| Literature DB >> 22924552 |
Yaíma L Lightfoot1, Jing Chen, Clayton E Mathews.
Abstract
Type 1 diabetes (T1D) is a chronic, multifactorial disorder that results from a contretemps of genetic and environmental factors. Autoimmune attack and functional inhibition of the insulin-producing β cells in the pancreas lead to the inability of β cells to metabolize glucose, and thus results the hallmark clinical symptom of diabetes: abnormally high blood glucose levels. Treatment and protection from T1D require a detailed knowledge of the molecular effectors and the mechanism(s) of cell death leading to β-cell demise. Primary islets and surrogate β cells have been utilized in vitro to investigate in isolation-specific mechanisms associated with progression to T1D in vivo. This review focuses on the data obtained from these experiments. Studies using transformed β cells of human sources are described.Entities:
Mesh:
Year: 2012 PMID: 22924552 PMCID: PMC3703770 DOI: 10.1111/j.1365-2362.2012.02711.x
Source DB: PubMed Journal: Eur J Clin Invest ISSN: 0014-2972 Impact factor: 4.686