MiR-142-5p promotes bone repair by maintaining osteoblast activity

被引:51
|
作者
Tu, Manli [1 ]
Tang, Juanjuan [4 ]
He, Hongbo [5 ]
Cheng, Peng [3 ]
Chen, Chao [2 ]
机构
[1] Cent S Univ, Xiangya Hosp 2, Inst Endocrinol & Metab, Changsha 410011, Hunan, Peoples R China
[2] Soochow Univ, Affiliated Hosp 1, Dept Endocrinol & Metab, Suzhou 215006, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Hosp 1, Dept Gerontol, Nanjing 210029, Jiangsu, Peoples R China
[4] Nanjing Med Univ, Hosp 1, Dept Gynaecol & Obstet, Nanjing 210029, Jiangsu, Peoples R China
[5] Cent S Univ, Xiangya Hosp, Dept Orthoped, 87 Xiangya Rd, Changsha 410008, Hunan, Peoples R China
关键词
MicroRNA; Bone fracture; Osteoblastogenesis; Wwp1; E3 LIGASE WWP1; UP-REGULATION; MECHANICAL-PROPERTIES; FRACTURE; DIFFERENTIATION; MICRORNA; PROLIFERATION; EXPRESSION; PROGRAM; MICE;
D O I
10.1007/s00774-016-0757-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
MicroRNAs play important roles in regulating bone regeneration and remodeling. However, the pathophysiological roles of microRNAs in bone repair remain unclear. Here we identify a significant upregulation of miR-142-5p correlated with active osteoblastogenesis during the bone healing process. In vitro, miR-142-5p promoted osteoblast activity and matrix mineralization by targeting the gene encoding WW-domain-containing E3 ubiquitin protein ligase 1. We also found that the expression of miR-142-5p in the callus of aged mice was lower than that in the callus of young mice and directly correlated with the age-related delay in bone healing. Furthermore, treatment with agomir-142-5p in the fracture areas stimulated osteoblast activity which repaired the bone fractures in aged mice. Thus, our study revealed that miR-142-5p plays a crucial role in healing fractures by maintaining osteoblast activity, and provided a new molecular target therapeutic strategy for bone healing.
引用
收藏
页码:255 / 264
页数:10
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