Bone Analysis of T-Cell Leukaemia Translocation-Associated Gene (TCTA)Transgenic Mice and Conditional Knockout Mice: Possibility that TCTA ProteinExpressed on Osteoclasts Plays a Role as a Novel Coupling Factor In Vivo

S. Kotake, Y. Nanke, T. Yago, M. Kawamoto, T. Kobashigawa, H. Yamanaka
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Abstract

T-cell leukemia translocation-associated gene (TCTA) protein is expressed ubiquitously in normal human tissues. However, its function has not been clarified. In 2009, we demonstrated that TCTA protein play an important role in human osteoclastogenesis and pit formation of mature human osteoclasts inducing the fusion process of osteoclastogenesis in vitro. In the current study, to clarify the role of TCTA protein in vivo, we generated TCTA gene transgenic, both systemic and osteoclast-specific, mice and osteoclast-specific conditional knockout mice and then analyzed their bones. Surprisingly, in the conditional knockout mice, bone volume decreased despite inhibited osteoclastogenesis. According to these findings, we speculated that TCTA protein expressed on osteoclasts plays a role as a E»coupling factorE¼ in vivo.
t细胞白血病易位相关基因(TCTA)转基因小鼠和条件敲除小鼠的骨分析:TCTA蛋白在破骨细胞上表达的可能性在体内作为一种新的偶联因子
T细胞白血病易位相关基因(TCTA)蛋白在正常人体组织中广泛表达。然而,其功能尚未明确。2009年,我们证明TCTA蛋白在人类破骨细胞生成和成熟人破骨细胞的凹坑形成中发挥重要作用,从而在体外诱导破骨细胞形成的融合过程。在目前的研究中,为了阐明TCTA蛋白在体内的作用,我们产生了TCTA基因转基因,包括系统性和破骨细胞特异性,小鼠和破骨细胞核特异性条件敲除小鼠,然后分析了它们的骨骼。令人惊讶的是,在条件敲除小鼠中,尽管破骨细胞生成受到抑制,但骨体积却减少了。根据这些发现,我们推测破骨细胞上表达的TCTA蛋白在体内作为E»偶联因子E¼发挥作用。
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