一种评估炎症微泡对人诱导的多能干细胞衍生心肌细胞Ca2+处理影响的方法。

IF 2.7 4区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Experimental Biology and Medicine Pub Date : 2025-08-28 eCollection Date: 2025-01-01 DOI:10.3389/ebm.2025.10461
Dania Fischer, Mishkaat Sha'sha'a, Judith Schenz, Aycan Tayan, Christina Mertens, Sebastian O Decker, Nadia Gallenstein, Maximilian Dietrich, Trim Lajqi, Anna Hafner, Markus A Weigand, Nina D Ullrich
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引用次数: 0

摘要

从脓毒症个体中分离的微囊泡(MV)被观察到影响全身血流动力学和心功能。本实验旨在分析tnf α诱导的内皮细胞MV (TMV)和脓毒症患者内皮细胞MV (SMV)对人诱导多能干细胞源性心肌细胞(hiPSC-CM)跳动频率和Ca2+瞬态动力学的影响。从20例脓毒症患者经tnf α刺激的原代人肺微血管内皮细胞(HPMEC)上清液和血浆中进行超离心分离,流式细胞术定量。在不同MV浓度的孵育时间点,使用Ca2+敏感比率指示剂fura-2测量hiPSC-CM中自发Ca2+瞬态。在孵育16 h时,较高的MV浓度表现出显著差异,特别是在衰减和跳动频率方面。尽管变异很大,但在10 × 106 MV/mL和16 h孵育时,TMV的频率与对照MV (CMV)相比显著降低。在这些实验环境下,脓毒症患者的SMV对Ca2+瞬态没有任何显着影响。从对照或tnf α处理的HPMEC中分离的MV影响Ca2+处理和hiPSC-CM的自发活性,但在不同条件下测量的效果并不一致。需要进一步完善实验条件,以确定内皮源性MV和心肌细胞之间串扰的确切条件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

An approach to evaluate the effect of inflammatory microvesicles on Ca<sup>2+</sup> handling in human-induced pluripotent stem cell-derived cardiomyocytes.

An approach to evaluate the effect of inflammatory microvesicles on Ca<sup>2+</sup> handling in human-induced pluripotent stem cell-derived cardiomyocytes.

An approach to evaluate the effect of inflammatory microvesicles on Ca<sup>2+</sup> handling in human-induced pluripotent stem cell-derived cardiomyocytes.

An approach to evaluate the effect of inflammatory microvesicles on Ca2+ handling in human-induced pluripotent stem cell-derived cardiomyocytes.

Microvesicles (MV) isolated from septic individuals were observed to impact systemic hemodynamics and cardiac function. The aim of this in vitro study was to analyze the effects of TNFα-induced endothelial MV (TMV) and MV from septic patients (SMV) on beating frequency and Ca2+ transient kinetics of human-induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CM). MV were isolated from supernatants of TNFα-stimulated primary human pulmonary microvascular endothelial cells (HPMEC) and plasma from 20 sepsis patients by ultracentrifugation and quantified using flow cytometry. Spontaneous Ca2+ transients were measured in hiPSC-CM using the Ca2+-sensitive ratiometric indicator fura-2 at different time points of incubation with different MV concentrations. At 16 h of incubation, higher MV concentrations showed significant differences, especially regarding decay and beating frequency. Despite high variability, at 10 × 106 MV/mL and 16 h of incubation, TMV significantly decreased frequency compared to control MV (CMV). SMV from septic patients did not reveal any significant effects on Ca2+ transients under these experimental settings. MV isolated from control or TNFα-treated HPMEC affected Ca2+ handling and spontaneous activity of hiPSC-CM, however, the measured effects were not consistent throughout the different conditions. Further refinement of the experiment conditions is needed to specify the exact conditions for crosstalk between endothelium-derived MV and cardiomyocytes.

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来源期刊
Experimental Biology and Medicine
Experimental Biology and Medicine 医学-医学:研究与实验
CiteScore
6.00
自引率
0.00%
发文量
157
审稿时长
1 months
期刊介绍: Experimental Biology and Medicine (EBM) is a global, peer-reviewed journal dedicated to the publication of multidisciplinary and interdisciplinary research in the biomedical sciences. EBM provides both research and review articles as well as meeting symposia and brief communications. Articles in EBM represent cutting edge research at the overlapping junctions of the biological, physical and engineering sciences that impact upon the health and welfare of the world''s population. Topics covered in EBM include: Anatomy/Pathology; Biochemistry and Molecular Biology; Bioimaging; Biomedical Engineering; Bionanoscience; Cell and Developmental Biology; Endocrinology and Nutrition; Environmental Health/Biomarkers/Precision Medicine; Genomics, Proteomics, and Bioinformatics; Immunology/Microbiology/Virology; Mechanisms of Aging; Neuroscience; Pharmacology and Toxicology; Physiology; Stem Cell Biology; Structural Biology; Systems Biology and Microphysiological Systems; and Translational Research.
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