Kim Nacksung, Kadono Yuho, Takami Masamichi, Lee Junwon, Lee Seoung-Hoon, Okada Fumihiko, Kim Jung Ha, Kobayashi Takashi, Odgren Paul R, Nakano Hiroyasu, Yeh Wen-Chen, Lee Sun-Kyeong, Lorenzo Joseph A, Choi Yongwon
Medical Research Center for Gene Regulation, Chonnam National University Medical School, Gwangju, Korea.
J Exp Med. 2005 Sep 5;202(5):589-95. doi: 10.1084/jem.20050978.
Osteoclasts are derived from myeloid lineage cells, and their differentiation is supported by various osteotropic factors, including the tumor necrosis factor (TNF) family member TNF-related activation-induced cytokine (TRANCE). Genetic deletion of TRANCE or its receptor, receptor activator of nuclear factor kappaB (RANK), results in severely osteopetrotic mice with no osteoclasts in their bones. TNF receptor-associated factor (TRAF) 6 is a key signaling adaptor for RANK, and its deficiency leads to similar osteopetrosis. Hence, the current paradigm holds that TRANCE-RANK interaction and subsequent signaling via TRAF6 are essential for the generation of functional osteoclasts. Surprisingly, we show that hematopoietic precursors from TRANCE-, RANK-, or TRAF6-null mice can become osteoclasts in vitro when they are stimulated with TNF-alpha in the presence of cofactors such as TGF-beta. We provide direct evidence against the current paradigm that the TRANCE-RANK-TRAF6 pathway is essential for osteoclast differentiation and suggest the potential existence of alternative routes for osteoclast differentiation.
破骨细胞源自髓系谱系细胞,其分化受到多种促骨因子的支持,包括肿瘤坏死因子(TNF)家族成员肿瘤坏死因子相关激活诱导细胞因子(TRANCE)。TRANCE或其受体核因子κB受体激活剂(RANK)的基因缺失会导致严重的骨石化小鼠,其骨骼中没有破骨细胞。TNF受体相关因子(TRAF)6是RANK的关键信号转导衔接蛋白,其缺乏会导致类似的骨石化。因此,目前的范式认为TRANCE-RANK相互作用以及随后通过TRAF6的信号传导对于功能性破骨细胞的生成至关重要。令人惊讶的是,我们发现,当在诸如转化生长因子-β等辅助因子存在的情况下用TNF-α刺激时,来自TRANCE、RANK或TRAF6基因敲除小鼠的造血前体在体外可以成为破骨细胞。我们提供了直接证据反驳当前的范式,即TRANCE-RANK-TRAF6途径对于破骨细胞分化至关重要,并表明破骨细胞分化可能存在替代途径。