[The primary culture of human tooth pulp cell].

Hu Zhao, Zhiqing Chen, Wei Bai
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Abstract

Objective: In this study, we established the optimal condition and duration for the primary culture of the human tooth pulp cell with collagenase digestion method.

Method: Pulp tissue was removed from healthy young human teeth extracted for orthodontic purposes, and then the pulp was digested by collagenase separately in duration of 30 mins, 1 hr, 2 hrs, 3 hrs. After the digestion, the viability and digestion efficiency were evaluated by microscopy and trypan-blue dying. The cytokeratin and vimentin were immunocytochemically detected to identify the cell phenotype. The tissue explant culture and trypsin digestion were set as controls.

Results: After digestion of 1 hr, 2 hrs, or 3 hrs, little tissue residue was left, while there is still much tissue remained after digestion of 30 mins. The viability decreased with the elongation of digestion duration.

Conclusion: 37 degrees C, continuing stirring and 1 hr of type I collagenase digestion are the optimal conditions for the primary culture of human tooth pulp with digestion method.

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【人牙髓细胞原代培养】。
目的:探讨胶原酶消化法培养人牙髓细胞的最佳条件和培养时间。方法:从正畸拔牙的健康青年牙齿中取出牙髓组织,分别用胶原酶消化牙髓,时间分别为30 min、1 hr、2 hr、3 hr。消化后,用显微镜和台盼蓝染色法评价细胞活力和消化效率。免疫细胞化学检测细胞角蛋白和波形蛋白,鉴定细胞表型。以组织外植体培养和胰蛋白酶消化为对照。结果:消化1小时、2小时、3小时后组织残留较少,消化30分钟后组织残留较多。随着消化时间的延长,活性降低。结论:37℃,持续搅拌,I型胶原酶消化1小时是消化法人牙髓原代培养的最佳条件。
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