用于单细胞鞭毛分析的微流控精子捕获器阵列,可实现无限制的二维鞭毛运动

IF 6.1 2区 工程技术 Q1 BIOCHEMICAL RESEARCH METHODS
Lab on a Chip Pub Date : 2024-09-12 DOI:10.1039/D4LC00515E
Kaiyu Wang, Antai Tao, Rongjing Zhang and Junhua Yuan
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引用次数: 0

摘要

精子捕获技术可固定精子,使其停止活动,对于长期分析单个精子至关重要。这些技术有利于卵胞浆内精子注射(ICSI)等辅助生殖技术,可以对精子进行选择性筛选。然而,高通量、非破坏性的精子捕获方法明显不足,这些方法允许鞭毛自由跳动,这对于准确反映不受束缚、自由游动的精子的行为至关重要。为了弥补这一差距,我们推出了一种新型微流体设备,专门用于捕获精子而不限制鞭毛运动。该设计利用了精子在三维和二维环境中与生俱来的边界追随行为,引导它们进入捕获区。一旦被捕获,精子头部就会被束缚住,而鞭毛则可以自由地表现出自然的跳动模式。利用这种装置,我们探索了超激活剂、温度以及它们对牛精子鞭毛动力学的综合影响。我们的设备提供的不受限制的鞭毛运动产生了两个显著优势:它反映了自由游动精子的鞭毛行为,确保研究结果与自然精子活动一致;它防止了鞭毛和捕获结构之间的成像重叠,简化了鞭毛跟踪和分析的自动化。这一技术进步有助于收集整个鞭毛的波形参数,解决了以往研究中因测量点不同而产生的不一致问题,并能精确提取精子的行为特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Microfluidic sperm trap array for single-cell flagellar analysis with unrestricted 2D flagellar movement†

Microfluidic sperm trap array for single-cell flagellar analysis with unrestricted 2D flagellar movement†

Sperm capture techniques that immobilize sperm to halt their motility are essential for the long-term analysis of individual sperm. These techniques are beneficial in assisted reproductive technologies such as intracytoplasmic sperm injection (ICSI) by allowing selective screening of sperm. However, there is a notable lack of high-throughput and non-destructive sperm capture methods that allow the flagellum to beat freely, which is crucial for accurately reflecting the behavior of unfettered, freely swimming sperm. To bridge this gap, we introduce a novel microfluidic device specifically engineered to capture sperm without restricting flagellar motion. The design utilizes sperm's innate boundary-following behavior in both 3D and 2D environments to direct them into a capture zone. Once captured, the sperm head is restrained while the flagellum remains free to exhibit natural beating patterns. Utilizing this device, we explore the effects of hyperactivating agents, temperature, and their combined influence on the dynamics of bovine sperm flagella. The unrestricted flagellar motion offered by our device yields two prominent advantages: it mirrors the flagellar behavior of free-swimming sperm, ensuring research findings are consistent with natural sperm activity, and it prevents imaging overlap between the flagellum and the capture structures, simplifying the automation of flagellar tracking and analysis. This technological advancement facilitates the collection of waveform parameters along the entire flagellum, addressing inconsistencies that have arisen in previous research due to differing measurement sites, and enabling precise extraction of sperm behavioral properties.

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来源期刊
Lab on a Chip
Lab on a Chip 工程技术-化学综合
CiteScore
11.10
自引率
8.20%
发文量
434
审稿时长
2.6 months
期刊介绍: Lab on a Chip is the premiere journal that publishes cutting-edge research in the field of miniaturization. By their very nature, microfluidic/nanofluidic/miniaturized systems are at the intersection of disciplines, spanning fundamental research to high-end application, which is reflected by the broad readership of the journal. Lab on a Chip publishes two types of papers on original research: full-length research papers and communications. Papers should demonstrate innovations, which can come from technical advancements or applications addressing pressing needs in globally important areas. The journal also publishes Comments, Reviews, and Perspectives.
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