Immunohistology of lymphoid and non-lymphoid cells in the thymus in relation to T lymphocyte differentiation

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Abstract
The present paper reports the distribution of lymphoid and non‐lymphoid cell types in the thymus of mice. To this purpose, we employed scanning electron microscopy and immunohistology. For immunohistology we used the immunoperoxidase method and incubated frozen sections of the thymus with (1) monoclonal antibodies detecting cell‐surface‐differentiation antigens on lymphoid cells, such as Thy‐1, T‐200, Lyt‐1, Lyt‐2, and MEL‐14; (2) Mococlonal antibodies detecting the major histocompatibility (MHC) antigens, H‐2K, I‐A, I‐E, and H‐2D; and (3) monoclonal antibodies directed against cell‐surface antigens associated with cells of the mononuclear phagocyte system, such as Mac‐1, Mac‐2, and Mac‐3. The results of this study indicate that subsets of T lymphocytes are not randomly distributed throughout the thymic parenchyma; rather they are localized in discrete domains. Two major and four minor subpopulations of thymocytes can be detected in frozen sections of the thymus: (1) the majority of cortical thymocytes are strongly Thy‐1+ (positive), strongly T‐200+, variable in Lyt‐1 expression, and strongly Lyt‐2+; (2) the majority of medullary thymocytes are weakly Thy‐1+, strongly T‐200+, strongly Lyt‐1+, and Lyt‐2− (negative); (3) a minority of medullary cells are weakly Thy‐1+, T‐200+, strongly Lyt‐1+, and strongly Lyt‐2+; (4) a small subpopulation of subcapsular lymphoblasts is Thy‐1+, T‐200+, and negative for the expression of Lyt‐1 and Lyt‐2 antigens; (5) a small subpopulation of subcapsular lymphoblasts is only Thy‐1+ but T‐200− and Lyt−; and (6) a small subpopulation of subcapsular lymphoblasts is negative for all antisera tested. Surprisingly, a few individual cells in the thymic cortex, but not in the medulla, react with antibodies directed to MEL‐14, a receptor involved in the homing of lymphocytes in peripheral lymphoid organs. MHC antigens (I‐A, I‐E, H‐2K) are mainly expressed on stromal cells in the thymus, as well as on medullary thymocytes. H‐2D is also expressed at a low density on cortical thymocytes. In general, anti‐MHC antibodies reveal epithelial‐reticular cells in the thymic cortex, in a fine dendritic staining pattern. In the medulla, the labeling pattern is more confluent and most probably associated with bone‐marrow‐derived interdigitating reticular cells and medullary thymocytes. We discuss the distribution of the various lymphoid and non‐lymphoid subpopulations within the thymic parenchyma in relation to recently published data on the differentiation of T lymphocytes.