期刊
NANOMATERIALS
卷 11, 期 2, 页码 -出版社
MDPI
DOI: 10.3390/nano11020275
关键词
bioreactor; tissue engineering; decellularization; liver; extracellular matrix; bioluminescence
类别
资金
- National Institute for Health Research [NIHR-RP-2014-04-046]
- UKRMP Universal cells to overcome HLA barriers in regenerative medicine
- OAK Foundation [W1095/OCAY-14-191]
- GOSHCC the Horizon 2020 grant [INTENS 668294]
Decellularised organ scaffolds in the field of in vitro liver disease models maintain original properties, but the scarcity of appropriate bioreactors hampers tissue engineering approaches. A novel specific bioreactor was designed for long-term 3D culture of whole liver constructs, supporting cell survival and function. The bioreactor allows non-invasive monitoring and analysis of bioengineered constructs, showing higher viability, distribution, and functionality under dynamic conditions compared to static culture.
In the field of in vitro liver disease models, decellularised organ scaffolds maintain the original biomechanical and biological properties of the extracellular matrix and are established supports for in vitro cell culture. However, tissue engineering approaches based on whole organ decellularized scaffolds are hampered by the scarcity of appropriate bioreactors that provide controlled 3D culture conditions. Novel specific bioreactors are needed to support long-term culture of bioengineered constructs allowing non-invasive longitudinal monitoring. Here, we designed and validated a specific bioreactor for long-term 3D culture of whole liver constructs. Whole liver scaffolds were generated by perfusion decellularisation of rat livers. Scaffolds were seeded with Luc(+)HepG2 and primary human hepatocytes and cultured in static or dynamic conditions using the custom-made bioreactor. The bioreactor included a syringe pump, for continuous unidirectional flow, and a circuit built to allow non-invasive monitoring of culture parameters and media sampling. The bioreactor allowed non-invasive analysis of cell viability, distribution, and function of Luc(+)HepG2-bioengineered livers cultured for up to 11 days. Constructs cultured in dynamic conditions in the bioreactor showed significantly higher cell viability, measured with bioluminescence, distribution, and functionality (determined by albumin production and expression of CYP enzymes) in comparison to static culture conditions. Finally, our bioreactor supports primary human hepatocyte viability and function for up to 30 days, when seeded in the whole liver scaffolds. Overall, our novel bioreactor is capable of supporting cell survival and metabolism and is suitable for liver tissue engineering for the development of 3D liver disease models.
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