Home LiteratureArticle Details
PMID: 15229375 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, P.H.S. Review

Rat models of type 1 diabetes: genetics, environment, and autoimmunity.

ILAR journal ·Vol. 45 ·No. 3 ·2004-00-00 ·Pages 278-91

Mordes JP, Bortell R, Blankenhorn EP, Rossini AA, Greiner DL

Abstract

For many years, the vast amount of data gathered from analysis of nonobese diabetic (NOD) and congenic NOD mice has eclipsed interest in the rat for the study of type 1 diabetes. The study of rat models has continued, however, and recently there has been a reanimation of interest for several reasons. First, genetic analysis of the rat has accelerated. Ian4L1, cblb, and Iddm4 are now known to play major roles in rat autoimmunity. Second, rats are amenable to study the interactions of genetics and environment that may be critical for disease expression in humans. Environmental perturbants that predictably enhance the expression of rat autoimmune diabetes include viral infection, toll-like receptor ligation, and depletion of regulatory T cell populations. Finally, data generated in the rat have correctly predicted the outcome of several human diabetes prevention trials, notably the failure of nicotinamide and low dose parenteral and oral insulin therapies.

MeSH Terms
Animals Autoimmunity/genetics Diabetes Mellitus, Type 1/genetics,immunology Disease Models, Animal Genetic Predisposition to Disease Immunogenetics Rats Rats, Inbred BB
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Mordes John P
Department of Medicine, University of Massachusetts, Medical School, Worcester, MA, USA.
Bortell Rita
Blankenhorn Elizabeth P
Rossini Aldo A
Greiner Dale L
Article Info
Journal
ILAR journal
Abbr.
ILAR J
ISSN
1084-2020
Published
2004-00-00
Pages
278-91
Language
English
Region
England
NLM ID
9516416
Subset
IM
Grants
NIDDK NIH HHS · DK25306 · United States
NIDDK NIH HHS · DK36024 · United States
NIDDK NIH HHS · DK49106 · United States
NIDDK NIH HHS · P01-DK053006 · United States
NIDDK NIH HHS · P30-DK32520 · United States
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