Lindoso Rafael S, Collino Federica, Bruno Stefania, Araujo Dayana S, Sant'Anna Julliana F, Tetta Ciro, Provero Paolo, Quesenberry Peter J, Vieyra Adalberto, Einicker-Lamas Marcelo, Camussi Giovanni
1 Department of Medical Sciences, Molecular Biotechnology Center, University of Torino , Turin, Italy .
Stem Cells Dev. 2014 Aug 1;23(15):1809-19. doi: 10.1089/scd.2013.0618. Epub 2014 May 20.
The mechanisms involved in renal repair by mesenchymal stromal cells (MSCs) are not entirely elucidated. The paracrine secretion of bioactive molecules has been implicated in the protective effects. Besides soluble mediators, MSCs have been shown to release extracellular vesicles (EVs), involved in renal repair process for different injury models. EVs have been shown to mediate communication between cells through the transference of several molecules, like protein, bioactive lipids, mRNA, and microRNAs (miRNAs). The miRNAs are noncoding RNAs that posttranscriptionally modulate gene expression and are involved in the regulation of several cellular processes, including those related to repair. The aim of the present study was to investigate the role of MSC-EVs in the modulation of miRNAs inside renal proximal tubular epithelial cells (PTECs) in an in vitro model of ischemia-reperfusion injury induced by ATP depletion. In this model we evaluated whether changes in miRNA expression were dependent on direct miRNA transfer or on transcription induction by MSC-EVs. The obtained results showed an enhanced incorporation of MSC-EVs in injured PTECs with protection from cell death. This biological effect was associated with EV-mediated miRNA transfer and with transcriptional modulation of miRNAs expressed by injured PTECs. Prediction of miRNA targets showed that miRNAs modulated in PTECs are involved in process of renal recovery with downregulation of coding-mRNAs associated with apoptosis, cytoskeleton reorganization, and hypoxia, such as CASP3 and 7, SHC1 and SMAD4. In conclusion, these results indicate that MSC-EVs may transfer and modulate the expression of several miRNAs involved in the repair and recovery process in PTECs.
间充质基质细胞(MSCs)参与肾脏修复的机制尚未完全阐明。生物活性分子的旁分泌分泌被认为具有保护作用。除了可溶性介质外,MSCs已被证明可释放细胞外囊泡(EVs),其参与不同损伤模型的肾脏修复过程。EVs已被证明可通过蛋白质、生物活性脂质、mRNA和微小RNA(miRNAs)等多种分子的转移介导细胞间通讯。miRNAs是非编码RNA,可在转录后调节基因表达,并参与包括与修复相关的几个细胞过程的调控。本研究的目的是在ATP耗竭诱导的缺血再灌注损伤体外模型中,研究MSC-EVs在调节肾近端小管上皮细胞(PTECs)内miRNAs中的作用。在该模型中,我们评估了miRNA表达的变化是否依赖于直接的miRNA转移或MSC-EVs的转录诱导。获得的结果显示,受损PTECs中MSC-EVs的掺入增加,细胞死亡得到保护。这种生物学效应与EV介导的miRNA转移以及受损PTECs表达的miRNAs的转录调节有关。miRNA靶标的预测表明,PTECs中被调节的miRNAs参与肾脏恢复过程,与凋亡、细胞骨架重组和缺氧相关的编码mRNA(如CASP3和7、SHC1和SMAD4)下调。总之,这些结果表明,MSC-EVs可能转移并调节PTECs修复和恢复过程中涉及的几种miRNAs的表达。