Cell fusion dynamics: mechanisms of multinucleation in osteoclasts and macrophages.

Hideaki Sabe, Yasuhito Yahara, Masaru Ishii
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Abstract

Cell-cell fusion is a vital biological process where the membranes of two or more cells merge to form a syncytium. This phenomenon is critical in various physiological and pathological contexts, including embryonic development, tissue repair, immune responses, and the progression of several diseases. Osteoclasts, which are cells from the monocyte/macrophage lineage responsible for bone resorption, have enhanced functionality due to cell fusion. Additionally, other multinucleated giant cells (MGCs) also arise from the fusion of monocytes and macrophages, typically during chronic inflammation and reactions to foreign materials such as prostheses or medical devices. Foreign body giant cells (FBGCs) and Langhans giant cells (LGCs) emerge only under pathological conditions and are involved in phagocytosis, antigen presentation, and the secretion of inflammatory mediators. This review provides a comprehensive overview of the mechanisms underlying the formation of multinucleated cells, with a particular emphasis on macrophages and osteoclasts. Elucidating the intracellular structures, signaling cascades, and fusion-mediating proteins involved in cell-cell fusion enhances our understanding of this fundamental biological process and helps identify potential therapeutic targets for disorders mediated by cell fusion.

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细胞融合动力学:破骨细胞和巨噬细胞的多核机制
细胞-细胞融合是一个重要的生物过程,在这一过程中,两个或多个细胞的细胞膜合并形成一个合胞体。这种现象在胚胎发育、组织修复、免疫反应和多种疾病的进展等各种生理和病理情况下都至关重要。破骨细胞是单核/巨噬细胞系的细胞,负责骨吸收,由于细胞融合,其功能得到增强。此外,其他多核巨细胞(MGC)也是由单核细胞和巨噬细胞融合产生的,通常发生在慢性炎症和对假体或医疗器械等外来材料的反应期间。异物巨细胞(FBGCs)和朗汉斯巨细胞(LGCs)只有在病理情况下才会出现,它们参与吞噬、抗原递呈和炎症介质的分泌。本综述全面概述了多核细胞的形成机制,并特别强调了巨噬细胞和破骨细胞。阐明细胞-细胞融合所涉及的细胞内结构、信号级联和融合介导蛋白,可加深我们对这一基本生物学过程的理解,并有助于确定细胞融合介导的疾病的潜在治疗靶点。
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Cell fusion dynamics: mechanisms of multinucleation in osteoclasts and macrophages. Designer immune cells. Macrophage depletion in inflamed rat knees prevents the activation of synovial mesenchymal stem cells by weakening Nampt and Spp1 signaling. The new era for the research on the regulation of microorganism-induced inflammation. Focusing on exosomes to overcome the existing bottlenecks of CAR-T cell therapy.
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