Institute for Medical Microbiology, Immunology, and Hygiene, Technische Universität München, Munich, Germany.
Trends Cell Biol. 2009 Oct;19(10):514-22. doi: 10.1016/j.tcb.2009.07.005. Epub 2009 Sep 3.
Fusion of macrophages leads to the formation of osteoclasts in bone and of multinucleated giant cells in granulomas. The precise function of granuloma-associated multinucleates giant cells is not clear but substantial progress has recently been made in identifying the molecular machinery involved in macrophage fusion. Signaling processes mediated by DAP12 and STAT6 induce a fusion-competent status. Chemotaxis through CCL2, cell-cell adhesion mediated by E-cadherin, exposure of phosphatidylserine, lipid recognition by CD36 and cytoskeletal rearrangements depending on RAC1 are prerequisites for successful macrophage fusion. We review current knowledge on the molecular mediators of giant cell formation, compare giant cells with osteoclasts and highlight key target areas for future research and medical relevance.
巨噬细胞融合导致骨中的破骨细胞和肉芽肿中的多核巨细胞形成。肉芽肿相关多核巨细胞的确切功能尚不清楚,但最近在鉴定参与巨噬细胞融合的分子机制方面取得了实质性进展。由 DAP12 和 STAT6 介导的信号转导过程诱导融合能力状态。通过 CCL2 的趋化作用、E-钙粘蛋白介导的细胞间粘附、磷脂酰丝氨酸的暴露、CD36 对脂质的识别以及依赖 RAC1 的细胞骨架重排是巨噬细胞融合成功的前提条件。我们综述了巨细胞形成的分子介质的最新知识,将巨细胞与破骨细胞进行了比较,并强调了未来研究和医学相关性的关键目标领域。