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J Clin Invest. 2005 Oct;115(10):2934-43. Epub 2005 Sep 22.

Cathepsin L is essential for onset of autoimmune diabetes in NOD mice.

Author information

1
Department of Pathology, Harvard Medical School, Boston, Massachusetts 02115, USA.

Abstract

Lysosomal proteases generate peptides presented by class II MHC molecules to CD4+ T cells. To determine whether specific lysosomal proteases might influence the outcome of a CD4+ T cell-dependent autoimmune response, we generated mice that lack cathepsin L (Cat L) on the autoimmune diabetes-prone NOD inbred background. The absence of Cat L affords strong protection from disease at the stage of pancreatic infiltration. The numbers of I-A(g7)-restricted CD4+ T cells are diminished in Cat L-deficient mice, although a potentially diabetogenic T cell repertoire persists. Within the CD4+ T cell compartments of Cat L-deficient mice, there is an increased proportion of regulatory T cells compared with that in Cat L-sufficient littermates. We suggest that it is this displaced balance of regulatory versus aggressive CD4+ T cells that protects Cat L-deficient mice from autoimmune disease. Our results identify Cat L as an enzyme whose activity is essential for the development of type I diabetes in the NOD mouse.

PMID:
16184198
PMCID:
PMC1224301
DOI:
10.1172/JCI25485
[Indexed for MEDLINE]
Free PMC Article

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