STATs and macrophage fusion.

JAK-STAT Pub Date : 2013-07-01 Epub Date: 2013-04-23 DOI:10.4161/jkst.24777
Takeshi Miyamoto
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引用次数: 17

Abstract

Macrophages play a pivotal role in host defense against multiple foreign materials such as bacteria, parasites and artificial devices. Some macrophage lineage cells, namely osteoclasts and foreign body giant cells (FBGCs), form multi-nuclear giant cells by the cell-cell fusion of mono-nuclear cells. Osteoclasts are bone-resorbing cells, and are formed in the presence of RANKL on the surface of bones, while FBGCs are formed in the presence of IL-4 or IL-13 on foreign materials such as artificial joints, catheters and parasites. Recently, fusiogenic mechanisms and the molecules required for the cell-cell fusion of these macrophage lineage cells were, at least in part, clarified. Dendritic cell specific transmembrane protein (DC-STAMP) and osteoclast stimulatory transmembrane protein (OC-STAMP), both of which comprise seven transmembrane domains, are required for both osteoclast and FBGC cell-cell fusion. STAT6 was demonstrated to be required for the cell-cell fusion of FBGCs but not osteoclasts. In this review, advances in macrophage cell-cell fusion are discussed.

Abstract Image

STATs和巨噬细胞融合。
巨噬细胞在宿主防御多种外来物质(如细菌、寄生虫和人工装置)中起着关键作用。一些巨噬细胞系细胞,即破骨细胞和异物巨细胞(FBGCs),通过单核细胞的细胞-细胞融合形成多核巨细胞。破骨细胞是骨吸收细胞,在骨表面有RANKL存在时形成,而FBGCs则在人工关节、导管、寄生虫等异物上有IL-4或IL-13存在时形成。最近,这些巨噬细胞谱系细胞的融合机制和细胞-细胞融合所需的分子至少部分得到了澄清。树突状细胞特异性跨膜蛋白(DC-STAMP)和破骨细胞刺激跨膜蛋白(OC-STAMP)都包含7个跨膜结构域,是破骨细胞和FBGC细胞-细胞融合所必需的。STAT6被证明是FBGCs细胞间融合所必需的,而不是破骨细胞。本文就巨噬细胞与细胞融合的研究进展作一综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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