Brown adipose tissue-specific insulin receptor knockout shows diabetic phenotype without insulin resistance (Publication with Expression of Concern. See vol. 129, pg. 437, 2019)

被引:60
作者
Guerra, C
Navarro, P
Valverde, AM
Arribas, M
Brüning, J
Kozak, LP
Kahn, CR
Benito, M [1 ]
机构
[1] Univ Complutense Madrid, Fac Farm, Dept Bioquim & Biol Mol, Madrid 28040, Spain
[2] Jackson Lab, Bar Harbor, ME 04609 USA
[3] Harvard Univ, Sch Med, Joslin Diabet Ctr, Boston, MA 02115 USA
关键词
D O I
10.1172/JCI13103
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Although insulin regulates metabolism in both brown and white adipocytes, the role of these tissues in energy storage and utilization is quite different. Recombination technology using the Cre-loxP approach allows inactivation of the insulin receptor in a tissue-specific manner. Mice lacking insulin receptors in brown adipocytes show an age-dependent loss of interscapular brown fat but increased expression of uncoupling protein-1 and -2. In parallel, these mice develop an insulin-secretion defect resulting in a progressive glucose intolerance, without insulin resistance. This model provides direct evidence for not only a role for the insulin receptors in brown fat adipogenesis, the data also suggest a novel role of brown adipose tissue in the regulation of insulin secretion and glucose homeostasis.
引用
收藏
页码:1205 / 1213
页数:9
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