Literature DB >> 2788823

Thymic cortical epithelial cells lack full capacity for antigen presentation.

R G Lorenz1, P M Allen.   

Abstract

Several recent studies have suggested that interactions between thymocytes and thymic stromal cells are essential for the development and elimination of antigen-reactive T lymphocytes. It is important, therefore, to characterize the stromal cells involved in presentation of antigen in the thymus. In a previous report, we demonstrated, using T-cell hybridomas, that three distinct types of antigen presenting cells in the thymus (cortical epithelial cells, macrophages, and dendritic cells) constitutively expressed self haemoglobin/Ia complexes. Here we report that one of these cell types, the cortical epithelial cell, does not induce stimulation of T-lymphocyte clones even though the antigen/Ia complex required for antigen-specific recognition is present. This lack of response occurs with both TH1 and TH2 clones. Responsiveness of the TH2 clone can be restored by adding the murine lymphokine interleukin-1 beta to the culture system.

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Year:  1989        PMID: 2788823     DOI: 10.1038/340557a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  16 in total

Review 1.  Questionable thymic nurse cell.

Authors:  M Pezzano; M Samms; M Martinez; J Guyden
Journal:  Microbiol Mol Biol Rev       Date:  2001-09       Impact factor: 11.056

Review 2.  Mechanisms of cell death.

Authors:  D J Fawthrop; A R Boobis; D S Davies
Journal:  Arch Toxicol       Date:  1991       Impact factor: 5.153

3.  A bone marrow-derived stroma cell line, ST2, can support the differentiation of fetal thymocytes from the CD4+ CD8+ double negative to the CD4+ CD8+ double positive differentiation stage in vitro.

Authors:  J Tong; H Kishi; T Matsuda; A Muraguchi
Journal:  Immunology       Date:  1999-08       Impact factor: 7.397

4.  Regulation of the costimulator B7, not class II major histocompatibility complex, restricts the ability of murine kidney tubule cells to stimulate CD4+ T cells.

Authors:  D T Hagerty; B D Evavold; P M Allen
Journal:  J Clin Invest       Date:  1994-03       Impact factor: 14.808

5.  Apoptosis of T lymphocytes in experimental autoimmune encephalomyelitis. Evidence for programmed cell death as a mechanism to control inflammation in the brain.

Authors:  M Schmied; H Breitschopf; R Gold; H Zischler; G Rothe; H Wekerle; H Lassmann
Journal:  Am J Pathol       Date:  1993-08       Impact factor: 4.307

6.  cAMP inhibits induction of interleukin 2 but not of interleukin 4 in T cells.

Authors:  T J Novak; E V Rothenberg
Journal:  Proc Natl Acad Sci U S A       Date:  1990-12       Impact factor: 11.205

7.  Mechanisms of tolerance induction in major histocompatibility complex class II-restricted T cells specific for a blood-borne self-antigen.

Authors:  T Zal; A Volkmann; B Stockinger
Journal:  J Exp Med       Date:  1994-12-01       Impact factor: 14.307

8.  Studies on T cell maturation on defined thymic stromal cell populations in vitro.

Authors:  E J Jenkinson; G Anderson; J J Owen
Journal:  J Exp Med       Date:  1992-09-01       Impact factor: 14.307

9.  Promiscuous gene expression in thymic epithelial cells is regulated at multiple levels.

Authors:  Jens Derbinski; Jana Gäbler; Benedikt Brors; Sascha Tierling; Sunitha Jonnakuty; Manfred Hergenhahn; Leena Peltonen; Jörn Walter; Bruno Kyewski
Journal:  J Exp Med       Date:  2005-06-27       Impact factor: 14.307

10.  Selective activation of the calcium signaling pathway by altered peptide ligands.

Authors:  J Sloan-Lancaster; T H Steinberg; P M Allen
Journal:  J Exp Med       Date:  1996-10-01       Impact factor: 14.307

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