Phenotypic Characterization of Chicken Bursal Stromal Elements
Author(s) -
Richard L. Boyd,
Trevor J. Wilson,
H.A. Ward,
Kathy Mitrangas
Publication year - 1990
Publication title -
journal of immunology research
Language(s) - English
Resource type - Journals
eISSN - 2314-8861
pISSN - 2314-7156
DOI - 10.1155/1990/97618
Subject(s) - stromal cell , biology , medulla , epithelium , stroma , phenotype , monoclonal antibody , cortex (anatomy) , pathology , parenchyma , thymocyte , microbiology and biotechnology , antigen , antibody , immunology , immunohistochemistry , gene , anatomy , genetics , cancer research , cd8 , medicine , botany , neuroscience
Many, if not all, of the different phases of intrabursal B-cell maturation are controlled by the stromal components. We have used an extensive panel of mAb to provide a detailed phenotypic profile of these cells. Antigenic specificities were defined for the entire surface epithelium, interfollicular surface epithelium, follicle-associated epithelium, basement membrane, basement membrane-associated epithelium. Several mAb were specific for the medulla, including those reactive with the stellate network of epithelial cells, isolated macrophages, and granular, apparently secreted antigens. One of these, MUI-92, appears to be bursa-specific. Two mAb reacted strongly with stellate cortical macrophages, one of which weakly stained similar cells in the medulla. MHC-class II antigens were expressed on endothelium of the corticomedullary junction, macrophagelike cells in the cortex, and medulla and B lymphocytes predominantly in the cortex. Collectively, these mAb have demonstrated the antigenically distinct nature of discrete regions in the bursa, but also the continuity of the surface epithelium with the corticomedullary junction and medulla. They represent excellent reagents for defining the stromal cell contribution of B-cell development.
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