miR-338-3p regulates osteoclastogenesis via targeting IKK gene

被引:14
|
作者
Niu, Dequn [1 ]
Gong, Zheng [2 ]
Sun, Xuemin [3 ]
Yuan, Jianchang [2 ]
Zheng, Tiantian [2 ]
Wang, Xun [2 ]
Fan, Xu [2 ]
Mao, Yingji [2 ]
Liu, Xianfu [4 ]
Tang, Baoding [2 ]
Fu, Yingxiao [2 ]
机构
[1] Bengbu Med Coll, Affiliated Hosp 2, Dept Obstet & Gynaecol, Bengbu 233000, Peoples R China
[2] Bengbu Med Coll, Dept Biosci, Bengbu 233000, Peoples R China
[3] Bengbu Med Coll, Dept Clin Med, Bengbu 233000, Peoples R China
[4] Bengbu Med Coll, Affiliated Hosp 1, Dept Surg Oncol, Bengbu 233000, Peoples R China
关键词
miR-338-3p; Osteoclastogenesis; IKK gene; BONE; DIFFERENTIATION; MICRORNAS;
D O I
10.1007/s11626-019-00325-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
This study determined the effects of miR-338-3p on osteoclast (OC) differentiation and activation. The change levels of miR-338-3p in differentiated OCs were investigated by microRNA microarray assay and quantitative real-time PCR analysis. The effects of miR-338-3p on the differentiation and activation of OCs were determined by tartrate-resistant acid phosphatase staining resorption activity assay and Western blot. Target genes of miR-338-3p were identified by target gene prediction and dual-luciferase reporter gene detection assay as well as Western blot. Results showed that miR-338-3p was markedly downregulated in differentiated OCs. miR-338-3p could inhibit the formation and absorption activity of OCs. Western blot showed that miR-338-3p could influence the change levels of OC differentiation-related proteins. Dual-luciferase reporter gene detection assay and Western blot both showed that miR-338-3p directly targeted IKK gene. In conclusion, miR-338-3p may affect the formation and activity of OCs by targeting the IKK gene.
引用
收藏
页码:243 / 251
页数:9
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