An in situ mechanical adjustable double crosslinking hyaluronic acid/ poly-lysine hydrogel matrix: Fabrication, characterization and cell morphology

Cell fate and morphologies are influenced by the mechanical property of matrix. However, the relevant works about the dynamic adjustable of matrix mechanical property is rare and most of them need extra stimulation, such as the controllable of the degradation. In this study, double crosslinking (DC) hydrogels are fabricated by sequential covalent crosslinking and electrostatic interactions between hyaluronic acid and poly-lysine. Without any extra stimulation or treatment, the compressive stress of DC-hydrogels increases from 22.4 +/- 9.4 kPa to 320.1 +/- 6.6 kPa with the elongation of incubation time in DMEM solution. The change of compressive stress of matrix induced the morphology of L929 fibroblast cells adjusted from the distributed round shape to spheroid cell clusters and finally to spread shape. RNA sequence analysis also demonstrated that the differentially gene expression and GO enrichment between the cells seeded on the DC-hydrogel with different incubation time. In addition, by increasing the electrostatic interactions ratio of the hydrogel, the biodegradation, compressive stress and energy dissipation of the DC-hydrogels were also significantly improved. Therefore, our study provides new and critical insights into the design strategy to achieve DC-hydrogels which can in situ alter cells morphology and open up a new avenue for the application of disease therapy. (c) 2021 Elsevier B.V. All rights reserved.

Automated summary

This study demonstrates the fabrication of double crosslinking hydrogels that can alter matrix compressive stress, influencing cell morphology without additional stimulation. By increasing electrostatic interactions ratio, the performance of the hydrogels can be significantly improved, providing new insights for disease therapy applications.