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.
{"title":"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.","authors":"Gamze Demirel, Olgu E Tok, Ranan G Aktas","doi":"10.1007/7651_2025_634","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":18490,"journal":{"name":"Methods in molecular biology","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-06-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Methods in molecular biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/7651_2025_634","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
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.
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.