Roles for cathepsins S, L, and B in insulitis and diabetes in the NOD mouse

J Autoimmun. 2010 Mar;34(2):96-104. doi: 10.1016/j.jaut.2009.07.003. Epub 2009 Aug 6.

Abstract

We developed a panel of non-obese diabetic (NOD) mice deficient in major lysosomal cysteine proteases (cathepsins S, L and B) to identify protease enzymes essential for autoimmune diabetes. Null alleles for cathepsins (Cts) S, L or B were introgressed onto the NOD genetic background with 19 Idd markers at homozygosity. Diabetes onset was determined among females aged up to 6 months. We evaluated insulitis and sialadenitis in tissues using histology and computer assisted morphology. NOD mice deficient in Ctss or Ctsb were partially protected from diabetes with incidence at 33% and 28%, respectively, versus wild-type NOD (69%; p < 0.00001). NODs lacking cathepsin L (Ctsl-/-) are completely protected from IDDM, as originally shown by others. Ctsl, Ctss, or Ctsb heterozygous mice were able to develop IDDM, although incidence levels were significantly lower for Ctsb+/- (50%) and Ctsl+/- (55%) as compared to NODs (69%; p < 0.03). Ctsl-/- mice contain functional, diabetogenic T cells and an enriched Foxp3+ regulatory T cell population, and diabetes resistance was due to the presence of an expanded population of regulatory T cells. These data provide additional information about the potency of the diabetogenic T cell population in Ctsl-/- mice which were comparable in potency to wild-type NOD mice. These data illustrate the critical contribution of each of these proteases in determining IDDM in the NOD mouse and provide a useful set of models for further studies.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age of Onset
  • Animals
  • CD4 Antigens / biosynthesis
  • Cathepsin B / genetics
  • Cathepsin B / immunology
  • Cathepsin B / metabolism*
  • Cathepsin L / genetics
  • Cathepsin L / immunology
  • Cathepsin L / metabolism*
  • Cathepsins / genetics
  • Cathepsins / immunology
  • Cathepsins / metabolism*
  • Cell Movement / genetics
  • Diabetes Mellitus, Type 1 / genetics
  • Diabetes Mellitus, Type 1 / metabolism*
  • Diabetes Mellitus, Type 1 / pathology
  • Diabetes Mellitus, Type 1 / physiopathology
  • Female
  • Forkhead Transcription Factors / biosynthesis
  • Lymphopenia
  • Mice
  • Mice, Congenic
  • Mice, Inbred C57BL
  • Mice, Inbred NOD
  • Mice, Knockout
  • Pancreatitis
  • Sialadenitis
  • T-Lymphocyte Subsets / pathology
  • T-Lymphocytes, Regulatory / pathology

Substances

  • CD4 Antigens
  • Forkhead Transcription Factors
  • Foxp3 protein, mouse
  • Cathepsins
  • Cathepsin B
  • Cathepsin L
  • cathepsin S