A multifunctional sensor for cell traction force, matrix remodeling and biomechanical assays in self-assembled 3D tissues in vitro

IF 16 1区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS Nature Protocols Pub Date : 2025-01-24 DOI:10.1038/s41596-024-01106-8
Bashar Emon, Md Saddam Hossain Joy, William C. Drennan, M. Taher A. Saif
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Abstract

Cell–matrix interactions, mediated by cellular force and matrix remodeling, result in dynamic reciprocity that drives numerous biological processes and disease progression. Currently, there is no available method for directly quantifying cell traction force and matrix remodeling in three-dimensional matrices as a function of time. To address this long-standing need, we developed a high-resolution microfabricated device that enables longitudinal measurement of cell force, matrix stiffness and the application of mechanical stimulation (tension or compression) to cells. Here a specimen comprising of cells and matrix self-assembles and self-integrates with the sensor. With primary fibroblasts, cancer cells and neurons we have demonstrated the feasibility of the sensor by measuring single or multiple cell force with a resolution of 1 nN and changes in tissue stiffness due to matrix remodeling by the cells. The sensor can also potentially be translated into a high-throughput system for clinical assays such as patient-specific drug and phenotypic screening. We present the detailed protocol for manufacturing the sensors, preparing experimental setup, developing assays with different tissues and for imaging and analyzing the data. Apart from microfabrication of the molds in a cleanroom (one time operation), this protocol does not require any specialized skillset and can be completed within 4–5 h. A high-resolution microfabricated device that enables longitudinal measurement of cell force, matrix stiffness and the application of mechanical tension or compression to cells in self-assembled 3D tissues.

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一种多功能传感器,用于体外自组装3D组织的细胞牵引力、基质重塑和生物力学分析。
细胞-基质相互作用,由细胞力和基质重塑介导,导致驱动许多生物过程和疾病进展的动态互惠。目前,还没有一种方法可以直接量化三维基质中细胞牵引力和基质重塑随时间的变化。为了解决这一长期存在的需求,我们开发了一种高分辨率的微加工设备,可以纵向测量细胞力、基质刚度和对细胞的机械刺激(张力或压缩)。在这里,由细胞和基质组成的试样与传感器自组装和自集成。对于原代成纤维细胞、癌细胞和神经元,我们已经证明了该传感器的可行性,通过测量单个或多个细胞的力,分辨率为1nn,以及细胞因基质重塑而导致的组织刚度变化。该传感器还可以潜在地转化为高通量系统,用于临床分析,如患者特异性药物和表型筛选。我们提出了制造传感器,准备实验装置,开发不同组织的分析以及成像和分析数据的详细协议。除了在洁净室中进行模具微加工(一次性操作)外,该方案不需要任何专业技能,可在4-5小时内完成。
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来源期刊
Nature Protocols
Nature Protocols 生物-生化研究方法
CiteScore
29.10
自引率
0.70%
发文量
128
审稿时长
4 months
期刊介绍: Nature Protocols focuses on publishing protocols used to address significant biological and biomedical science research questions, including methods grounded in physics and chemistry with practical applications to biological problems. The journal caters to a primary audience of research scientists and, as such, exclusively publishes protocols with research applications. Protocols primarily aimed at influencing patient management and treatment decisions are not featured. The specific techniques covered encompass a wide range, including but not limited to: Biochemistry, Cell biology, Cell culture, Chemical modification, Computational biology, Developmental biology, Epigenomics, Genetic analysis, Genetic modification, Genomics, Imaging, Immunology, Isolation, purification, and separation, Lipidomics, Metabolomics, Microbiology, Model organisms, Nanotechnology, Neuroscience, Nucleic-acid-based molecular biology, Pharmacology, Plant biology, Protein analysis, Proteomics, Spectroscopy, Structural biology, Synthetic chemistry, Tissue culture, Toxicology, and Virology.
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