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沙鼠(肥尾沙鼠)输出小管中的G蛋白偶联雌激素受体1、雌激素受体和雄激素受体。

G protein-coupled oestrogen receptor 1, oestrogen receptors and androgen receptor in the sand rat (Psammomys obesus) efferent ducts.

作者信息

Menad R, Fernini M, Lakabi L, Soudani N, Smaï S, Bonnet X, Gernigon-Spychalowicz T, Moudilou E, Exbrayat J-M

出版信息

Folia Morphol (Warsz). 2020;79(4):756-766. doi: 10.5603/FM.a2020.0053. Epub 2020 May 27.

Abstract

BACKGROUND

The efferent ducts are mainly involved in the reabsorption of the seminiferous tubular fluid. Testosterone and oestrogens regulate efferent ducts functions via their receptors.

MATERIALS AND METHODS

This paper presents an experimental investigation on the location of the P450 aromatase, the 17-b oestradiol (E2), the androgen receptor (AR), the oestrogen receptor 1 (ESR1), the oestrogen receptor 2 (ESR2) and the G protein-coupled oestrogen receptor 1 (GPER1) in the efferent ducts using Psammomys obesus as an animal model to highlight the effect of the season on the histology and the distribution of these receptors.

RESULTS

We observed a proliferation of the connective tissue, decreasing in the height of the epithelium during the resting season compared to the breeding season. Ciliated cells expressed P450 aromatase, AR, E2, ESR1, ESR2 and GPER1 during both seasons. Basal cells showed a positive staining for the ESR1 and the GPER1 during both season, the AR and E2 during the breeding season and ESR2 during the resting season.

CONCLUSIONS

Our result shows that the expression of androgen receptor and oestrogen receptors in the efferent ducts vary by season witch suggest that they are largely involved in the regulation of the efferent ducts functions.

摘要

背景

输出小管主要参与生精小管液的重吸收。睾酮和雌激素通过其受体调节输出小管的功能。

材料与方法

本文以欧氏沙鼠为动物模型,对输出小管中细胞色素P450芳香化酶、17-β雌二醇(E2)、雄激素受体(AR)、雌激素受体1(ESR1)、雌激素受体2(ESR2)和G蛋白偶联雌激素受体1(GPER1)的定位进行了实验研究,以突出季节对这些受体的组织学和分布的影响。

结果

我们观察到结缔组织增生,与繁殖季节相比,静止季节上皮高度降低。在两个季节中,纤毛细胞均表达细胞色素P450芳香化酶、AR、E2、ESR1、ESR2和GPER1。在两个季节中,基底细胞ESR1和GPER1染色均呈阳性,繁殖季节AR和E2染色呈阳性,静止季节ESR2染色呈阳性。

结论

我们研究结果表明,输出小管中雄激素受体和雌激素受体的表达随季节变化,这表明它们在很大程度上参与了输出小管功能的调节。

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