Role for neuronal insulin resistance in neurodegenerative diseases

被引:492
作者
Schubert, M
Gautam, D
Surjo, D
Ueki, K
Baudler, S
Schubert, D
Kondo, T
Alber, J
Galldiks, N
Küstermann, E
Arndt, S
Jacobs, AH
Krone, W
Kahn, CR
Brüning, JC
机构
[1] Univ Cologne, Inst Genet, D-50931 Cologne, Germany
[2] Univ Cologne, Ctr Mol Med Cologne, D-50931 Cologne, Germany
[3] Univ Cologne, Inst Anat, D-50931 Cologne, Germany
[4] Univ Cologne, Dept Neurol, D-50931 Cologne, Germany
[5] Max Planck Inst Neurol Res, D-50931 Cologne, Germany
[6] Univ Cologne, Klin 2, D-50924 Cologne, Germany
[7] Univ Cologne, Poliklin Innere Med, D-50924 Cologne, Germany
[8] Ctr Mol Med Cologne, D-50924 Cologne, Germany
[9] Harvard Univ, Sch Med, Joslin Diabet Ctr, Boston, MA 02115 USA
关键词
D O I
10.1073/pnas.0308724101
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
Impairment of insulin signaling in the brain has been linked to neurodegenerative diseases. To test the hypothesis that neuronal insulin resistance contributes to defects in neuronal function, we have performed a detailed analysis of brain/neuron-specific insulin receptor knockout (NIRKO) mice. We find that NIRKO mice exhibit a complete loss of insulin-mediated activation of phosphatidylinositol 3-kinase and inhibition of neuronal apoptosis. In intact animals, this loss results in markedly reduced phosphorylation of Akt and GSK3beta, leading to substantially increased phosphorylation of the microtubule-associated protein Tau, a hallmark of neurodegenerative diseases. Nevertheless, these animals exhibit no alteration in neuronal proliferation/survival, memory, or basal brain glucose metabolism. Thus, lack of insulin signaling in the brain may lead to changes in Akt and GSK3beta activity and Tau hyperphosphorylation but must interact with other mechanisms for development of Alzheimer's disease.
引用
收藏
页码:3100 / 3105
页数:6
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