Associated Tissue Bank, Faculty of Medicine, Pavol Jozef Safarik University and Louis Pasteur University Hospital, Trieda SNP 1, 04011, Kosice, Slovakia.
Institute of Geotechnics of the Slovak Academy of Sciences, Watsonova 45, 040 01, Kosice, Slovakia.
Stem Cell Rev Rep. 2024 Nov;20(8):2318-2335. doi: 10.1007/s12015-024-10790-8. Epub 2024 Sep 21.
Chorionic mesenchymal stromal cells (CHO-MSCs) and their extracellular vesicles (EVs) are becoming increasingly popular, since chorion is ethically harmless and an easily accessible source of MSCs. However, until now there is only a limited number of studies with a thorough characterization of CHO-MSCs derived EVs and their miRNA profile. In this study, we monitored changes in the EV-miRNA profile between early and late passage of human CHO-MSCs. First, senescence of CHO-MSCs was induced by serial passaging and confirmed by morphological changes, shortened telomeres and changes in the expression of selected genes. The expression of MSCs-specific surface markers CD73, CD90, CD105 did not change with increasing passages. Next, EVs and their miRNA profiles were compared between early vs late passage cells. Number of EVs and their size were not significantly changed. Seven of the top 10 most expressed EV-miRNAs were common to both early and late passages. A differential expression study between early and late passages identified 37 significantly differentially expressed EV-miRNAs, out of which 23 were found to be associated with pathways of cellular senescence based on KEGG pathway analysis. A set of 9 miRNAs were identified as the most frequently associated with senescence and/or with the most altered expression between early and late passages, out of which miR-145-5p, miR-335-5p and miR-199b-3p were the most significant downregulated miRNAs in late passages. The most upregulated EV-miRNAs were miR-1307-3p, miR-3615 and miR320b. Targeting these miRNAs in future experiments may prolong the therapeutic potential of CHO-MSCs and their EVs.
绒毛膜间充质基质细胞(CHO-MSCs)及其细胞外囊泡(EVs)越来越受欢迎,因为绒毛膜在伦理上是无害的,并且是间充质干细胞的易得来源。然而,到目前为止,只有少数研究对源自 CHO-MSCs 的 EVs 及其 miRNA 图谱进行了全面表征。在这项研究中,我们监测了人源 CHO-MSCs 早期和晚期传代之间 EV-miRNA 图谱的变化。首先,通过连续传代诱导 CHO-MSCs 衰老,并通过形态学变化、端粒缩短和选定基因表达的变化来确认。随着传代次数的增加,间充质干细胞特异性表面标志物 CD73、CD90 和 CD105 的表达没有变化。接下来,比较了早期和晚期传代细胞之间的 EV 和它们的 miRNA 图谱。EV 的数量及其大小没有显著变化。早期和晚期传代中前 10 位表达最多的 EV-miRNAs 中有 7 个是共同的。早期和晚期传代之间的差异表达研究鉴定出 37 个差异表达的 EV-miRNAs,其中 23 个根据 KEGG 途径分析与细胞衰老途径有关。确定了一组 9 个 miRNA 作为与衰老最相关和/或在早期和晚期传代之间表达变化最显著的 miRNA,其中 miR-145-5p、miR-335-5p 和 miR-199b-3p 是晚期传代中下调最显著的 miRNA。上调表达最多的 EV-miRNAs 是 miR-1307-3p、miR-3615 和 miR320b。在未来的实验中靶向这些 miRNA 可能会延长 CHO-MSCs 和它们的 EV 的治疗潜力。