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体内巨细胞的形成。

Formation of giant cells in vivo.

作者信息

Kraus B

出版信息

Immunobiology. 1982 Apr;161(3-4):290-7. doi: 10.1016/S0171-2985(82)80085-5.

Abstract

In vivo, the development of multinucleate giant cells in granulomas always proceeds in accordance with a given mode (simultaneous phagocytosis--fusion--unordered multinucleate giant cells--ordered multinucleate giant cells). This mode is both quantitatively and qualitatively modifiable, showing a dependence on the quantity, shape, size, and digestibility of the phagocytic material: on uncoated coverslips implanted i.p. in rats, only a few small syncytia develop, bit by bit, on coverslips coated with phagocytotic material, on the other hand, numerous very large, always initially unordered, multinucleate syncytia showing simultaneous aggregation around large phagocytic objects are seen. These can develop into ordered giant cells of the Langhans type, by re-distribution of the cytoplasmic contents, but only when most of the phagocytosed material has been digested. Actively phagocytosing mononuclear macrophages, which coalesce or have already fused to form syncytia frequently develop various types of junctions that probably have the same function in granulomas as in epithelia. Pentalaminar structures in multinucleate giant cells are frequently observed in close conjunction with residual phagocytic material and obviously represent outer cell-membranes that have coalesced during fusion and been incorporated into the cytoplasm. The clear zones surrounding such areas probably represent an element of the cytoskeleton.

摘要

在体内,肉芽肿中多核巨细胞的形成总是按照特定模式进行(同时吞噬——融合——无序多核巨细胞——有序多核巨细胞)。这种模式在数量和质量上均可改变,表现出对吞噬物质的数量、形状、大小和可消化性的依赖性:将未包被的盖玻片腹腔植入大鼠体内时,只会逐渐形成少量小的多核体;而在涂有吞噬物质的盖玻片上,则会看到大量非常大的、最初总是无序的多核体,它们围绕大的吞噬物体同时聚集。只有当大部分吞噬物质被消化后,这些多核体才能通过细胞质内容物的重新分布发展为朗汉斯型有序巨细胞。积极吞噬的单核巨噬细胞聚集或已经融合形成多核体时,常常会形成各种类型的连接,这些连接在肉芽肿中的功能可能与在上皮细胞中的功能相同。多核巨细胞中的五层层状结构经常与残留的吞噬物质紧密相连,显然代表了在融合过程中合并并融入细胞质的外部细胞膜。围绕这些区域的透明带可能代表细胞骨架的一个成分。

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