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microRNA-203 promotes proliferation, differentiation, and migration of osteoblasts by upregulation of Msh homeobox 2  期刊论文  

  • 编号:
    3ded0427-14f6-4a83-9878-93c2cde50f0c
  • 作者:
  • 语种:
    英文
  • 期刊:
    JOURNAL OF CELLULAR PHYSIOLOGY ISSN:0021-9541 2019 年 234 卷 10 期 (17639 - 17648) ; OCT
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  • 摘要:

    Despite the improvements in fracture healing, about 10% of patients undergo abnormal healing. As a tumor suppressor, upregulation of microRNA (miR)-203 has been observed in osteogenic differentiation. Herein, we aimed to explore the functional role of miR-203 in osteoblasts as well as the underlying mechanisms. The expression of miR-203 in MC3T3-E1 cells that underwent osteogenic differentiation was determined by quantitative reverse transcription PCR (qRT-PCR). The effects of aberrantly expressed miR-203 on cell viability, migration, and expressions of proteins associated with proliferation, migration, and osteogenic differentiation were measured by using a Cell Counting Kit-8 assay, Transwell cell migration assay, and western blot/qRT-PCR, respectively. The possible downstream factor of miR-203 was subsequently studied. Finally, involvements of the mitogen-activated protein kinase (MAPK)/activator of transcription (STAT) pathways were assessed by western blot. We found thatthe miR-203 level was increased in osteogenic differentiation of MC3T3-E1 cells with increasing duration time (28th day, p<0.001). After cell transfection, we interestingly found that miR-203 overexpression could increase cell viability (p<0.05), promote proliferation, migration (p<0.05), and osteogenic differentiation, and upregulate Msh homeobox 2 (Msx2) expression. Furthermore, Msx2 knockdown was proved to abrogate the effects of miR-203 overexpression on MC3T3-E1 cells. Finally, phosphorylated levels of key kinases in the MAPK/STAT pathways were increased by miR-203 overexpression via upregulating Msx2 expression. In conclusion, miR-203 overexpression promoted proliferation, migration, and osteogenic differentiation of MC3T3-E1 cells through upregulating Msx2along with activation of the MAPK/STAT pathways.

  • 推荐引用方式
    GB/T 7714:
    Liu Haochuan,Chen Bing,Li Yi, et al. microRNA-203 promotes proliferation, differentiation, and migration of osteoblasts by upregulation of Msh homeobox 2 [J].JOURNAL OF CELLULAR PHYSIOLOGY,2019,234(10):17639-17648.
  • APA:
    Liu Haochuan,Chen Bing,Li Yi.(2019).microRNA-203 promotes proliferation, differentiation, and migration of osteoblasts by upregulation of Msh homeobox 2 .JOURNAL OF CELLULAR PHYSIOLOGY,234(10):17639-17648.
  • MLA:
    Liu Haochuan, et al. "microRNA-203 promotes proliferation, differentiation, and migration of osteoblasts by upregulation of Msh homeobox 2" .JOURNAL OF CELLULAR PHYSIOLOGY 234,10(2019):17639-17648.
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