A Simplified and Robust Immunofluorescence Labeling Method for Complex 3D Cell Cultures: Minimizing Manipulation and Maximizing Data in Whole-Mount Analysis of Organoids, Spheroids, and Co-culture Models.

Q4 Biochemistry, Genetics and Molecular Biology
Gamze Demirel, Olgu E Tok, Ranan G Aktas
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引用次数: 0

Abstract

Whole-mount imaging and labeling of 3D organoids and spheroids offer unparalleled insights into spatial biology, organogenesis, disease mechanisms, and cancer cell dynamics within a physiologically relevant 3D context. Those techniques in biomedical research, yet its application to complex 3D cell culture models, remain fraught with challenges. Current methods often suffer from sample damage and loss, in addition to lengthy and complex protocols involving multiple steps and reagent preparations. To address these challenges, we describe a novel approach that overcomes limitations of conventional techniques by preserving sample integrity, minimizing sample manipulation, and eliminating the need for multiple reagents. The current method facilitates comprehensive sample analysis, significantly improving the efficiency and accuracy of protein visualization. It is compatible with a wide range of samples, including organoids and spheroids in hydrogels, organ-on-chip models, and co-culture systems.

复杂3D细胞培养的一种简化和稳健的免疫荧光标记方法:在类器官,球体和共培养模型的全mount分析中,最小化操作和最大化数据。
三维类器官和球体的全载成像和标记在生理学相关的三维环境中为空间生物学、器官发生、疾病机制和癌细胞动力学提供了无与伦比的见解。生物医学研究中的这些技术,在复杂的3D细胞培养模型中的应用,仍然充满了挑战。目前的方法除了涉及多个步骤和试剂制备的冗长和复杂的方案外,还经常遭受样品损坏和损失。为了解决这些挑战,我们描述了一种新的方法,通过保持样品完整性,最大限度地减少样品操作,并消除了对多种试剂的需求,克服了传统技术的局限性。目前的方法有利于全面的样品分析,显著提高了蛋白质可视化的效率和准确性。它与广泛的样品兼容,包括水凝胶中的类器官和球体,器官芯片模型和共培养系统。
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
Methods in molecular biology
Methods in molecular biology Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
2.00
自引率
0.00%
发文量
3536
期刊介绍: For over 20 years, biological scientists have come to rely on the research protocols and methodologies in the critically acclaimed Methods in Molecular Biology series. The series was the first to introduce the step-by-step protocols approach that has become the standard in all biomedical protocol publishing. Each protocol is provided in readily-reproducible step-by-step fashion, opening with an introductory overview, a list of the materials and reagents needed to complete the experiment, and followed by a detailed procedure that is supported with a helpful notes section offering tips and tricks of the trade as well as troubleshooting advice.
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