权益分类	功能权益	普通用户	{{item.name}}会员
{{category.name}}	{{benefitItem.name}}

Osteocalcin as a Regulator of Energy Metabolism

骨钙素作为能量代谢的调节剂

基本信息

批准号：
8260469
负责人：
Gerard Karsenty
金额：
$ 48.31万
依托单位：
COLUMBIA UNIVERSITY HEALTH SCIENCES
依托单位国家：
美国
项目类别：
财政年份：
1998
资助国家：
美国
起止时间：
1998-04-01 至 2013-04-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8260469
关键词：
Adipocytes Affect Alleles Biological Biology Blood Bone remodeling Cell Culture Techniques Cell Proliferation Cells Cues Data Endocrine Energy Metabolism Enzymes Fatty acid glycerol esters Feedback Fostering Genes Genetic Goals Grant Health Hormones Image Insulin Laboratories Leptin Metabolic Metabolic syndrome Molecular Mus Non-Insulin-Dependent Diabetes Mellitus Obesity Osteoblasts Osteocalcin Osteogenesis Oxidoreductase Pathway interactions Phenotype Protein Tyrosine Phosphatase Proteins Publishing Regulation Secondary to Serum Signaling Molecule Skeleton Testing Therapeutic Vitamin K Wild Type Mouse adipocyte biology adiponectin base bone bone cell carboxylate carboxylation extracellular fight against glucose metabolism hormone regulation human PTPRT protein in vivo insulin secretion insulin sensitivity insulin signaling interest mouse model pancreatic juice research study tool

项目摘要

DESCRIPTION (provided by applicant): The fact that an adipocyte-derived hormone like leptin regulates bone remodeling raises the project that bone cells may in turn influence adipocyte biology. While testing this hypothesis we identified a gene, Esp, encoding a tyrosine phosphatase whose osteoblast-specific deletion results in an increase in insulin and adiponectin secretion by pancreatic cells and adipocytes respectively. Looking for substrates of the Esp gene product we noted that Osteocalcin-deficient mice had a phenotype that is the mirror image of the one observed in Esp-deficient mice. Osteocalcin -/- mice display a decrease in insulin and in adiponectin secretion. Moreover, removing one allele of osteocalcin sufficed to correct the entire metabolic phenotype of the Esp -/- mice. Based on these and additional published preliminary data we have shown that osteocalcin is a hormone regulating insulin secretion and sensitivity we now intend to foster our molecular understanding of how osteocalcin regulates energy metabolism. To achieve this goal we propose the following specific aims: 1. To demonstrate that gamma carboxylase is a target of OST-PTP, the Esp gene product in vivo 2. To generate mice lacking, in osteoblasts only, the Vitamin K epoxy reductase C1, another enzyme involved in carboxylation of osteocalcin 3. To determine whether bones, through osteocalcin, are responsible of the increase in insulin secretion observed in absence of leptin 4. To define how insulin signaling in osteoblasts regulates osteocalcin expression or bioactivity. PUBLIC HEALTH RELEVANCE. Type 2 diabetes and obesity is a growing public concern. Here we identified a potential new hormone regulating glucose metabolism. This hormone may be an important therapeutic tool in the fight against the metabolic syndrome.

描述（由申请人提供）：事实上，脂肪细胞衍生的激素如瘦素调节骨重塑，提出了骨细胞可能反过来影响脂肪细胞生物学的项目。在验证这一假设时，我们确定了一个编码酪氨酸磷酸酶的基因Esp，其成骨细胞特异性缺失导致胰腺细胞和脂肪细胞分别增加胰岛素和脂联素分泌。寻找Esp基因产物的底物，我们注意到骨钙素缺陷小鼠的表型是在Esp缺陷小鼠中观察到的表型的镜像。骨钙素-/-小鼠显示胰岛素和脂联素分泌减少。此外，去除骨钙素的一个等位基因足以纠正Esp -/-小鼠的整个代谢表型。基于这些和其他已发表的初步数据，我们已经表明骨钙素是一种调节胰岛素分泌和敏感性的激素，我们现在打算促进我们对骨钙素如何调节能量代谢的分子理解。为实现这一目标，我们提出以下具体目标：1.为了证明γ羧化酶是OST-PTP的靶标，Esp基因在体内的产物2。为了产生缺乏的小鼠，仅在成骨细胞中，维生素K环氧还原酶C1，另一种参与骨钙素3羧化的酶。为了确定骨骼是否通过骨钙素负责在缺乏瘦素4的情况下观察到的胰岛素分泌增加。目的：探讨成骨细胞中胰岛素信号通路对骨钙素表达和生物活性的调节作用。公共卫生相关性。2型糖尿病和肥胖是一个日益增长的公众关注。在这里，我们确定了一个潜在的新激素调节葡萄糖代谢。这种激素可能是对抗代谢综合征的重要治疗工具。

项目成果

期刊论文数量（16）

专著数量（0）

科研奖励数量（0）

会议论文数量（0）

专利数量（0）

Insulin signaling in osteoblasts integrates bone remodeling and energy metabolism.

DOI：
10.1016/j.cell.2010.06.003
发表时间：
2010-07-23
期刊：
Cell
影响因子：
64.5
作者：
Ferron M;Wei J;Yoshizawa T;Del Fattore A;DePinho RA;Teti A;Ducy P;Karsenty G
通讯作者：
Karsenty G

Co-dependence of bone and energy metabolisms.