The aim of this study was to further elucidate our previous observation on molecular interaction of GM3, CD4 and p56(lck) in microdomains of human peripheral blood lymphocytes (PBL). We analyzed GM3 distribution by immunoelectron microscopy and the association between GM3 and CD4-p56(lck) complex by scanning confocal microscopy and co-immunoprecipitation experiments. Scanning confocal microscopy analysis showed an uneven signal distribution of GM3 molecules over the surface of human lymphocytes. Nearly complete colocalization areas indicated that CD4 molecules were distributed in GMS-enriched plasma membrane domains. Co-immunoprecipitation experiments revealed that CD4 and p56(lck) were immunoprecipitated by IgG anti-GM3, demonstrating that GM3 tightly binds to the CD4-p56(lck) complex in human PBL. In order to verify whether GM3 association with CD4 molecules may depend on the presence of p56(lck), we analyzed this association in U937, a CD4 + and p56(lck) negative cell line, The immunoprecipitation with anti-GM3 revealed the presence of a 58 kDa band immunostained with anti-CD4 Ab, suggesting that the GM3-CD4 interaction does not require its association with p56(lck). These findings support the view that GM3 enriched-domains may represent a functional multimolecular complex involved in signal transduction and cell activation.
Association between GM3 and CD4-lck complex in human peripheral blood lymphocytes / Sorice, Maurizio; Garofalo, Tina; Misasi, Roberta; Longo, Agostina; J., Mikulak; V., Dolo; Pontieri, Giuseppe; Pavan, Antonio. - In: GLYCOCONJUGATE JOURNAL. - ISSN 0282-0080. - STAMPA. - 17:3-4(2000), pp. 247-252. [10.1023/a:1026501609699]
Association between GM3 and CD4-lck complex in human peripheral blood lymphocytes
SORICE, Maurizio;GAROFALO, TINA;MISASI, Roberta;LONGO, Agostina;PONTIERI, Giuseppe;PAVAN, Antonio
2000
Abstract
The aim of this study was to further elucidate our previous observation on molecular interaction of GM3, CD4 and p56(lck) in microdomains of human peripheral blood lymphocytes (PBL). We analyzed GM3 distribution by immunoelectron microscopy and the association between GM3 and CD4-p56(lck) complex by scanning confocal microscopy and co-immunoprecipitation experiments. Scanning confocal microscopy analysis showed an uneven signal distribution of GM3 molecules over the surface of human lymphocytes. Nearly complete colocalization areas indicated that CD4 molecules were distributed in GMS-enriched plasma membrane domains. Co-immunoprecipitation experiments revealed that CD4 and p56(lck) were immunoprecipitated by IgG anti-GM3, demonstrating that GM3 tightly binds to the CD4-p56(lck) complex in human PBL. In order to verify whether GM3 association with CD4 molecules may depend on the presence of p56(lck), we analyzed this association in U937, a CD4 + and p56(lck) negative cell line, The immunoprecipitation with anti-GM3 revealed the presence of a 58 kDa band immunostained with anti-CD4 Ab, suggesting that the GM3-CD4 interaction does not require its association with p56(lck). These findings support the view that GM3 enriched-domains may represent a functional multimolecular complex involved in signal transduction and cell activation.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.