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PMID: 15662003 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Type 2 diabetes-a matter of beta-cell life and death?

Science (New York, N.Y.) ·Vol. 307 ·No. 5708 ·2005-01-21 ·Pages 380-4

Rhodes CJ

Abstract

In type 2 diabetes, the beta cells of the pancreas fail to produce enough insulin to meet the body's demand, in part because of an acquired decrease in beta-cell mass. In adults, pancreatic beta-cell mass is controlled by several mechanisms, including beta-cell replication, neogenesis, hypertrophy, and survival. Here, I discuss evidence supporting the notion that increased beta-cell apoptosis is an important factor contributing to beta-cell loss and the onset of type 2 diabetes. Interestingly, a key signaling molecule that promotes beta-cell growth and survival, insulin receptor substrate 2 (IRS-2), is a member of a family of proteins whose inhibition contributes to the development of insulin resistance in the liver and other insulin-responsive tissues. Thus, the IRS-2 pathway appears to be a crucial participant in the tenuous balance between effective pancreatic beta-cell mass and insulin resistance.

MeSH Terms
Adaptation, Physiological Animals Apoptosis Cell Count Cell Division Cell Size Cell Survival Cytokines/metabolism Diabetes Mellitus, Type 2/physiopathology Homeostasis Humans Hyperglycemia/physiopathology Hyperlipidemias/physiopathology Insulin/metabolism Insulin Receptor Substrate Proteins Insulin Resistance Intracellular Signaling Peptides and Proteins Islets of Langerhans/cytology,physiology Lipid Metabolism Obesity/physiopathology Phosphoproteins/metabolism Signal Transduction
Chemicals
Cytokines IRS2 protein, human Insulin Insulin Receptor Substrate Proteins Intracellular Signaling Peptides and Proteins Phosphoproteins
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Rhodes Christopher J
Pacific Northwest Research Institute, 720 Broadway, Seattle, WA 98122, USA. cjr@pnri.org
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
1095-9203
Published
2005-01-21
Pages
380-4
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIDDK NIH HHS · DK-55267 · United States
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