Laboratory of Reproductive Physiology, Graduate School of Environmental and Life Science, Okayama University, 1-1-1, Tsushimanaka, Kita-Ku, Okayama, 700-8530, Japan.
Japan Society for the Promotion of Science, Tokyo, Japan.
Mol Biol Rep. 2020 Feb;47(2):1003-1012. doi: 10.1007/s11033-019-05192-w. Epub 2019 Nov 18.
The oviductal epithelium is composed of ciliated and non-ciliated cells. The proportions of these cells change during the estrous cycle. However, the mechanism underlying this cyclic change in the cell proportions remains unclear. Our previous study indicated that ciliated cells are derived from non-ciliated cells. Here, we aimed to investigate the mechanism regulating the changes in the populations of ciliated and non-ciliated cells during the estrous cycle. To this end, we examined the numbers of cells that were positive for acetylated-α-tubulin (cilia marker), Ki67 (proliferation marker), PAX8 (non-ciliated cell marker), and FOXJ1 and MYB (ciliogenesis markers) in the epithelial cells at four different estrous stages (Stage I: days 1-4 after ovulation, Stage II: days 5-10, Stage III: days 11-17, and Stage IV: days 18-20) by immunohistochemistry. The oviductal epithelial cells expressed either FOXJ1 or PAX8. All the acetylated-α-tubulin cells were positive for FOXJ1, although there were a few acetylated-α-tubulin/FOXJ1 cells. MYB was expressed in both the FOXJ1 and PAX8 cells, but it was not expressed in the Ki67 cells. The numbers of Ki67 and MYB cells were the highest in Stage IV, while the numbers of FOXJ1 and acetylated-α-tubulin cells were the highest in the following Stage I, suggesting that ciliogenesis is associated with the estrous cycle. Thus, based on immunological classification, the oviductal epithelium contains at least seven types of cells at different translational/transcriptional states, and their number is regulated by the estrous cycle. This cyclic event might provide an optimal environment for gamete transport, fertilization, and embryonic development.
输卵管上皮由纤毛细胞和非纤毛细胞组成。这些细胞的比例在发情周期中发生变化。然而,这种细胞比例周期性变化的机制尚不清楚。我们之前的研究表明,纤毛细胞是由非纤毛细胞衍生而来的。在这里,我们旨在研究调节发情周期中纤毛细胞和非纤毛细胞群体变化的机制。为此,我们通过免疫组织化学检查了在四个不同发情阶段(排卵后第 1-4 天的阶段 I、第 5-10 天的阶段 II、第 11-17 天的阶段 III 和第 18-20 天的阶段 IV)上皮细胞中对乙酰化-α-微管蛋白(纤毛标记物)、Ki67(增殖标记物)、PAX8(非纤毛细胞标记物)和 FOXJ1 和 MYB(纤毛发生标记物)呈阳性的细胞数量。输卵管上皮细胞表达 FOXJ1 或 PAX8。尽管存在少数乙酰化-α-微管蛋白/FOXJ1 细胞,但所有乙酰化-α-微管蛋白细胞均呈 FOXJ1 阳性。MYB 表达于 FOXJ1 和 PAX8 细胞中,但不表达于 Ki67 细胞中。Ki67 和 MYB 细胞的数量在阶段 IV 中最高,而 FOXJ1 和乙酰化-α-微管蛋白细胞的数量在随后的阶段 I 中最高,这表明纤毛发生与发情周期有关。因此,基于免疫分类,输卵管上皮至少包含七种处于不同翻译/转录状态的细胞类型,其数量受发情周期调节。这种周期性事件可能为配子运输、受精和胚胎发育提供最佳环境。