山羊子宫组织中RGMb的表达:RGMb在子宫内膜上皮细胞增殖和凋亡中的可能作用

IF 1.8 4区 生物学 Q3 DEVELOPMENTAL BIOLOGY
Yang Xue, Xiaomeng Pei, Yuting Xia, Hengguang Chen, Hao Yu, Wei Wang, Dagan Mao
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引用次数: 0

摘要

骨形态发生蛋白(BMPs)在子宫中起着重要作用。排斥引导分子b (RGMb);已被证实是bmp的辅助受体,通过果蝇母亲对抗十肢截瘫蛋白(Smads)和丝裂原活化蛋白激酶(MAPK)途径发挥作用。我们假设RGMb通过Smads和MAPK途径调节子宫功能。目的探讨RGMb在山羊子宫中的表达及其在子宫内膜上皮细胞(EECs)中的潜在作用。方法采用免疫组化(IHC)方法检测RGMb在山羊子宫组织中的定位,分离EECs并转染siRNA,研究RGMb在子宫组织增殖和凋亡中的作用。采用western blot (WB)和real-time PCR (RT-PCR)检测Smads和MAPK成员的表达水平。免疫组化结果显示,RGMb存在于山羊子宫内膜腔细胞、腺上皮细胞和圆形肌纤维中,但不存在于基质细胞中。RT-PCR结果显示,RGMb siRNA抑制增殖相关基因cyclin D1 (CCND1, P=0.0291)、cyclin依赖性激酶2 (CDK2, P=0.0107)和增殖细胞核抗原(PCNA, P=0.0508)的表达,导致EECs活力降低(P=0.0010)。WB结果显示,转染RGMb siRNA后,切割型caspase 3/caspase 3的表达比(P=0.0013)显著升高。磷酸化细胞外信号调节激酶1/2 (P - erk1 /2, P=0.0068)和P - smad1 /5/8 (P=0.0011)的表达水平也显著降低,而P - p38 MAPK的表达水平无明显差异(P < 0.05)。结论RGMb可能通过Smads和ERK信号通路参与山羊脑脊液细胞增殖和凋亡的调控。意义RGMb参与调节山羊子宫内膜上皮细胞的增殖和凋亡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RGMb expression in goat uterine tissues: possible role of RGMb in the proliferation and apoptosis of endometrial epithelial cells.

Context Bone morphogenetic proteins (BMPs) play an important role in the uteri. Repulsive guidance molecule b (RGMb; a.k.a. Dragon) has been confirmed as the coreceptor of BMPs to function through drosophila mothers against decapentaplegic protein (Smads) and mitogen-activated protein kinases (MAPK) pathways. We hypothesise that RGMb regulates the uterine function through the Smads and MAPK pathways. Aims This study aimed to investigate the expression of RGMb in goat uteri and the potential role of RGMb in the endometrial epithelial cells (EECs). Methods The localisation of RGMb in goat uterine tissues was detected by immunohistochemistry (IHC), EECs were isolated and transfected with siRNA to investigate the role of RGMb in proliferation, and apoptosis. The expression levels of Smads and MAPK members was measured by western blot (WB) and real-time PCR (RT-PCR). Key results IHC showed that RGMb was localised in goat endometrial luminal cells, glandular epithelial cells, and circular muscle fibres, but not in stromal cells. RT-PCR results showed that treatment with RGMb siRNA suppressed the expressions of proliferation-related genes cyclin D1 (CCND1 , P =0.0291), cyclin-dependent kinase 2 (CDK2 P =0.0107), and proliferating cell nuclear antigen (PCNA, P =0.0508), leading to the reduced viability of EECs (P =0.0010). WB results showed that the expression ratio of cleaved-caspase 3/caspase 3 (P =0.0013) was markedly increased after RGMb siRNA transfection. Likewise, the level of phospho-extracellular signal-regulated kinase 1/2 (p-ERK1/2, P =0.0068) and p-Smad1/5/8 (P =0.0011) decreased significantly, while there were no appreciable differences in the level of p-P38 MAPK expression (P >0.05). Conclusions RGMb might participate in the regulation of cell proliferation and apoptosis through Smads and ERK signalling pathways in goat EECs. Implications RGMb is involved in regulating the proliferation and apoptosis in goat endometrial epithelial cells.

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来源期刊
CiteScore
2.10
自引率
10.50%
发文量
317
审稿时长
2 months
期刊介绍: Reproduction, Fertility and Development is an international journal for the publication of original and significant contributions on vertebrate reproductive and developmental biology. Subject areas include, but are not limited to: physiology, biochemistry, cell and molecular biology, endocrinology, genetics and epigenetics, behaviour, immunology and the development of reproductive technologies in humans, livestock and wildlife, and in pest management. Reproduction, Fertility and Development is a valuable resource for research scientists working in industry or academia on reproductive and developmental biology, clinicians and veterinarians interested in the basic science underlying their disciplines, and students. Reproduction, Fertility and Development is the official journal of the International Embryo Technology Society and the Society for Reproductive Biology. Reproduction, Fertility and Development is published with the endorsement of the Commonwealth Scientific and Industrial Research Organisation (CSIRO) and the Australian Academy of Science.
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