MicroRNA-195a-5p inhibits mouse medullary thymic epithelial cells proliferation by directly targeting Smad7

被引:17
|
作者
Guo, Dongguang [1 ]
Ye, Yaqiong [1 ]
Qi, Junjie [1 ]
Xu, Lifeng [1 ]
Zhang, Lihua [1 ]
Tan, Xiaotong [1 ]
Tan, Zhigang [1 ]
Yu, Xiaofang [1 ]
Zhang, Yuan [1 ]
Ma, Yongjiang [1 ]
Li, Yugu [1 ]
机构
[1] South China Agr Univ, Coll Vet Med, Guangzhou 510642, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
miR-195a-5p; mouse thymic epithelial cell; cell proliferation; Smad7; TGF-BETA RECEPTOR; CYCLE ARREST; EXPRESSION; THYMOCYTE; MICRORNAS; INCREASES; GENES; AGE;
D O I
10.1093/abbs/gmv136
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
MiR-195 has been implicated in inhibiting cell proliferation in different types of tumors. Whether it contributes to the process of thymic epithelial cells (TECs) proliferation remains unclear. In this study, we found that miR-195a-5p was highly up-regulated in the TECs isolated from the aging mice. Further experiments showed that miR-195a-5p mimic transfection inhibited the proliferation of mouse medullary thymic epithelial cell line 1 (MTEC1), whereas the transfection of miR-195a-5p inhibitor in MTEC1 had the opposite effect. In addition, miR-195a-5p had no obvious effect on MTEC1 apoptosis. Furthermore, Smad7, a negative regulator of transforming growth factor beta pathway, was confirmed as a direct target of miR-195a-5p by luciferase assays. Taken together, our results indicate that miR-195a-5p inhibits MTEC1 proliferation, at least in part, via down-regulation of Smad7.
引用
收藏
页码:290 / 297
页数:8
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