中国组织工程研究
中國組織工程研究
중국조직공정연구
Journal of Clinical Rehabilitative Tissue Engineering Research
2014年
20期
3257-3262
,共6页
宋敏%董万涛%陈秉虎%柴居堂%黎彦龙%韦宏%陈秉雄
宋敏%董萬濤%陳秉虎%柴居堂%黎彥龍%韋宏%陳秉雄
송민%동만도%진병호%시거당%려언룡%위굉%진병웅
组织构建%骨组织工程%组织构建综述%V-ATPase a3%破骨细胞%骨折愈合%国家自然科学基金
組織構建%骨組織工程%組織構建綜述%V-ATPase a3%破骨細胞%骨摺愈閤%國傢自然科學基金
조직구건%골조직공정%조직구건종술%V-ATPase a3%파골세포%골절유합%국가자연과학기금
V-ATPase a3%osteoclasts%fracture healing
背景:V-ATPase a3转运系统在破骨细胞对于骨吸收机制中起重要作用。<br> 目的:归纳总结V-ATPase a3转运系统在骨折修复中的表达,以及V-ATPase a3转运系统抑制剂对于骨折愈合的影响,进而能更好的指导临床。<br> 方法:在国内外期刊数据库中检索近10年内国内外文献,按检索关键词检索相关文献,筛选出符合纳入标准的文献,对其文献进行质量评估后采纳。<br> 结果与结论:V-ATPase a3转运系统广泛存在于真核细胞的细胞质膜和细胞器膜上,V-ATPase a3有2个结构域V0和V1,V0结构域是质子转运的通道,V1结构域主要是水解ATP供能。V-ATPase a3转运系统集中存在于破骨细胞皱褶缘上,逆浓度梯度转运H+,为破骨细胞提供酸性环境,溶解无机物,为水解酶创造微环境降解有机物,参与骨吸收。因而V-ATPase a3转运系统在骨折的修复与重塑中选作研究靶点。
揹景:V-ATPase a3轉運繫統在破骨細胞對于骨吸收機製中起重要作用。<br> 目的:歸納總結V-ATPase a3轉運繫統在骨摺脩複中的錶達,以及V-ATPase a3轉運繫統抑製劑對于骨摺愈閤的影響,進而能更好的指導臨床。<br> 方法:在國內外期刊數據庫中檢索近10年內國內外文獻,按檢索關鍵詞檢索相關文獻,篩選齣符閤納入標準的文獻,對其文獻進行質量評估後採納。<br> 結果與結論:V-ATPase a3轉運繫統廣汎存在于真覈細胞的細胞質膜和細胞器膜上,V-ATPase a3有2箇結構域V0和V1,V0結構域是質子轉運的通道,V1結構域主要是水解ATP供能。V-ATPase a3轉運繫統集中存在于破骨細胞皺褶緣上,逆濃度梯度轉運H+,為破骨細胞提供痠性環境,溶解無機物,為水解酶創造微環境降解有機物,參與骨吸收。因而V-ATPase a3轉運繫統在骨摺的脩複與重塑中選作研究靶點。
배경:V-ATPase a3전운계통재파골세포대우골흡수궤제중기중요작용。<br> 목적:귀납총결V-ATPase a3전운계통재골절수복중적표체,이급V-ATPase a3전운계통억제제대우골절유합적영향,진이능경호적지도림상。<br> 방법:재국내외기간수거고중검색근10년내국내외문헌,안검색관건사검색상관문헌,사선출부합납입표준적문헌,대기문헌진행질량평고후채납。<br> 결과여결론:V-ATPase a3전운계통엄범존재우진핵세포적세포질막화세포기막상,V-ATPase a3유2개결구역V0화V1,V0결구역시질자전운적통도,V1결구역주요시수해ATP공능。V-ATPase a3전운계통집중존재우파골세포추습연상,역농도제도전운H+,위파골세포제공산성배경,용해무궤물,위수해매창조미배경강해유궤물,삼여골흡수。인이V-ATPase a3전운계통재골절적수복여중소중선작연구파점。
BACKGROUND:The V-ATPase a3 transport system plays a crucial role on bone resorption mechanism of the osteoclasts. <br> 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. <br> 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. <br> 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.