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New insights into the biology of osteocalcin

期刊

BONE
卷 82, 期 -, 页码 42-49

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.bone.2015.05.046

关键词

Osteocalcin; Osteoblast; Metabolism; Diabetes

资金

  1. Merit Review grant [BX001234]
  2. Veterans Administration
  3. National Institute of Diabetes and Digestive and Kidney Diseases of the NIH [DK099134]
  4. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R01DK099134, P30DK079637] Funding Source: NIH RePORTER
  5. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [T32GM008752] Funding Source: NIH RePORTER
  6. Veterans Affairs [I01BX001234] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Osteocalcin is among the 'most abundant proteins in bone and is produced exclusively by osteoblasts. Initially believed to be an inhibitor of bone mineralization, recent studies suggest a broader role for osteocalcin that extends to the regulation of whole body metabolism, reproduction, and cognition. Circulating undercarboxylated osteocalcin, which is regulated by insulin, acts in a feed-forward loop to increase beta-cell proliferation as well as insulin production and secretion, while skeletal muscle and adipose tissue respond to osteocalcin by increasing their sensitivity to insulin, Osteocalcin also acts in the brain to increase neurotransmitter production and in the testes to stimulate testosterone production. At least one putative receptor for osteocalcin, Gprc6a, is expressed by adipose, skeletal muscle, and the Leydig cells of the testes and appears to mediate osteocalcin's effects in these tissues. In this review, we summarize these new discoveries, which suggest that the ability of osteocalcin to function both locally in bone and as a hormone depends on a novel post-translational mechanism that alters osteocalcin's affinity for the bone matrix and bioavailability. This article is part of a Special Issue entitled Bone and diabetes. (C) 2015 Elsevier Inc. All rights reserved.

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