从微流体到微生理系统:过去,现在和未来

María Virumbrales-Muñoz , Jose M. Ayuso
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引用次数: 7

摘要

十多年来,我们看到微流体领域取得了重大进展,导致了微生理系统的概念。这些系统在2010年代初出现,作为多功能的体外平台,使研究人员能够在体外模拟组织的复杂性。早期的模型侧重于展示流体物理在微观尺度上的优势,并展示概念验证实验。随着技术的发展,微流控模型变得越来越复杂,并显示出它们在器官水平上模拟复杂生物反应的能力,创造了器官芯片平台的概念。在“微生理系统”的旗帜下,目前的平台评估了在高度组织的情况下涉及许多细胞类型的复杂动力学。最近的模型利用先进的成像和多组学技术来研究各种各样的细胞和分子过程,从癌症和中风到生殖生物学和传染病。在这篇文章中,我们强调了这些时期的主要特征,并概述了微生理系统领域当前和未来的趋势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
From microfluidics to microphysiological systems: Past, present, and future

For over a decade, we have seen significant strides in the microfluidics field that have led to the concept of microphysiological systems. These systems emerged in the early 2010s as versatile in vitro platforms that allowed researchers to mimic tissue complexity in vitro. Early models focused on showing the advantages of fluid physics at the microscale and demonstrating proof-of-concept experiments. As the technology evolved, microfluidic models became more complex and showed their capacity to mimic complex biological responses at an organ level, coining the concept of organ-on-a-chip platforms. Gathered under the banner of “microphysiological systems”, current platforms evaluate complex dynamics that involve numerous cell types in highly organized scenarios. Recent models have leveraged advanced imaging and multi-omics techniques to study a large variety of cellular and molecular processes, from cancer and strokes to reproductive biology and infectious diseases. In this piece, we highlight the main hallmarks of each of these periods and outline current and upcoming trends in the field of microphysiological systems.

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来源期刊
Organs-on-a-chip
Organs-on-a-chip Analytical Chemistry, Biochemistry, Genetics and Molecular Biology (General), Cell Biology, Pharmacology, Toxicology and Pharmaceutics (General)
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