牙周膜干细胞
运行x2
化学
牙周纤维
细胞生物学
小RNA
转染
细胞分化
下调和上调
内分泌学
内科学
碱性磷酸酶
体外
成骨细胞
生物
医学
生物化学
牙科
酶
基因
作者
Lei Zhen,Xuewei Jiang,Yan Chen,Desheng Fan
出处
期刊:PubMed
[National Institutes of Health]
日期:2017-01-01
卷期号:9 (5): 2384-2393
被引量:31
摘要
, the high expression of miR-31 is associated with the impaired osteogenic differentiation ability of PDLSCs in high glucose environment. Furthermore, miR-31 inhibitors increased mineralized bone matrix formation and raised Runx2, Osx and OCN expression at both mRNA and protein levels. However, PDLSCs pretreated with miR-31 mimics decreased bone matrix formation and reduced Runx2, Osx and OCN expression level in high glucose microenvironment. Moreover, Satb2 was identified as a target of miR-31 which directly binds to its 3'-untranslated region. To further elucidate the effect of Satb2 in miR-31-mediated osteogenic differentiation, PDLSCs were transfected with Satb2 siRNA and miR-31 inhibitors. The results showed that Satb2 siRNA inhibited osteogenic differentiation of PDLSCs in HG, whereas miR-31 inhibitors reversed the repression of osteogenic differentiation in Satb2 siRNA transfected PDLSCs. Taken together, these results demonstrate that miR-31 is involved in the high glucose-suppressed osteogenic differentiation of PDLSCs by targeting Satb2.
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