利用微流体技术解码细胞在受控环境下迁移的物理原理。

IF 2.9 Q2 BIOPHYSICS
Biophysics reviews Pub Date : 2024-07-29 eCollection Date: 2024-09-01 DOI:10.1063/5.0199161
Young Joon Suh, Alan T Li, Mrinal Pandey, Cassidy S Nordmann, Yu Ling Huang, Mingming Wu
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引用次数: 0

摘要

活细胞可以完成人造微型/纳米机器人尚未能完成的不可思议的任务。例如,白细胞可以在几分钟内感知并移动到病原体攻击的部位。经过数十亿年的进化,细胞功能的稳健性和精确性日臻完善。在这种情况下,我们要问的问题是,细胞是否遵循一套物理原则来感知、适应和迁移。微流控技术的出现,为细胞迁移研究提供了再现定义明确的细胞环境的有利技术,其跟踪单细胞动态的能力使研究结果可用于理论建模。在这篇综述中,我们将重点介绍微流控平台的发展,该平台可为三维细胞迁移研究再现细胞生物物理(如机械应力)和生物化学(如营养物质和细胞因子)环境。我们总结了细胞(包括细菌、藻类和哺乳动物细胞)对微流控系统学到的化学梯度做出反应的基本原理。我们还讨论了从生物物理线索下的细胞迁移研究中获得的新生物学见解,以及未来在控制良好的生物物理环境下进一步定量研究细胞功能的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Decoding physical principles of cell migration under controlled environment using microfluidics.

Living cells can perform incredible tasks that man-made micro/nano-sized robots have not yet been able to accomplish. One example is that white blood cells can sense and move to the site of pathogen attack within minutes. The robustness and precision of cellular functions have been perfected through billions of years of evolution. In this context, we ask the question whether cells follow a set of physical principles to sense, adapt, and migrate. Microfluidics has emerged as an enabling technology for recreating well-defined cellular environment for cell migration studies, and its ability to follow single cell dynamics allows for the results to be amenable for theoretical modeling. In this review, we focus on the development of microfluidic platforms for recreating cellular biophysical (e.g., mechanical stress) and biochemical (e.g., nutrients and cytokines) environments for cell migration studies in 3D. We summarize the basic principles that cells (including bacteria, algal, and mammalian cells) use to respond to chemical gradients learned from microfluidic systems. We also discuss about novel biological insights gained from studies of cell migration under biophysical cues and the need for further quantitative studies of cell function under well-controlled biophysical environments in the future.

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