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骨髓来源的人多能基质细胞中的微小RNA表达

MicroRNA expression in bone marrow-derived human multipotent Stromal cells.

作者信息

Bellayr Ian H, Kumar Abhinav, Puri Raj K

机构信息

Tumor Vaccines and Biotechnology Branch, Division of Cellular and Gene Therapies, Center for Biologics and Evaluation Research, US Food and Drug Administration, Silver Spring, MD, USA.

出版信息

BMC Genomics. 2017 Aug 11;18(1):605. doi: 10.1186/s12864-017-3997-7.

Abstract

BACKGROUND

Multipotent stromal cells (MSCs) are being studied in the field of regenerative medicine for their multi-lineage differentiation and immunoregulatory capacity. MicroRNAs (miRNAs) are short non-coding RNAs that are responsible for regulating gene expression by targeting transcripts, which can impact MSC functions such as cellular proliferation, differentiation, migration and cell death. miRNAs are expressed in MSCs; however, the impact of miRNAs on cellular functions and donor variability is not well understood. Eight MSC lines were expanded to passages 3, 5 and 7, and their miRNA expression was evaluated using microarray technology.

RESULTS

Statistical analyses of our data revealed that 71 miRNAs out of 939 examined were expressed by this set of MSC lines at all passages and the expression of 11 miRNAs were significantly different between passages 3 and 7, while the expression of 7 miRNAs was significantly different between passages 3 and 5. The expression of these identified miRNAs was evaluated using RT-qPCR for both the first set of MSC lines (n = 6) and a second set of MSC lines (n = 7) expanded from passages 4 to 8. By RT-qPCR only 2 miRNAs, miR-638 and miR-572 were upregulated at passage 7 compared to passage 3 in the first set of MSC lines by 1.71 and 1.54 fold, respectively; and upregulated at passage 8 compared to passage 4 in the second set of MSC lines, 1.35 and 1.59 fold, respectively.

CONCLUSIONS

The expression of miR-638 and miR-572 can distinguish MSCs from two different passages of cell culture. These results may be useful in establishing critical quality attributes of MSCs and determining whether changes in these two miRNAs impact cellular functions.

摘要

背景

多能间充质干细胞(MSCs)因其多向分化和免疫调节能力而在再生医学领域受到研究。微小RNA(miRNAs)是短的非编码RNA,通过靶向转录本调控基因表达,这会影响MSCs的细胞增殖、分化、迁移和细胞死亡等功能。miRNAs在MSCs中表达;然而,miRNAs对细胞功能和供体变异性的影响尚不清楚。8个MSCs系扩增至第3、5和7代,并使用微阵列技术评估其miRNA表达。

结果

对我们的数据进行统计分析发现,在检测的939个miRNAs中,这组MSCs系在所有传代中均表达71个miRNAs,11个miRNAs在第3代和第7代之间的表达有显著差异,7个miRNAs在第3代和第5代之间的表达有显著差异。使用RT-qPCR对从第4代扩增至第8代的第一组MSCs系(n = 6)和第二组MSCs系(n = 7)评估这些已鉴定miRNAs的表达。通过RT-qPCR,在第一组MSCs系中,与第3代相比,仅2个miRNAs,即miR-638和miR-572在第7代分别上调1.71倍和1.54倍;在第二组MSCs系中,与第4代相比,在第8代分别上调1.35倍和1.59倍。

结论

miR-638和miR-572的表达可以区分细胞培养两个不同传代的MSCs。这些结果可能有助于确定MSCs的关键质量属性,以及确定这两个miRNAs的变化是否影响细胞功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4cc6/5553681/ce2cd365e84a/12864_2017_3997_Fig1_HTML.jpg

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