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参考基因的关键选择:鉴定miR-191-5p用于骨髓间充质基质细胞和HS27a/HS5细胞系中miRNAs表达的标准化。

The crucial choice of reference genes: identification of miR-191-5p for normalization of miRNAs expression in bone marrow mesenchymal stromal cell and HS27a/HS5 cell lines.

作者信息

Costé É, Rouleux-Bonnin F

机构信息

CNRS ERL7001 GICC Team LNOx, University of Tours, Tours, France.

出版信息

Sci Rep. 2020 Oct 20;10(1):17728. doi: 10.1038/s41598-020-74685-7.

Abstract

Bone marrow mesenchymal stromal cells (BM-MSCs) have a critical role in tissue regeneration and in the hematopoietic niche due to their differentiation and self-renewal capacities. These mechanisms are finely tuned partly by small non-coding microRNA implicated in post-transcriptional regulation. The easiest way to quantify them is RT-qPCR followed by normalization on validated reference genes (RGs). This study identified appropriate RG for normalization of miRNA expression in BM-MSCs and HS27a and HS5 cell lines in various conditions including normoxia, hypoxia, co-culture, as model for the hematopoietic niche and after induced differentiation as model for regenerative medicine. Six candidates, namely miR-16-5p, miR-34b-3p, miR-103a-3p, miR-191-5p, let-7a-5p and RNU6A were selected and their expression verified by RT-qPCR. Next, a ranking on stability of the RG candidates were performed with two algorithms geNorm and RefFinder and the optimal number of RGs needed to normalize was determined. Our results indicate miR-191-5p as the most stable miRNA in all conditions but also that RNU6a, usually used as RG is the less stable gene. This study demonstrates the interest of rigorously evaluating candidate miRNAs as reference genes and the importance of the normalization process to study the expression of miRNAs in BM-MSCs or derived cell lines.

摘要

骨髓间充质基质细胞(BM-MSCs)因其分化和自我更新能力,在组织再生和造血微环境中发挥着关键作用。这些机制部分由参与转录后调控的小非编码微小RNA精细调节。对它们进行定量的最简单方法是逆转录定量聚合酶链反应(RT-qPCR),随后在经过验证的参考基因(RGs)上进行标准化。本研究确定了在多种条件下,包括常氧、缺氧、共培养(作为造血微环境模型)以及诱导分化后(作为再生医学模型),用于标准化BM-MSCs以及HS27a和HS5细胞系中miRNA表达的合适参考基因。选择了六个候选基因,即miR-16-5p、miR-34b-3p、miR-103a-3p、miR-191-5p、let-7a-5p和RNU6A,并通过RT-qPCR验证了它们的表达。接下来,使用geNorm和RefFinder两种算法对候选参考基因的稳定性进行排序,并确定标准化所需的最佳参考基因数量。我们的结果表明,miR-191-5p在所有条件下都是最稳定的miRNA,但通常用作参考基因的RNU6a却是稳定性最差的基因。本研究证明了严格评估候选miRNA作为参考基因的重要性,以及标准化过程对于研究BM-MSCs或其衍生细胞系中miRNA表达的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aede/7576785/bb17999c97a7/41598_2020_74685_Fig1_HTML.jpg

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