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Low‐density cells isolated from the rat thymus resemble branched cortical macrophages and have a reduced capability of rescuing double‐positive thymocytes from apoptosis in the BB‐DP rat
Author(s) -
Sommandas Vinod,
Rutledge Elizabeth A.,
Van Yserloo Brian,
Fuller Jessica,
Lernmark Åke,
Drexhage Hemmo A.
Publication year - 2007
Publication title -
journal of leukocyte biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.819
H-Index - 191
eISSN - 1938-3673
pISSN - 0741-5400
DOI - 10.1189/jlb.0407213
Subject(s) - biology , congenic , autoimmunity , apoptosis , microbiology and biotechnology , thymocyte , endocrinology , medicine , t cell , immunology , gene , immune system , biochemistry
Biobreeding‐diabetes prone (BB‐DP) rats spontaneously develop organ‐specific autoimmunity and are severely lymphopenic and particularly deficient in ART2 + regulatory T cells. A special breed, the so‐called BB‐diabetic‐resistant (DR) rats, are not lymphopenic and do not develop organ‐specific autoimmunity. The genetic difference between both strains is the lymphopenia ( lyp ) gene. Intrathymic tolerance mechanisms are important to prevent autoimmunity, and next to thymus epithelial cells, thymus APC play a prominent part in this tolerance. We here embarked on a study to detect defects in thymus APC of the BB‐DP rat and isolated thymus APC using a protocol based on the low‐density and nonadherent character of the cells. We used BB‐DP, BB‐DR, wild‐type F344, and F344 rats congenic for the lyp gene‐containing region. The isolated thymus, nonadherent, low‐density cells appeared to be predominantly ED2 + branched cortical macrophages and not OX62 + thymus medullary and cortico‐medullary dendritic cells. Functionally, these ED2 + macrophages were excellent stimulators of T cell proliferation, but it is more important that they rescued double‐positive thymocytes from apoptosis. The isolated thymus ED2 + macrophages of the BB‐DP and the F344. lyp/lyp rat exhibited a reduced T cell stimulatory capacity as compared with such cells of nonlymphopenic rats. They had a strongly diminished capability of rescuing thymocytes from apoptosis (also of ART2 + T cells) and showed a reduced Ian5 expression (as lyp/lyp thymocytes do). Our experiments strongly suggest that branched cortical macrophages play a role in positive selection of T cells in the thymus and point to defects in these cells in BB‐DP rats.