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血液因素对两种不同心力衰竭模型内皮细胞代谢和功能的影响。

Impact of blood factors on endothelial cell metabolism and function in two diverse heart failure models.

机构信息

Department of Anesthesiology and Pain Medicine, Anesthesia and Pain Research Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.

Veterans Administration San Diego Healthcare System, San Diego, CA, United States of America.

出版信息

PLoS One. 2023 Feb 13;18(2):e0281550. doi: 10.1371/journal.pone.0281550. eCollection 2023.

Abstract

Role of blood-based factors in development and progression of heart failure (HF) is poorly characterized. Blood contains factors released during pathophysiological states that may impact cellular function and provide mechanistic insights to HF management. We tested effects of blood from two distinct HF models on cardiac metabolism and identified possible cellular targets of the effects. Blood plasma was obtained from daunorubicin- and myocardial infarction-induced HF rabbits (Dauno-HF and MI-HF) and their controls (Dauno-Control and MI-Control). Effects of plasma on bioenergetics of myocardial tissue from healthy mice and cellular cardiac components were assessed using high-resolution respirometry and Seahorse flux analyzer. Since endothelial cell respiration was profoundly affected by HF plasma, effects of plasma on endothelial cell barrier function and death were further evaluated. Western-blotting and electron microscopy were performed to evaluate mitochondrial proteins and morphology. Brief exposure to HF plasma decreased cardiac tissue respiration. Endothelial cell respiration was most impacted by exposure to HF plasma. Endothelial cell monolayer integrity was decreased by incubation with Dauno-HF plasma. Apoptosis and necrosis were increased in cells incubated with Dauno-HF plasma for 24 h. Down-regulation of voltage-dependent anion-selective channel (VDAC)-1, translocase of outer membrane 20 (Tom20), and mitochondrial fission factor (MFF) in cells exposed to Dauno-HF plasma and mitochondrial signal transducer and activator of transcription 3 (Stat3) and MFF in cells exposed to MI-HF plasma were observed. Mitochondrial structure was disrupted in cells exposed to HF plasma. These findings indicate that endothelial cells and mitochondrial structure and function may be primary target where HF pathology manifests and accelerates. High-throughput blood-based screening of HF may provide innovative ways to advance disease diagnosis and management.

摘要

血液因子在心力衰竭(HF)的发生和发展中的作用尚未得到充分描述。血液中包含在病理生理状态下释放的因子,这些因子可能影响细胞功能,并为 HF 的治疗提供机制见解。我们检测了两种不同 HF 模型的血液对心脏代谢的影响,并确定了这些影响的可能细胞靶标。从柔红霉素诱导的 HF 兔(Dauno-HF)和心肌梗死诱导的 HF 兔(MI-HF)及其对照(Dauno-Control 和 MI-Control)中获得血浆。使用高分辨率呼吸测定法和 Seahorse 通量分析仪评估血浆对来自健康小鼠的心肌组织的生物能量学和细胞心脏成分的影响。由于内皮细胞呼吸受到 HF 血浆的显著影响,因此进一步评估了血浆对内皮细胞屏障功能和死亡的影响。进行 Western 印迹和电子显微镜检查以评估线粒体蛋白和形态。短暂暴露于 HF 血浆会降低心脏组织的呼吸。内皮细胞呼吸受 HF 血浆暴露的影响最大。与 Dauno-HF 血浆孵育会降低内皮细胞单层的完整性。与 Dauno-HF 血浆孵育 24 小时会增加细胞凋亡和坏死。暴露于 Dauno-HF 血浆的细胞中电压依赖性阴离子选择通道(VDAC)-1、外膜 20 转位酶(Tom20)和线粒体分裂因子(MFF)下调,以及暴露于 MI-HF 血浆的细胞中线粒体信号转导和转录激活因子 3(Stat3)和 MFF 下调。暴露于 HF 血浆的细胞中线粒体结构被破坏。这些发现表明,内皮细胞和线粒体的结构和功能可能是 HF 病理表现和加速的主要靶标。HF 的高通量基于血液的筛选可能为疾病诊断和治疗提供创新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03bd/9924994/9cc108022292/pone.0281550.g001.jpg

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