牙体牙髓牙周病学杂志
牙體牙髓牙週病學雜誌
아체아수아주병학잡지
CHINESE JOURNAL OF CONSERVATIVE DENTISTRY
2015年
4期
187-192
,共6页
肖敏%陈博%李明伟%何文喜%余擎
肖敏%陳博%李明偉%何文喜%餘擎
초민%진박%리명위%하문희%여경
牙髓干细胞%周期性机械压应力%增殖%矿化
牙髓榦細胞%週期性機械壓應力%增殖%礦化
아수간세포%주기성궤계압응력%증식%광화
human dental pulp stem cells%cyclic mechanical stress%proliferation%mineralization
目的:研究不同大小的周期性机械压应力刺激对人牙髓干细胞(hDPSCs)体外增殖和矿化的影响。方法:用体外离心力加压模式,对各组hDPSCs施加30 min/d、大小分别为170、210、250 g的周期性机械压应力刺激,以不加力组作为对照。分别利用CCK-8试剂盒及碱性磷酸酶(ALP)试剂盒检测各组hDPSCs的增殖情况及ALP活性;茜素红染色检测各组hDPSCs的矿化能力;透射电镜观察各组hDPSCs的超微结构。结果:3种大小的机械压应力刺激均可显著抑制hDPSCs增殖、ALP活性显著下降(P<0.05);各加力组形成的矿化结节明显减少,且以250 g的应力刺激对矿化能力的抑制最为显著(P<0.05)。结论:一定大小、频率范围内的周期性机械压应力刺激可抑制人牙髓干细胞体外增殖和矿化,且对矿化的抑制作用与周期性机械压应力大小成正相关。
目的:研究不同大小的週期性機械壓應力刺激對人牙髓榦細胞(hDPSCs)體外增殖和礦化的影響。方法:用體外離心力加壓模式,對各組hDPSCs施加30 min/d、大小分彆為170、210、250 g的週期性機械壓應力刺激,以不加力組作為對照。分彆利用CCK-8試劑盒及堿性燐痠酶(ALP)試劑盒檢測各組hDPSCs的增殖情況及ALP活性;茜素紅染色檢測各組hDPSCs的礦化能力;透射電鏡觀察各組hDPSCs的超微結構。結果:3種大小的機械壓應力刺激均可顯著抑製hDPSCs增殖、ALP活性顯著下降(P<0.05);各加力組形成的礦化結節明顯減少,且以250 g的應力刺激對礦化能力的抑製最為顯著(P<0.05)。結論:一定大小、頻率範圍內的週期性機械壓應力刺激可抑製人牙髓榦細胞體外增殖和礦化,且對礦化的抑製作用與週期性機械壓應力大小成正相關。
목적:연구불동대소적주기성궤계압응력자격대인아수간세포(hDPSCs)체외증식화광화적영향。방법:용체외리심력가압모식,대각조hDPSCs시가30 min/d、대소분별위170、210、250 g적주기성궤계압응력자격,이불가력조작위대조。분별이용CCK-8시제합급감성린산매(ALP)시제합검측각조hDPSCs적증식정황급ALP활성;천소홍염색검측각조hDPSCs적광화능력;투사전경관찰각조hDPSCs적초미결구。결과:3충대소적궤계압응력자격균가현저억제hDPSCs증식、ALP활성현저하강(P<0.05);각가력조형성적광화결절명현감소,차이250 g적응력자격대광화능력적억제최위현저(P<0.05)。결론:일정대소、빈솔범위내적주기성궤계압응력자격가억제인아수간세포체외증식화광화,차대광화적억제작용여주기성궤계압응력대소성정상관。
AIM:To explore the effects of mechanical stress on the proliferation and differentiation of human dental pulp stem cells(hDPSCs).METHODS:Human DPSCs were cultured and subjected to cyclic mechanical stress at 170 g,210 g and 250 g respectively for 30 min every day.Untreated DPSCs served as controls.After that,cell pro-liferation and ALP activity was examined by CCK-8 and ALP kit respectively.The formation of mineralized nodules was determined using half-quantitative Alizarin Red S assay.Cell ultrastructure was observed by the transmission electron microscope.RESULTS:CCK-8 results demonstrated that cell proliferation was reduced(P<0.05),ALP activity and mineralization capacity of stress-treated DPSCs were descended by the stress treatment.The 250 g group had the most significant inhibition(P<0.05).CONCLUSION:Cyclic mechanical stress can inhibit the proliferation and minerali-zation of hDPSCs in vitro in a stress value dependent manner.