Chinese Journal of Tissue Engineering Research ›› 2017, Vol. 21 ›› Issue (25): 4038-4043.doi: 10.3969/j.issn.2095-4344.2017.25.017

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Long non-coding RNA DANCR enhances chondrogenic differentiation and proliferation of human synovium-derived mesenchymal stem cells  

Yang Chao1, Zhang Lei2, Zhou Li-wu2, Zhao Jian-ning2   

  1. 1Department of Orthopedics, Clinical College of Medical School of Nanjing University, Nanjing 210000, Jiangsu Province, China; 2Department of Orthopedics, Nanjing General Hospital of Nanjing Military Command, Nanjing 210002, Jiangsu Province, China
  • Revised:2017-04-06 Online:2017-09-08 Published:2017-10-09
  • Contact: Zhang Lei, M.D., Attending physician, Department of Orthopedics, Nanjing General Hospital of Nanjing Military Command, Nanjing 210002, Jiangsu Province, China; Zhao Jian-ning, Chief physician, Department of Orthopedics, Nanjing General Hospital of Nanjing Military Command, Nanjing 210002, Jiangsu Province, China
  • About author:Yang Chao, Studying for master’s degree, Department of Orthopedics, Clinical College of Medical School of Nanjing University, Nanjing 210000, Jiangsu Province, China
  • Supported by:

    the Clinical Medical Research Foundation of Jiangsu Province of China, No. BL2012002; Postdoctoral Science Foundation of China, No. 2016M592956; the Funding Project of Nanjing General Hospital of Nanjing Military Command in China, No. 2016003

Abstract:

BACKGROUND: A number of studies have shown that long non-coding RNA DANCR can play an important role in various pathophysiological processes through Wnt/β-catenin signaling pathway.
OBJECTIVE: To explore the effect of long non-coding RNA DANCR on the proliferation and chondrogenesis of synovium-derived mesenchymal stem cells.
METHODS: Passage 3 synovium-derived mesenchymal stem cells were obtained and transfected with pcDNA3.1-GP (control) and pcDNA3.1-GP(DANCR Homo) (experimental). Cell viability was estimated at 1, 2, 3, 4, 5, 6 and 7 days after DANCR transfection. The passage 3 cells were cultured in the chondriogenic medium for 14 days. And the chondrogenesis potential of cells was examined by toluidine blue staining. The chondrogenic-specific marker genes Aggrecan, Type II collagen (Col2) and Sox9 were determined by Real-time PCR.
RESULTS AND CONCLUSION: The synovium-derived mesenchymal stem cells exhibited “S”-shaped curves in the two groups, with cell arrest at 1-2 days and rapid proliferation beginning at 3 days. Cell counting kit-8 assay and toluidine blue staining showed overexpressing DANCR significantly promoted proliferation in synovium-derived mesenchymal stem cells. The aggregates from synovium-derived mesenchymal stem cells in the experimental group had a greater amount of toluidine blue staining than the control group. In addition, we detected the higher expression of chondrogenic specific marker genes, such as Col2, Sox9 and Aggrecan, in the experimental group than the control group at 14 days after chondrogenic induction (P < 0.05). These results demonstrate that long non-coding RNA DANCR could enhance chondrogenic differentiation and proliferation of human synovium-derived mesenchymal stem cells and increase the expression of chondrogenic specific marker genes.

中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程

Key words: Stem Cells, Mesenchymal Stem Cells, Cell Proliferation, Cell Differentiation, Tissue Engineering

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