Meraviglia Viviana, Azzimato Valerio, Piacentini Luca, Chiesa Mattia, Kesharwani Rupesh K, Frati Caterina, Capogrossi Maurizio C, Gaetano Carlo, Pompilio Giulio, Colombo Gualtiero I, Rossini Alessandra
Laboratory of Vascular Biology and Regenerative Medicine, Centro Cardiologico Monzino IRCCS, Milano, Italy; Center for Biomedicine, European Academy Bozen/Bolzano (EURAC) (affiliated Institute of the University of Lübeck), Bolzano, Italy.
Laboratory of Vascular Biology and Regenerative Medicine, Centro Cardiologico Monzino IRCCS, Milano, Italy; Department of Pharmacology, Chemotherapy and Medical Toxicology, Università degli Studi di Milano, Milano, Italy.
PLoS One. 2014 Sep 18;9(9):e107269. doi: 10.1371/journal.pone.0107269. eCollection 2014.
MicroRNAs are key modulators at molecular level in different biological processes, including determination of cell fate and differentiation. Herein, microRNA expression profiling experiments were performed on syngeneic cardiac (CStC) and bone marrow (BMStC) mesenchymal stromal cells cultured in standard growth medium and then in vitro exposed to adipogenic, osteogenic, cardiomyogenic and endothelial differentiation media. Analysis identified a tissue-specific microRNA signature composed of 16 microRNAs that univocally discriminated cell type of origin and that were completely unaffected by in vitro differentiation media: 4 microRNAs were over-expressed in cardiac stromal cells, and 12 were overexpressed or present only in bone marrow stromal cells. Further, results revealed microRNA subsets specifically modulated by each differentiation medium, irrespective of the cell type of origin, and a subset of 7 microRNAs that were down-regulated by all media with respect to growth medium. Finally, we identified 16 microRNAs that were differentially modulated by the media when comparing the two tissues of origin. The existence of a tissue-specific microRNA signature surviving to any differentiation stimuli, strongly support the role if microRNAs determining cell identity related to tissue origin. Moreover, we identified microRNA subsets modulated by different culture conditions in a tissue-specific manner, pointing out their importance during differentiation processes.
微小RNA是不同生物学过程中分子水平的关键调节因子,包括细胞命运的决定和分化。在此,我们对在标准生长培养基中培养,然后体外暴露于成脂、成骨、心肌生成和内皮分化培养基中的同基因心脏(CStC)和骨髓(BMStC)间充质基质细胞进行了微小RNA表达谱实验。分析确定了一个由16种微小RNA组成的组织特异性微小RNA特征,这些微小RNA能够明确区分细胞来源类型,并且完全不受体外分化培养基的影响:4种微小RNA在心脏基质细胞中过表达,12种在骨髓基质细胞中过表达或仅存在于骨髓基质细胞中。此外,结果显示,无论细胞来源类型如何,每种分化培养基都能特异性调节微小RNA亚群,并且相对于生长培养基,有7种微小RNA亚群被所有培养基下调。最后,我们确定了16种微小RNA,在比较两种来源组织时,它们受培养基的差异调节。存在一种在任何分化刺激下都能存活的组织特异性微小RNA特征,有力地支持了微小RNA在决定与组织来源相关的细胞身份方面的作用。此外,我们以组织特异性方式鉴定了受不同培养条件调节的微小RNA亚群,指出了它们在分化过程中的重要性。
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