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发现 14-3-3 ζ 作为心肌肥厚的潜在生物标志物。

Discovery of 14-3-3 zeta as a potential biomarker for cardiac hypertrophy.

机构信息

Center for Advanced Biomolecular Recognition, Korea Institute of Science and Technology, Seoul 02792; Division of Bio-Medical Science & Technology, KIST School, University of Science and Technology, Seoul 02792, Korea.

Cardiovascular Center, Korea University Guro Hospital, Korea University Medicine, Seoul 08308, Korea.

出版信息

BMB Rep. 2023 Jun;56(6):341-346. doi: 10.5483/BMBRep.2022-0194.

DOI:10.5483/BMBRep.2022-0194
PMID:36977605
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10315568/
Abstract

Acute myocardial infarction (AMI) is a multifaceted syndrome influenced by the functions of various extrinsic and intrinsic pathways and pathological processes, which can be detected in circulation using biomarkers. In this study, we investigated the secretome protein profile of induced-hypertrophy cardiomyocytes to identify next-generation biomarkers for AMI diagnosis and management. Hypertrophy was successfully induced in immortalized human cardiomyocytes (T0445) by 200 nM ET-1 and 1 μM Ang II. The protein profiles of hypertrophied cardiomyocyte secretomes were analyzed by nano-liquid chromatography with tandem mass spectrometry and differentially expressed proteins that have been identified by Ingenuity Pathway Analysis. The levels of 32 proteins increased significantly (>1.4 fold), whereas 17 proteins (<0.5 fold) showed a rapid decrease in expression. Proteomic analysis showed significant upregulation of six 14-3-3 protein isoforms in hypertrophied cardiomyocytes compared to those in control cells. Multi-reaction monitoring results of human plasma samples showed that 14-3-3 protein-zeta levels were significantly elevated in patients with AMI compared to those of healthy controls. These findings elucidated the role of 14-3-3 protein-zeta in cardiac hypertrophy and cardiovascular disorders and demonstrated its potential as a novel biomarker and therapeutic strategy. [BMB Reports 2023; 56(6): 341-346].

摘要

急性心肌梗死(AMI)是一种多方面的综合征,受各种外在和内在途径及病理过程的影响,可以通过生物标志物在循环中检测到。在这项研究中,我们研究了诱导肥大心肌细胞的分泌组蛋白谱,以确定用于 AMI 诊断和管理的下一代生物标志物。通过 200 nM ET-1 和 1 μM Ang II 成功诱导永生人类心肌细胞(T0445)肥大。通过纳升液相色谱-串联质谱分析肥大心肌细胞分泌组的蛋白质谱,并通过 Ingenuity 通路分析鉴定差异表达的蛋白质。32 种蛋白质的水平显著增加(>1.4 倍),而 17 种蛋白质(<0.5 倍)的表达迅速下降。蛋白质组学分析表明,与对照细胞相比,肥大心肌细胞中六种 14-3-3 蛋白同工型的表达显著上调。人血浆样本的多反应监测结果显示,AMI 患者的 14-3-3 蛋白-ζ水平明显高于健康对照组。这些发现阐明了 14-3-3 蛋白-ζ在心脏肥大和心血管疾病中的作用,并证明了它作为一种新型生物标志物和治疗策略的潜力。[BMB 报告 2023;56(6):341-346]。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a06a/10315568/f91430ebbaad/bmb-56-6-341-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a06a/10315568/fc59b830abd4/bmb-56-6-341-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a06a/10315568/1a6413356450/bmb-56-6-341-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a06a/10315568/644dbc15e163/bmb-56-6-341-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a06a/10315568/f91430ebbaad/bmb-56-6-341-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a06a/10315568/fc59b830abd4/bmb-56-6-341-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a06a/10315568/1a6413356450/bmb-56-6-341-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a06a/10315568/644dbc15e163/bmb-56-6-341-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a06a/10315568/f91430ebbaad/bmb-56-6-341-f4.jpg

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