Synergistic induction of nuclear factor-κB by transforming growth factor-β and tumour necrosis factor-α is mediated by protein kinase A-dependent RelA acetylation

Author:

Ishinaga Hajime1,Jono Hirofumi1,Lim Jae Hyang1,Komatsu Kensei1,Xu Xiangbin1,Lee Jiyun1,Woo Chang-Hoon2,Xu Haidong1,Feng Xin-Hua3,Chen Lin-Feng4,Yan Chen2,Li Jian-Dong1

Affiliation:

1. Department of Microbiology & Immunology, University of Rochester Medical Center, Rochester, NY 14642, U.S.A.

2. Aab Cardiovascular Research Institute, University of Rochester Medical Center, West Henrietta, NY 14586, U.S.A.

3. Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, TX 77030, U.S.A.

4. Department of Biochemistry, University of Illinois at Urbana-Champaign, Urbana, IL 61801, U.S.A.

Abstract

The TGF-β (transforming growth factor-β) pathway represents an important signalling pathway involved in regulating diverse biological processes, including cell proliferation, differentiation and inflammation. Despite the critical role for TGF-β in inflammatory responses, its role in regulating NF-κB (nuclear factor-κB)-dependent inflammatory responses still remains unknown. In the present study we show that TGF-β1 synergizes with proinflammatory cytokine TNF-α (tumour necrosis factor-α) to induce NF-κB activation and the resultant inflammatory response in vitro and in vivo. TGF-β1 synergistically enhances TNF-α-induced NF-κB DNA binding activity via induction of RelA acetylation. Moreover, synergistic enhancement of TNF-α-induced RelA acetylation and DNA-binding activity by TGF-β1 is mediated by PKA (protein kinase A). Thus the present study reveals a novel role for TGF-β in inflammatory responses and provides new insight into the regulation of NF-κB by TGF-β signalling.

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference42 articles.

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