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Immune Network ; : 55-62, 2013.
Artigo em Inglês | WPRIM | ID: wpr-147332

RESUMO

Swiprosin-1 exhibits the highest expression in CD8+ T cells and immature B cells and has been proposed to play a role in lymphocyte biology through actin remodeling. However, regulation of swiprosin-1 gene expression is poorly understood. Here we report that swiprosin-1 is up-regulated in T cells by PKC pathway. Targeted inhibition of the specific protein kinase C (PKC) isotypes by siRNA revealed that PKC-theta is involved in the expression of swiprosin-1 in the human T cells. In contrast, down-regulation of swiprosin-1 by A23187 or ionomycin suggests that calcium-signaling plays a negative role. Interestingly, swiprosin-1 expression is only reduced by treatment with NF-kappaB inhibitors but not by NF-AT inhibitor, suggesting that the NF-kappaB pathway is critical for regulation of swiprosin-1 expression. Collectively, these results suggest that swiprosin-1 is a PKC-theta-inducible gene and that it may modulate the late phase of T cell activation after antigen challenge.


Assuntos
Humanos , Actinas , Biologia , Calcimicina , Regulação para Baixo , Expressão Gênica , Ionomicina , Linfócitos , NF-kappa B , Células Precursoras de Linfócitos B , Proteína Quinase C , Proteínas Quinases , RNA Interferente Pequeno , Linfócitos T
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