Year: 2023
Type: article
Abstract: Despite decades of effort, the preservation of complex organs for transplantation remains a significant barrier that exacerbates the organ shortage crisis. Progress in organ preservation research is significantly hindered by suboptimal research tools that force investigators to sacrifice translatability over throughput. For instance, simple model systems, such as single cell monolayers or co-cultures, lack native tissue structure and functional assessment, while mammalian whole organs are complex systems with confounding variables not compatible with high-throughput experimentation. In response, diverse fields and industries have bridged this experimental gap through the development of rich and robust resources for the use of zebrafish as a model organism. Through this study, we aim to demonstrate the value zebrafish pose for the fields of solid organ preservation and transplantation, especially with respect to experimental transplantation efforts. A wide array of methods were customized and validated for preservation-specific experimentation utilizing zebrafish, including the development of assays at multiple developmental stages (larvae and adult), methods for loading and unloading preservation agents, and the development of viability scores to quantify functional outcomes. Using this platform, the largest and most comprehensive screen of cryoprotectant agents (CPAs) was performed to determine their toxicity and efficiency at preserving complex organ systems using a high subzero approach called partial freezing (i.e., storage in the frozen state at -10°C). As a result, adult zebrafish cardiac function was successfully preserved after 5 days of partial freezing storage. In combination, the methods and techniques developed have the potential to drive and accelerate research in the fields of solid organ preservation and transplantation.
Source: The FASEB Journal
Language: English
Subfield: Surgery
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Estimated APC paid: $3,390
Funders: National Science Foundation, Foundation for the National Institutes of Health, American Heart Association, Massachusetts General Hospital, National Institutes of Health, National Heart, Lung, and Blood Institute, National Institute of General Medical Sciences, National Institute of Diabetes and Digestive and Kidney Diseases
Awards: G102216896, G1330203626, G1410383544, G1558119636, G1560286954, G159185806, G1656549027, G1670029188, G1772008459, G2010549676, G2022062059, High subzero preservation of liver for transplantation, G2596098297, G2631298735, G2788952747, G3506141840, G4004993690, G4151902639, G4279048994, G4776902722, G5689005019, G6628441132, G707340384, Exploring the role of Hippo signaling and elevated cardiomyocyte ploidy as barriers for zebrafish heart regeneration, G738160294, NSF Engineering Research Center for Advanced Technologies for Preservation of Biological Systems (ATP-Bio), G9000042905, G9000078997, G9000174082, G9000194663, G9000344418, A quantitative viability metric for liver transplantation using Resonance Raman Spectroscopy, Whole heart suspended animation: leveraging the zebrafish to solve the organ shortage., G985574109
OpenAlex ID: W4386818296
