| Literature DB >> 26002466 |
Bin Yang1, Wei Li2, Qichang Zheng1, Tao Qin3, Kun Wang1, Jinjin Li1, Bing Guo1, Qihong Yu1, Yuzhe Wu1, Yang Gao1, Xiang Cheng1, Shaobo Hu1, Stanley Naveen Kumar1, Sanguang Liu4, Zifang Song5.
Abstract
Stromal-derived Factor-1 (SDF-1) derived from vascular smooth muscle cells (VSMCs) contributes to vascular repair and remodeling in various vascular diseases. In this study, the mechanism underlying regulation of SDF-1 expression by interleukin-1α (IL-1α) was investigated in primary rat VSMCs. We found IL-1α promotes SDF-1 expression by up-regulating CCAAT-enhancer-binding protein β (C/EBPβ) in an IκB kinase β (IKKβ) signaling-dependent manner. Moreover, IL-1α-induced expression of C/EBPβ and SDF-1 was significantly potentiated by knockdown of transforming growth factor β-activated kinase 1 (TAK1), an upstream activator of IKKβ signaling. In addition, we also demonstrated that TAK1/p38 mitogen-activated protein kinase (p38 MAPK) signaling exerted negative effect on IL-1α-induced expression of C/EBPβ and SDF-1 through counteracting ROS-dependent up-regulation of nuclear factor erythroid 2-related factor 2 (NRF2). In conclusion, TAK1 acts as an important regulator of IL-1α-induced SDF-1 expression in VSMCs, and modulating activity of TAK1 may serve as a potential strategy for modulating vascular repair and remodeling.Entities:
Keywords: CCAAT-enhancer-binding protein β; Interleukin-1; Nuclear factor erythroid 2-related factor 2; Stromal-derived factor-1; Transforming growth factor β-activated kinase 1; p38 mitogen-activated protein kinase
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Year: 2015 PMID: 26002466 DOI: 10.1016/j.bbrc.2015.05.047
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575