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IL-4-induced AID expression and its relevance to IgA class switch recombination.
Kim, Ran Ju; Kim, Hyun-A; Park, Jae-Bong; Park, Seok-Rae; Jeon, Seong-Hyun; Seo, Goo-Young; Seo, Dong-Wan; Seo, Su Ryeon; Chun, Gie-Taek; Kim, Nam-Soo; Yie, Se-Won; Byeon, Woo-Hyeon; Kim, Pyeung-Hyeun.
Afiliação
  • Kim RJ; Department of Molecular Bioscience, School of Bioscience and Biotechnology, Kangwon National University, Chunchon 200-701, Republic of Korea.
Biochem Biophys Res Commun ; 361(2): 398-403, 2007 Sep 21.
Article em En | MEDLINE | ID: mdl-17645870
ABSTRACT
Activation-induced cytidine deaminase (AID) is an inducible gene that plays a critical role in Ig class switch recombination and somatic hypermutation in B cells. We explored the mechanisms by which IL-4 induces AID expression in mouse B cells. IL-4 increased AID expression and over-expression of Stat6 further augmented IL-4-induced promoter activity. The involvement of Stat6 in the promoter activity was confirmed using ChIP assays and site-directed mutagenesis. Treatment with H89, a PKA inhibitor, markedly decreased IL-4-induced AID expression, and over-expression of CREB enhanced it. These results indicate that Stat6 and PKA/CREB are involved in IL-4-induced AID expression. The relevance of these signal transducing molecules was verified using the TGFbeta1-induced IgA isotype switching model. Our results indicate that IL-4, through Stat6 and PKA/CREB, induces AID expression leading to Ig isotype switching event.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Recombinação Genética / Imunoglobulina A / Interleucina-4 / Switching de Imunoglobulina / Citidina Desaminase Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2007 Tipo de documento: Article
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Recombinação Genética / Imunoglobulina A / Interleucina-4 / Switching de Imunoglobulina / Citidina Desaminase Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2007 Tipo de documento: Article