Microfluidic tools to model, monitor, and modulate the gut-brain axis.

IF 2.4 4区 工程技术 Q2 BIOCHEMICAL RESEARCH METHODS
Biomicrofluidics Pub Date : 2025-03-07 eCollection Date: 2025-03-01 DOI:10.1063/5.0253041
Hyehyun Kim, Gregory Girardi, Allison Pickle, Testaverde S Kim, Erkin Seker
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引用次数: 0

Abstract

The gut-brain axis (GBA) connects the gastrointestinal tract and the central nervous system (CNS) via the peripheral nervous system and humoral (e.g., circulatory and lymphatic system) routes. The GBA comprises a sophisticated interaction between various mammalian cells, gut microbiota, and systemic factors. This interaction shapes homeostatic and pathophysiological processes and plays an important role in the etiology of many disorders including neuropsychiatric conditions. However, studying the underlying processes of GBA in vivo, where numerous confounding factors exist, is challenging. Furthermore, conventional in vitro models fall short of capturing the GBA anatomy and physiology. Microfluidic platforms with integrated sensors and actuators are uniquely positioned to enhance in vitro models by representing the anatomical layout of cells and allowing to monitor and modulate the biological processes with high spatiotemporal resolution. Here, we first briefly describe microfluidic technologies and their utility in modeling the CNS, vagus nerve, gut epithelial barrier, blood-brain barrier, and their interactions. We then discuss the challenges and opportunities for each model, including the use of induced pluripotent stem cells and incorporation of sensors and actuator modalities to enhance the capabilities of these models. We conclude by envisioning research directions that can help in making the microfluidics-based GBA models better-suited to provide mechanistic insight into pathophysiological processes and screening therapeutics.

微流控工具建模,监测和调节肠脑轴。
肠脑轴(GBA)通过周围神经系统和体液(如循环和淋巴系统)途径连接胃肠道和中枢神经系统(CNS)。大湾区包括各种哺乳动物细胞、肠道微生物群和系统因素之间复杂的相互作用。这种相互作用形成了体内平衡和病理生理过程,并在包括神经精神疾病在内的许多疾病的病因学中起着重要作用。然而,在体内研究GBA的潜在过程具有挑战性,其中存在许多混杂因素。此外,传统的体外模型无法捕捉大湾区的解剖和生理特征。集成传感器和执行器的微流控平台具有独特的定位,可以通过代表细胞的解剖布局来增强体外模型,并允许以高时空分辨率监测和调节生物过程。在这里,我们首先简要介绍微流体技术及其在模拟中枢神经系统、迷走神经、肠上皮屏障、血脑屏障及其相互作用方面的应用。然后,我们讨论了每个模型的挑战和机遇,包括使用诱导多能干细胞和结合传感器和执行器模式来增强这些模型的能力。最后,我们展望了可以帮助基于微流体的GBA模型更好地为病理生理过程和筛选治疗提供机制见解的研究方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biomicrofluidics
Biomicrofluidics 生物-纳米科技
CiteScore
5.80
自引率
3.10%
发文量
68
审稿时长
1.3 months
期刊介绍: Biomicrofluidics (BMF) is an online-only journal published by AIP Publishing to rapidly disseminate research in fundamental physicochemical mechanisms associated with microfluidic and nanofluidic phenomena. BMF also publishes research in unique microfluidic and nanofluidic techniques for diagnostic, medical, biological, pharmaceutical, environmental, and chemical applications. BMF offers quick publication, multimedia capability, and worldwide circulation among academic, national, and industrial laboratories. With a primary focus on high-quality original research articles, BMF also organizes special sections that help explain and define specific challenges unique to the interdisciplinary field of biomicrofluidics. Microfluidic and nanofluidic actuation (electrokinetics, acoustofluidics, optofluidics, capillary) Liquid Biopsy (microRNA profiling, circulating tumor cell isolation, exosome isolation, circulating tumor DNA quantification) Cell sorting, manipulation, and transfection (di/electrophoresis, magnetic beads, optical traps, electroporation) Molecular Separation and Concentration (isotachophoresis, concentration polarization, di/electrophoresis, magnetic beads, nanoparticles) Cell culture and analysis(single cell assays, stimuli response, stem cell transfection) Genomic and proteomic analysis (rapid gene sequencing, DNA/protein/carbohydrate arrays) Biosensors (immuno-assay, nucleic acid fluorescent assay, colorimetric assay, enzyme amplification, plasmonic and Raman nano-reporter, molecular beacon, FRET, aptamer, nanopore, optical fibers) Biophysical transport and characterization (DNA, single protein, ion channel and membrane dynamics, cell motility and communication mechanisms, electrophysiology, patch clamping). Etc...
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