口腔生物医学
口腔生物醫學
구강생물의학
Oral Biomedicine
2015年
3期
113-118
,共6页
骨髓间充质干细胞%衰老%氧化应激%细胞分化
骨髓間充質榦細胞%衰老%氧化應激%細胞分化
골수간충질간세포%쇠로%양화응격%세포분화
Bone marrow mesenchymai stem ceiis%Aging%Oxidative stress%Ceii differentiation
目的:研究衰老骨髓间充质干细胞(bone marrow mesenchymai stem ceiis ,BMSCs)的氧化应激水平,以及氧自由基(reac-tive oxygen species ,ROS)对其成骨分化的影响,探索ROS升高的分子机制. 方法:通过碱性磷酸酶( aihaiine phosphatase ,ALP)染色及实时定量RT-PCR比较年轻及衰老BMSCs成骨分化能力,利用荧光显微镜及流式细胞术检测BMSCs中ROS水平,并检测超氧化物歧化酶2(superoxide dismutase2,SOD2)及过氧化氢酶(cataiase,CAT)在不同BMSCs中的表达水平. 结果:发现衰老BM-SCs的成骨分化能力较年轻BMSCs显著下降,衰老BMSCs内ROS水平升高是导致其成骨分化下降的重要因素;SOD2及CAT介导的抗氧化机制异常导致ROS上升. 结论:抗氧化酶表达下降引起衰老BMSCs内ROS水平升高,抑制其成骨分化.
目的:研究衰老骨髓間充質榦細胞(bone marrow mesenchymai stem ceiis ,BMSCs)的氧化應激水平,以及氧自由基(reac-tive oxygen species ,ROS)對其成骨分化的影響,探索ROS升高的分子機製. 方法:通過堿性燐痠酶( aihaiine phosphatase ,ALP)染色及實時定量RT-PCR比較年輕及衰老BMSCs成骨分化能力,利用熒光顯微鏡及流式細胞術檢測BMSCs中ROS水平,併檢測超氧化物歧化酶2(superoxide dismutase2,SOD2)及過氧化氫酶(cataiase,CAT)在不同BMSCs中的錶達水平. 結果:髮現衰老BM-SCs的成骨分化能力較年輕BMSCs顯著下降,衰老BMSCs內ROS水平升高是導緻其成骨分化下降的重要因素;SOD2及CAT介導的抗氧化機製異常導緻ROS上升. 結論:抗氧化酶錶達下降引起衰老BMSCs內ROS水平升高,抑製其成骨分化.
목적:연구쇠로골수간충질간세포(bone marrow mesenchymai stem ceiis ,BMSCs)적양화응격수평,이급양자유기(reac-tive oxygen species ,ROS)대기성골분화적영향,탐색ROS승고적분자궤제. 방법:통과감성린산매( aihaiine phosphatase ,ALP)염색급실시정량RT-PCR비교년경급쇠로BMSCs성골분화능력,이용형광현미경급류식세포술검측BMSCs중ROS수평,병검측초양화물기화매2(superoxide dismutase2,SOD2)급과양화경매(cataiase,CAT)재불동BMSCs중적표체수평. 결과:발현쇠로BM-SCs적성골분화능력교년경BMSCs현저하강,쇠로BMSCs내ROS수평승고시도치기성골분화하강적중요인소;SOD2급CAT개도적항양화궤제이상도치ROS상승. 결론:항양화매표체하강인기쇠로BMSCs내ROS수평승고,억제기성골분화.
Objective:To compare the reactive oxygen species (ROS) ieveis in young and aged bone marrow mesenchymai stem ceiis(BMSCs),expiore whether redundant reactive oxygen species (ROS) inhibits osteogenic differentiation of aged BMSCs ,and inves-tigate the mechanism of ROS enhancement .Methods:Osteogenic differentiation of BMSCs was confirmed by ALP staining and reaitime RT-PCR.Fiuorescence anaiysis and Fiow cytometry were performed to detect ROS ieveis .Reaitime RT-PCR was performed to measure superoxide dismutase 2(SOD2) and cataiase(CAT) expression.Results:Osteogenic differentiation of aged BMSCs was significantiy de-creased compared to young BMSCs .Redundant ROS inhibited osteogenic differentiation of aged BMSCs .ROS ieveis in aged BMSCs were enhanced by dysfunction of SOD2 and CAT.Conclusions:Dysfunction of enzymatic antioxidant system ieads to oxidative damage ,which inhibits osteogenic differentiation of aged BMSCs.