Literature DB >> 1372574

Multiple TCR V beta usage by infiltrates of young NOD mouse islets of Langerhans. A polymerase chain reaction analysis.

S H Waters1, J J O'Neil, D T Melican, M C Appel.   

Abstract

Because a restricted repertoire of T-cell receptor (TCR) V beta gene expression has been reported in other autoimmune diseases, the possibility of similarly restricted V beta gene expression by T-cell infiltrates of NOD mouse islets was examined. With isolated islets from 4- to 12-wk-old NOD mice, a prospective polymerase chain reaction analysis with 18 V beta-specific oligonucleotide primers was performed on the noncloned and unexpanded islet-infiltrating T cells. The methodology used permitted the detection of a minimum of 50 T cells. In contrast to the restricted TCR V beta gene usage reported for other autoimmune diseases, infiltrates of even the youngest mice were characterized by expression of multiple V beta gene segments.

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Year:  1992        PMID: 1372574     DOI: 10.2337/diab.41.3.308

Source DB:  PubMed          Journal:  Diabetes        ISSN: 0012-1797            Impact factor:   9.461


  11 in total

1.  Beta cell expression of endogenous xenotropic retrovirus distinguishes diabetes-susceptible NOD/Lt from resistant NON/Lt mice.

Authors:  H R Gaskins; M Prochazka; K Hamaguchi; D V Serreze; E H Leiter
Journal:  J Clin Invest       Date:  1992-12       Impact factor: 14.808

2.  Recruitment of multiple V beta genes in the TCR repertoire against a single pathogenic thyroglobulin epitope.

Authors:  V P Rao; R S Russell; G Carayanniotis
Journal:  Immunology       Date:  1997-08       Impact factor: 7.397

3.  In search of TCR restriction in autoreactive T cell in human autoimmunity: why is it so elusive?

Authors:  C Navarrete; G F Bottazzo
Journal:  Clin Exp Immunol       Date:  1993-02       Impact factor: 4.330

4.  T-cell receptor V beta repertoire of L3T4+ regulatory T cells in anti-L3T4 antibody-induced tolerant NOD mice.

Authors:  A Sakamoto; M Furukawa; I Iwamoto; T Koike; H Tomioka; T Sumida
Journal:  Immunology       Date:  1994-12       Impact factor: 7.397

5.  Two genetic loci regulate T cell-dependent islet inflammation and drive autoimmune diabetes pathogenesis.

Authors:  C J Fox; A D Paterson; S M Mortin-Toth; J S Danska
Journal:  Am J Hum Genet       Date:  2000-06-09       Impact factor: 11.025

Review 6.  Mechanisms of autoimmunity in the non-obese diabetic mouse: effector/regulatory cell equilibrium during peak inflammation.

Authors:  Nadir Askenasy
Journal:  Immunology       Date:  2016-02-08       Impact factor: 7.397

7.  Restricted islet-cell reactive T cell repertoire of early pancreatic islet infiltrates in NOD mice.

Authors:  Felix J Baker; Mark Lee; Yueh-hsiu Chien; Mark M Davis
Journal:  Proc Natl Acad Sci U S A       Date:  2002-06-24       Impact factor: 11.205

8.  Major histocompatibility complex class I-restricted T cells are required for all but the end stages of diabetes development in nonobese diabetic mice and use a prevalent T cell receptor alpha chain gene rearrangement.

Authors:  T P DiLorenzo; R T Graser; T Ono; G J Christianson; H D Chapman; D C Roopenian; S G Nathenson; D V Serreze
Journal:  Proc Natl Acad Sci U S A       Date:  1998-10-13       Impact factor: 11.205

9.  T cell populations in the pancreatic lymph node naturally and consistently expand and contract in NOD mice as disease progresses.

Authors:  Idania Marrero; Allen Vong; Yang Dai; Joanna D Davies
Journal:  Mol Immunol       Date:  2012-05-10       Impact factor: 4.407

10.  Autoreactive effector/memory CD4+ and CD8+ T cells infiltrating grafted and endogenous islets in diabetic NOD mice exhibit similar T cell receptor usage.

Authors:  Ramiro Diz; Alaina Garland; Benjamin G Vincent; Mark C Johnson; Nicholas Spidale; Bo Wang; Roland Tisch
Journal:  PLoS One       Date:  2012-12-14       Impact factor: 3.240

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