Acyclic retinoid inhibits functional interaction of transcription factors Kruppel-like factor 5 and retinoic acid receptor-alpha

Acyclic retinoid inhibits functional interaction of transcription factors Kruppel-like factor 5 and retinoic acid receptor-alpha
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DOI:
10.1016/j.febslet.2008.04.040
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发表时间:
2008-05-28
期刊:
影响因子:
3.5
通讯作者:
Nagai, Ryozo
Nagai, Ryozo
中科院分区:
生物学3区
文献类型:
--
作者:
Kada, Nanae;Suzuki, Toru;Nagai, Ryozo

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我们发现,转录因子Kruppel样因子5(KLF 5),这是重要的心血管重塑,与视黄酸受体α(RAR α)相互作用,调节下游基因的表达。在这里,我们研究了无环类维生素A(ACR)是否调节KLF 5和抑制血管重塑。免疫共沉淀和pull-down结合实验表明ACR减弱了KLF 5和RAR α的功能性相互作用。ACR通过调节血小板衍生生长因子A(PDGF-A)链的反式激活来影响KLF 5功能。ACR可能是一种新的血管治疗靶向KLF 5在心血管病理。(C)2008年由Elsevier B. V.代表欧洲生物化学学会联合会出版。
We show that transcription factor Kruppel-like factor 5 (KLF5), which is important in cardiovascular remodeling, interacts with retinoic acid receptor-alpha (RAR alpha) to regulate downstream gene expression. Here, we investigated whether acyclic retinoid (ACR) regulates KLF5 and inhibits vascular remodeling. Co-immunoprecipitation and pull-down binding assay showed that ACR attenuates functional interaction of KLF5 and RAR alpha. ACR affects KLF5 functions by regulating transactivation of platelet-derived growth factor A (PDGF-A) chain. ACR may be a new vascular therapy to target KLF5 in cardiovascular pathology. (C) 2008 Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.