Isolation, Extraction, and Analysis of Cells After Confined Migration

IF 2.2
Xu Gao, Yixuan Li, Jia Wen Nicole Lee, Jianxuan Zhou, Vaishnavi Rangaraj, Avery Rui Sun, Jennifer L. Young, Andrew W. Holle
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引用次数: 0

Abstract

Cell migration through confined microenvironments is a critical biological process that underlies numerous physiological and pathological events, including immune cell trafficking, tissue morphogenesis, and cancer metastasis. Although polydimethylsiloxane-based microchannel devices have enabled detailed studies of confined migration, the efficient collection of cells post-migration for downstream molecular analyses remains a major challenge. Existing approaches often rely on harsh mechanical dissociation that compromises cell viability and integrity and do not permit in situ collection of cell lysates. To overcome these limitations, we have developed the Trap-based Recovery After Permeation (TRAP) chip, a pump-free microfluidic platform that integrates controlled confined migration with efficient post-migration cell or lysate collection. The TRAP chip incorporates microchannel arrays terminating in a precisely engineered trap region that enables gentle recovery of cells or cellular components without exposing them to high shear forces or requiring large buffer volumes. This innovation ensures the viability of recovered cells and expands the applicability of confined migration assays beyond imaging-based studies. We demonstrate that the TRAP chip facilitates the extraction of post-confinement cells for mechanical characterization, including measurement of Young's modulus, as well as the isolation of proteins and RNA suitable for downstream assays such as western blot and qPCR. The TRAP chip thus represents a significant advancement in microfluidic technologies, offering a robust, reproducible, and minimally invasive approach for studying the mechanobiology of confined migration, with broad potential for applications in basic research, cellular engineering, and translational studies where cell behavior under physical confinement is of critical importance. © 2025 The Author(s). Current Protocols published by Wiley Periodicals LLC.

Basic Protocol 1: Fabrication of TRAP and control chips

Basic Protocol 2: Cell seeding and live cell isolation from TRAP chips

Alternate Protocol: Biomolecular extraction from TRAP chips

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隔离、提取和细胞在受限迁移后的分析
细胞在受限微环境中的迁移是一个重要的生物学过程,是许多生理和病理事件的基础,包括免疫细胞运输、组织形态发生和癌症转移。尽管基于聚二甲基硅氧烷的微通道设备已经能够对受限迁移进行详细的研究,但有效收集迁移后的细胞用于下游分子分析仍然是一个主要挑战。现有的方法通常依赖于苛刻的机械解离,这损害了细胞的活力和完整性,并且不允许原位收集细胞裂解物。为了克服这些限制,我们开发了基于陷阱的渗透后回收(TRAP)芯片,这是一种无泵的微流体平台,将受控的受限迁移与高效的迁移后细胞或裂解物收集集成在一起。TRAP芯片集成了微通道阵列,在一个精确设计的陷阱区域终止,使细胞或细胞成分能够温和地恢复,而无需将它们暴露在高剪切力或需要大的缓冲体积。这一创新确保了恢复细胞的活力,并扩大了基于成像研究的限制性迁移分析的适用性。我们证明,TRAP芯片有助于提取禁闭后细胞进行力学表征,包括杨氏模量的测量,以及适用于下游分析(如western blot和qPCR)的蛋白质和RNA的分离。因此,TRAP芯片代表了微流控技术的重大进步,为研究受限迁移的机械生物学提供了一种强大的、可重复的、微创的方法,在基础研究、细胞工程和转化研究中具有广泛的应用潜力,在这些领域,细胞在物理限制下的行为是至关重要的。©2025作者。Wiley期刊有限责任公司发表的当前协议:基本协议1:制造TRAP和控制芯片;基本协议2:从TRAP芯片中提取细胞种子和活细胞;备选协议:从TRAP芯片中提取生物分子
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CiteScore
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