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用于脑神经元细胞力学生物学研究的工程化细胞培养微环境

Engineered cell culture microenvironments for mechanobiology studies of brain neural cells.

作者信息

Castillo Ransanz Lucía, Van Altena Pieter F J, Heine Vivi M, Accardo Angelo

机构信息

Department of Child and Adolescence Psychiatry, Amsterdam Neuroscience, Emma Children's Hospital, Amsterdam UMC Location Vrije Universiteit Amsterdam, Amsterdam, Netherlands.

Department of Precision and Microsystems Engineering, Delft University of Technology, Delft, Netherlands.

出版信息

Front Bioeng Biotechnol. 2022 Dec 14;10:1096054. doi: 10.3389/fbioe.2022.1096054. eCollection 2022.

DOI:10.3389/fbioe.2022.1096054
PMID:36588937
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9794772/
Abstract

The biomechanical properties of the brain microenvironment, which is composed of different neural cell types, the extracellular matrix, and blood vessels, are critical for normal brain development and neural functioning. Stiffness, viscoelasticity and spatial organization of brain tissue modulate proliferation, migration, differentiation, and cell function. However, the mechanical aspects of the neural microenvironment are largely ignored in current cell culture systems. Considering the high promises of human induced pluripotent stem cell- (iPSC-) based models for disease modelling and new treatment development, and in light of the physiological relevance of neuromechanobiological features, applications of engineered neuronal microenvironments should be explored thoroughly to develop more representative brain models. In this context, recently developed biomaterials in combination with micro- and nanofabrication techniques 1) allow investigating how mechanical properties affect neural cell development and functioning; 2) enable optimal cell microenvironment engineering strategies to advance neural cell models; and 3) provide a quantitative tool to assess changes in the neuromechanobiological properties of the brain microenvironment induced by pathology. In this review, we discuss the biological and engineering aspects involved in studying neuromechanobiology within scaffold-free and scaffold-based 2D and 3D iPSC-based brain models and approaches employing primary lineages (neural/glial), cell lines and other stem cells. Finally, we discuss future experimental directions of engineered microenvironments in neuroscience.

摘要

由不同神经细胞类型、细胞外基质和血管组成的脑微环境的生物力学特性,对于正常脑发育和神经功能至关重要。脑组织的硬度、粘弹性和空间组织调节细胞增殖、迁移、分化及细胞功能。然而,当前细胞培养系统很大程度上忽略了神经微环境的力学方面。鉴于基于人诱导多能干细胞(iPSC)的模型在疾病建模和新治疗方法开发方面具有巨大潜力,且考虑到神经机械生物学特征的生理相关性,应深入探索工程化神经元微环境的应用,以开发更具代表性的脑模型。在此背景下,最近开发的生物材料与微纳制造技术相结合:1)能够研究力学特性如何影响神经细胞发育和功能;2)有助于制定优化的细胞微环境工程策略,以推进神经细胞模型的发展;3)提供一种定量工具,用于评估病理状态下脑微环境神经机械生物学特性的变化。在本综述中,我们讨论了在无支架和基于支架的二维及三维iPSC脑模型以及采用原代谱系(神经/胶质)、细胞系和其他干细胞的方法中,研究神经机械生物学所涉及的生物学和工程学方面。最后,我们讨论了神经科学中工程化微环境未来的实验方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4585/9794772/5947fb08e0d5/fbioe-10-1096054-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4585/9794772/53e7d2607eb1/fbioe-10-1096054-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4585/9794772/933fa575f017/fbioe-10-1096054-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4585/9794772/f64af7edb803/fbioe-10-1096054-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4585/9794772/2bb32de68a61/fbioe-10-1096054-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4585/9794772/44fea1d0bd6b/fbioe-10-1096054-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4585/9794772/72e3fa5785dd/fbioe-10-1096054-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4585/9794772/5947fb08e0d5/fbioe-10-1096054-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4585/9794772/53e7d2607eb1/fbioe-10-1096054-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4585/9794772/933fa575f017/fbioe-10-1096054-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4585/9794772/f64af7edb803/fbioe-10-1096054-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4585/9794772/2bb32de68a61/fbioe-10-1096054-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4585/9794772/44fea1d0bd6b/fbioe-10-1096054-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4585/9794772/72e3fa5785dd/fbioe-10-1096054-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4585/9794772/5947fb08e0d5/fbioe-10-1096054-g007.jpg

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