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Differential Expression Of Adhesion Molecules Within The Human Thymus

Development of a diverse, MHC-restricted yet self-tolerant T-cell repertoire occurs within the thymus, and requires contact between developing T cells and their stromal microenvironment. Such interactions are likely to depend on the combinatorial effect of specific adhesion molecules. As a prelimina...

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Detalles Bibliográficos
Autores principales: Reza, Julie Naima, Ritter, Mary A.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 1994
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2275941/
https://www.ncbi.nlm.nih.gov/pubmed/7620326
http://dx.doi.org/10.1155/1994/49301
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author Reza, Julie Naima
Ritter, Mary A.
author_facet Reza, Julie Naima
Ritter, Mary A.
author_sort Reza, Julie Naima
collection PubMed
description Development of a diverse, MHC-restricted yet self-tolerant T-cell repertoire occurs within the thymus, and requires contact between developing T cells and their stromal microenvironment. Such interactions are likely to depend on the combinatorial effect of specific adhesion molecules. As a preliminary step to determining their role in T-cell development, we have studied the distribution of LFA-1/ICAM-1, CD2/LFA-3, VLA-4/VCAM-1, and HECA 452-antigen/E-Selectin ligand pairs on frozen sections of human thymus. Using two color-immunohistochemistry, and a variety of cell-lineage markers that reveal the nature of the cells on which these adhesion molecules are located, we find a differential distribution of adhesion molecules, with some being shared by both endothelial and epithelial cells. We also identify the VCAM-1-positive subpopulation as cortical macrophages. The relevance of these findings to thymopoiesis is discussed.
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spelling pubmed-22759412008-03-31 Differential Expression Of Adhesion Molecules Within The Human Thymus Reza, Julie Naima Ritter, Mary A. Dev Immunol Research Article Development of a diverse, MHC-restricted yet self-tolerant T-cell repertoire occurs within the thymus, and requires contact between developing T cells and their stromal microenvironment. Such interactions are likely to depend on the combinatorial effect of specific adhesion molecules. As a preliminary step to determining their role in T-cell development, we have studied the distribution of LFA-1/ICAM-1, CD2/LFA-3, VLA-4/VCAM-1, and HECA 452-antigen/E-Selectin ligand pairs on frozen sections of human thymus. Using two color-immunohistochemistry, and a variety of cell-lineage markers that reveal the nature of the cells on which these adhesion molecules are located, we find a differential distribution of adhesion molecules, with some being shared by both endothelial and epithelial cells. We also identify the VCAM-1-positive subpopulation as cortical macrophages. The relevance of these findings to thymopoiesis is discussed. Hindawi Publishing Corporation 1994 /pmc/articles/PMC2275941/ /pubmed/7620326 http://dx.doi.org/10.1155/1994/49301 Text en Copyright © 1994 Hindawi Publishing Corporation. http://creativecommons.org/licenses/by/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Reza, Julie Naima
Ritter, Mary A.
Differential Expression Of Adhesion Molecules Within The Human Thymus
title Differential Expression Of Adhesion Molecules Within The Human Thymus
title_full Differential Expression Of Adhesion Molecules Within The Human Thymus
title_fullStr Differential Expression Of Adhesion Molecules Within The Human Thymus
title_full_unstemmed Differential Expression Of Adhesion Molecules Within The Human Thymus
title_short Differential Expression Of Adhesion Molecules Within The Human Thymus
title_sort differential expression of adhesion molecules within the human thymus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2275941/
https://www.ncbi.nlm.nih.gov/pubmed/7620326
http://dx.doi.org/10.1155/1994/49301
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