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
9期
515-518,528
,共5页
徐畅%魏亚红%王玉敏%张莉%韩晓谦%韩婷婷%高玉光
徐暢%魏亞紅%王玉敏%張莉%韓曉謙%韓婷婷%高玉光
서창%위아홍%왕옥민%장리%한효겸%한정정%고옥광
Jun家族蛋白%釉原蛋白%免疫组化%RT-PCR
Jun傢族蛋白%釉原蛋白%免疫組化%RT-PCR
Jun가족단백%유원단백%면역조화%RT-PCR
Jun family proteins%amelogenin%immunohistochemistry%RT-PCR
目的:探讨Jun家族蛋白JunB、c-Jun 和JunD在小鼠釉质发育中的作用. 方法: 应用免疫组化染色检测JunB、c-Jun 和JunD在不同发育阶段小鼠牙胚成釉细胞中的表达;分别以0. 5 μg和2. 0 μg的JunB、c-Jun 和JunD转染小鼠成釉细胞后,运用RT-PCR观察其对釉原蛋白amelogenin mRNA表达的影响.结果:免疫组化染色结果显示:釉质分泌期时,JunB在成釉细胞核中无显著表达,JunD呈弱表达,而c-Jun表达明显;釉质转型期时,JunB和JunD 表达增强且JunD 早于JunB, c-Jun持续表达明显; 在釉质成熟期时, JunB、c-Jun和JunD均显著表达. RT-PCR检测显示:高剂量JunB可明显抑制amelogenin的表达(P<0. 05);低剂量c-Jun可明显促进amelogenin的表达(P<0. 05);JunD对amelogenin的表达无显著影响. 结论:在釉质发育早期,c-Jun可通过上调釉原蛋白的表达参与釉质发育. 在釉质发育后期,JunB可通过抑制釉原蛋白的分泌促进釉质的成熟. JunD对amelogenin表达无显著影响.
目的:探討Jun傢族蛋白JunB、c-Jun 和JunD在小鼠釉質髮育中的作用. 方法: 應用免疫組化染色檢測JunB、c-Jun 和JunD在不同髮育階段小鼠牙胚成釉細胞中的錶達;分彆以0. 5 μg和2. 0 μg的JunB、c-Jun 和JunD轉染小鼠成釉細胞後,運用RT-PCR觀察其對釉原蛋白amelogenin mRNA錶達的影響.結果:免疫組化染色結果顯示:釉質分泌期時,JunB在成釉細胞覈中無顯著錶達,JunD呈弱錶達,而c-Jun錶達明顯;釉質轉型期時,JunB和JunD 錶達增彊且JunD 早于JunB, c-Jun持續錶達明顯; 在釉質成熟期時, JunB、c-Jun和JunD均顯著錶達. RT-PCR檢測顯示:高劑量JunB可明顯抑製amelogenin的錶達(P<0. 05);低劑量c-Jun可明顯促進amelogenin的錶達(P<0. 05);JunD對amelogenin的錶達無顯著影響. 結論:在釉質髮育早期,c-Jun可通過上調釉原蛋白的錶達參與釉質髮育. 在釉質髮育後期,JunB可通過抑製釉原蛋白的分泌促進釉質的成熟. JunD對amelogenin錶達無顯著影響.
목적:탐토Jun가족단백JunB、c-Jun 화JunD재소서유질발육중적작용. 방법: 응용면역조화염색검측JunB、c-Jun 화JunD재불동발육계단소서아배성유세포중적표체;분별이0. 5 μg화2. 0 μg적JunB、c-Jun 화JunD전염소서성유세포후,운용RT-PCR관찰기대유원단백amelogenin mRNA표체적영향.결과:면역조화염색결과현시:유질분비기시,JunB재성유세포핵중무현저표체,JunD정약표체,이c-Jun표체명현;유질전형기시,JunB화JunD 표체증강차JunD 조우JunB, c-Jun지속표체명현; 재유질성숙기시, JunB、c-Jun화JunD균현저표체. RT-PCR검측현시:고제량JunB가명현억제amelogenin적표체(P<0. 05);저제량c-Jun가명현촉진amelogenin적표체(P<0. 05);JunD대amelogenin적표체무현저영향. 결론:재유질발육조기,c-Jun가통과상조유원단백적표체삼여유질발육. 재유질발육후기,JunB가통과억제유원단백적분비촉진유질적성숙. JunD대amelogenin표체무현저영향.
AIM:To investigate the role of Jun family proteins in enamel development of mouse. METH-ODS:Immunohistochemical staining was applied to detect the expression of JunB, c-Jun and JunD in mouse tooth germ ameloblasts. RT-PCR was employed to evaluate the effect on the mRNA expression of amelogenin after transfec-tion of the ameloblasts by JunB, C-Jun and JunD at 0. 5 μg and 2. 0 μg respectively. RESULTS: At the secretion stage, JunB was not expressed and JunD was weakly expressed in ameloblasts nuclei, but c-Jun was obviously ex-pressed. At the transition stage, JunB and JunD expression were increased and JunD was earlier than JunB. c-Jun continuously exhibited strong expression. At the maturation stage, all of the proteins were strongly expressed. Transfec-tion results showed that high dose of JunB inhibited the expression of amelogenin. Low dose of c-Jun evidently en-hanced the expression of amelogenin JunD had no significant effect on amelogenin expression. CONCLUTION:c-Jun may up-regulate the expression of amelogenin at the early stage of enamel development. JunB may suppress the secre-tion of amelogenin and promote the maturation of enamel at the late stage of enamel development. JunD has no significant effect on amelogenin.