Serine Phosphorylation of Insulin Receptor Substrate 1 by Inhibitor κB Kinase Complex
Pennington Biomedical Research Center · Louisiana State University · +2 more institutions
Abstract
Insulin resistance contributes importantly to the pathophysiology of type 2 diabetes mellitus. One mechanism mediating insulin resistance may involve the phosphorylation of serine residues in insulin receptor substrate-1 (IRS-1), leading to impairment in the ability of IRS-1 to activate downstream phosphatidylinositol 3-kinase-dependent pathways. Insulin-resistant states and serine phosphorylation of IRS-1 are associated with the activation of the inhibitor kappaB kinase (IKK) complex. However, the precise molecular mechanisms by which IKK may contribute to the development of insulin resistance are not well understood. In this study, using phosphospecific antibodies against rat IRS-1 phosphorylated at Ser(307)…
Citation impact
- FWCI
- 10.40
- Percentile
- 100%
- References
- 64
Authors
7- ZGZhan‐Guo GaoCorresponding
Pennington Biomedical Research Center
- DHDaniel Hwang
Pennington Biomedical Research Center, Louisiana State University
- FBFredly Bataille
National Institutes of Health, National Center for Complementary and Integrative Health
- MLMichael Lefevre
Pennington Biomedical Research Center, Louisiana State University
- DADavid A. York
Pennington Biomedical Research Center, Louisiana State University
Topics & keywords
- Insulin receptor
- Insulin receptor substrate
- Phosphorylation
- Serine
- IRS1
- Chemistry
- Substrate (aquarium)
- Cell biology
- Good health and well-being