| Literature DB >> 31437458 |
Zehan Li1, Xingyun Ge1, Jiamin Lu1, Minxia Bian1, Na Li1, Xiao Wu1, Yuzhi Li1, Ming Yan2, Jinhua Yu3.
Abstract
Biological phenotypes of mesenchymal stem cells (MSCs) are regulated by a series of biochemical elements, including microRNAs, hormones and growth factors. Our previous study illustrated a significant role of miR-141-3p during the osteogenic differentiation of stem cells from apical papilla (SCAPs). Nevertheless, the functions of miR-141-3p in regulating the proliferative ability and senescence of SCAPs have not been determined. This study identified that overexpression of miR-141-3p inhibited the proliferative ability of SCAPs. Meanwhile, the senescence of SCAPs was ahead of time. Conversely, transfection of miR-141-3p inhibitor promoted the proliferative ability of SCAPs and delayed their senescence. Yes-associated protein (YAP) was predicted as the downstream target gene of miR-141-3p by online softwares (miRDB, miRTarBase, miRWalk, and TargetScan), and was further verified by dual-luciferase reporter gene assay. Additionally, knockdown of YAP inhibited the proliferation and accelerated the senescence of SCAPs. Collectively, these findings proposed a novel direction that miR-141-3p impeded proliferative ability and promoted senescence of SCAPs through post-transcriptionally downregulating YAP.Entities:
Keywords: Proliferation; Senescence; Stem cells; YAP; miR-141-3p
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Year: 2019 PMID: 31437458 DOI: 10.1016/j.yexcr.2019.111562
Source DB: PubMed Journal: Exp Cell Res ISSN: 0014-4827 Impact factor: 3.905