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Mesenchymal stem cells rejuvenate cardiac muscle through regulating macrophage polarization

机译:间充质干细胞通过调节巨噬细胞极化使心肌恢复活力

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摘要

We have shown that the effects of transplantation of CD146+ mesenchymal stem cells (MSCs) on myocardial regeneration after myocardial infarction (MI) exceeds the effects of transplantation of MSCs, likely resulting from reduction of aging-associated cellular reactive oxygen species in injured cardiac muscle cells (CMCs). Since the role of macrophages in the MSC-mediated recovery of heart function after MI remains unclear, this question was thus addressed in the current study. We found that transplantation of MSCs did not alter the total number of the macrophages in the injured heart, but induced their polarization towards a M2-phenotype. Moreover, administration of tumor necrosis factor alpha (TNFα) into MSC-transplanted mice, which prevented M2-polarization of macrophages, abolished the effects of MSCs on recovery of heart function and on the reduction of infarcted cardiac tissue. Thus, our data suggest that MSCs may rejuvenate CMCs after ischemic injury at least partially through induction of M2-polarization of macrophages.
机译:我们已经表明,CD146 +间充质干细胞(MSCs)移植对心肌梗死(MI)后心肌再生的影响超过了MSCs移植的影响,这可能是由于受损心肌细胞中与衰老相关的细胞活性氧物质减少所致(CMC)。由于巨噬细胞在心肌梗死后MSC介导的心功能恢复中的作用尚不清楚,因此该问题已在本研究中得到解决。我们发现,MSCs的移植并没有改变受伤心脏中巨噬细胞的总数,而是诱导了它们向M2型的分化。此外,向移植了MSC的小鼠中施用肿瘤坏死因子α(TNFα)可阻止M2极化巨噬细胞,从而消除了MSC对心脏功能恢复和梗死心脏组织减少的影响。因此,我们的数据表明,MSCs可在缺血性损伤后至少部分地通过诱导巨噬细胞的M2极化来使CMC恢复活力。

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