Insulin Regulates Astrocytic Glucose Handling Through Cooperation With IGF-I

Author:

Fernandez Ana M.12,Hernandez-Garzón Edwin12,Perez-Domper Paloma12,Perez-Alvarez Alberto13,Mederos Sara1,Matsui Takashi4,Santi Andrea12,Trueba-Saiz Angel12,García-Guerra Lucía25,Pose-Utrilla Julia25,Fielitz Jens67,Olson Eric N.8,Fernandez de la Rosa Ruben9,Garcia Garcia Luis9,Pozo Miguel Angel9,Iglesias Teresa25,Araque Alfonso1,Soya Hideaki4,Perea Gertrudis1,Martin Eduardo D.10,Torres Aleman Ignacio12

Affiliation:

1. Cajal Institute, Consejo Superior de Investigaciones Científicas, Madrid, Spain

2. CIBERNED, Madrid, Spain

3. Center for Molecular Neurobiology Hamburg, Hamburg, Germany

4. Laboratory of Exercise Biochemistry and Neuroendocrinology, University of Tsukuba, Tsukuba, Japan

5. Instituto de Investigaciones Biomédicas “Alberto Sols,” Consejo Superior de Investigaciones Científicas-Universidad Autónoma de Madrid, Madrid, Spain

6. Experimental and Clinical Research Center, Charité-Universitätsmedizin, Max Delbrück Center for Molecular Medicine, Berlin, Germany

7. Brandenburg Heart Center and Medical University of Brandenburg, Brandenburg, Germany

8. University of Texas Southwestern Medical Center, Dallas, TX

9. Pluridisciplinary Institute, Complutense University of Madrid, Madrid, Spain

10. Science and Technology Park, Institute for Research in Neurological Disabilities, University of Castilla-La Mancha, Albacete, Spain

Abstract

Brain activity requires a flux of glucose to active regions to sustain increased metabolic demands. Insulin, the main regulator of glucose handling in the body, has been traditionally considered not to intervene in this process. However, we now report that insulin modulates brain glucose metabolism by acting on astrocytes in concert with IGF-I. The cooperation of insulin and IGF-I is needed to recover neuronal activity after hypoglycemia. Analysis of underlying mechanisms show that the combined action of IGF-I and insulin synergistically stimulates a mitogen-activated protein kinase/protein kinase D pathway resulting in translocation of GLUT1 to the cell membrane through multiple protein-protein interactions involving the scaffolding protein GAIP-interacting protein C terminus and the GTPase RAC1. Our observations identify insulin-like peptides as physiological modulators of brain glucose handling, providing further support to consider the brain as a target organ in diabetes.

Funder

MINECO

CIBERNED

Comunidad de Madrid

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

Cited by 64 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3