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磷酸蛋白质组学和功能分析揭示了人类精子中κ阿片受体下游的精子特异性蛋白变化。

Phosphoproteomic and Functional Analyses Reveal Sperm-specific Protein Changes Downstream of Kappa Opioid Receptor in Human Spermatozoa.

机构信息

From the ‡Department of Physiology, Faculty of Medicine and Nursing, University of the Basque Country (UPV/EHU), Leioa, Bizkaia, Spain, 49840;; Biocruces Bizkaia Health Research Institute, Barakaldo, Bizkaia, Spain, 48903.

Department of Biochemistry and Molecular Biology, Faculty of Pharmacy, University of the Basque Country (UPV/EHU), Vitoria-Gasteiz, Araba, Spain, 01006.

出版信息

Mol Cell Proteomics. 2019 Mar 15;18(Suppl 1):S118-S131. doi: 10.1074/mcp.RA118.001133. Epub 2019 Jan 8.

Abstract

G-protein coupled receptors (GPCRs) belong to the seven transmembrane receptor superfamily that transduce signals via G proteins in response to external stimuli to initiate different intracellular signaling pathways which culminate in specific cellular responses. The expression of diverse GPCRs at the plasma membrane of human spermatozoa suggests their involvement in the regulation of sperm fertility. However, the signaling events downstream of many GPCRs in spermatozoa remain uncharacterized. Here, we selected the kappa-opioid receptor (KOR) as a study model and applied phosphoproteomic approach based on TMT labeling and LC-MS/MS analyses. Quantitative coverage of more than 5000 proteins with over 3500 phosphorylation sites revealed changes in the phosphorylation levels of sperm-specific proteins involved in the regulation of the sperm fertility in response to a specific agonist of KOR, U50488H. Further functional studies indicate that KOR could be involved in the regulation of sperm fertile capacity by modulation of calcium channels. Our findings suggest that human spermatozoa possess unique features in the molecular mechanisms downstream of GPCRs which could be key regulators of sperm fertility and improved knowledge of these specific processes may contribute to the development of useful biochemical tools for diagnosis and treatment of male infertility.

摘要

G 蛋白偶联受体(GPCRs)属于七次跨膜受体超家族,可通过 G 蛋白响应外部刺激转导信号,从而启动不同的细胞内信号通路,最终导致特定的细胞反应。人类精子质膜上表达多种 GPCRs,表明它们参与了精子活力的调节。然而,许多 GPCR 在精子中的信号事件仍未被描述。在这里,我们选择了κ阿片受体(KOR)作为研究模型,并应用了基于 TMT 标记和 LC-MS/MS 分析的磷酸蛋白质组学方法。超过 5000 种蛋白质的定量覆盖范围,其中包含 3500 多个磷酸化位点,揭示了在特定 KOR 激动剂 U50488H 作用下,参与调节精子活力的精子特异性蛋白的磷酸化水平的变化。进一步的功能研究表明,KOR 可能通过调节钙通道参与调节精子的生育能力。我们的研究结果表明,人类精子在 GPCR 下游的分子机制中具有独特的特征,这些特征可能是精子活力的关键调节剂,对这些特定过程的深入了解可能有助于开发用于男性不育症诊断和治疗的有用生化工具。

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