Armstrong M Y, Richards F F
Yale MacArthur Center for Molecular Parasitology, Yale University School of Medicine, New Haven, CT 06510.
J Protozool. 1989 Jan-Feb;36(1):24S-27S. doi: 10.1111/j.1550-7408.1989.tb02677.x.
A short-term cell culture is used to propagate and purify rat-derived Pneumocystis carinii (Pc). An aliquot of pelleted material washed out of the lungs of rats with moderate to severe Pc pneumonia is cultured for 7 to 10 days on the adherent mink lung cell line Mv 1 Lu, and the rest of the material is frozen down in medium with 10% glycerol. Although it has not been established that substantial multiplication of Pc occurs in culture, the Pc organisms harvested from the supernatant at the end of the culture period are relatively free of both host and feeder cells. This is in marked contrast with the lung wash inoculum in which the Pc organisms are heavily contaminated with rat cells and enmeshed in a highly sticky material. Lung wash preparations frozen down in glycerol and stored at -70 degrees C for as long as 6 months or more can be successfully cultured upon thawing with no apparent loss of viability of the Pc organisms.
短期细胞培养用于繁殖和纯化大鼠源卡氏肺孢子虫(Pc)。从患有中度至重度Pc肺炎的大鼠肺中冲洗出的沉淀物质的一部分,在贴壁貂肺细胞系Mv 1 Lu上培养7至10天,其余物质在含有10%甘油的培养基中冷冻保存。虽然尚未确定Pc在培养物中会大量繁殖,但在培养期结束时从上清液中收获的Pc生物体相对不含宿主细胞和饲养细胞。这与肺灌洗接种物形成鲜明对比,在肺灌洗接种物中,Pc生物体被大鼠细胞严重污染,并包裹在一种高度粘性的物质中。在甘油中冷冻并在-70℃下储存长达6个月或更长时间的肺灌洗制剂,解冻后可以成功培养,且Pc生物体的活力没有明显损失。