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Mesenchymal Stem Cells and Their Conditioned Medium Improve Integration of Purified Induced Pluripotent Stem Cell–Derived Cardiomyocyte Clusters into Myocardial Tissue

机译:间充质干细胞及其条件培养基可提高纯化的诱导多能干细胞衍生的心肌细胞簇整合入心肌组织的能力

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摘要

Induced pluripotent stem cell–derived cardiomyocytes (iPS-CMs) might become therapeutically relevant to regenerate myocardial damage. Purified iPS-CMs exhibit poor functional integration into myocardial tissue. The aim of this study was to investigate whether murine mesenchymal stem cells (MSCs) or their conditioned medium (MScond) improves the integration of murine iPS-CMs into myocardial tissue. Vital or nonvital embryonic murine ventricular tissue slices were cocultured with purified clusters of iPS-CMs in combination with murine embryonic fibroblasts (MEFs), MSCs, or MScond. Morphological integration was assessed by visual scoring and functional integration by isometric force and field potential measurements. We observed a moderate morphological integration of iPS-CM clusters into vital, but a poor integration into nonvital, slices. MEFs and MSCs but not MScond improved morphological integration of CMs into nonvital slices and enabled purified iPS-CMs to confer force. Coculture of vital slices with iPS-CMs and MEFs or MSCs resulted in an improved electrical integration. A comparable improvement of electrical coupling was achieved with the cell-free MScond, indicating that soluble factors secreted by MSCs were involved in electrical coupling. We conclude that cells such as MSCs support the engraftment and adhesion of CMs, and confer force to noncontractile tissue. Furthermore, soluble factors secreted by MSCs mediate electrical coupling of purified iPS-CM clusters to myocardial tissue. These data suggest that MSCs may increase the functional engraftment and therapeutic efficacy of transplanted iPS-CMs into infarcted myocardium.
机译:诱导的多能干细胞衍生的心肌细胞(iPS-CM)可能在治疗上与再生心肌损伤有关。纯化的iPS-CM在心肌组织中的功能整合较差。这项研究的目的是调查鼠间充质干细胞(MSCs)或它们的条件培养基(MScond)是否能改善鼠iPS-CM与心肌组织的整合。将重要或非重要的胚胎鼠心室组织切片与iPS-CM的纯化簇结合鼠胚成纤维细胞(MEF),MSC或MScond共培养。通过视觉评分评估形态学整合,通过等距力和场电势测量评估功能整合。我们观察到iPS-CM群集适度整合到重要的形态,但整合到非重要切片中却很差。 MEF和MSC而不是MScond改善了CM到非重要切片的形态学整合,并使纯化的iPS-CM能够赋予力量。将重要切片与iPS-CM和MEF或MSC共培养可改善电整合。无细胞MScond达到了可比的电耦合改善,表明MSC分泌的可溶性因子参与了电耦合。我们得出的结论是,诸如MSC的细胞支持CM的植入和粘附,并向非收缩性组织赋予力量。此外,MSC分泌的可溶性因子介导纯化的iPS-CM簇与心肌组织的电耦合。这些数据表明,MSC可能会增加将iPS-CM移植到梗死心肌中的功能植入和治疗效果。

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