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用于 3D 脑类器官原位特征分析的无创无标记成像分析流程。

Non-invasive label-free imaging analysis pipeline for in situ characterization of 3D brain organoids.

机构信息

George W. Woodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, GA, 30318, USA.

Georgia Institute of Technology, Interdisciplinary Program in Bioengineering, Atlanta, GA, 30332, USA.

出版信息

Sci Rep. 2024 Sep 27;14(1):22331. doi: 10.1038/s41598-024-72038-2.

DOI:10.1038/s41598-024-72038-2
PMID:39333572
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11436713/
Abstract

Brain organoids provide a unique opportunity to model organ development in a system similar to human organogenesis in vivo. Brain organoids thus hold great promise for drug screening and disease modeling. Conventional approaches to organoid characterization predominantly rely on molecular analysis methods, which are expensive, time-consuming, labor-intensive, and involve the destruction of the valuable three-dimensional (3D) architecture of the organoids. This reliance on end-point assays makes it challenging to assess cellular and subcellular events occurring during organoid development in their 3D context. As a result, the long developmental processes are not monitored nor assessed. The ability to perform non-invasive assays is critical for longitudinally assessing features of organoid development during culture. In this paper, we demonstrate a label-free high-content imaging approach for observing changes in organoid morphology and structural changes occurring at the cellular and subcellular level. Enabled by microfluidic-based culture of 3D cell systems and a novel 3D quantitative phase imaging method, we demonstrate the ability to perform non-destructive high-resolution quantitative image analysis of the organoid. The highlighted results demonstrated in this paper provide a new approach to performing live, non-destructive monitoring of organoid systems during culture.

摘要

脑类器官为在类似于体内器官发生的系统中对器官发育进行建模提供了独特的机会。因此,脑类器官在药物筛选和疾病建模方面具有很大的应用前景。传统的类器官表征方法主要依赖于分子分析方法,这些方法昂贵、耗时、劳动强度大,并且涉及对类器官有价值的三维 (3D) 结构的破坏。这种对终点测定法的依赖使得难以评估类器官发育过程中发生的细胞和亚细胞事件。因此,无法评估长期的发育过程。进行非侵入性测定的能力对于在培养过程中纵向评估类器官发育的特征至关重要。在本文中,我们展示了一种无标记的高内涵成像方法,用于观察类器官形态的变化和发生在细胞和亚细胞水平上的结构变化。通过基于微流控的 3D 细胞系统培养和一种新颖的 3D 定量相位成像方法,我们展示了对类器官进行非破坏性高分辨率定量图像分析的能力。本文中强调的结果提供了一种新的方法,可以在培养过程中对类器官系统进行实时、非破坏性的监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b39/11436713/ef41738beab4/41598_2024_72038_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b39/11436713/2fcf7388ae71/41598_2024_72038_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b39/11436713/a4d64d6d9b19/41598_2024_72038_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b39/11436713/0661bd3aad8a/41598_2024_72038_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b39/11436713/e23610d507f5/41598_2024_72038_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b39/11436713/86935cea47c1/41598_2024_72038_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b39/11436713/1974342f304e/41598_2024_72038_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b39/11436713/ef41738beab4/41598_2024_72038_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b39/11436713/2fcf7388ae71/41598_2024_72038_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b39/11436713/a4d64d6d9b19/41598_2024_72038_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b39/11436713/0661bd3aad8a/41598_2024_72038_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b39/11436713/e23610d507f5/41598_2024_72038_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b39/11436713/86935cea47c1/41598_2024_72038_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b39/11436713/1974342f304e/41598_2024_72038_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b39/11436713/ef41738beab4/41598_2024_72038_Fig7_HTML.jpg

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Multiscale light-sheet organoid imaging framework.
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