Antidiabetic Effects of IGFBP2, a Leptin-Regulated Gene

被引:231
作者
Hedbacker, Kristina [1 ]
Birsoy, Kivanc [1 ]
Wysocki, Robert W. [1 ,2 ]
Asilmaz, Esra [1 ]
Ahima, Rexford S. [3 ,4 ]
Farooqi, I. Sadaf [5 ]
Friedman, Jeffrey M. [1 ,2 ]
机构
[1] Rockefeller Univ, Mol Genet Lab, New York, NY 10065 USA
[2] Howard Hughes Med Inst, New York, NY 10065 USA
[3] Univ Penn, Sch Med, Dept Med, Div Endocrinol Diabet & Metab, Philadelphia, PA 19104 USA
[4] Univ Penn, Sch Med, Inst Diabet Obes & Metab, Philadelphia, PA 19104 USA
[5] Univ Cambridge, Addenbrookes Hosp, Inst Metab Sci, Metab Res Labs, Cambridge CB2 0QQ, England
关键词
GROWTH-FACTOR-I; GENOME-WIDE ASSOCIATION; REVERSES INSULIN-RESISTANCE; FACTOR-BINDING PROTEIN; DIET-INDUCED OBESITY; OB/OB MICE; CONGENITAL LIPODYSTROPHY; EXTRACELLULAR-MATRIX; REPLACEMENT THERAPY; DIABETES-MELLITUS;
D O I
10.1016/j.cmet.2009.11.007
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We tested whether leptin can ameliorate diabetes independent of weight loss by defining the lowest dose at which leptin treatment of ob/ob mice reduces plasma glucose and insulin concentration. We found that a leptin dose of 12.5 ng/hr significantly lowers blood glucose and that 25 ng/hr of leptin normalizes plasma glucose and insulin without significantly reducing body weight, establishing that leptin exerts its most potent effects on glucose metabolism. To find possible mediators of this effect, we profiled liver mRNA using microarrays and identified IGF Binding Protein 2 (IGFBP2) as being regulated by leptin with a similarly high potency. Overexpression of IGFBP2 by an adenovirus reversed diabetes in insulin-resistant ob/ob, Ay/a, and diet-induced obese mice, as well as insulin-deficient streptozotocin-treated mice. Hyperinsulinemic clamp studies showed a 3-fold improvement in hepatic insulin sensitivity following IGFBP2 treatment of ob/ob mice. These results show that IGFBP2 can regulate glucose metabolism, a finding with potential implications for the pathogenesis and treatment of diabetes.
引用
收藏
页码:11 / 22
页数:12
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