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IL-4-induced AID expression and its relevance to IgA class switch recombination.

作者信息

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

机构信息

Department of Molecular Bioscience, School of Bioscience and Biotechnology, Kangwon National University, Chunchon 200-701, Republic of Korea.

出版信息

Biochem Biophys Res Commun. 2007 Sep 21;361(2):398-403. doi: 10.1016/j.bbrc.2007.07.022. Epub 2007 Jul 16.

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.

摘要

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