miR-152 induces human dental pulp stem cell senescence by inhibiting SIRT7 expression

被引:45
|
作者
Gu, Shensheng [1 ]
Ran, Shujun [1 ]
Liu, Bin [1 ]
Liang, Jingping [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Shanghai Key Lab Stomatol, Dept Endodont,Peoples Hosp 9, Zhizaoju Rd 639, Shanghai 200011, Peoples R China
基金
中国国家自然科学基金;
关键词
dental pulp stem cells; miR-152; senescence; SIRT7; HEPATOCELLULAR-CARCINOMA; TUMOR-SUPPRESSOR; MICRORNAS; DISEASE; CANCER; TISSUE; BMI1;
D O I
10.1002/1873-3468.12138
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human dental pulp stem cells (HDPSCs) have potential applications in regenerative medicine. The molecular mechanisms underlying HDPSC senescence are not completely understood. Here, we investigated the significance of miR-152 in HDPSC senescence. We show that miR-152 is upregulated during HDPSC senescence and its overexpression in early passaged HDPSCs induced senescence. Sirtuin 7 (SIRT7) was identified as a target of miR-152. SIRT7 was downregulated in senescent HDPSCs, whereas miR-152 inhibition upregulated SIRT7 and suppressed the senescent phenotype and SIRT7 overexpression rescued miR-152-induced senescence. Our results demonstrate that the miR-152/SIRT7 axis plays a key role in the regulation of HDPSC senescence and provide a candidate target to improve the functional and therapeutic potential of HDPSCs.
引用
收藏
页码:1123 / 1131
页数:9
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