A major pathological feature of type 2 diabetes is skeletal muscle insulin resistance. Contraction of skeletal muscle results in a very large increase in glucose uptake independent of insulin. The complete signal transduction pathways mediating contraction and insulin stimulated glucose uptake in skeletal muscle are not known, nor is it understood if or where these signaling pathways converge. Novel research from the Goodyear laboratory has recently provided evidence that the Akt Substrate of 160 kDa (AS160) regulates both contraction and insulin stimulated glucose transport in skeletal muscle. Therefore, the primary objective of my research project is to determine how AS160 regulates glucose transport in skeletal muscle. Determining how AS160 regulates glucose uptake requires elucidation of the temporal-spatial dynamics of the AS160 protein network in response to both contraction and insulin. This will be accomplished by determining the subcellular localization of AS160, identifying sites on the AS160 molecule that are phosphorylated, and disovering novel AS160 interacting proteins. These studies will provide important mechanistic data that could eventually lead to novel therapies for the treatment of type 2 diabetes. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32DK075851-01
Application #
7111210
Study Section
Special Emphasis Panel (ZRG1-F06-E (20))
Program Officer
Hyde, James F
Project Start
2006-04-01
Project End
2009-03-31
Budget Start
2006-04-01
Budget End
2007-03-31
Support Year
1
Fiscal Year
2006
Total Cost
$45,976
Indirect Cost
Name
Joslin Diabetes Center
Department
Type
DUNS #
071723084
City
Boston
State
MA
Country
United States
Zip Code
02215
Treebak, Jonas T; Taylor, Eric B; Witczak, Carol A et al. (2010) Identification of a novel phosphorylation site on TBC1D4 regulated by AMP-activated protein kinase in skeletal muscle. Am J Physiol Cell Physiol 298:C377-85
An, Ding; Toyoda, Taro; Taylor, Eric B et al. (2010) TBC1D1 regulates insulin- and contraction-induced glucose transport in mouse skeletal muscle. Diabetes 59:1358-65
Taylor, Eric B; An, Ding; Kramer, Henning F et al. (2008) Discovery of TBC1D1 as an insulin-, AICAR-, and contraction-stimulated signaling nexus in mouse skeletal muscle. J Biol Chem 283:9787-96
Kramer, Henning F; Taylor, Eric B; Witczak, Carol A et al. (2007) Calmodulin-binding domain of AS160 regulates contraction- but not insulin-stimulated glucose uptake in skeletal muscle. Diabetes 56:2854-62
Kramer, Henning F; Witczak, Carol A; Taylor, Eric B et al. (2006) AS160 regulates insulin- and contraction-stimulated glucose uptake in mouse skeletal muscle. J Biol Chem 281:31478-85