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巨噬细胞细胞毒性机制的研究。

Studies on the mechanism of macrophage cytotoxicity.

作者信息

Zippel D

出版信息

Exp Pathol. 1985;27(1):3-15. doi: 10.1016/s0232-1513(85)80052-9.

Abstract

The interactions with tumor target cells of resident and BCG-activated murine peritoneal macrophages (M phi) as well as of BCG-activated M phi additionally stimulated by a lymphokine-like factor were investigated in order to get some insight into the cytolytic process mediated by activated M phi. The lymphokine-like factor enhancing the cytotoxicity of BCG-activated M phi (MCF) was isolated and partially purified from cell-free fluid of rat Zajdela ascites hepatoma. M phi cytotoxicity was determined by a modified 51Cr release assay. Scanning and transmission electron microscopic findings suggested a two-step mechanism of target cell lysis: a first step of specific attachment of processes of M phi on the target cell surface and a second step with transport of lysosome-like vesicles to the target cells obviously with liberation of these vesicles in the immediate vicinity of target cells resulting in a local accumulation of cytolytic substances. This interpretation was supported by findings after treatment of interacting effector and target cells with amphotericin B and bestatin which substances were modifying M phi cytotoxicity. MCF caused only an augmentation of M phi cytotoxicity without qualitative differences to the cytolytic action of merely BCG-activated M phi.

摘要

为了深入了解活化巨噬细胞介导的细胞溶解过程,研究了驻留的和经卡介苗(BCG)激活的小鼠腹腔巨噬细胞(M phi)以及经卡介苗激活后又受到类淋巴因子刺激的M phi与肿瘤靶细胞的相互作用。从大鼠扎伊德拉腹水肝癌的无细胞液中分离并部分纯化了增强卡介苗激活的M phi(MCF)细胞毒性的类淋巴因子。通过改良的51Cr释放试验测定M phi细胞毒性。扫描电镜和透射电镜结果提示靶细胞裂解的两步机制:第一步是M phi的突起特异性附着于靶细胞表面,第二步是类似溶酶体的小泡向靶细胞转运,显然这些小泡在靶细胞紧邻区域释放,导致细胞溶解物质局部积聚。用两性霉素B和贝他汀处理相互作用的效应细胞和靶细胞后的结果支持了这一解释,这两种物质可改变M phi细胞毒性。MCF仅增强了M phi细胞毒性,与单纯卡介苗激活的M phi的细胞溶解作用在性质上无差异。

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