首页> 外文期刊>Journal of Pathology: Journal of the Pathological Society of Great Britain and Ireland >Lineage tracing suggests that ovarian endosalpingiosis does not result from escape of oviductal epithelium
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Lineage tracing suggests that ovarian endosalpingiosis does not result from escape of oviductal epithelium

机译:谱系追踪表明,卵巢内皮表源于产卵性上皮逸出

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Abstract Most high‐grade serous carcinomas are thought to arise from Fallopian tube epithelium (FTE), but some likely arise outside of the tube, perhaps from ectopic tubal‐type epithelium known as endosalpingiosis. Importantly, the origin of endosalpingiosis is poorly understood. The proximity of the tubal fimbriae to the ovaries has led to the proposal that disruptions in the ovarian surface that occur during ovulation may allow detached FTE to implant in the ovary and form tubal‐type glands and cysts. An alternative model suggests that cells present in ectopic locations outside the Müllerian tract retain the capacity for multi‐lineage differentiation and can form glands with tubal‐type epithelium. We used double transgenic Ovgp1‐iCreER T2 ;R26R LSL‐eYFP mice, which express an eYFP reporter protein in OVGP1‐positive tissues following transient tamoxifen (TAM) treatment, to track the fate of oviductal epithelial cells. Cohorts of adult mice were given TAM to activate eYFP expression in oviductal epithelium, and ovaries were examined at time points ranging from 2?days to 12?months post‐TAM. To test whether superovulation might increase acquisition of endosalpingiosis, additional cohorts of TAM‐treated mice underwent up to five cycles of superovulation and ovaries were examined at 1, 6, and 12?months post‐TAM. Ovaries were sectioned in their entirety to identify endosalpingiosis. Immunohistochemical staining for PAX8, tubulin, OVGP1, and eYFP was employed to study endosalpingiosis lesions. Ovarian endosalpingiosis was identified in 14.2% of TAM‐treated adult mice. The endosalpingiotic inclusion glands and cysts were lined by secretory and ciliated cells and expressed PAX8, tubulin, OVGP1, and eYFP. Neither age nor superovulation was associated with a significant increase in endosalpingiosis. Endosalpingiosis was also occasionally present in the ovaries of pre‐pubertal mice. The findings imply that ovarian endosalpingiosis in the mouse does not likely arise as a consequence of detachment and implantation of tubal epithelium and other mechanisms may be relevant. ? 2019 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
机译:摘要旨在从输卵管上皮(FTE)产生的大多数高级浆液癌,但是一些可能在管外面出现,也许来自称为底座的异位输卵管型上皮。重要的是,终结性的起源很难理解。输卵管FIMBRIAE对卵巢的接近导致了在排卵期间发生的卵巢表面中断的提议可以允许分离的FTE植入卵巢并形成输卵管型腺体和囊肿。替代模型表明,Müllerian道外的异位位置存在于Müllerian的异位位置,保留了多谱分化的能力,并且可以形成具有输卵管型上皮的腺体。我们使用双转基因OVGP1-ICREER T2; R26R LSL-EYFP小鼠,其在瞬时Tamoxifen(TAM)处理后,在OVGP1阳性组织中表达EyFP报告蛋白,以跟踪输卵管上皮细胞的命运。给予成人小鼠的群组是给予TAM以激活OVIDuctal上皮中的EyFP表达,并在2个月到12个月的时间点检查卵巢.TAM后的时间点。为了测试超级化是否可能增加对底座的药物,额外的TAM处理小鼠的额外队列在1,6和12个月的1,6和12个月内检查了高达五个循环的超级超级化和卵巢。卵巢完全分开以识别内部表层。用于PAX8,微管蛋白,OVGP1和EYFP的免疫组织化学染色,用于研究骨果作用病变。在14.2%的TAM治疗的成人小鼠中鉴定了卵巢骨化合物。通过分泌细胞和纤毛细胞衬里衬里衬有含有腺体和囊肿,并表达PAX8,管蛋白,OVGP1和EYFP。既不是年龄也没有超级化与内部化合物的显着增加有关。结核表也偶尔存在于青春期前小鼠的卵巢中。结果暗示小鼠中的卵巢骨质作品,由于分离和输卵管上皮的植入,其他机制可能是相关的。还2019年英国和爱尔兰病理学协会。 John Wiley&amp出版; SONS,LTD.

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