Differential Expression Of Adhesion Molecules Within The Human Thymus
Author(s) -
Julie N. Reza,
Mary A. Ritter
Publication year - 1994
Publication title -
journal of immunology research
Language(s) - English
Resource type - Journals
eISSN - 2314-8861
pISSN - 2314-7156
DOI - 10.1155/1994/49301
Subject(s) - cell adhesion molecule , microbiology and biotechnology , biology , stromal cell , cell adhesion , neural cell adhesion molecule , major histocompatibility complex , lineage (genetic) , adhesion , antigen , cell , immunology , chemistry , genetics , cancer research , gene , organic chemistry
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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