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器官培养中的人输卵管:病原微生物损伤的制备、维持及定量分析

Human fallopian tubes in organ culture: preparation, maintenance, and quantitation of damage by pathogenic microorganisms.

作者信息

McGee Z A, Johnson A P, Taylor-Robinson D

出版信息

Infect Immun. 1976 Feb;13(2):608-18. doi: 10.1128/iai.13.2.608-618.1976.

Abstract

An experimental organ culture model has been developed in which rates of damage to fallopian tube mucosa by agents of sexually transmitted diseases can be quantitated. This required assessment of the effect on organ cultures of such variables as the anatomic area of the fallopian tube employed, endocrinological status of the donor, and composition of media. Organ cultures established from the ampulla of tubes of nonpregnant, premenopausal women and maintained with Eagle minimal essential medium containing 0.05 M N-2-hydroxyethylpiperazine-N'-2-ethanesulfonic acid buffer were most suitable for quantitative studies. Various means of quantitating damage to fallopian tube mucosa were evaluated. Of these, sequential estimations of ciliary vigor and percentage of the periphery of fallopian tube pieces with active cilia proved the most successful. To assess the specificity of the model, fallopian tube organ cultures were infected with Neisseria gonorrhoeae or N. pharyngis, a commensal Neisseria. Damage by N. gonorrhoeae was significantly greater than that by N. pharyngis at each period of observation (P less than 0.001), suggesting that, by using the model, differences in virulence can be determined in vitro that reflect differences in virulence for humans. This model is a potentially valuable tool for studying the interaction of human genital mucosa with known or suspected agents of sexually transmitted diseases.

摘要

已经建立了一种实验性器官培养模型,在该模型中,可以对性传播疾病病原体对输卵管黏膜的损伤率进行定量分析。这需要评估诸如所采用的输卵管解剖区域、供体的内分泌状态以及培养基成分等变量对器官培养的影响。从非孕、绝经前妇女的输卵管壶腹部建立的器官培养物,并用含有0.05 M N-2-羟乙基哌嗪-N'-2-乙磺酸缓冲液的伊格尔最低必需培养基进行维持,最适合进行定量研究。评估了多种定量输卵管黏膜损伤的方法。其中,对纤毛活力的连续评估以及带有活动纤毛的输卵管片段周边百分比的评估最为成功。为了评估该模型的特异性,将输卵管器官培养物用淋病奈瑟菌或咽奈瑟菌(一种共生奈瑟菌)感染。在每个观察期,淋病奈瑟菌造成的损伤均显著大于咽奈瑟菌造成的损伤(P小于0.001),这表明通过使用该模型,可以在体外确定反映对人类毒力差异的毒力差异。该模型是研究人类生殖黏膜与已知或疑似性传播疾病病原体相互作用的潜在有价值工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8706/420652/94b75f20c71e/iai00218-0309-a.jpg

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