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Expression of the H‐2 Antigenic Complex on Murine Haematopoietic Stem Cells
Author(s) -
FITCHEN J. H.,
HAYS E. F.,
FERRONE S.
Publication year - 1982
Publication title -
scandinavian journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.934
H-Index - 88
eISSN - 1365-3083
pISSN - 0300-9475
DOI - 10.1111/j.1365-3083.1982.tb00682.x
Subject(s) - antigen , haematopoiesis , monoclonal antibody , stem cell , microbiology and biotechnology , biology , antibody , bone marrow , immunology
We used hybridoma‐derived monoclonal antibody to H‐2K k antigens and xenoantibodies to β 2 ‐microglobulin (β 2 ) to study the expression of the H‐2 antigenic molecular complex on murine hematopoietic stem cells and the effect of long‐term culture in vitro on the expression of these antigens. Monoclonal anti‐H‐2K k antibody produced potent complement‐dependent inhibition of pluripotent (CFU‐S), myeloid (CFU‐C), and erythroid (CFU‐E) stem cells from the bone marrow of C3H and AKR (H‐2 k ) mice and was without effect on stem cells from Balb/C (H‐2 d ) mice. Anti‐β 2 m xenoantibodies inhibited stem cells from all three strains. Stem cells could not be ‘rescued’ from the inhibitory effects of the antibodies by the addition of thymocytes to marrow cells after antibody treatment. Both the anti‐H‐2K k monoclonal antibody and the anti‐β 2 m xenoantibodies produced potent inhibition of AKR (H‐2 k ) CFU‐C that had been maintained in culture for up to 6 weeks. These results indicate that murine CFU‐S, CFU‐C, and CFU‐E express H‐2 antigens and that the expression of these antigens by CFU‐C is not altered during long‐term culture.
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