细胞介导的细胞毒性的超微结构

Iren Vollenweider, P. Groscurth
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引用次数: 21

摘要

接触依赖细胞介导的细胞毒性已被发现由淋巴细胞、巨噬细胞甚至粒细胞执行,淋巴系的细胞毒性效应细胞分为介导MHC相关细胞毒性的细胞毒性T淋巴细胞(CTL),以及介导非MHC限制性细胞毒性的效应细胞,如自然杀伤细胞(NK)细胞、显示NK样活性的T淋巴细胞和淋巴因子激活的杀伤细胞(LAK)细胞。在形态学研究中,这些细胞很难区分:它们都表现出大颗粒淋巴细胞(LGLs)的特征,其特征是低核与细胞质比和亲氮颗粒。在超微结构上发现溶酶体颗粒,显示一个电子密集的核心,被许多小囊泡或小的电子半透明晕包围。在这些颗粒中发现了穿孔素、丝氨酸酯酶和蛋白聚糖等成孔蛋白。其特点是NK细胞中的平行管状阵列(PTA)和LAK细胞中的核包涵体。在形态学上可以区分两种类型的杀伤事件。一方面,在效应细胞结合后靶细胞表面形成膜病变,在细胞溶解的晚期,靶细胞被完全解体的膜包围。然而,细胞核只显示出微小的变化。另一种被称为细胞凋亡的方式是,靶细胞的细胞膜保持完整,但细胞核和细胞器很早就在细胞内解体。这些形态学上不同类型的细胞杀伤是否对应于细胞介导的细胞毒性的功能不同途径仍有待解决。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ultrastructure of cell mediated cytotoxicity

Contact dependent cell mediated cytotoxicity has been found to be executed by lymphocytes, macrophages, and even granulocytes, Cytotoxic effector cells of the lymphatic lineage are divided into cytotoxic T lymphocytes (CTL), mediating MHC related cytotoxicity, and in effectors mediating non-MHC restricted cytotoxicity such as natural killer (NK) cells, T lymphocytes displaying NK-like activity and lymphokine activated killer (LAK) cells. In morphologic studies these cells are hardly to be distinguished: they all show features of large granular lymphocytes (LGLs), which are characterized by a low nuclear to cytoplasmic ratio and azurophilic granules. Ultrastructurally lysosomal granules, showing an electron dense core that is either surrounded by numerous small vesicles or by a small electron translucent halo, have been found. Pore-forming proteins such as perforin, as well as serine esterases and proteoglycans have been pointed out in these granules. Specialities are parallel tubular arrays (PTA) in NK cells and nuclear inclusion bodies in LAK cells.

Morphologically two types of killing event may be distinguished. In one way membrane lesions develop at the surface of target cells upon binding of effector cells and in advanced stages of cytolysis the target cells are sorrounded by a completely disintegrated membrane. The nuclei, however, show only minor changes. In the other way, called apoptosis, the cell membrane of the targets remains intact, but the nucleus and cell organelles very early disintegrate intracellularly. Whether these morphologically different types of cell killing correspond to the functionally different pathways of cell mediated cytotoxicity remains to be resolved.

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