北京口腔医学
北京口腔醫學
북경구강의학
BEIJING JOURNAL OF STOMATOLOGY
2014年
6期
311-315
,共5页
郑颖%张建鹏%王劲松%樊闪%石乃琳%陈宁宁%张洋%张春梅
鄭穎%張建鵬%王勁鬆%樊閃%石迺琳%陳寧寧%張洋%張春梅
정영%장건붕%왕경송%번섬%석내림%진저저%장양%장춘매
牙髓细胞%牙髓再生%I型胶原浓度%I型胶原收缩
牙髓細胞%牙髓再生%I型膠原濃度%I型膠原收縮
아수세포%아수재생%I형효원농도%I형효원수축
Dental pulp cells%Pulp regeneration%Collagen I concentration%Collagen I contraction
目的:探讨牙髓组织再生研究中不同浓度的I型胶原支架对牙髓细胞的分布及数量的影响,确定最佳胶原材料的浓度。方法实验组将10μl移液枪头一端封闭,做为人工根管;对照组为两端开放的10μl移液枪头。体外培养转染绿色荧光蛋白的C57BL/6小鼠牙髓细胞,并将其分别接种于1%,2%和3%的I型胶原支架中,注入10μl的实验组和对照组移液枪头内,于6孔板中培养2周。荧光显微镜下观察牙髓细胞的分布,胰蛋白酶消化后计算各浓度中牙髓细胞的数目。结果对照组各浓度的胶原支架内牙髓细胞均生长良好。实验组1%和2%的I型胶原中的牙髓细胞生长良好,且细胞计数无显著性差异( P>0.05);浓度为3%的胶原中牙髓细胞在人工根管的中、上段少有生长,且与1%和2%的胶原支架中的牙髓细胞数目差异有统计学意义(P<0.01)。结论 I型胶原支架材料浓度从1%提高到2%,可减少材料的收缩,并能保证细胞生长良好,2%的I型胶原浓度是牙髓组织再生中最佳浓度。
目的:探討牙髓組織再生研究中不同濃度的I型膠原支架對牙髓細胞的分佈及數量的影響,確定最佳膠原材料的濃度。方法實驗組將10μl移液鎗頭一耑封閉,做為人工根管;對照組為兩耑開放的10μl移液鎗頭。體外培養轉染綠色熒光蛋白的C57BL/6小鼠牙髓細胞,併將其分彆接種于1%,2%和3%的I型膠原支架中,註入10μl的實驗組和對照組移液鎗頭內,于6孔闆中培養2週。熒光顯微鏡下觀察牙髓細胞的分佈,胰蛋白酶消化後計算各濃度中牙髓細胞的數目。結果對照組各濃度的膠原支架內牙髓細胞均生長良好。實驗組1%和2%的I型膠原中的牙髓細胞生長良好,且細胞計數無顯著性差異( P>0.05);濃度為3%的膠原中牙髓細胞在人工根管的中、上段少有生長,且與1%和2%的膠原支架中的牙髓細胞數目差異有統計學意義(P<0.01)。結論 I型膠原支架材料濃度從1%提高到2%,可減少材料的收縮,併能保證細胞生長良好,2%的I型膠原濃度是牙髓組織再生中最佳濃度。
목적:탐토아수조직재생연구중불동농도적I형효원지가대아수세포적분포급수량적영향,학정최가효원재료적농도。방법실험조장10μl이액창두일단봉폐,주위인공근관;대조조위량단개방적10μl이액창두。체외배양전염록색형광단백적C57BL/6소서아수세포,병장기분별접충우1%,2%화3%적I형효원지가중,주입10μl적실험조화대조조이액창두내,우6공판중배양2주。형광현미경하관찰아수세포적분포,이단백매소화후계산각농도중아수세포적수목。결과대조조각농도적효원지가내아수세포균생장량호。실험조1%화2%적I형효원중적아수세포생장량호,차세포계수무현저성차이( P>0.05);농도위3%적효원중아수세포재인공근관적중、상단소유생장,차여1%화2%적효원지가중적아수세포수목차이유통계학의의(P<0.01)。결론 I형효원지가재료농도종1%제고도2%,가감소재료적수축,병능보증세포생장량호,2%적I형효원농도시아수조직재생중최가농도。
Objective To investigate the optimal concentration of collagen I for the proliferation and distribution of dental pulp cells in pulp regeneration. Methods The 10μl pipette tips were capped to structurally mimic artificial root canals. The bland sterile 10μl pipette tips were used as the control group. GFP positive dental pulp cells were obtained from GFP C57BL/6 mouse. Predetermined amount of GPF positive dental pulp cells were mixed with 1%, 2% and 3% collagen I, respectively. The collagen I gel encapsulated with dental pulp cells were then injected into the artificial root canals and cultured for 2 weeks in 6 wells. The distribution and proliferation of dental pulp cells were observed under fluorescent microscope and the cell amount was also counted. Results The proliferation and distribution had no significant difference in the control group. In artificial root canals, there was no significant difference between 1% and 2% collagen I. However, when the concentration of collagen I increased to 3%, there was only a small fraction of cells survived in the artificial root canals. Conclusion 2% collagen I is the optimal concentration for pulp regeneration.