CircRNA AFF4 promotes osteoblast cells proliferation and inhibits apoptosis via the Mir-7223-5p/PIK3R1 axis

被引:50
|
作者
Mi, Bobin [1 ]
Xiong, Yuan [1 ]
Chen, Lang [1 ]
Yan, Chenchen [1 ]
Endo, Yori [2 ]
Liu, Yi [1 ]
Liu, Jing [1 ]
Hu, Liangcong [1 ]
Hu, Yiqiang [1 ]
Sun, Yun [3 ]
Cao, Faqi [1 ]
Zhou, Wu [1 ]
Liu, Guohui [1 ]
机构
[1] Huazhong Univ Sci & Technol, Union Hosp, Dept Orthoped, Tongji Med Coll, Wuhan 430022, Hubei, Peoples R China
[2] Harvard Med Sch, Brigham & Womens Hosp, Div Plast Surg, Boston, MA 02215 USA
[3] Huazhong Univ Sci & Technol, Union Hosp, Dept Neurosurg, Tongji Med Coll, Wuhan 430022, Hubei, Peoples R China
来源
AGING-US | 2019年 / 11卷 / 24期
基金
美国国家科学基金会;
关键词
circRNA; fracture healing; miRNA;
D O I
10.18632/aging.102524
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Fracture healing is a complex process involving various cell types, cytokines, and mRNAs. Here, we report the roles of the circRNA AFF4/miR-7223-5p/PIK3R1 axis during fracture healing. We found that increased expression of PIK3R1 during fracture healing is directly associated with augmented proliferation and decreased apoptosis of MC3T3-E1 cells. Furthermore, miR-7223-5p targeted PI3KR1 and inhibited MC3T3-E1 proliferation while promoting apoptosis. CircRNA AFF4 acted as a sponge of miR-7223-5p, thereby promoting MC3T3-E1 cell proliferation and inhibiting apoptosis. Local injection of circRNA AFF4 into femoral fracture sites promoted fracture healing in vivo while the injection of miR-7223-5p delayed healing. These findings suggest that CircRNA AFF4 promotes fracture healing by targeting the miR-7223-5p/PIK3R1 axis, and suggests miR-7223-5p, CircRNA AFF4, and the miR-7223-5p/PIK3R1 axis are potential therapeutic targets for improving fracture healing.
引用
收藏
页码:11988 / 12001
页数:14
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