Kowalik M K, Martyniak M, Rekawiecki R, Kotwica J
Department of Physiology and Toxicology of Reproduction, Institute of Animal Reproduction and Food Research of the Polish Academy of Sciences, Olsztyn 10-748, Poland.
Department of Physiology and Toxicology of Reproduction, Institute of Animal Reproduction and Food Research of the Polish Academy of Sciences, Olsztyn 10-748, Poland.
Domest Anim Endocrinol. 2016 Apr;55:83-96. doi: 10.1016/j.domaniend.2015.12.001. Epub 2015 Dec 17.
The oviduct plays a crucial role in the transport and maturation of gametes and ensures suitable conditions for fertility and early embryo development. One regulator of oviduct function is progesterone (P4), which affects the cell by interacting with nuclear progesterone receptors (PGRs) and through nongenomic mechanisms, presumably involving membrane PGRs. The aim of this study was to evaluate the expression of messenger RNAS (mRNAs) and proteins for progesterone receptor membrane component (PGRMC) 1 and 2 and membrane progestin receptors (mPR) α, β, and γ and to use immunohistochemistry to demonstrate their cell-specific localization in the bovine oviduct. Oviducts ipsilateral and contralateral to the corpus luteum or to the dominant follicle were collected from cows on days 6 to 12 (midluteal stage) and 18 to 20 (follicular stage) of the estrous cycle and divided into 3 parts (infundibulum, ampulla, and isthmus). There were no differences (P > 0.05) in the PGRMC1, PGRMC2, mPRα, β, and γ mRNA expression between ipsi- and contralateral oviducts. However, the same parts of the oviduct collected during the different stages of the estrous cycle showed higher (P < 0.05) mRNA levels of PGRMC1, PGRMC2, and mPRα on days 18 to 20 than on days 6 to 12 of the estrous cycle. mPRα and mPRβ mRNA levels were higher (P < 0.05) in the infundibulum than in the isthmus, whereas PGRMC1 expression was higher (P < 0.05) in the infundibulum than in ampulla. Immunohistochemistry was used to detect PGRMC1, PGRMC2, PRα, β, and γ proteins in all parts of both oviducts from days 6 to 12 and 18 to 20 of the estrous cycle. There were no differences in the staining intensity and cellular localization of the studied proteins between the ipsi- and contralateral oviducts and between the studied stages of the estrous cycle. A strong positive reaction was observed in luminal cells, but this reaction was less evident in myocytes and stromal cells. All proteins were also localized to the endothelial cells of blood vessels. These results suggest that membrane progesterone receptors, may be involved in the regulation of oviduct motility, secretory function, and blood flow in this organ.
输卵管在配子的运输和成熟过程中起着关键作用,并确保生育和早期胚胎发育的适宜条件。输卵管功能的一个调节因子是孕酮(P4),它通过与核孕酮受体(PGRs)相互作用以及通过非基因组机制(可能涉及膜孕酮受体)影响细胞。本研究的目的是评估孕酮受体膜成分(PGRMC)1和2以及膜孕激素受体(mPR)α、β和γ的信使核糖核酸(mRNAs)和蛋白质的表达,并使用免疫组织化学方法证明它们在牛输卵管中的细胞特异性定位。在发情周期的第6至12天(黄体中期)和第18至20天(卵泡期)从母牛收集与黄体或优势卵泡同侧和对侧的输卵管,并将其分为3部分(漏斗部、壶腹部和峡部)。同侧和对侧输卵管之间的PGRMC1、PGRMC2、mPRα、β和γ mRNA表达没有差异(P>0.05)。然而,在发情周期不同阶段收集的输卵管相同部位,在发情周期的第18至20天,PGRMC1、PGRMC2和mPRα的mRNA水平高于第6至12天(P<0.05)。mPRα和mPRβ的mRNA水平在漏斗部高于峡部(P<0.05),而PGRMC1的表达在漏斗部高于壶腹部(P<0.05)。使用免疫组织化学方法检测发情周期第6至12天和第18至20天两侧输卵管所有部位的PGRMC1、PGRMC2、PRα、β和γ蛋白。同侧和对侧输卵管之间以及发情周期的不同研究阶段之间,所研究蛋白质的染色强度和细胞定位没有差异。在腔面细胞中观察到强阳性反应,但在肌细胞和基质细胞中这种反应不太明显。所有蛋白质也定位于血管内皮细胞。这些结果表明,膜孕酮受体可能参与该器官输卵管运动、分泌功能和血流的调节。