Insulin resistance and a diabetes mellitus-like syndrome in mice lacking the protein kinase Akt2 (PKBβ)

被引:1516
作者
Cho, H
Mu, J
Kim, JK
Thorvaldsen, JL
Chu, QW
Crenshaw, EB
Kaestner, KH
Bartolomei, MS
Shulman, GI
Birnbaum, MJ [1 ]
机构
[1] Univ Penn, Sch Med, Dept Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Cell & Dev Biol, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Med, Dept Neurosci, Philadelphia, PA 19104 USA
[4] Univ Penn, Sch Med, Dept Genet, Philadelphia, PA 19104 USA
[5] Yale Univ, Sch Med, Dept Internal Med, New Haven, CT 06520 USA
[6] Univ Penn, Dept Biol, Philadelphia, PA 19104 USA
关键词
D O I
10.1126/science.292.5522.1728
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Glucose homeostasis depends on insulin responsiveness in target tissues, most importantly, muscle and Liver. The critical initial steps in insulin action include phosphorylation of scaffolding proteins and activation of phosphatidylinositol 3-kinase. These early events Lead to activation of the serine-threonine protein kinase Akt, also known as protein kinase B. We show that mice deficient in Akt2 are impaired in the ability of insulin to Lower blood glucose because of defects in the action of the hormone on Liver and skeletal muscle. These data establish Akt2 as an essential gene in the maintenance of normal glucose homeostasis.
引用
收藏
页码:1728 / 1731
页数:4
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