Bio-based hydrogels as three-dimensional (3D) constructs have attracted attention in advanced tissue engineering. Compared with conventional two-dimensional (2D) cell culture, cells grown in 3D scaffolds are expected to demonstrate the inherent behavior of living organisms of cellular spheroids. Herein, we constructed cell-laden nanofiber-based hydrogels in combination with 2,2,6,6-tetramethylpiperidine 1-oxyl-oxidized cellulose nanofiber (TOCNF) and chitosan nanofiber (CsNF) for bioadaptive liver tissue engineering. The carboxylates of TOCNF and amines of CsNF were directly crosslinked via EDC/NHS chemistry. The rheological properties of the solutions for the nanofibers and hydrogels revealed sufficient physical properties for the injection, printing, and plotting process, as well as significant encapsulation of living cells. As-designed hydrogels exhibited excellent viscoelastic properties with typical shear-thinning behavior, and had a storage modulus of 1234 Pa ± 68 Pa, suitable for cell culture. Non-cytotoxicity was confirmed using a live/dead assay with mouse-derived fibroblast NIH/3T3 cells. Human hepatocellular carcinoma HepG2 cells could be cultured on a gel surface (2D environment) and encapsulated in the gel structure (3D environment), which enabled 10 d growth with high gene expression level of albumin of HepG2 spheroids in the 3D gels. The biodegradable cell-laden hydrogels are expected to mimic the cellular microenvironment and provide potential for bioadaptive 3D cell cultures in biomedical applications.
Keywords: 3D bioprinting; cell encapsulation; chitosan nanofiber; injectable hydrogel; nanocellulose.
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