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New Insights Into Sperm Ultrastructure Through Enhanced Scanning Electron Microscopy

机译:通过增强扫描电子显微镜通过增强扫描电子显微镜进行精子超微结构的新见解

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The analysis of spermatozoa morphology is fundamental to understand male fertility and the etiology of infertility. Traditionally scanning electron microscopy (SEM) has been used to define surface topology. Recently, however, it has become a critical tool for three-dimensional analysis of internal cellular ultrastructure. Modern SEM provides nanometer-scale resolution, but the meaningfulness of such information is proportional to the quality of the sample preservation. In this study, we demonstrate that sperm quickly and robustly adhere to gold-coated surfaces. Leveraging this property, we developed three step-by-step protocols fulfilling different needs for sperm imaging: chemically fixed monolayers for SEM examination of the external morphology, and two high-pressure freezing-based protocols for fast SEM examination of full cell internal morphology and focused ion-beam SEM (FIB-SEM) tomography. These analyses allow previously unappreciated insights into mouse sperm ultrastructure, including the identification of novel structures within the fibrous sheath and domain-specific interactions between the plasma membrane and exosome-like structures.
机译:对精子形态的分析是理解男性生育能力和不孕症的病因的基础。传统上扫描电子显微镜(SEM)已被用于定义表面拓扑。然而,最近,它已成为内部蜂窝超微结构的三维分析的关键工具。现代SEM提供纳米规模的分辨率,但这些信息的有意义性与样品保存的质量成正比。在这项研究中,我们证明精子快速且鲁棒地粘附到镀金表面上。利用这一财产,我们开发了三个逐步的协议,满足了对精子成像的不同需求:化学固定单层用于SEM检查外部形态,以及用于全细胞内部形态的快速SEM检查的两种高压冻结协议。聚焦离子束SEM(FIB-SEM)断层扫描。这些分析允许先前未被覆盖的小鼠精子超微结构的见解,包括识别纤维护套内的新型结构和质膜和外孔状结构之间的域特异性相互作用。

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