| Literature DB >> 26837421 |
Dongguang Guo1, Yaqiong Ye1, Junjie Qi1, Lifeng Xu1, Lihua Zhang1, Xiaotong Tan1, Zhigang Tan1, Xiaofang Yu1, Yuan Zhang1, Yongjiang Ma1, Yugu Li2.
Abstract
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 β 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. Published by Oxford University Press ABBS Editorial Office in association with Oxford University Press on behalf of the Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences 2016. This work is written by (a) US Government employee(s) and is in the public domain in the US.Entities:
Keywords: cell proliferation, Smad7; miR-195a-5p; mouse thymic epithelial cell
Mesh:
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Year: 2016 PMID: 26837421 PMCID: PMC4885129 DOI: 10.1093/abbs/gmv136
Source DB: PubMed Journal: Acta Biochim Biophys Sin (Shanghai) ISSN: 1672-9145 Impact factor: 3.848