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Functional ultrasound imaging for assessment of extracellular matrix scaffolds used for liver organoid formation
Open accessAbstract
A method of 3D functional ultrasound imaging has been developed to enable non-destructive assessment of extracellular matrix scaffolds that have been prepared by decellularization protocols and are intended for recellularization to create organoids. A major challenge in organ decellularization is retaining patent micro-vascular structures crucial for nutrient access and functionality of organoids. The imaging method described here provides statistical distributions of flow rates throughout the tissue volumes, 3D vessel network architecture visualization, characterization of microvessel volumes and sizes, and delineation of matrix from vascular circuits. The imaging protocol was tested on matrix scaffolds that are tissue-specific, but not species-specific, matrix extracts, prepared by a process that preserved >98% of the collagens, collagen-associated matrix components, and matrix-bound growth factors and cytokines. Image-derived data are discussed with respect to assessment of scaffolds followed by proof-of-concept studies in organoid establishment using Hep3B, a human hepatoblast-like cell line. Histology showed that the cells attached to scaffolds with patent vasculature within minutes, achieved engraftment at near 100%, expressed liver-specific functions within 24 h, and yielded evidence of proliferation and increasing differentiation of cells throughout the two weeks of culture studies. This imaging method should prove valuable in analyses of such matrix scaffolds.
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Gessner et al.'s protocol yielded efficient decellularization while preserving the ECM ultrastructure and the macro- and micro-vascular network.
“Their protocol yielded efficient decellularization while preserving the ECM ultrastructure and the macro- and micro-vascular network.”
From Liver tissue engineering using decellularized scaffolds: Current progress, challenges, and opportunities (2024) · cites this paper as [162]
Gessner et al. used phospholipase and nucleases (DNase and RNase) in combination with detergent for rat liver decellularization.
“Gessner et al. used phospholipase and nucleases (DNase and RNase) in combination with detergent for rat liver decellularization [162].”
From Liver tissue engineering using decellularized scaffolds: Current progress, challenges, and opportunities (2024) · cites this paper as [162]
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Decellularization for the retention of tissue niches
Moffat, D., Ye, K., & Jin, S. (2022) · Journal of Tissue Engineering · doi:10.1177/20417314221101151 · Cited by 152
Hussein, K. H., Ahmadzada, B., Correa, J. C., Sultan, A., Wilken, S., Amiot, B., & Nyberg, S. L. (2024) · Bioactive Materials · doi:10.1016/j.bioactmat.2024.06.001 · Cited by 28
“Gessner et al. used phospholipase and nucleases (DNase and RNase) in combination with detergent for rat liver decellularization [162].”
Background
Metadata
- Authors
- Gessner, R. C., Hanson, A. D., Feingold, S., Cashion, A. T., Corcimaru, A., Wu, B. T., Mullins, C. R., Aylward, S. R., Reid, L. M., & Dayton, P. A.
- Affiliations
- University of North Carolina at Chapel Hill (US)
- Kitware (United States) (US)
- Corresponding author
- Reid, Lola M.
- Dayton, Paul A.
- Venue
- Biomaterials
- Publisher
- Elsevier BV
- Published
- 2013-12
- Volume
- 34
- Issue
- 37
- Pages
- 9341-9351
- ISSN
- 0142-9612 (ISSN-L)
- PMC
- PMC4597479
- OpenAlex
- W2001059760
- Cited by
- 44
- References
- 1
- Citations by year
- 2025: 2 · 2024: 1 · 2023: 4 · 2022: 4 · 2021: 5 · 2019: 6 · 2018: 3 · 2017: 4 · 2016: 4 · 2015: 5 · 2014: 5
- FWCI
- 4.60
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Biomaterials (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Carolina Digital Repository (University of North Carolina at Chapel Hill) (submittedVersion)
- UNC Libraries
- Funders
- National Science Foundation
- Siemens Medical Solutions USA
- National Institutes of Health (5r43ca165621-02, CA016086, 1 R43 CA165621, DK-34987)
- National Cancer Institute (R43 CA165621, CA016086, R01CA170665, 1R43CA165621, R21CA182322, P30CA016086)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK 34987, P30‐DK34987, P30DK034987)
- Topics
- Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
- Physical Sciences › Engineering › Biomedical Engineering › 3D Printing in Biomedical Research
- Physical Sciences › Engineering › Biomedical Engineering › Photoacoustic and Ultrasonic Imaging
- Keywords
- functional ultrasound imaging, extracellular matrix scaffolds, liver organoids, recellularization, microvascular networks, flow rate distribution, Hep3B cells, liver regeneration
- MeSH terms
- Animals, Cell Line, Extracellular Matrix, Humans, Liver, Organoids, Ultrasonography, Rats, Wistar, Rats, Tissue Scaffolds
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