LINC00473 rescues human bone marrow mesenchymal stem cells from apoptosis induced by dexamethasone through the PEBP1-mediated Akt/Bad/Bcl-2 signaling pathway

被引:11
作者
Xu, Yingxing [1 ,2 ]
Jiang, Yaping [2 ,3 ]
Wang, Yingzhen [1 ,2 ]
Zhao, Zhiping [1 ,2 ]
Li, Tao [1 ,2 ]
机构
[1] Qingdao Univ, Dept Joint Surg, Affiliated Hosp, 59 Haier Rd, Qingdao 266003, Shandong, Peoples R China
[2] Qingdao Univ, Med Dept, Qingdao 266071, Shandong, Peoples R China
[3] Qingdao Univ, Dept Stomatol, Affiliated Hosp, Qingdao 266003, Shandong, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
lncRNA LINC00473; human bone marrow mesenchymal stem cells; dexamethasone; apoptosis; phosphatidylethanolamine-binding protein 1; Akt; Bad; Bcl-2 signaling pathway; FEMORAL-HEAD; STROMAL CELLS; OSTEOGENIC DIFFERENTIATION; INDUCED OSTEONECROSIS; GENE; INHIBITION; PROTEIN; ROLES;
D O I
10.3892/ijmm.2020.4788
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The inhibition of the proliferation and apoptosis of bone marrow-derived mesenchymal stem cells (BMSCs) triggered by the excessive use of glucocorticoids, is considered a potential mechanism for the pathogenesis of steroid-induced osteonecrosis of the femoral head (SONFH). Long non-coding RNAs (lncRNAs) have been proven to influence the proliferation, apoptosis and differentiation of BMSCs by regulating the expression of critical genes. A previous microarray analysis by the authors confirmed the significant downregulation of LINC00473 in human BMSCs (hBMSCs) from patients with SONFH. However, the underlying role and molecular mechanisms of LINC00473 on dexamethasone (Dex)-stimulated hBMSCs remains unknown. In the present study, the expression of LINC00473 was determined in the hBMSCs of patients with SONFH and control patients. In addition, the protective effects and underlying molecular mechanisms of LINC00473 in Dex-stimulated hBMSCs were investigated. The results revealed that LINC00473 expression was significantly down-regulated in hBMSCs from patients with SONFH compared with the controls, and that the upregulation of LINC00473 attenuated the inhibitory effects exerted by 1 mu M Dex on the proliferation and apoptosis of hBMSCs. Moreover, the upregulation of LINC00473 significantly promoted the protein expression of phosphorylated (p-)Akt, p-Bcl-2-associated death promoter (p-Bad) and B-cell lymphoma 2 (Bcl-2), whereas it decreased the cleavage of caspase-3, thus preventing the Dex-induced apoptosis of hBMSCs. Of note, the regulatory effects of LINC00473 on the Akt/Bad/Bcl-2 signaling pathway and its anti-apoptotic effects were similar to those of SC79 (an Akt activator), and were inhibited by MK-2206 (an Akt inhibitor). In further experiments, it was found that the upregulation of LINC00473 markedly promoted the phosphorylation of Akt in Dex-stimulated hBMSCs, and increased the protein level of phosphatidylethanolamine-binding protein 1 (PEBP1). Alternatively, the promoting effect on Akt phosphorylation induced by LINC00473 was significantly attenuated following the knockdown of PEBP1. Furthermore, the upregulation of PEBP1 triggered a marked increase in the levels of Akt phosphorylation in Dex-stimulated hBMSCs, which was line with the upregulation of LINC00473. Taken together, the results of the present study demonstrate that LINC00473 has the ability to rescue hBMSCs from Dex-induced apoptosis through the PEBP1-mediated activation of the Akt/Bad/Bcl-2 signaling pathway.
引用
收藏
页码:171 / 182
页数:12
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