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肌球蛋白IIA是人自然杀伤细胞中细胞毒性颗粒胞吐作用所必需的。

Myosin IIA is required for cytolytic granule exocytosis in human NK cells.

作者信息

Andzelm Milena M, Chen Xi, Krzewski Konrad, Orange Jordan S, Strominger Jack L

机构信息

Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA.

出版信息

J Exp Med. 2007 Oct 1;204(10):2285-91. doi: 10.1084/jem.20071143. Epub 2007 Sep 17.

Abstract

Natural killer (NK) cell cytotoxicity involves the formation of an activating immunological synapse (IS) between the effector and target cell through which granzymes and perforin contained in lytic granules are delivered to the target cell via exocytosis. Inhibition of nonmuscle myosin II in human NK cells with blebbistatin or ML-9 impaired neither effector-target cell conjugation nor formation of a mature activating NK cell IS (NKIS; formation of an actin ring and polarization of the microtubule-organizing center and cytolytic granules to the center of the ring). However, membrane fusion of lytic granules, granzyme secretion, and NK cell cytotoxicity were all effectively blocked. Specific knockdown of the myosin IIA heavy chain by RNA interference impaired cytotoxicity, membrane fusion of lytic granules, and granzyme secretion. Thus, myosin IIA is required for a critical step between NKIS formation and granule exocytosis.

摘要

自然杀伤(NK)细胞的细胞毒性涉及效应细胞与靶细胞之间形成活化免疫突触(IS),通过该突触,溶解颗粒中所含的颗粒酶和穿孔素通过胞吐作用传递至靶细胞。用肌球蛋白抑制剂(blebbistatin)或ML-9抑制人NK细胞中的非肌肉肌球蛋白II,既不影响效应细胞与靶细胞的结合,也不影响成熟活化NK细胞免疫突触(NKIS;肌动蛋白环的形成以及微管组织中心和溶细胞颗粒向环中心的极化)的形成。然而,溶解颗粒的膜融合、颗粒酶分泌和NK细胞的细胞毒性均被有效阻断。通过RNA干扰特异性敲低肌球蛋白IIA重链会损害细胞毒性、溶解颗粒的膜融合和颗粒酶分泌。因此,肌球蛋白IIA是NKIS形成与颗粒胞吐之间关键步骤所必需的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab47/2118468/98934f3da00d/jem2042285f01.jpg

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