Tunneling nanotube formation is essential for the regulation of osteoclastogenesis

破骨细胞 细胞生物学 兰克尔 细胞融合 细胞内 化学 多核 细胞 脂质双层融合 生物 生物化学 基因 激活剂(遗传学) 受体
作者
Akira Takahashi,Akiko Kukita,Yin-Ji Li,Jing-Qi Zhang,Hisayuki Nomiyama,Takayoshi Yamaza,Yasunori Ayukawa,Kiyoshi Koyano,Toshio Kukita
出处
期刊:Journal of Cellular Biochemistry [Wiley]
卷期号:114 (6): 1238-1247 被引量:57
标识
DOI:10.1002/jcb.24433
摘要

Osteoclasts are the multinucleated giant cells formed by cell fusion of mononuclear osteoclast precursors. Despite the finding of several membrane proteins involving DC-STAMP as regulatory proteins required for fusion among osteoclast precursors, cellular and molecular events concerning this process are still ambiguous. Here we identified Tunneling Nanotubes (TNTs), long intercellular bridges with small diameters, as the essential cellular structure for intercellular communication among osteoclast precursors in prior to cell fusion. Formation of TNTs was highly associated with osteoclastogenesis and it was accompanied with the significant induction of the M-Sec gene, an essential gene for TNT formation. M-Sec gene expression was significantly upregulated by RANKL-treatment in osteoclast precursor cell line. Blockage of TNT formation by Latrunclin B or by M-Sec siRNA significantly suppressed osteoclastogenesis. We have detected the rapid intercellular transport of not only the membrane phospholipids labeled with DiI but also the DC-STAMP-GFP fusion protein through TNTs formed among osteoclast precursors during osteoclastogenesis. Transportation of such regulatory molecules through TNTs would be essential for the process of the specific cell fusion among osteoclast precursors.
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