Hiramatsu Kiyoshi, Asaba Yutaro, Takeshita Sunao, Nimura Yuji, Tatsumi Sawako, Katagiri Nobuyoshi, Niida Shumpei, Nakajima Toshihiro, Tanaka Sakae, Ito Masako, Karsenty Gerard, Ikeda Kyoji
Department of Bone and Joint Disease, Research Institute, National Center for Geriatrics and Gerontology (NCGG), 36-3 Gengo, Morioka, Obu, Aichi 474-8522, Japan.
Endocrinology. 2007 Jun;148(6):2708-15. doi: 10.1210/en.2007-0215. Epub 2007 Mar 15.
We previously identified gamma-glutamyltransferase (GGT) by expression cloning as a factor inducing osteoclast formation in vitro. To examine its pathogenic role in vivo, we generated transgenic mice that overexpressed GGT in a tissue-specific manner utilizing the Cre-loxP recombination system. Systemic as well as local production of GGT accelerated osteoclast development and bone resorption in vivo by increasing the sensitivity of bone marrow macrophages to receptor activator of nuclear factor-kappaB ligand, an essential cytokine for osteoclastogenesis. Mutated GGT devoid of enzyme activity was as potent as the wild-type molecule in inducing osteoclast formation, suggesting that GGT acts not as an enzyme but as a cytokine. Recombinant GGT protein increased receptor activator of nuclear factor-kappaB ligand expression in marrow stromal cells and also stimulated osteoclastogenesis from bone marrow macrophages at lower concentrations. Thus, GGT is implicated as being involved in diseases characterized by accelerated osteoclast development and bone destruction and provides a new target for therapeutic intervention.
我们之前通过表达克隆鉴定出γ-谷氨酰转移酶(GGT)是一种在体外诱导破骨细胞形成的因子。为了研究其在体内的致病作用,我们利用Cre-loxP重组系统构建了以组织特异性方式过表达GGT的转基因小鼠。GGT的全身及局部产生通过增加骨髓巨噬细胞对核因子-κB受体激活剂配体(破骨细胞生成所必需的细胞因子)的敏感性,加速了体内破骨细胞的发育和骨吸收。缺乏酶活性的突变型GGT在诱导破骨细胞形成方面与野生型分子一样有效,这表明GGT并非作为一种酶起作用,而是作为一种细胞因子。重组GGT蛋白增加了骨髓基质细胞中核因子-κB受体激活剂配体的表达,并且在较低浓度下也刺激了骨髓巨噬细胞的破骨细胞生成。因此,GGT被认为与以破骨细胞发育加速和骨破坏为特征的疾病有关,并为治疗干预提供了一个新的靶点。