{"title":"Engineering and Evaluating Vascularized Organotypic Spheroids On-Chip","authors":"James J. Tronolone, Nadin Mohamed, Christopher P. Chaftari, Yuxiang Sun, Tanmay Mathur, Abhishek Jain","doi":"10.1002/cpz1.70058","DOIUrl":null,"url":null,"abstract":"<p>Organotypic spheroids are evolving as a mainstream in vitro modeling platform, but it is crucial to integrate vascular tissue and perfusion for maintaining their longevity, stability, and physiological relevance. Current vascularization methods remain underdeveloped, and several protocols are poorly reproducible and are limited to use by a few select groups who have designed these methods. To achieve standardization, we offer a step-by-step guide to vascularize organotypic spheroids in case studies of pancreatic islets and cancer spheroids. Our systematic approach spans microfluidic chip design, spheroid fabrication, and vascularization techniques (vasculogenesis and angiogenesis) while describing critical tissue engineering methods. We also include additional insights and operating guidelines within our protocols that characterize and quantitate these models with molecular assays as well as our integrated computational algorithms of mass transport through formed capillary vessels. These protocols contribute to establishing reproducibility, standardization, and enhanced adoption by other contemporary organ-chip researchers, who want to engineer vascularized organoid-based microphysiological platforms. © 2024 Wiley Periodicals LLC.</p><p><b>Basic Protocol 1</b>: Design and fabrication of microfluidic chips for vascularized spheroids</p><p><b>Basic Protocol 2</b>: Organotypic spheroid fabrication</p><p><b>Basic Protocol 3</b>: Vascularized spheroids on-chip</p><p><b>Basic Protocol 4</b>: Functionality assays</p><p><b>Support Protocol 1</b>: Cell Culture</p><p><b>Support Protocol 2</b>: Immunocytochemistry</p>","PeriodicalId":93970,"journal":{"name":"Current protocols","volume":"4 11","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current protocols","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpz1.70058","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Organotypic spheroids are evolving as a mainstream in vitro modeling platform, but it is crucial to integrate vascular tissue and perfusion for maintaining their longevity, stability, and physiological relevance. Current vascularization methods remain underdeveloped, and several protocols are poorly reproducible and are limited to use by a few select groups who have designed these methods. To achieve standardization, we offer a step-by-step guide to vascularize organotypic spheroids in case studies of pancreatic islets and cancer spheroids. Our systematic approach spans microfluidic chip design, spheroid fabrication, and vascularization techniques (vasculogenesis and angiogenesis) while describing critical tissue engineering methods. We also include additional insights and operating guidelines within our protocols that characterize and quantitate these models with molecular assays as well as our integrated computational algorithms of mass transport through formed capillary vessels. These protocols contribute to establishing reproducibility, standardization, and enhanced adoption by other contemporary organ-chip researchers, who want to engineer vascularized organoid-based microphysiological platforms. © 2024 Wiley Periodicals LLC.
Basic Protocol 1: Design and fabrication of microfluidic chips for vascularized spheroids
Basic Protocol 2: Organotypic spheroid fabrication
Basic Protocol 3: Vascularized spheroids on-chip
Basic Protocol 4: Functionality assays
Support Protocol 1: Cell Culture
Support Protocol 2: Immunocytochemistry
芯片上血管有组织球体的工程设计与评估
有机球体正逐渐发展成为主流体外建模平台,但要保持其寿命、稳定性和生理相关性,整合血管组织和灌注至关重要。目前的血管化方法仍不完善,一些方案的可重复性很差,仅限于少数设计这些方法的小组使用。为了实现标准化,我们在胰岛和癌症球形体的案例研究中提供了一个分步指南,指导如何对器官型球形体进行血管化。我们的系统方法涵盖微流控芯片设计、球形体制造和血管化技术(血管生成和血管生成),同时介绍了关键的组织工程方法。我们还在操作规程中加入了更多的见解和操作指南,通过分子检测以及我们的综合计算算法对这些模型进行表征和量化,并通过已形成的毛细血管进行质量传输。这些规程有助于建立可重复性、标准化,并提高其他当代器官芯片研究人员的采用率,这些研究人员希望设计出基于血管的类器官微生理学平台。© 2024 Wiley Periodicals LLC.基本方案 1:设计和制造用于血管化球体的微流控芯片 基本方案 2:制造器官型球体 基本方案 3:芯片上的血管化球体 基本方案 4:功能测定 支持方案 1:细胞培养 支持方案 2:免疫细胞化学。
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