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J. physiol. biochem ; 66(1): 39-46, mar. 2010.
Artigo em Inglês | IBECS | ID: ibc-122848

RESUMO

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Human leukocyte antigen (HLA)-G is an immunomodulatory molecule discovered for the first time in the maternal–fetal interface. In cancer context, where high number of natural killer (NK) cells is described, the presence of HLA-G in its soluble form is thought to be essential for NK cellssignaling. To evaluate intracellular signaling in NK cells upon HLA-G soluble forms stimulation, we investigate the role of soluble HLA-G (HLA-G5- and HLA-G1 shedding form) stimulation on classical nuclear factor (NF)–κB pathway activation. We reported that these two forms of soluble HLA-G could activate NF–κB in NK cells. NF–κB activation in NK cells does implicate neither phosphatidylinositol 3-kinase (PI3K) nor MEK (MAP kinase kinase) as demonstrated after specific inhibition experiments. We demonstrated elsewhere that NF–κB activation in NK cells is not implicated in cytotoxicity inhibition by HLA-G. Our findings may suggest the important role played by NF–κB activation after soluble HLA-G stimulation in other NK cells function (AU)


Assuntos
Humanos , Células Matadoras Naturais/fisiologia , Antígenos HLA-G/fisiologia , NF-kappa B/fisiologia , Fatores Imunológicos/farmacocinética , Fosfatidilinositol 3-Quinase/fisiologia , Quinases de Proteína Quinase Ativadas por Mitógeno/fisiologia
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