Journal article
Establishment and characterization of turtle liver organoids provides a potential model to decode their unique adaptations
Communications biology, Vol.7(1), 218
02/22/2024
DOI: 10.1038/s42003-024-05818-1
PMCID: PMC10883927
PMID: 38388772
Abstract
Painted turtles are remarkable for their freeze tolerance and supercooling ability along with their associated resilience to hypoxia/anoxia and oxidative stress, rendering them an ideal biomedical model for hypoxia-induced injuries (including strokes), tissue cooling during surgeries, and organ cryopreservation. Yet, such research is hindered by their seasonal reproduction and slow maturation. Here we developed and characterized adult stem cell-derived turtle liver organoids (3D self-assembled in vitro structures) from painted, snapping, and spiny softshell turtles spanning ~175My of evolution, with a subset cryopreserved. This development is, to the best of our knowledge, a first for this vertebrate Order, and complements the only other non-avian reptile organoids from snake venom glands. Preliminary characterization, including morphological, transcriptomic, and proteomic analyses, revealed organoids enriched in cholangiocytes. Deriving organoids from distant turtles and life stages demonstrates that our techniques are broadly applicable to chelonians, permitting the development of functional genomic tools currently lacking in herpetological research. Such platform could potentially support studies including genome-to-phenome mapping, gene function, genome architecture, and adaptive responses to climate change, with implications for ecological, evolutionary, and biomedical research.
Details
- Title: Subtitle
- Establishment and characterization of turtle liver organoids provides a potential model to decode their unique adaptations
- Creators
- Christopher Zdyrski - Iowa State UniversityVojtech Gabriel - Iowa State UniversityThea B Gessler - Iowa State UniversityAbigail Ralston - 3D Health Solutions Inc., Ames, IA, USAItzel Sifuentes-Romero - Iowa State UniversityDebosmita Kundu - Iowa State UniversitySydney Honold - Iowa State UniversityHannah Wickham - Iowa State UniversityNicholas E Topping - Iowa State UniversityDipak Kumar Sahoo - Iowa State UniversityBasanta Bista - Iowa State UniversityJeffrey Tamplin - University of Northern IowaOscar Ospina - Moffitt Cancer CenterPablo Piñeyro - Iowa State UniversityMarco Arriaga - The University of Texas Rio Grande ValleyJacob A Galan - The University of Texas Rio Grande ValleyDavid K Meyerholz - University of IowaKarin Allenspach - Iowa State UniversityJonathan P Mochel - University of GeorgiaNicole Valenzuela - Iowa State University
- Resource Type
- Journal article
- Publication Details
- Communications biology, Vol.7(1), 218
- DOI
- 10.1038/s42003-024-05818-1
- PMID
- 38388772
- PMCID
- PMC10883927
- NLM abbreviation
- Commun Biol
- eISSN
- 2399-3642
- Language
- English
- Date published
- 02/22/2024
- Academic Unit
- Pathology
- Record Identifier
- 9984560422102771
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