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Metabolic Syndrome Induces Release of Smaller Extracellular Vesicles fromPorcine Mesenchymal Stem Cells

机译:代谢综合症诱导释放较小的细胞外囊泡猪间充质干细胞

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摘要

Mesenchymal stromal/stem cells (MSCs) belong to the endogenous cellular reparative system, and can be used exogenously in cell-based therapy. MSCs release extracellular vesicles (EVs), including exosomes and microvesicles, which mediate some of their therapeutic activity through intercellular communication. We have previously demonstrated that metabolic syndrome (MetS) modifies the cargo packed within swine EV, but whether it influences their phenotypical characteristics remains unclear. This study tested the hypothesis that MetS shifts the size distribution of MSC-derived EVs. Adipose tissue-derived MSC-EV subpopulations from Lean (n = 6) and MetS (n = 6) pigs were characterized for number and size using nanoparticle-tracking analysis, flow cytometry, and transmission electron microscopy. Expression of exosomal genes was determined using next-generation RNA-sequencing (RNA-seq). The number of EV released from Lean and MetS pig MSCs was similar, yet MetS-MSCs yielded a higher proportion of small-size EVs (202.4 ± 17.7 nm vs. 280.3 ± 15.1 nm), consistent with exosomes. RNA-seq showed that their EVs were enriched with exosomal markers. Lysosomal activity remained unaltered in MetS-MSCs. Therefore, MetS alters the size distribution of MSC-derived EVs in favor of exosome release. These observations may reflect MSC injury and membrane recycling in MetS or increased expulsion of wasteproducts, and may have important implications for development of adequate cell-basedtreatments.
机译:间充质基质/干细胞(MSC)属于内源性细胞修复系统,可在基于细胞的治疗中外源性使用。 MSC释放细胞外囊泡(EVs),包括外泌体和微囊泡,它们通过细胞间通讯介导某些治疗活性。先前我们已经证明了代谢综合症(MetS)会改变猪EV内包装的货物,但是尚不清楚它是否影响其表型特征。这项研究验证了MetS改变了MSC衍生电动汽车尺寸分布的假设。使用纳米颗粒追踪分析,流式细胞仪和透射电子显微镜对瘦肉猪(n = 6)和大都会MetS(n = 6)的脂肪组织来源的MSC-EV亚群进行了数量和大小的表征。使用下一代RNA测序(RNA-seq)确定外泌体基因的表达。从精益和MetS猪MSC中释放的EV数量相似,但MetS-MSC产生的小尺寸EV比例更高(202.4±17.7 nm对280.3±15.1 nm),与外泌体一致。 RNA-seq显示其电动汽车富含外泌体标记。在MetS-MSC中,溶酶体的活性保持不变。因此,MetS改变MSC衍生的EV的大小分布,有利于外泌体释放。这些观察结果可能反映了MetS中的MSC损伤和膜回收或废物排出量增加产品,可能会对基于细胞的适当细胞的发育产生重要影响治疗。

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