| Literature DB >> 2649381 |
E Houssaint1, O Lassila, O Vainio.
Abstract
Genetically polymorphic cell surface antigen, Bu-1, is expressed on B cells as well as on a subset of macrophages. Bu-1+ cells are also present in embryonic spleen and bone marrow, and these could represent prebursal precursors for B cells and Bu-1+ macrophages. To test the repopulation capacity of these cells we sorted 14-day embryonic spleen cells from Bu-1a-homozygous donors into Bu-1a+ and Bu-1a- fractions and transferred them into age-matched irradiated Bu-1b-homozygous recipients. Four to six weeks after hatching, the recipients were analyzed for Bu-1 chimerism. The results demonstrate that B cell precursors are exclusively present in the Bu-1+ population of 14-day embryonic spleen, whereas the Bu-1+ macrophage subpopulation can be repopulated by either the Bu-1+ or the Bu-1- fraction of these embryonic cells. Bone marrow cells from young chickens could also repopulate the Bu-1+ macrophage subset but not the B cell compartment, thus confirming previous data that postnatal bone marrow does not contain B cell precursors. These results demonstrate that all B cell precursors in the 14-day embryonic spleen carry the Bu-1 antigen, and suggest that there is no lineage relationship between the Bu-1+ cells and macrophages.Entities:
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Year: 1989 PMID: 2649381 DOI: 10.1002/eji.1830190204
Source DB: PubMed Journal: Eur J Immunol ISSN: 0014-2980 Impact factor: 5.532