TY - JOUR
T1 - Immunochemical Characterization of Differentiation and Age-related Cell Surface Antigens Expressed by Chicken Erythrocytes
AU - Kline, Kimberly
AU - Allison, James P.
AU - McIntyre, Bradley W.
AU - Sanders, Bob G.
PY - 1984/8/1
Y1 - 1984/8/1
N2 - Hematopoietic-lymphoid membrane antigens that are related to ceil differentiation and development, referred to as chicken fetal antigen (CFA) and chicken adult antigen (CAA) were im-munochemically characterized; Mr 220,000; Mr 170,000; Mr 130,000; M, 99,000; M, 88,000; M, 50,000; and M, 24,000 CFA molecules are detected on embryonic RBC, and M, 210,000; M, 130,000; Mr 102,000; M, 56,000; M, 48,000; and Mr 43,000 CAA molecules are detected on adult RBC. Limited peptide mapping analyses showed all of the CFA and CAA molecules to be distinct entities. Both the M, 50,000 CFA and the M, 43,000 CAA molecules exhibited multiple isomorphic variants when analyzed by 2-dimensional electrophoresis. Analyses involving neuraminidase treatments and limited peptide mapping showed the M, 50,000 CFA isomorphic variants to be chemically identical with the isoelectric point variations being due to sialic add differences. In addition to multiple isomorphic variants, the molecular weight and charge differences of which were diminished by neuraminidase treatments, the M, 43,000 CAA molecules exhibited a doublet pattern suggesting that the polyclonal antisera may be detecting chicken major histocompatibility complex products. Analyses of the M, 50,000 CFA molecules immunoprecipitated with monoclonal antibody 190-4 confirmed that the monoclonal antibody recognizes a serological subset of the M, 50,000 CFA molecules but showed that it did not recognize a unique molecularly detectable subset among the 18 isomorphic variants discernable by 2-dimensional electrophoretic analyses. Cocapping analyses with splenic lymphocytes showed CFA and CAA to occur as distinct membrane entities on lymphocytes.
AB - Hematopoietic-lymphoid membrane antigens that are related to ceil differentiation and development, referred to as chicken fetal antigen (CFA) and chicken adult antigen (CAA) were im-munochemically characterized; Mr 220,000; Mr 170,000; Mr 130,000; M, 99,000; M, 88,000; M, 50,000; and M, 24,000 CFA molecules are detected on embryonic RBC, and M, 210,000; M, 130,000; Mr 102,000; M, 56,000; M, 48,000; and Mr 43,000 CAA molecules are detected on adult RBC. Limited peptide mapping analyses showed all of the CFA and CAA molecules to be distinct entities. Both the M, 50,000 CFA and the M, 43,000 CAA molecules exhibited multiple isomorphic variants when analyzed by 2-dimensional electrophoresis. Analyses involving neuraminidase treatments and limited peptide mapping showed the M, 50,000 CFA isomorphic variants to be chemically identical with the isoelectric point variations being due to sialic add differences. In addition to multiple isomorphic variants, the molecular weight and charge differences of which were diminished by neuraminidase treatments, the M, 43,000 CAA molecules exhibited a doublet pattern suggesting that the polyclonal antisera may be detecting chicken major histocompatibility complex products. Analyses of the M, 50,000 CFA molecules immunoprecipitated with monoclonal antibody 190-4 confirmed that the monoclonal antibody recognizes a serological subset of the M, 50,000 CFA molecules but showed that it did not recognize a unique molecularly detectable subset among the 18 isomorphic variants discernable by 2-dimensional electrophoretic analyses. Cocapping analyses with splenic lymphocytes showed CFA and CAA to occur as distinct membrane entities on lymphocytes.
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M3 - Article
C2 - 6378372
AN - SCOPUS:0021139050
SN - 0008-5472
VL - 44
SP - 3576
EP - 3583
JO - Cancer Research
JF - Cancer Research
IS - 8
ER -