Osteocytic connexin 43 channels affect fracture healing

被引:17
作者
Chen, Yunhe [1 ]
Chen, Meng [1 ]
Xue, Tong [1 ]
Li, Guobin [1 ]
Wang, Dongen [1 ]
Shang, Peng [2 ]
Jiang, Jean X. [3 ]
Xu, Huiyun [1 ,2 ,4 ]
机构
[1] Northwestern Polytech Univ, Sch Life Sci, Key Lab Space Biosci & Biotechnol, Xian, Shaanxi, Peoples R China
[2] Northwestern Polytech Univ Shenzhen, Res & Dev Inst Shenzhen, Key Lab Space Biosci & Biotechnol, Shenzhen 710072, Guangdong, Peoples R China
[3] Univ Texas Hlth Sci Ctr San Antonio, Dept Biochem & Struct Biol, San Antonio, TX 78229 USA
[4] Northwestern Polytech Univ, Res Ctr Special Environm Biomech & Med Engn, Xian, Shaanxi, Peoples R China
基金
中国国家自然科学基金; 美国国家卫生研究院;
关键词
Cx43; fracture healing; gap junction; hemichannel; transgenic mouse model; SCLEROSTIN ANTIBODY; GAP-JUNCTIONS; BONE; HEMICHANNELS; RELEASE; MICE; OSTEOCLASTOGENESIS; OSTEOBLAST; REPAIR;
D O I
10.1002/jcp.28581
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The cross-talk between cells is very critical for moving forward fracture healing in an orderly manner. Connexin (Cx) 43-formed gap junctions and hemichannels mediate the communication between adjacent cells and cells and extracellular environment. Loss of Cx43 in osteoblasts/osteocytes results in delayed fracture healing. For investigating the role of two channels in osteocytes in bone repair, two transgenic mouse models with Cx43 dominant negative mutants driven by a 10kb-DMP1 promoter were generated: R76W (gap junctions are blocked, whereas hemichannels are promoted) and Delta 130-136 (both gap junctions and hemichannels are blocked). R76W mice (promotion of hemichannels) showed a significant increase of new bone formation, whereasdelayed osteoclastogenesis and healing was observed in Delta 130-136 (impairment of gap junctions), but not in R76W mice (hemichannel promotion may recover the delay). These results suggest that gap junctions and hemichannels play some similar and cooperative roles in bone repair.
引用
收藏
页码:19824 / 19832
页数:9
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