临床口腔医学杂志
臨床口腔醫學雜誌
림상구강의학잡지
JOURNAL OF CLINICAL STOMATOLOGY
2014年
6期
336-339
,共4页
常秀梅%张克荣%王书文%齐香微
常秀梅%張剋榮%王書文%齊香微
상수매%장극영%왕서문%제향미
牙囊细胞%分化%矿化%LIM矿化蛋白-1
牙囊細胞%分化%礦化%LIM礦化蛋白-1
아낭세포%분화%광화%LIM광화단백-1
dental follicle cells%differentiation%mineralizzation%LIM-1 mineralization protein-1
目的:研究人牙囊细胞成骨分化前后LIM矿化蛋白-1的表达。探讨LIM矿化蛋白-1在牙囊细胞向牙周组织分化过程中的作用。方法:组织块加酶消化法分离培养人牙囊细胞,实验组培养液中加入矿化诱导剂,对照组不加矿化诱导剂。培养4周后,免疫细胞化学检测骨涎蛋白的表达;Von Kossa染色检测矿化结节的形成。矿化诱导前后,采用RT-PCR技术检测LIM矿化蛋白-1。结果:培养4周,实验组矿化结节形成,骨涎蛋白免疫细胞化学呈阳性表达, Von Kossa染色阳性;对照组未形成矿化结节,骨涎蛋白表达弱阳性,Von Kossa染色阴性。 RT-PCR结果显示LIM矿化蛋白-1在实验组强阳性表达,对照组弱表达。结论:LIM矿化蛋白-1与胚胎期人牙囊细胞的体外矿化过程相关,提示LIM矿化蛋白-1可能在胚胎期牙囊细胞的分化、矿化中发挥一定作用。
目的:研究人牙囊細胞成骨分化前後LIM礦化蛋白-1的錶達。探討LIM礦化蛋白-1在牙囊細胞嚮牙週組織分化過程中的作用。方法:組織塊加酶消化法分離培養人牙囊細胞,實驗組培養液中加入礦化誘導劑,對照組不加礦化誘導劑。培養4週後,免疫細胞化學檢測骨涎蛋白的錶達;Von Kossa染色檢測礦化結節的形成。礦化誘導前後,採用RT-PCR技術檢測LIM礦化蛋白-1。結果:培養4週,實驗組礦化結節形成,骨涎蛋白免疫細胞化學呈暘性錶達, Von Kossa染色暘性;對照組未形成礦化結節,骨涎蛋白錶達弱暘性,Von Kossa染色陰性。 RT-PCR結果顯示LIM礦化蛋白-1在實驗組彊暘性錶達,對照組弱錶達。結論:LIM礦化蛋白-1與胚胎期人牙囊細胞的體外礦化過程相關,提示LIM礦化蛋白-1可能在胚胎期牙囊細胞的分化、礦化中髮揮一定作用。
목적:연구인아낭세포성골분화전후LIM광화단백-1적표체。탐토LIM광화단백-1재아낭세포향아주조직분화과정중적작용。방법:조직괴가매소화법분리배양인아낭세포,실험조배양액중가입광화유도제,대조조불가광화유도제。배양4주후,면역세포화학검측골연단백적표체;Von Kossa염색검측광화결절적형성。광화유도전후,채용RT-PCR기술검측LIM광화단백-1。결과:배양4주,실험조광화결절형성,골연단백면역세포화학정양성표체, Von Kossa염색양성;대조조미형성광화결절,골연단백표체약양성,Von Kossa염색음성。 RT-PCR결과현시LIM광화단백-1재실험조강양성표체,대조조약표체。결론:LIM광화단백-1여배태기인아낭세포적체외광화과정상관,제시LIM광화단백-1가능재배태기아낭세포적분화、광화중발휘일정작용。
Objective:To investigate Expression of LIM mineralization protein-1 after osteogenic differentiation of hu-man dental follicle cells compared with undifferented. Method:Human dental follicle cells were cultured in the presence of dexamethasone,asorbic acid and B-glycerophosphate for bone-like mineralized nodule formation ,characterized by Von Kos-sa staining and immunocyto chemistry of bone sialoprotein.Expression of LIM mineralization protein-1 was analzed by re-verse transcriptase-polymerase chain reaction. Result:LIM mineralization protein-1 were expressed both before mineraliza-tion and after,generally held at astatistically significantly higher level compared with the control. Conclusion:LIM mineral-ization protein-1 is found to be involved in the mineralization of human dental follicle cells.LIM mineralization protein-1 may play a role in the diferentiation and mineralization of human dental follicle cells.