4.7 Article

Photocrosslinkable liver extracellular matrix hydrogels for the generation of 3D liver microenvironment models

Journal

SCIENTIFIC REPORTS
Volume 11, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41598-021-94990-z

Keywords

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Funding

  1. National Breast Cancer Foundation of Australia [PF-16-004]

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Liver extracellular matrix (ECM)-based hydrogels have been prepared using detergent-based protocols to generate photocrosslinkable methacrylated liver ECM (LivMA) hydrogels. The mechanical properties of the hydrogels were tunable, showing distinct compressive modulus dependent on the hydrogel concentration. The cytocompatibility of the hydrogels for encapsulated Human Hepatocytes cells was demonstrated after one week of culture, making LivMA hydrogels a potential platform for liver disease research and drug studies.
Liver extracellular matrix (ECM)-based hydrogels have gained considerable interest as biomimetic 3D cell culture environments to investigate the mechanisms of liver pathology, metabolism, and toxicity. The preparation of current liver ECM hydrogels, however, is based on time-consuming thermal gelation and limits the control of mechanical properties. In this study, we used detergent-based protocols to produce decellularized porcine liver ECM, which in turn were solubilized and functionalized with methacrylic anhydride to generate photocrosslinkable methacrylated liver ECM (LivMA) hydrogels. Firstly, we explored the efficacy of two protocols to decellularize porcine liver tissue using varying combinations of commonly used chemical agents such as Triton X-100, Sodium Dodecyl Sulphate (SDS) and Ammonium hydroxide. Then, we demonstrated successful formation of stable, reproducible LivMA hydrogels from both the protocols by photocrosslinking. The LivMA hydrogels obtained from the two decellularization protocols showed distinct mechanical properties. The compressive modulus of the hydrogels was directly dependent on the hydrogel concentration, thereby demonstrating the tuneability of mechanical properties of these hydrogels. Immortalized Human Hepatocytes cells were encapsulated in the LivMA hydrogels and cytocompatibility of the hydrogels was demonstrated after one week of culture. In summary, the LivMA hydrogel system provides a simple, photocrosslinkable platform, which can potentially be used to simulate healthy versus damaged liver for liver disease research, drug studies and cancer metastasis modelling.

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