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血管生成素样蛋白 3:一种具有系统和细胞自主功能的新兴代谢心脏治疗靶点。

Angiopoietin-like protein 3, an emerging cardiometabolic therapy target with systemic and cell-autonomous functions.

机构信息

Minerva Foundation Institute for Medical Research, Helsinki, Finland; Molecular and Integrative Biosciences, University of Helsinki, Finland.

Minerva Foundation Institute for Medical Research, Helsinki, Finland.

出版信息

Biochim Biophys Acta Mol Cell Biol Lipids. 2020 Dec;1865(12):158791. doi: 10.1016/j.bbalip.2020.158791. Epub 2020 Aug 8.

Abstract

Angiopoietin like protein 3 (ANGPTL3) is best known for its function as an inhibitor of lipoprotein and endothelial lipases. Due to the capacity of genetic or pharmacologic ANGPTL3 suppression to markedly reduce circulating lipoproteins, and the documented cardioprotection upon such suppression, ANGPTL3 has become an emerging therapy target for which both antibody and antisense oligonucleotide (ASO) therapeutics are being clinically tested. While the antibody is relatively selective for circulating ANGPTL3, the ASO also depletes the intra-hepatocellular protein, and there is emerging evidence for cell-autonomous functions of ANGPTL3 in the liver. These include regulation of hepatocyte glucose and fatty acid uptake, insulin sensitivity, LDL/VLDL remnant uptake, VLDL assembly/secretion, polyunsaturated fatty acid (PUFA) and PUFA-derived lipid mediator content, and gene expression. In this review we elaborate on (i) why ANGPTL3 is considered one of the most promising new cardiometabolic therapy targets, and (ii) the present evidences for its intra-hepatocellular or cell-autonomous functions.

摘要

血管生成素样蛋白 3(ANGPTL3)最著名的功能是作为脂蛋白和内皮脂肪酶的抑制剂。由于遗传或药理学抑制 ANGPTL3 可以显著降低循环脂蛋白,并且这种抑制作用有明确的心脏保护作用,因此 ANGPTL3 已成为一种新兴的治疗靶点,抗体和反义寡核苷酸(ASO)治疗剂都正在进行临床测试。虽然抗体对循环 ANGPTL3 具有相对选择性,但 ASO 也会耗尽肝细胞内的蛋白质,并且有越来越多的证据表明 ANGPTL3 在肝脏中有细胞自主功能。这些功能包括调节肝细胞对葡萄糖和脂肪酸的摄取、胰岛素敏感性、LDL/VLDL 残粒的摄取、VLDL 的组装/分泌、多不饱和脂肪酸(PUFA)和 PUFA 衍生的脂质介质含量以及基因表达。在这篇综述中,我们详细阐述了:(i)为什么 ANGPTL3 被认为是最有前途的新心脏代谢治疗靶点之一;(ii)目前关于其肝细胞内或细胞自主功能的证据。

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