The sympathetic tone mediates leptin's inhibition of insulin secretion by modulating osteocalcin bioactivity

被引:194
作者
Hinoi, Eiichi [1 ,3 ]
Gao, Nan [2 ]
Jung, Dae Young [4 ]
Yadav, Vijay [1 ]
Yoshizawa, Tatsuya [1 ]
Myers, Martin G., Jr. [5 ,6 ]
Chua, Streamson C., Jr. [7 ,8 ]
Kim, Jason K. [4 ]
Kaestner, Klaus H. [2 ,3 ]
Karsenty, Gerard [1 ]
机构
[1] Columbia Univ, Coll Phys & Surg, Dept Genet & Dev, New York, NY 10032 USA
[2] Univ Penn, Dept Genet, Philadelphia, PA 19104 USA
[3] Univ Penn, Inst Diabet Obes & Metab, Philadelphia, PA 19104 USA
[4] Penn State Univ, Coll Med, Dept Cellular & Mol Physiol, Hershey, PA 17033 USA
[5] Univ Michigan, Sch Med, Dept Internal Med, Ann Arbor, MI 48109 USA
[6] Univ Michigan, Sch Med, Dept Mol & Integrat Physiol, Ann Arbor, MI 48109 USA
[7] Albert Einstein Coll Med, Dept Med, Bronx, NY 12461 USA
[8] Albert Einstein Coll Med, Dept Neurosci, Bronx, NY 12461 USA
基金
美国国家卫生研究院; 日本学术振兴会;
关键词
D O I
10.1083/jcb.200809113
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The osteoblast-secreted molecule osteocalcin favors insulin secretion, but how this function is regulated in vivo by extracellular signals is for now unknown. In this study, we show that leptin, which instead inhibits insulin secretion, partly uses the sympathetic nervous system to fulfill this function. Remarkably, for our purpose, an osteoblast-specific ablation of sympathetic signaling results in a leptin-dependent hyperinsulinemia. In osteoblasts, sympathetic tone stimulates expression of Esp, a gene inhibiting the activity of osteocalcin, which is an insulin secretagogue. Accordingly, Esp inactivation doubles hyperinsulinemia and delays glucose intolerance in ob/ob mice, whereas Osteocalcin inactivation halves their hyperinsulinemia. By showing that leptin inhibits insulin secretion by decreasing osteocalcin bioactivity, this study illustrates the importance of the relationship existing between fat and skeleton for the regulation of glucose homeostasis.
引用
收藏
页码:1235 / 1242
页数:8
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