A Platelet Membrane Glycoprotein (GP) Deficiency in Healthy Blood Donors: Naka Platelets Lack Detectable GPIV (CD36)

It has recently been shown that the Naka antigen, which is absent in 3% to 11% of Japanese blood donors, is expressed on platelet glycoprotein IV (GPIV; CD36) (Tomiyama et al, BLOOD, 75:684, 1990). In the present studies, flow cytometry was used to distinguish differences in the reactivity of Naka+...

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Veröffentlicht in:Blood 1990-11, Vol.76 (9), p.1698-1703
Hauptverfasser: Yamamoto, Naomasa, Ikeda, Hisami, Tandon, Narendra N., Herman, Jay, Tomiyama, Yoshiaki, Mitani, Takako, Sekiguchi, Sadayoshi, Lipsky, Robert, Kralisz, Urszula, Jamieson, G.A.
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Sprache:eng
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Zusammenfassung:It has recently been shown that the Naka antigen, which is absent in 3% to 11% of Japanese blood donors, is expressed on platelet glycoprotein IV (GPIV; CD36) (Tomiyama et al, BLOOD, 75:684, 1990). In the present studies, flow cytometry was used to distinguish differences in the reactivity of Naka+ and Naka- platelets with both OKM5, a monoclonal antibody that recognizes an epitope on GPIV, and with polyclonal anti-GPIV antibody. OKM5 was also used to screen 871 platelet concentrates prepared from healthy US blood donors. Three of these showed markedly deficient binding of 125l-OKM5 or an incidence of 0.34%. Two of these donors were re-accessed and showed less than 1% binding of 125l-OKM5 as compared with 10,300 ± 1,500 binding sites per platelet in controls (n = 4). Platelets from these two US donors were radiolabeled (125l, 3H) and compared with control platelets and with platelets from Japanese Naka+ and Naka- donors by crossed Immunoelectrophoresis, protein blots, immunoprecipitation, and two-dimensional gel electrophoresis. GPIV could not be detected by any of these techniques in the Naka- platelets nor in the donors whose platelets showed deficient binding of OKM5. These results suggest that GPIV functions as an isoantigen rather than an alloantigen in immunizing Naka- platelet recipients. This is the first report of the absence of a major platelet membrane GP in healthy blood donors.
ISSN:0006-4971
1528-0020
DOI:10.1182/blood.V76.9.1698.1698