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成骨细胞中的γ-谷氨酰羧化酶调节小鼠的葡萄糖代谢。

γ-Glutamyl carboxylase in osteoblasts regulates glucose metabolism in mice.

作者信息

Shiba Sachiko, Ikeda Kazuhiro, Azuma Kotaro, Hasegawa Tomoka, Amizuka Norio, Horie-Inoue Kuniko, Inoue Satoshi

机构信息

Division of Gene Regulation and Signal Transduction, Research Center for Genomic Medicine, Saitama Medical University, Saitama, Japan.

Department of Geriatric Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.

出版信息

Biochem Biophys Res Commun. 2014 Oct 24;453(3):350-5. doi: 10.1016/j.bbrc.2014.09.091. Epub 2014 Sep 27.

Abstract

Vitamin K-dependent γ-glutamyl carboxylase (GGCX) is an enzyme that catalyzes the conversion of glutamic acid to gamma-carboxyglutamic acid in substrate proteins. Among GGCX target proteins, recent evidence indicates that osteocalcin regulates insulin sensitivity and secretion. However, the precise contribution of GGCX to glucose metabolism remains to be clarified. To address this question, we generated osteoblast-specific Ggcx-deficient (i.e., conditional knockout [cKO]) mice using collagen type 1 α1 (Col1)-Cre mice. Ggcx cKO mice exhibited altered metabolism compared with their controls; serum glucose levels could be maintained with low amounts of insulin, and the weight of white adipose tissue (WAT) significantly decreased in Ggcx cKO mice. Our findings suggest that GGCX expressed in osteoblasts is critical for the maintenance of blood glucose and WAT.

摘要

维生素K依赖的γ-谷氨酰羧化酶(GGCX)是一种催化底物蛋白中谷氨酸向γ-羧基谷氨酸转化的酶。在GGCX的靶蛋白中,最近有证据表明骨钙素调节胰岛素敏感性和分泌。然而,GGCX对葡萄糖代谢的确切作用仍有待阐明。为了解决这个问题,我们使用I型胶原α1(Col1)-Cre小鼠构建了成骨细胞特异性Ggcx缺陷(即条件性敲除[cKO])小鼠。与对照小鼠相比,Ggcx cKO小鼠的代谢发生了改变;低剂量胰岛素即可维持血清葡萄糖水平,且Ggcx cKO小鼠的白色脂肪组织(WAT)重量显著降低。我们的研究结果表明,成骨细胞中表达的GGCX对维持血糖和白色脂肪组织至关重要。

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