Decellularized caprine liver extracellular matrix as a 2D substrate coating and 3D hydrogel platform for vascularized liver tissue engineering
Open accessAbstract
Development of a vascularized liver tissue construct is a need of an hour to circumvent the current demand of liver transplantation in health care sector. An appropriate matrix must support liver cell viability, functionality, and development of microvasculature. With this perspective, here, we report the use of decellularized caprine liver extracellular matrix (CLECM) derived hydrogel for tissue engineering applications. First, CLECM was used as a substrate coating material for 2D hepatocyte culture. HepG2 cells cultured on CLECM-coated surface showed higher albumin, urea, glycogen, and GAGs synthesis in comparison with collagen-coated surface (taken as control for the study). Thereafter, the cells were encapsulated in CLECM hydrogels for 3D culture. In CLECM hydrogels, HepG2 cells showed highly differentiated and polarized phenotype with the appearance of bile canaliculi-like structures and enhanced expression of mature hepatocyte markers. We further showed that CLECM hydrogels also supported the development of microvasculature in vitro, thus making it a suitable candidate for development of a prevascularized liver tissue construct. In conclusion, we proved the superiority of CLECM over collagen for 2D/3D human hepatocyte and endothelial cell culture. CLECM could serve as an efficient biomaterial platform in the development of a liver tissue construct for application in tissue engineering.
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dLECM hydrogels invariably supported high cell compatibility, with viability above 90% as determined by Live/Dead, MTT, and CCK-8 assays.
“hydrogels invariably supported high cell compatibility, with viability above 90 % as determined by Live/Dead, MTT, and CCK-8 assays [16,26].”
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Liver tissue engineering and cell sources: issues and challenges
Palakkan, A. A., Hay, D. C., PR, A. K., TV, K., & Ross, J. A. (2013) · Liver International · doi:10.1111/liv.12134 · Cited by 130 · see citing works
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Tao, M., Ao, T., Mao, X., Yan, X., Javed, R., Hou, W., Wang, Y., Sun, C., Lin, S., Yu, T., et al. (2021) · Bioactive Materials · doi:10.1016/j.bioactmat.2021.02.010 · Cited by 119 · see citing works
Bhatt, S., Krishnakumar, J., Mounica, K. L., & Nune, M. (2025) · Macromolecular Materials and Engineering · doi:10.1002/mame.202400451 · Cited by 6 · see citing works
Majidi, Z., Sarvi, M. M., Rajabi, M. A., Firouzian, H., Seyhoun, I., & Majidi Zolbin, M. (2026) · Regenerative Therapy · doi:10.1016/j.reth.2025.11.006 · Cited by 5 · see citing works
- Authors
- Agarwal, T., Narayan, R., Maji, S., Ghosh, S. K., & Maiti, T. K.
- Affiliations
- Indian Institute of Technology Kharagpur (IN)
- Corresponding author
- Maiti, Tapas Kumar
- Venue
- Journal of Tissue Engineering and Regenerative Medicine
- Publisher
- Wiley
- Published
- 2017-11-23
- Volume
- 12
- Issue
- 3
- Pages
- e1678-e1690
- ISSN
- 1932-6254 (ISSN-L)
- 1932-7005
- OpenAlex
- W2766217622
- Cited by
- 46
- References
- 2
- Citations by year
- 2026: 2 · 2025: 3 · 2024: 8 · 2023: 9 · 2022: 5 · 2021: 9 · 2020: 4 · 2019: 4 · 2018: 2
- FWCI
- 2.80
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Journal of Tissue Engineering and Regenerative Medicine (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Department of Science and Technology, Ministry of Science and Technology, India
- Council of Scientific and Industrial Research, India
- Topics
- Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
- Physical Sciences › Engineering › Biomedical Engineering › 3D Printing in Biomedical Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Medicine › Hydrogels: synthesis, properties, applications
- Keywords
- goat liver, hydrogels, 3D cell culture, HepG2 cells, hepatocyte differentiation, microcirculation, endothelial cells, liver tissue engineering
- MeSH terms
- Animals, Extracellular Matrix, Goats, Humans, Liver, Male, Solubility, Neovascularization, Physiologic, Coated Materials, Biocompatible, Hydrogels, Hepatocytes, Tissue Engineering, Hep G2 Cells, Human Umbilical Vein Endothelial Cells
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