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骨桥蛋白和 Gremlin 1 蛋白在缺血性心力衰竭心肌细胞中的表达。

Expression of Osteopontin and Gremlin 1 Proteins in Cardiomyocytes in Ischemic Heart Failure.

机构信息

Laboratory of Cardiac Pathology, Institute of Cardiology, Lithuanian University of Health Sciences, LT-50161 Kaunas, Lithuania.

Laboratory of Molecular Cardiology, Institute of Cardiology, Lithuanian University of Health Sciences, LT-50161 Kaunas, Lithuania.

出版信息

Int J Mol Sci. 2024 Jul 28;25(15):8240. doi: 10.3390/ijms25158240.

Abstract

A relevant role of osteopontin (OPN) and gremlin 1 (Grem1) in regulating cardiac tissue remodeling and formation of heart failure (HF) are documented, with the changes of OPN and Grem1 levels in blood plasma due to acute ischemia, ischemic heart disease-induced advanced HF or dilatative cardiomyopathy being the primary focus in most of these studies. However, knowledge on the early OPN and Grem1 proteins expression changes within cardiomyocytes during remodeling due to chronic ischemia remains insufficient. The aim of this study was to determine the OPN and Grem1 proteins expression changes in human cardiomyocytes at different stages of ischemic HF. A semi-quantitative immunohistochemical analysis was performed in 105 myocardial tissue samples obtained from the left cardiac ventricles. Increased OPN immunostaining intensity was already detected in the stage A HF group, compared to the control group ( < 0.001), and continued to increase in the stage B HF ( < 0.001), achieving the peak of immunostaining in the stages C/D HF group ( < 0.001). Similar data of Grem1 immunostaining intensity changes in cardiomyocytes were documented. Significantly positive correlations were detected between OPN, Grem1 expression in cardiomyocytes and their diameter as well as the length, in addition to positive correlation between OPN and Grem1 expression changes within cardiomyocytes. These novel findings suggest that OPN and Grem1 contribute significantly to reorganization of cellular geometry from the earliest stage of cardiomyocyte remodeling, providing new insights into the ischemic HF pathogenesis.

摘要

骨桥蛋白(OPN)和 GREM1 在调节心肌组织重构和心力衰竭(HF)形成中具有重要作用,这些研究主要集中在由于急性缺血、缺血性心脏病引起的晚期 HF 或扩张型心肌病导致的血浆 OPN 和 GREM1 水平变化上。然而,对于慢性缺血导致心肌细胞重构过程中 OPN 和 GREM1 蛋白早期表达变化的认识仍然不足。本研究旨在确定在缺血性 HF 的不同阶段人类心肌细胞中 OPN 和 GREM1 蛋白的表达变化。对取自左心室的 105 个心肌组织样本进行了半定量免疫组织化学分析。与对照组相比,HF 组 A 期的 OPN 免疫染色强度已经增加(<0.001),并在 HF 组 B 期继续增加(<0.001),在 HF 组 C/D 期达到免疫染色强度的峰值(<0.001)。在心肌细胞中 GREM1 免疫染色强度变化也记录到了类似的数据。在心肌细胞中 OPN 和 GREM1 的表达与细胞直径以及长度之间存在显著的正相关,此外,心肌细胞中 OPN 和 GREM1 的表达变化之间也存在正相关。这些新发现表明,OPN 和 GREM1 从心肌细胞重构的最早阶段就对细胞几何形状的重组有重要贡献,为缺血性 HF 的发病机制提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5793/11311846/ecc19dfbcbe7/ijms-25-08240-g001.jpg

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