Literature DB >> 25762784

NF-κB downregulates Cbl-b through binding and suppressing Cbl-b promoter in T cell activation.

Yong Liu1, Yao Li2, LiMin Zhang3, MingQiang Li4, Chao Li5, ChengBiao Xue6, Xia Huang3, Ping Zhou7.   

Abstract

T cell activation causes the translocation of NF-κB dimers from the cytoplasm into the nucleus where NF-κB regulates inflammatory and immune response genes. Cbl-b is a negative regulator of T cell activation. However, the correlation between NF-κB activity and Cbl-b expression remains unclear. We showed that IκBαΔN-Tg T cells exhibited less NF-κB activity but higher levels of Cbl-b when compared with wild-type T cells. Furthermore, ursolic acid suppressed NF-κB activation and inhibited the downregulation of Cbl-b in wild-type T cells. NF-κBp65 specifically bound to an 11-bp NF-κB consensus sequence (gcaggaagtcc) in the Cbl-b promoter. Binding of NF-κB to this sequence suppressed Cbl-b transcription, thereby resulting in the negative regulation of Cbl-b expression. In addition, Cbl-b knockout led to the loss of cardiac allograft tolerance in IκBαΔN-Tg mice. These results indicated that NF-κB downregulated Cbl-b by binding and suppressing Cbl-b promoter in T cell activation. Our findings provide a novel role for NF-κB signaling in T cell activation.
Copyright © 2015 by The American Association of Immunologists, Inc.

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Year:  2015        PMID: 25762784     DOI: 10.4049/jimmunol.1402104

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  5 in total

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4.  Intestinal mucosa-derived DNA methylation signatures in the penetrating intestinal mucosal lesions of Crohn's disease.

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5.  FGFC1 Exhibits Anti-Cancer Activity via Inhibiting NF-κB Signaling Pathway in EGFR-Mutant NSCLC Cells.

Authors:  Jingwen Feng; Songlin Li; Bing Zhang; Namin Duan; Rui Zhou; Shike Yan; Jeevithan Elango; Ning Liu; Wenhui Wu
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  5 in total

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