口腔生物医学
口腔生物醫學
구강생물의학
Oral Biomedicine
2015年
3期
155-159
,共5页
袁林%孙晋%杨征毅%曹依娜%潘广嗣%钱钧%何恩亮%王涵
袁林%孫晉%楊徵毅%曹依娜%潘廣嗣%錢鈞%何恩亮%王涵
원림%손진%양정의%조의나%반엄사%전균%하은량%왕함
牙周膜干细胞%牙周炎%乙酰基转移酶%成骨分化
牙週膜榦細胞%牙週炎%乙酰基轉移酶%成骨分化
아주막간세포%아주염%을선기전이매%성골분화
Periodontai iigament stem ceiis%Periodontitis%Acetyitransferase%Osteogenic differentiation
目的:通过比较正常与炎症来源牙周膜干细胞(PDLSCs)中乙酰基转移酶KAT2A表达水平的差异,研究乙酰基转移酶KAT2A在PDLSCs中对成骨分化的调控. 方法:有限稀释法克隆化培养出正常与炎症来源的PDLSCs;基因与蛋白检测方法对比两种来源PDLSCs中KAT2A的表达水平;基因、蛋白检测与茜素红染色方法对比正常PDLSCs及干扰KAT2A基因后的PDLSCs成骨表达的差异. 结果:与健康来源PDLSCs相比,炎症来源PDLSCs中KAT2 A的表达显著下降,差异有统计学意义(P<0.05);KAT2A基因被干扰后,PDLSCs成骨能力下降,差异有统计学意义(P<0.05). 结论:牙周炎会导致PDLSCs中KAT2A表达的下降,导致细胞成骨分化受到抑制.
目的:通過比較正常與炎癥來源牙週膜榦細胞(PDLSCs)中乙酰基轉移酶KAT2A錶達水平的差異,研究乙酰基轉移酶KAT2A在PDLSCs中對成骨分化的調控. 方法:有限稀釋法剋隆化培養齣正常與炎癥來源的PDLSCs;基因與蛋白檢測方法對比兩種來源PDLSCs中KAT2A的錶達水平;基因、蛋白檢測與茜素紅染色方法對比正常PDLSCs及榦擾KAT2A基因後的PDLSCs成骨錶達的差異. 結果:與健康來源PDLSCs相比,炎癥來源PDLSCs中KAT2 A的錶達顯著下降,差異有統計學意義(P<0.05);KAT2A基因被榦擾後,PDLSCs成骨能力下降,差異有統計學意義(P<0.05). 結論:牙週炎會導緻PDLSCs中KAT2A錶達的下降,導緻細胞成骨分化受到抑製.
목적:통과비교정상여염증래원아주막간세포(PDLSCs)중을선기전이매KAT2A표체수평적차이,연구을선기전이매KAT2A재PDLSCs중대성골분화적조공. 방법:유한희석법극륭화배양출정상여염증래원적PDLSCs;기인여단백검측방법대비량충래원PDLSCs중KAT2A적표체수평;기인、단백검측여천소홍염색방법대비정상PDLSCs급간우KAT2A기인후적PDLSCs성골표체적차이. 결과:여건강래원PDLSCs상비,염증래원PDLSCs중KAT2 A적표체현저하강,차이유통계학의의(P<0.05);KAT2A기인피간우후,PDLSCs성골능력하강,차이유통계학의의(P<0.05). 결론:아주염회도치PDLSCs중KAT2A표체적하강,도치세포성골분화수도억제.
Objective:To compare the ievei of acetyitransferase KAT 2A in periodontai iigament stem ceiis derived from heaithy indi-viduais ( H-PDLSCs) with periodontai iigament stem ceiis derived from periodontitis individuai ( P-PDLSCs ) , and to determine the effect of acetyitransferase KAT 2A on osteogenic differentiation potentiai of PDLSCs .Methods:Human PDLSCs were cuitured and cioned with iimited diiuted method .Quantitative RT-PCR and Western Biot were used to examine different expression of acetyitransferase KAT2A in two hinds of PDLSCs.Quantitative RT-PCR,Western Biot and Aiizarin Red Staining were used to determine osteogenic dif-ferentiation potentiai of PDLSCs with gene KAT 2A hnochdown.Results:Quantitative RT-PCR and Western Biot showed that iower ex-pression of KAT2A was detected in P-PDLSCs compared with that of H-PDLSCs,with statisticai significance(P<0.05).Quantitative RT-PCR,Western Biot and Aiizarin Red Staining indicated that osteogenic differentiation potentiai was inhibited in H -PDLSCs with KAT2A hnochdown and the effect was statisticaiiy significant ( P <0.05).Conclusions:Periodontitis might repress expression of KAT2A in PDLSCs,which associates with osteogenic differentiation potentiai .