素及其在T淋巴细胞介导的细胞溶解中的作用。

Perforin and its role in T lymphocyte-mediated cytolysis.

作者信息

Lowin B, Krähenbühl O, Müller C, Dupuis M, Tschopp J

机构信息

Institute of Biochemistry, University of Lausanne, Epalinges, Switzerland.

出版信息

Experientia. 1992 Oct 15;48(10):911-20. doi: 10.1007/BF01919138.

Abstract

The killing mediated by cytotoxic T lymphocytes (CTL) represents an important mechanism in the immune defence against tumors and virus infections. The lytic mechanism has been proposed to consist of a polarized secretion of granule-stored molecules, occurring on effector-target cell contact. By electron microscopy, membrane deposited, pore-like lesions are detected on the target cell membrane during cytolysis by CTL. These structures resembled strikingly pores formed during complement attack. Granules of CTL isolated by nitrogen cavitation and Percoll gradient centrifugation were shown to retain cytotoxic activity. Further purification of proteins stored in these granules led to the discovery of a membranolytic protein named perforin which was capable of polymerizing into pore-like structures. In addition to this cytolytic protein, a set of serine esterases was found as well as lysosomal enzymes and proteoglycans, whose function are not yet clearly defined. The role of perforin in the cytotoxic process is currently being explored by ablating the active gene in mice.

摘要

细胞毒性T淋巴细胞(CTL)介导的杀伤作用是机体抵抗肿瘤和病毒感染免疫防御中的重要机制。据推测,其溶解机制包括在效应细胞与靶细胞接触时,颗粒储存分子的极化分泌。通过电子显微镜观察,在CTL介导的细胞溶解过程中,可在靶细胞膜上检测到膜沉积的孔状损伤。这些结构与补体攻击时形成的孔极为相似。通过氮空化和Percoll梯度离心分离得到的CTL颗粒显示保留了细胞毒性活性。对这些颗粒中储存的蛋白质进一步纯化,发现了一种名为穿孔素的膜溶解蛋白,它能够聚合成孔状结构。除了这种细胞溶解蛋白外,还发现了一组丝氨酸酯酶以及溶酶体酶和蛋白聚糖,其功能尚未明确界定。目前正在通过敲除小鼠中的活性基因来探索穿孔素在细胞毒性过程中的作用。

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