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Heterogeneous Nuclear Ribonucleoprotein A2B1 Exerts a Regulatory Role in Lipopolysaccharide-stimulated 38B9 B Cell Activation
Immune Network ; : 437-450, 2017.
Artigo em Inglês | WPRIM | ID: wpr-10874
ABSTRACT
Major histocompatibility complex (MHC) class II molecules, which are recognized for their primary function of presenting an antigen to the T cell receptor, are involved in various signaling pathways in B cell activation. We identified heterogeneous nuclear ribonucleoprotein (hnRNP) A2B1 as an MHC class II molecule-associated protein involved in MHC class II-mediated signal transduction in lipopolysaccharide (LPS)-stimulated 38B9 B cells. Although the function of hnRNP A2B1 in the nucleus is primarily known, the level of hnRNP A2B1 in the cytoplasm was increased in LPS-stimulated 38B9 cells, while it was not detected in the cytoplasm of non-treated 38B9 cells. The silencing of hnRNP A2B1 expression using siRNA disturbed B cell maturation by regulation of mitogen-activated protein kinase signaling, NF-κB activation, and protein kinase B activation. These results suggest that hnRNP A2B1 is associated with MHC class II molecules and is involved in B cell activation signaling pathways in LPS-stimulated 38B9 cells.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Proteínas Quinases / Linfócitos B / Receptores de Antígenos de Linfócitos T / Transdução de Sinais / Citoplasma / Ribonucleoproteínas Nucleares Heterogêneas / RNA Interferente Pequeno / Proteínas Proto-Oncogênicas c-akt / Complexo Principal de Histocompatibilidade Idioma: Inglês Revista: Immune Network Ano de publicação: 2017 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Proteínas Quinases / Linfócitos B / Receptores de Antígenos de Linfócitos T / Transdução de Sinais / Citoplasma / Ribonucleoproteínas Nucleares Heterogêneas / RNA Interferente Pequeno / Proteínas Proto-Oncogênicas c-akt / Complexo Principal de Histocompatibilidade Idioma: Inglês Revista: Immune Network Ano de publicação: 2017 Tipo de documento: Artigo