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miR-301b~miR-130b-PPARγ 轴是不同组织来源的间充质干细胞成脂能力的基础。

miR-301b~miR-130b-PPARγ axis underlies the adipogenic capacity of mesenchymal stem cells with different tissue origins.

机构信息

Central Laboratory, Affiliated Hospital of Jining Medical University, Jining, 272029, Shandong Province, China.

Department of Graduate School, Jining Medical University, Jining, 272000, Shandong Province, China.

出版信息

Sci Rep. 2017 Apr 25;7(1):1160. doi: 10.1038/s41598-017-01294-2.

Abstract

Mesenchymal stem cells (MSCs) have been widely used in regenerative medicine and cellular therapy due to their multi-lineage differentiation potential and immunomodulatory function. The applicability of MSCs also depends on their cellular sources and in vivo functions. Here in this study, we systematically compared the morphologic characteristics, immunophenotypes and the adipogenic differentiation of MSCs derived from umbilical cord (UC), adipose tissue (Ad) and bone marrow (BM). We found that the three tissues-derived MSCs displayed decreased adipogenic capacity in the order: Ad-MSC > BM-MSC > UC-MSC, and no morphologic and immunophenotypic differences were observed. Mechanistic investigation revealed a miR-301bmiR-130b-PPARγ axis, whose expression pattern in UC-MSC, Ad-MSC and BM-MSC significantly correlates with their adipogenic capacity. Our results come up with a potential mechanism to elucidate the differential adipogenesis of Ad-MSC, BM-MSC and UC-MSC, which would provide instructional advice for which source of MSCs to choose according to a certain clinical purpose. Furthermore, the miR-301bmiR-130b-PPARγ axis may also be used as a potential therapeutic target for the disorders associated with MSCs-mediated abnormal adipogenesis.

摘要

间充质干细胞(MSCs)因其多向分化潜能和免疫调节功能而广泛应用于再生医学和细胞治疗。MSCs 的适用性还取决于其细胞来源和体内功能。在本研究中,我们系统比较了来源于脐带(UC)、脂肪组织(Ad)和骨髓(BM)的 MSCs 的形态特征、免疫表型和脂肪分化能力。我们发现,三种组织来源的 MSCs 的脂肪分化能力依次降低:Ad-MSC>BM-MSC>UC-MSC,且未观察到形态和免疫表型差异。机制研究揭示了一个 miR-301bmiR-130b-PPARγ 轴,其在 UC-MSC、Ad-MSC 和 BM-MSC 中的表达模式与它们的脂肪分化能力显著相关。我们的研究结果提出了一种潜在的机制来阐明 Ad-MSC、BM-MSC 和 UC-MSC 的脂肪分化差异,这将为根据特定的临床目的选择哪种来源的 MSCs 提供指导建议。此外,miR-301bmiR-130b-PPARγ 轴也可能作为与 MSCs 介导的异常脂肪分化相关疾病的潜在治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14df/5430834/70a9092f836a/41598_2017_1294_Fig1_HTML.jpg

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