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本文引用的文献

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microRNAs: important regulators of stem cells.微小RNA:干细胞的重要调节因子。
Stem Cell Res Ther. 2017 May 11;8(1):110. doi: 10.1186/s13287-017-0551-0.
2
MicroRNA-145 regulates the differentiation of human adipose-derived stem cells to smooth muscle cells via targeting Krüppel-like factor 4.微小RNA-145通过靶向Krüppel样因子4调控人脂肪来源干细胞向平滑肌细胞的分化。
Mol Med Rep. 2017 Jun;15(6):3787-3795. doi: 10.3892/mmr.2017.6478. Epub 2017 Apr 13.
3
Promotion Effects of miR-375 on the Osteogenic Differentiation of Human Adipose-Derived Mesenchymal Stem Cells.miR-375对人脂肪间充质干细胞成骨分化的促进作用
Stem Cell Reports. 2017 Mar 14;8(3):773-786. doi: 10.1016/j.stemcr.2017.01.028. Epub 2017 Mar 2.
4
Effects of miR-146a on the osteogenesis of adipose-derived mesenchymal stem cells and bone regeneration.miR-146a 对脂肪间充质干细胞成骨分化及骨再生的影响。
Sci Rep. 2017 Feb 16;7:42840. doi: 10.1038/srep42840.
5
Adipose-derived circulating miRNAs regulate gene expression in other tissues.脂肪来源的循环微小RNA可调节其他组织中的基因表达。
Nature. 2017 Feb 23;542(7642):450-455. doi: 10.1038/nature21365. Epub 2017 Feb 15.
6
Identification of Potential Plasma microRNA Stratification Biomarkers for Response to Allogeneic Adipose-Derived Mesenchymal Stem Cells in Rheumatoid Arthritis.鉴定潜在的血浆 microRNA 分层生物标志物,以预测类风湿关节炎患者对同种异体脂肪间充质干细胞治疗的反应。
Stem Cells Transl Med. 2017 Apr;6(4):1202-1206. doi: 10.1002/sctm.16-0356. Epub 2017 Jan 3.
7
miR-450a-5p within rat adipose tissue exosome-like vesicles promotes adipogenic differentiation by targeting WISP2.大鼠脂肪组织外泌体样囊泡中的miR-450a-5p通过靶向WISP2促进脂肪生成分化。
J Cell Sci. 2017 Mar 15;130(6):1158-1168. doi: 10.1242/jcs.197764. Epub 2017 Feb 6.
8
MiR-218 Induces Neuronal Differentiation of ASCs in a Temporally Sequential Manner with Fibroblast Growth Factor by Regulation of the Wnt Signaling Pathway.miR-218 通过调控 Wnt 信号通路以时序性方式诱导 ASC 向神经元分化。
Sci Rep. 2017 Jan 3;7:39427. doi: 10.1038/srep39427.
9
Insulin producing cells generation by overexpression of miR-375 in adipose-derived mesenchymal stem cells from diabetic patients.通过在糖尿病患者脂肪来源间充质干细胞中过表达miR-375来生成胰岛素产生细胞。
Biologicals. 2017 Mar;46:23-28. doi: 10.1016/j.biologicals.2016.12.004. Epub 2016 Dec 22.
10
microRNA-145 Mediates the Inhibitory Effect of Adipose Tissue-Derived Stromal Cells on Prostate Cancer.微小RNA-145介导脂肪组织来源的基质细胞对前列腺癌的抑制作用。
Stem Cells Dev. 2016 Sep 1;25(17):1290-8. doi: 10.1089/scd.2016.0093. Epub 2016 Aug 18.

[微小RNA调控脂肪来源干细胞分化的研究进展]

[Research progress of miRNA regulation in differentiation of adipose-derived stem cells].

作者信息

Zhou Lanting, Feng Yanting, Dai Jingxing, Ouyang Jun

机构信息

Medical College, Hubei University of Arts and Science, Xiangyang Hubei, 441053, P.R.China;Department of Anatomy, Southern Medical University, Guangzhou Guangdong, 510515, P.R.China.

Department of Anatomy, Southern Medical University, Guangzhou Guangdong, 510515, P.R.China.

出版信息

Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2017 Dec 15;31(12):1506-1511. doi: 10.7507/1002-1892.201706076.

DOI:10.7507/1002-1892.201706076
PMID:29806396
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8498276/
Abstract

OBJECTIVE

To review the research progress of miRNA regulation in the differentiation of adipose-derived stem cells (ADSCs).

METHODS

The recent literature associated with miRNAs and differentiation of ADSCs was reviewed. The regulatory mechanism was analyzed in detail and summarized.

RESULTS

The results indicate that the expression of miRNAs changes during differentiation of ADSCs. In addition, miRNAs regulate the differentiation of ADSCs into adipocytes, osteoblasts, chondrocytes, neurons, and hepatocytes by regulating the signaling pathways involved in cell differentiation.

CONCLUSION

Through controlling the differentiation of ADSCs by miRNAs, the suitable seed cell for tissue engineering can be established. The review will provide a theoretical basis for molecular targeted therapy and stem cell therapy in clinic.

摘要

目的

综述微小RNA(miRNA)调控脂肪来源干细胞(ADSCs)分化的研究进展。

方法

回顾近期与miRNA和ADSCs分化相关的文献。详细分析并总结其调控机制。

结果

结果表明,在ADSCs分化过程中miRNA的表达发生变化。此外,miRNA通过调控参与细胞分化的信号通路来调节ADSCs向脂肪细胞、成骨细胞、软骨细胞、神经元和肝细胞的分化。

结论

通过miRNA控制ADSCs的分化,可为组织工程建立合适的种子细胞。本综述将为临床分子靶向治疗和干细胞治疗提供理论依据。