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蛋白质组学和脂质组学揭示前蛋白转化酶枯草溶菌素9(PCSK9)除降低胆固醇之外的作用:一篇综述

Proteomics and Lipidomics to unveil the contribution of PCSK9 beyond cholesterol lowering: a narrative review.

作者信息

Gianazza Erica, Macchi Chiara, Banfi Cristina, Ruscica Massimiliano

机构信息

Unit of Functional Proteomics, Metabolomics and Network Analysis, Centro Cardiologico Monzino IRCCS, Milan, Italy.

Department of Pharmacological and Biomolecular Sciences "Rodolfo Paoletti", Università degli Studi di Milano, Milan, Italy.

出版信息

Front Cardiovasc Med. 2023 Jun 12;10:1191303. doi: 10.3389/fcvm.2023.1191303. eCollection 2023.

DOI:10.3389/fcvm.2023.1191303
PMID:37378405
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10291627/
Abstract

Proprotein convertase subtilisin/kexin type 9 (PCSK9), one of the key regulators of the low-density lipoprotein receptor (LDLR), can play a direct role in atheroma development. Although advances in the understandings of genetic polymorphisms have enabled to reveal the role of in the complex pathophysiology of cardiovascular diseases (CVDs), increasing lines of evidence support non-cholesterol-related processes mediated by PCSK9. Owing to major improvements in mass spectrometry-based technologies, multimarker proteomic and lipidomic panels hold the promise to identify novel lipids and proteins potentially related to PCSK9. Within this context, this narrative review aims to provide an overview of the most significant proteomics and lipidomics studies related to PCSK9 effects beyond cholesterol lowering. These approaches have enabled to unveil non-common targets of PCSK9, potentially leading to the development of novel statistical models for CVD risk prediction. Finally, in the era of precision medicine, we have reported the impact of PCSK9 on extracellular vesicles (EVs) composition, an effect that could contribute to an increased prothrombotic status in CVD patients. The possibility to modulate EVs release and cargo could help counteract the development and progression of the atherosclerotic process.

摘要

前蛋白转化酶枯草溶菌素/kexin 9型(PCSK9)是低密度脂蛋白受体(LDLR)的关键调节因子之一,可在动脉粥样硬化发展中发挥直接作用。尽管对基因多态性的认识取得了进展,能够揭示其在心血管疾病(CVD)复杂病理生理学中的作用,但越来越多的证据支持PCSK9介导的非胆固醇相关过程。由于基于质谱技术的重大改进,多标志物蛋白质组学和脂质组学分析有望识别与PCSK9潜在相关的新型脂质和蛋白质。在此背景下,本叙述性综述旨在概述与PCSK9降低胆固醇以外作用相关的最重要蛋白质组学和脂质组学研究。这些方法已能够揭示PCSK9的非常见靶点,可能导致开发用于CVD风险预测的新型统计模型。最后,在精准医学时代,我们报道了PCSK9对细胞外囊泡(EVs)组成的影响,这一效应可能导致CVD患者血栓形成前状态增加。调节EVs释放和货物的可能性有助于对抗动脉粥样硬化过程发展和进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e28d/10291627/438589efed72/fcvm-10-1191303-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e28d/10291627/a5b2403fcd9a/fcvm-10-1191303-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e28d/10291627/438589efed72/fcvm-10-1191303-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e28d/10291627/a5b2403fcd9a/fcvm-10-1191303-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e28d/10291627/438589efed72/fcvm-10-1191303-g002.jpg

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2
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Eur Heart J. 2023 May 7;44(18):1594-1607. doi: 10.1093/eurheartj/ehad161.
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Identification of PCSK9-like human gene knockouts using metabolomics, proteomics, and whole-genome sequencing in a consanguineous population.
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Heliyon. 2024 Nov 6;10(22):e40127. doi: 10.1016/j.heliyon.2024.e40127. eCollection 2024 Nov 30.
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