Thymic epithelial defects and predisposition to autoimmune disease in BB rats
- PMID: 7992854
- PMCID: PMC1887500
Thymic epithelial defects and predisposition to autoimmune disease in BB rats
Abstract
We report an association between thymic epithelial defects and predisposition to autoimmunity. Diabetes-prone (DP) BB rats develop spontaneous hyperglycemia and are deficient in T cell subsets expressing the RT6 alloantigen. Diabetes resistant (DR) BB rats become diabetic if depleted of RT6+ T cells. The inciting immune system defects are unknown. We made the following observations: 1) Regions of thymic cortex and medulla devoid of thymic epithelium exist in DP-BB, DR-BB, and Lewis rats, all of which are susceptible to autoimmune disorders. Such defects were absent in eight normal rat strains. 2) Thymic epithelial defects are absent at birth, but present in BB rats at 4 weeks of age. 3) The genetic predisposition to thymic epithelial defects is an autosomal dominant trait. 4) The observation of thymic defects in (DP x WF)F1 rats led to the prediction that such animals, which never develop spontaneous autoimmunity, might be susceptible to its induction. Following depletion of RT6+ T cells we observed diabetes in 91%, and thyroiditis in 43%, of treated F1 animals (n = 23). Pancreatic insulitis was uniformly present. Because thymic epithelium participates in the positive and negative selection of developing thymocytes, we propose that thymic epithelial defects may play an important role in the predisposition of BB rats to autoimmunity.
Similar articles
-
Ontogeny and immunohistochemical localization of thymus-dependent and thymus-independent RT6+ cells in the rat.Am J Pathol. 1996 Jun;148(6):2043-56. Am J Pathol. 1996. PMID: 8669488 Free PMC article.
-
Recapitulation of normal and abnormal BioBreeding rat T cell development in adult thymus organ culture.J Immunol. 1999 Apr 1;162(7):4003-12. J Immunol. 1999. PMID: 10201921
-
Absence of RT6+ T cells in diabetes-prone biobreeding/Worcester rats is due to genetic and cell developmental defects.J Immunol. 1988 Dec 15;141(12):4146-51. J Immunol. 1988. PMID: 3058800
-
The spontaneously diabetic BB rat: sites of the defects leading to autoimmunity and diabetes mellitus. A review.Curr Top Microbiol Immunol. 1990;156:1-14. doi: 10.1007/978-3-642-75239-1_1. Curr Top Microbiol Immunol. 1990. PMID: 2199161 Review.
-
Thymic neuroendocrine self-antigens. Role in T-cell development and central T-cell self-tolerance.Ann N Y Acad Sci. 2000;917:710-23. doi: 10.1111/j.1749-6632.2000.tb05435.x. Ann N Y Acad Sci. 2000. PMID: 11268399 Review.
Cited by
-
The iddm4 locus segregates with diabetes susceptibility in congenic WF.iddm4 rats.Diabetes. 2002 Nov;51(11):3254-62. doi: 10.2337/diabetes.51.11.3254. Diabetes. 2002. PMID: 12401717 Free PMC article.
-
Ontogeny and immunohistochemical localization of thymus-dependent and thymus-independent RT6+ cells in the rat.Am J Pathol. 1996 Jun;148(6):2043-56. Am J Pathol. 1996. PMID: 8669488 Free PMC article.
-
Genetic susceptibility in type 1 diabetes and its associated autoimmune disorders.Rev Endocr Metab Disord. 2003 Sep;4(3):243-53. doi: 10.1023/a:1025100328425. Rev Endocr Metab Disord. 2003. PMID: 14501175 Review. No abstract available.
-
Lymphopenia in the BB rat model of type 1 diabetes is due to a mutation in a novel immune-associated nucleotide (Ian)-related gene.Genome Res. 2002 Jul;12(7):1029-39. doi: 10.1101/gr.412702. Genome Res. 2002. PMID: 12097339 Free PMC article.
References
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Medical