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用于实时评估和监测心脏组织工程构建体的高速成像系统的开发。

Development of a high-speed imaging system for real time evaluation and monitoring of cardiac engineered tissues.

作者信息

Belzil Antoine, Gélinas Roselle, Comtois Philippe

机构信息

Research Centre, Montreal Heart Institute, Montréal, QC, Canada.

Department of Pharmacology and Physiology, Universite de Montreal, Montréal, QC, Canada.

出版信息

Front Bioeng Biotechnol. 2024 Aug 12;12:1403044. doi: 10.3389/fbioe.2024.1403044. eCollection 2024.

DOI:10.3389/fbioe.2024.1403044
PMID:39188370
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11345265/
Abstract

Stem cell derived cardiac monolayers have high potential for tissue regeneration, drug testing and disease modeling. However, current differentiation protocols are still sub-optimal, resulting in cultures with variable yields and properties. We propose a high-speed lenseless imaging system, integrated with an electrical stimulation unit, to optimize the generation of these cultures. This tool relies on the variations of cellular patterns, during contraction, measured by digital imaging. The imaging system can monitor cardiac cell sheet function and structure, providing the necessary tools to quickly evaluate engineered monolayer. It can record high speed videos and capture high resolution images, from which tissue spatial organization and contractile characteristics can be obtained. Validation of the system was performed using cardiomyocytes derived from human induced pluripotent stem cell and neonatal rat cardiomyocytes. The imaging system allows the observation, acquisition and analysis of important data relating to contractile activity development of cardiac cells, making it a promising tool for optimization in cardiac tissue engineering.

摘要

干细胞衍生的心脏单层细胞在组织再生、药物测试和疾病建模方面具有很高的潜力。然而,目前的分化方案仍然不够理想,导致培养物的产量和特性存在差异。我们提出了一种集成了电刺激单元的高速无透镜成像系统,以优化这些培养物的生成。该工具依赖于通过数字成像测量的收缩过程中细胞模式的变化。成像系统可以监测心脏细胞片的功能和结构,提供快速评估工程单层细胞所需的工具。它可以记录高速视频并捕获高分辨率图像,从中可以获得组织的空间组织和收缩特性。使用源自人诱导多能干细胞的心肌细胞和新生大鼠心肌细胞对该系统进行了验证。该成像系统允许观察、获取和分析与心脏细胞收缩活动发展相关的重要数据,使其成为心脏组织工程优化的一个有前途的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/11345265/004c7e9927a5/fbioe-12-1403044-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/11345265/293c9e79870f/fbioe-12-1403044-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/11345265/9788b8844418/fbioe-12-1403044-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/11345265/4ff9a6870f12/fbioe-12-1403044-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/11345265/e7b32ff7c0f7/fbioe-12-1403044-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/11345265/9651af112104/fbioe-12-1403044-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/11345265/0337def927e4/fbioe-12-1403044-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/11345265/6c8394aeda32/fbioe-12-1403044-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/11345265/2f0bdef686ee/fbioe-12-1403044-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/11345265/004c7e9927a5/fbioe-12-1403044-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/11345265/293c9e79870f/fbioe-12-1403044-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/11345265/9788b8844418/fbioe-12-1403044-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/11345265/4ff9a6870f12/fbioe-12-1403044-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/11345265/e7b32ff7c0f7/fbioe-12-1403044-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/11345265/9651af112104/fbioe-12-1403044-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/11345265/0337def927e4/fbioe-12-1403044-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/11345265/6c8394aeda32/fbioe-12-1403044-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/11345265/2f0bdef686ee/fbioe-12-1403044-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f6/11345265/004c7e9927a5/fbioe-12-1403044-g009.jpg

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本文引用的文献

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Front Genet. 2024 Apr 19;15:1375467. doi: 10.3389/fgene.2024.1375467. eCollection 2024.
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Novel Analysis Method for Beating Cells Videomicroscopy Data: Functional Characterization of Culture Samples.跳动细胞视频显微镜数据的新型分析方法:培养样本的功能表征
Front Physiol. 2022 Feb 15;13:733706. doi: 10.3389/fphys.2022.733706. eCollection 2022.
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Characterization of a Human Induced Pluripotent Stem Cell-Derived Cardiomyocyte Model for the Study of Variant Pathogenicity: Validation of a Mutation.
用于研究变异致病性的人诱导多能干细胞衍生心肌细胞模型的表征:一种突变的验证
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Heart Disease and Stroke Statistics-2017 Update: A Report From the American Heart Association.《2017年心脏病和中风统计数据更新:美国心脏协会报告》
Circulation. 2017 Mar 7;135(10):e146-e603. doi: 10.1161/CIR.0000000000000485. Epub 2017 Jan 25.
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Electrical Stimulation Enhances Cardiac Differentiation of Human Induced Pluripotent Stem Cells for Myocardial Infarction Therapy.电刺激增强人诱导多能干细胞向心肌梗死治疗中的心肌分化。
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