Kohn D F, Chinookoswong N
Infect Immun. 1980 May;28(2):601-9. doi: 10.1128/iai.28.2.601-609.1980.
Ependymal organ culture was used as a model to study the effect of Mycoplasma pulmonis on the ciliated ependyma of the rat. Reduced ciliary activity or ciliostasis occurred 48 to 72 h after infection. Scanning electron microscopy showed that numerous organisms were associated with the cytoplasmic membrane of host cells beginning at 24 h, and transmission electron microscopy indicated that M. pulmonis cytadsorbs to the cell surface. Lesions observed in the organ cultures were limited to changes at the cell surface. These changes included reduction in microvilli density, matting of cilia into bundles, collapse of the cilia onto the cell surface, deciliation of the ependymal cells, and flattening of the cell surface. The results indicated that the response of the ependymal cell to M. pulmonis is similar to that which occurrs in Mycoplasma-infected tracheal and oviduct organ culture systems.
采用室管膜器官培养作为模型,研究肺炎支原体对大鼠纤毛室管膜的影响。感染后48至72小时出现纤毛活性降低或纤毛静止。扫描电子显微镜显示,从24小时开始,大量微生物与宿主细胞质膜相关联,透射电子显微镜表明肺炎支原体细胞吸附在细胞表面。在器官培养中观察到的病变仅限于细胞表面的变化。这些变化包括微绒毛密度降低、纤毛缠结成束、纤毛倒伏在细胞表面、室管膜细胞脱纤毛以及细胞表面变平。结果表明,室管膜细胞对肺炎支原体的反应与支原体感染的气管和输卵管器官培养系统中发生的反应相似。