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γ-Glutamyl carboxylase in osteoblasts regulates glucose metabolism in mice.
Shiba, Sachiko; Ikeda, Kazuhiro; Azuma, Kotaro; Hasegawa, Tomoka; Amizuka, Norio; Horie-Inoue, Kuniko; Inoue, Satoshi.
Affiliation
  • Shiba S; Division of Gene Regulation and Signal Transduction, Research Center for Genomic Medicine, Saitama Medical University, Saitama, Japan.
  • Ikeda K; Division of Gene Regulation and Signal Transduction, Research Center for Genomic Medicine, Saitama Medical University, Saitama, Japan.
  • Azuma K; Department of Geriatric Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Hasegawa T; Department of Developmental Hard Tissue, Graduate School of Dental Medicine, Hokkaido University, Hokkaido, Japan.
  • Amizuka N; Department of Developmental Hard Tissue, Graduate School of Dental Medicine, Hokkaido University, Hokkaido, Japan.
  • Horie-Inoue K; Division of Gene Regulation and Signal Transduction, Research Center for Genomic Medicine, Saitama Medical University, Saitama, Japan.
  • Inoue S; Division of Gene Regulation and Signal Transduction, Research Center for Genomic Medicine, Saitama Medical University, Saitama, Japan; Department of Anti-Aging Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan. Electronic address: INOUE-GER@h.u-tokyo.ac.jp.
Biochem Biophys Res Commun ; 453(3): 350-5, 2014 Oct 24.
Article in En | MEDLINE | ID: mdl-25264202
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.
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Full text: 1 Database: MEDLINE Main subject: Osteoblasts / Carbon-Carbon Ligases / Glucose Limits: Animals Language: En Year: 2014 Type: Article

Full text: 1 Database: MEDLINE Main subject: Osteoblasts / Carbon-Carbon Ligases / Glucose Limits: Animals Language: En Year: 2014 Type: Article