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首页> 外文期刊>Molecular and Cellular Endocrinology >Involvement of the bone morphogenetic protein/receptor system during follicle development in the bovine ovary: Hormonal regulation of the expression of bone morphogenetic protein 7 (BMP-7) and its receptors (ActRII and ALK-2).
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Involvement of the bone morphogenetic protein/receptor system during follicle development in the bovine ovary: Hormonal regulation of the expression of bone morphogenetic protein 7 (BMP-7) and its receptors (ActRII and ALK-2).

机译:牛卵巢卵泡发育过程中骨形态发生蛋白/受体系统的参与:骨形态发生蛋白7(BMP-7)及其受体(ActRII和ALK-2)表达的激素调节。

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摘要

Bone morphogenetic proteins (BMPs) are crucial factors in follicular growth and development. Among the BMP ligands, BMP-7 which use ActRII as their type II receptor, strongly bind to ALK-2 as their type I receptor. However, whether their receptors are expressed and the regulatory mechanisms controlling their expression during the process of bovine follicle development are still unknown. The aim of the present study was to clarify the involvement of the receptor system for BMP-7 in follicular selection by examining the effects of follicle-stimulating hormone (FSH) and estradiol (E2) on the regulation of ActRII and ALK-2 mRNA expression in bovine granulosa cells (GCs). To observe mRNA expression, follicles were obtained from heifers and GCs were classified into two groups: pre-selection follicles (PRF; follicles with an average diameter of 7 mm and low E2) and post-selection follicles (POF; follicles with an average diameter of 15 mm and high E2). The theca cell (TC) layer and GCs were harvested from aspirated follicles. For in vitro studies, GCs were obtained from bovine follicles of 4-7 mm diameter and cultured in Dulbecco's modified Eagle's/F12 (DMEM/F-12) medium with 10% fetal calf serum for 24h. The medium was then replaced with serum-free DMEM/F-12 supplemented with different doses of E2 (1, 10,100 ng/ml), FSH (1, 5, 10 ng/ml) or combinations of 1 ng/ml of E2 with different FSH doses (1, 5, 10 ng/ml). Total RNA was extracted from GCs and the mRNA expression of ActRII and ALK-2 was estimated by the quantitative PCR method using LightCycler. The expression of BMP-7 mRNA in TCs did not differ between the PRF and POF. ActRII and ALK-2 expression was detected in GCs from bovine antral follicles and was higher in the GCs of POF than in those of PRF, while the expression of the ActRII and ALK-2 genes in the TCs was not different between PRF and POF. Treatment of GCs with E2 (10 ng/ml) alone increased the expression of both ActRII and ALK-2 mRNAs, whereas FSH alone had no effect. However, ActRII and ALK-2 mRNA levels were up-regulated by the combination of E2 (1 ng/ml) and FSH (5 ng/ml). The results of the present study provide the first evidence that FSH and E2 regulate the expression of the ActRII and ALK-2 genes in bovine GCs. Thus, our data suggest that the BMP7/ActRII/ALK-2 system may be critically involved in the process of selection of bovine follicles.
机译:骨形态发生蛋白(BMP)是卵泡生长发育的关键因素。在BMP配体中,使用ActRII作为其II型受体的BMP-7与ALK-2作为其I型受体牢固结合。然而,在牛卵泡发育过程中它们的受体是否表达以及调控其表达的调节机制仍然未知。本研究的目的是通过检查促卵泡激素(FSH)和雌二醇(E2)对ActRII和ALK-2 mRNA表达调节的影响,阐明BMP-7受体系统在卵泡选择中的作用。在牛颗粒细胞(GCs)中。为了观察mRNA的表达,从小母牛处获得卵泡,并将GC分为两类:选择卵泡(PRF;平均直径为7毫米且E2低的卵泡)和选择卵泡(POF;平均直径的卵泡)。 15毫米和较高的E2)。从吸出的卵泡中收获theca细胞(TC)层和GC。为了进行体外研究,从直径为4-7 mm的牛卵泡中获得GC,并在含10%胎牛血清的Dulbecco改良的Eagle's / F12(DMEM / F-12)培养基中培养24小时。然后将培养基替换为无血清DMEM / F-12,其中补充了不同剂量的E2(1、10,100 ng / ml),FSH(1、5、10 ng / ml)或1 ng / ml E2与不同的FSH剂量(1、5、10 ng / ml)。从GC中提取总RNA,并使用LightCycler通过定量PCR方法估算ActRII和ALK-2的mRNA表达。 PRF和POF之间TC中BMP-7 mRNA的表达没有差异。在牛窦卵泡的GC中检测到ActRII和ALK-2的表达,并且在POF的GC中比在PRF中的ActRII和ALK-2的表达更高,而TCR中的ActRII和ALK-2基因的表达在PRF和POF之间没有差异。单独使用E2(10 ng / ml)处理GC会增加ActRII和ALK-2 mRNA的表达,而单独使用FSH则没有效果。但是,E2(1 ng / ml)和FSH(5 ng / ml)的组合上调了ActRII和ALK-2 mRNA的水平。本研究的结果提供了第一个证据,FSH和E2调节牛GC中ActRII和ALK-2基因的表达。因此,我们的数据表明BMP7 / ActRII / ALK-2系统可能在选择牛卵泡过程中起关键作用。

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