Molecular mechanism of osteoclast, bone resorption and fracture healing by V-ATPase a3 transport system
10.3969/j.issn.2095-4344.2014.20.026
- VernacularTitle:V-ATPase a3转运系统影响破骨细胞、骨吸收及骨折愈合的分子机制
- Author:
Min SONG
;
Wantao DONG
;
Binghu CHEN
;
Jutang CHAI
;
Yanlong LI
;
Hong WEI
;
Bingxiong CHEN
- Publication Type:Journal Article
- Keywords:
V-ATPase a3;
osteoclasts;
fracture healing
- From:
Chinese Journal of Tissue Engineering Research
2014;(20):3257-3262
- CountryChina
- Language:Chinese
-
Abstract:
BACKGROUND:The V-ATPase a3 transport system plays a crucial role on bone resorption mechanism of the osteoclasts.
OBJECTIVE:To observe the expression of V-ATPase a3 transport system in fracture repair and the effect of V-ATPase a3 transport system inhibitor on fracture healing.
METHODS:We retrieved related literatures in the periodicals database with the key words, and screen them according to the inclusion criteria. The literatures were included in this study after the evaluation of quality.
RESULTS AND CONCLUSION:V-ATPase a3 transport system widely exists in the cytoplasm membrane and organel e membrane of eukaryotic cells. V-ATPase a3 has two structural domains:V0 and V1. V0 structural domain is the proton transport channel, V1 structural domain is mainly the hydrolysis of ATP. V-ATPase a3 transport system focuses on the fril ed edge of osteoclasts, H+is transported to form a high concentration, dissolves inorganic minerals and provides the acidic environment for hydrolytic enzymes, thus being involved in bone resorption. So V-ATPase a3 transport system is selected as the research target in the fracture repair and reshape.
