Polack B, Ceré N, Le Rhun D, Guillot J, Chermette R
URA INRA-DGER Immuno-Pathologie Cellulaire et Moléculaire, Ecole Nationale Vétérinaire d'Alfort, Maisons-Alfort, France.
J Eukaryot Microbiol. 1997 Nov-Dec;44(6):22S. doi: 10.1111/j.1550-7408.1997.tb05749.x.
Cultivation of Pneumocystis carinii from rabbit onto cell monolayers was intended. Three cell types were used: rat lung derived cell line L2 and canine kidney derived cell line MDCK, and primary epithelial rabbit lung cells derived from 20 days old foetuses. These primary cells were also immortalized by transfection of the coding sequences for the large and small T antigens of the SV40 virus. P. carinii were extracted from lungs of corticoid treated young rabbits and were purified on Ficoll. In vitro development of P. carinii was assessed by counting the number of attached parasites on cells after staining. No development was observed on L2 nd MDCK cell lines. On the contrary, a development was observed on rabbit derived cells with a threefold increase of attached parasites on the third day of culture. Immortalized cells allowed also multiplication of attached P. carinii. These results are similar to those obtained with culture of rodent P. carinii onto cell monolayers.
旨在将卡氏肺孢子虫从兔体培养到细胞单层上。使用了三种细胞类型:大鼠肺源细胞系L2和犬肾源细胞系MDCK,以及来自20日龄胎儿的兔肺原代上皮细胞。这些原代细胞也通过转染SV40病毒大T抗原和小T抗原的编码序列而永生化。卡氏肺孢子虫从经皮质激素处理的幼兔肺中提取,并在菲可(Ficoll)上纯化。通过对染色后细胞上附着的寄生虫数量进行计数来评估卡氏肺孢子虫的体外发育情况。在L2和MDCK细胞系上未观察到发育情况。相反,在兔源细胞上观察到了发育情况,培养第三天附着的寄生虫数量增加了三倍。永生化细胞也允许附着的卡氏肺孢子虫增殖。这些结果与将啮齿类卡氏肺孢子虫培养到细胞单层上所获得的结果相似。