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阻断 IRE1 激酶-FMRP 信号通路可阻止动脉粥样硬化进展。

Intercepting IRE1 kinase-FMRP signaling prevents atherosclerosis progression.

机构信息

Department of Cardiology, Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA.

Department of Molecular Biology and Genetics, National Nanotechnology Center, Bilkent University, Ankara, Turkey.

出版信息

EMBO Mol Med. 2022 Apr 7;14(4):e15344. doi: 10.15252/emmm.202115344. Epub 2022 Feb 22.

Abstract

Fragile X Mental Retardation protein (FMRP), widely known for its role in hereditary intellectual disability, is an RNA-binding protein (RBP) that controls translation of select mRNAs. We discovered that endoplasmic reticulum (ER) stress induces phosphorylation of FMRP on a site that is known to enhance translation inhibition of FMRP-bound mRNAs. We show ER stress-induced activation of Inositol requiring enzyme-1 (IRE1), an ER-resident stress-sensing kinase/endoribonuclease, leads to FMRP phosphorylation and to suppression of macrophage cholesterol efflux and apoptotic cell clearance (efferocytosis). Conversely, FMRP deficiency and pharmacological inhibition of IRE1 kinase activity enhances cholesterol efflux and efferocytosis, reducing atherosclerosis in mice. Our results provide mechanistic insights into how ER stress-induced IRE1 kinase activity contributes to macrophage cholesterol homeostasis and suggests IRE1 inhibition as a promising new way to counteract atherosclerosis.

摘要

脆性 X 智力低下蛋白(FMRP),因在遗传性智力障碍中发挥作用而广为人知,是一种 RNA 结合蛋白(RBP),可控制特定 mRNA 的翻译。我们发现内质网(ER)应激会导致 FMRP 在一个已知可增强与 FMRP 结合的 mRNA 翻译抑制的位点上发生磷酸化。我们表明 ER 应激诱导的肌醇需求酶 1(IRE1)的激活,一种内质网驻留的应激感应激酶/内切核酸酶,导致 FMRP 磷酸化,并抑制巨噬细胞胆固醇流出和凋亡细胞清除(吞噬作用)。相反,FMRP 缺失和 IRE1 激酶活性的药理学抑制增强了胆固醇流出和吞噬作用,减少了小鼠的动脉粥样硬化。我们的研究结果为 ER 应激诱导的 IRE1 激酶活性如何促进巨噬细胞胆固醇稳态提供了机制上的见解,并表明 IRE1 抑制可能是对抗动脉粥样硬化的一种有前途的新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a23f/8988208/a4bf5706ecd7/EMMM-14-e15344-g006.jpg

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