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在人宫颈癌细胞(HeLa细胞)上持续培养刚地弓形虫。

Continual cultivation of Toxoplasma gondii on HeLa cells.

作者信息

Valkoun A

出版信息

Folia Parasitol (Praha). 1983;30(4):289-94.

PMID:6662403
Abstract

Continual cultivation of Toxoplasma gondii in monolayers of HeLa cells has been performed for 6 years. The toxoplasmas were then used for serial cultivation experiments. While searching for optimal conditions for toxoplasma inoculation it was found that infected HeLa cells which were scraped off the glass were a more suitable inoculum than those released by trypsinization. The optimal dose was one zoite per 12 host cells, medium level height at adsorption 2 mm and adsorption time 90 min at 37 degrees C. The concentration of sodium bicarbonate ranging from 8.7 to 26.1 mM had no effect on the multiplication of toxoplasmas. In serial passages in Roux bottles, when the medium was changed every 2-3 days, the average yield of toxoplasmas was 6.2 X 10(6) per ml of medium (after the second change of medium, i.e., 7 days after inoculation). The toxoplasmas obtained in serial passages were suitable for purification studies, for preparation of small amounts of antigens and as an inoculum for suspension cultures.

摘要

在HeLa细胞单层中连续培养刚地弓形虫已进行了6年。然后将这些弓形虫用于连续培养实验。在寻找弓形虫接种的最佳条件时发现,从玻璃上刮下的感染HeLa细胞比胰蛋白酶消化释放的细胞更适合作为接种物。最佳剂量是每12个宿主细胞接种1个速殖子,吸附时培养基水平高度为2毫米,37℃下吸附时间为90分钟。碳酸氢钠浓度在8.7至26.1 mM范围内对弓形虫的增殖没有影响。在Roux瓶中连续传代时,每2 - 3天更换一次培养基,弓形虫的平均产量为每毫升培养基6.2×10⁶个(在第二次更换培养基后,即接种后7天)。连续传代获得的弓形虫适用于纯化研究、制备少量抗原以及作为悬浮培养的接种物。

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