哈尔滨医科大学学报
哈爾濱醫科大學學報
합이빈의과대학학보
JOURNAL OF HARBIN MEDICAL UNIVERSITY
2009年
2期
143-146
,共4页
于清华%高玫梅%韩彦玲%周少云
于清華%高玫梅%韓彥玲%週少雲
우청화%고매매%한언령%주소운
牙髓细胞%分离培养%酶类
牙髓細胞%分離培養%酶類
아수세포%분리배양%매류
dental pulp cells%cell isolated cuhure%enzymes
目的 建立用酶消化组织块培养人牙髓细胞的方法.方法 用酶消化组织块进行人牙髓细胞体外培养,倒置显微镜和透射电镜分别观察牙髓细胞形态、生长情况和超微结构,取第5代牙髓细胞测定生长曲线、免疫组化法鉴定组织来源,并检测其矿化能力.结果 用酶消化组织块培养的人牙髓细胞成纤维细胞样,接种4天大部分组织块能有效贴附于培养瓶壁,第7天可见组织块边缘有细胞延展生长,第14天复层生长,呈网状,可顺利传代;牙髓细胞抗波形蛋白染色阳性,抗角蛋白染色阴性;细胞I型胶原染色阳性,连续培养的牙髓细胞可形成矿化结节,符合牙髓细胞的形态学特征和生物学特性.结论 酶消化组织块培养人牙髓细胞方法简单可行,具有较高的成功率.
目的 建立用酶消化組織塊培養人牙髓細胞的方法.方法 用酶消化組織塊進行人牙髓細胞體外培養,倒置顯微鏡和透射電鏡分彆觀察牙髓細胞形態、生長情況和超微結構,取第5代牙髓細胞測定生長麯線、免疫組化法鑒定組織來源,併檢測其礦化能力.結果 用酶消化組織塊培養的人牙髓細胞成纖維細胞樣,接種4天大部分組織塊能有效貼附于培養瓶壁,第7天可見組織塊邊緣有細胞延展生長,第14天複層生長,呈網狀,可順利傳代;牙髓細胞抗波形蛋白染色暘性,抗角蛋白染色陰性;細胞I型膠原染色暘性,連續培養的牙髓細胞可形成礦化結節,符閤牙髓細胞的形態學特徵和生物學特性.結論 酶消化組織塊培養人牙髓細胞方法簡單可行,具有較高的成功率.
목적 건립용매소화조직괴배양인아수세포적방법.방법 용매소화조직괴진행인아수세포체외배양,도치현미경화투사전경분별관찰아수세포형태、생장정황화초미결구,취제5대아수세포측정생장곡선、면역조화법감정조직래원,병검측기광화능력.결과 용매소화조직괴배양적인아수세포성섬유세포양,접충4천대부분조직괴능유효첩부우배양병벽,제7천가견조직괴변연유세포연전생장,제14천복층생장,정망상,가순리전대;아수세포항파형단백염색양성,항각단백염색음성;세포I형효원염색양성,련속배양적아수세포가형성광화결절,부합아수세포적형태학특정화생물학특성.결론 매소화조직괴배양인아수세포방법간단가행,구유교고적성공솔.
Objective To establish the tissue black enzymolytic method in cultures of human dental pulp cells.Methods The human dental pulp cells were cultured with tissue-explants enzymatic digestion method.The morphological characters and uhrastructure of the cells were observed by inverted microscope and transmission electron microscope.The cells were immunohistochemically detected to identify the cell phenotype,the ability of mineralization.Results Cultures of human dental pulp cells were fibroblast-like and well-attached to wall 4 days after passage,and became growth after 7 days,muhilayered after 14 days.Anti-vimentin was positive,anti-cytokeratin was negative and type I collagen expression was positive by immunohistochemical staining.Cellular nodules were formed in human dental pulp cell after consecutive cuhure.Their morphological and biologic characteristics were similar to those of dental pulp cells.Conclusion The tissue black enzymolytic method in cultures of human dental pulp cells is simple and feasible.The method has a high success rate.