实用口腔医学杂志
實用口腔醫學雜誌
실용구강의학잡지
Journal of Practical Stomatology
2015年
5期
648-652
,共5页
孙素%方明%沈丽娟%王冠林%第五海浪%肖玉鸿
孫素%方明%瀋麗娟%王冠林%第五海浪%肖玉鴻
손소%방명%침려연%왕관림%제오해랑%초옥홍
HEMA%牙髓细胞%增殖%迁移
HEMA%牙髓細胞%增殖%遷移
HEMA%아수세포%증식%천이
HEMA%Dental pulp cells%Proliferation%Migration
目的:研究树脂单体甲基丙烯酸β-羟乙酯(HEMA)对人牙髓细胞(hDPCs)增殖和迁移的影响。方法:组织块法体外原代培养获得 hDPCs,以含不同浓度 HEMA 的 DMEM培养基与第3~5代 hDPCs 共同培养,用 MTT 实验检测 HEMA 作用于hDPCs 24、48、72 h 的增殖情况,Transwell 法观察细胞的迁移能力。结果:HEMA 在体外一定程度上抑制了 hDPCs 的增殖(与对照组比较,P <0.05),并呈时间浓度依赖性,24 h 组的细胞活力值均显著高于48 h 和72 h 组(P <0.05)。HEMA 减少了 hD-PCs 的迁移数(P <0.05)。结论:HEMA 体外能抑制人牙髓细胞的增殖和迁移。
目的:研究樹脂單體甲基丙烯痠β-羥乙酯(HEMA)對人牙髓細胞(hDPCs)增殖和遷移的影響。方法:組織塊法體外原代培養穫得 hDPCs,以含不同濃度 HEMA 的 DMEM培養基與第3~5代 hDPCs 共同培養,用 MTT 實驗檢測 HEMA 作用于hDPCs 24、48、72 h 的增殖情況,Transwell 法觀察細胞的遷移能力。結果:HEMA 在體外一定程度上抑製瞭 hDPCs 的增殖(與對照組比較,P <0.05),併呈時間濃度依賴性,24 h 組的細胞活力值均顯著高于48 h 和72 h 組(P <0.05)。HEMA 減少瞭 hD-PCs 的遷移數(P <0.05)。結論:HEMA 體外能抑製人牙髓細胞的增殖和遷移。
목적:연구수지단체갑기병희산β-간을지(HEMA)대인아수세포(hDPCs)증식화천이적영향。방법:조직괴법체외원대배양획득 hDPCs,이함불동농도 HEMA 적 DMEM배양기여제3~5대 hDPCs 공동배양,용 MTT 실험검측 HEMA 작용우hDPCs 24、48、72 h 적증식정황,Transwell 법관찰세포적천이능력。결과:HEMA 재체외일정정도상억제료 hDPCs 적증식(여대조조비교,P <0.05),병정시간농도의뢰성,24 h 조적세포활력치균현저고우48 h 화72 h 조(P <0.05)。HEMA 감소료 hD-PCs 적천이수(P <0.05)。결론:HEMA 체외능억제인아수세포적증식화천이。
Objective:To assess the effects of HEMA on the proliferation and migration of human dental pulp cells(hDPCs).Meth-ods:hDPCs were obtained using tissue explant culture technique in vitro,and then cells of the 3rd -5th passages were treated by differ-ent concentrations of HEMA for 24,48 and 72 h respectively.Cell proliferation was examined by MTT assay.Cell migration was ob-served by Transwell method.Results:The proliferation ability of hDPCs decreased when exposed to HEMA in both time and concentra-tion dependent manner(vs control,P <0.05).Cell proliferation at 24 h expossure was statistically higher than that at 48 h and 72 h(P<0.05).The migration of hDPCs was significantly reduced in HEMA groups at different concentrations(vs control,P <0.05).Con-clusion:HEMA inhibits the proliferation and migration of human dental pulp cells in vitro.