In vitro, β-cells tend to reduce their ability to aggregate into islets and lose insulin-producing ability, likely due to insufﬁcient cell–cell and cell–matrix interactions that are essential for β-cell retention, viability and functionality. In response to these needs, surfaces of succinylated chitosan-based beads (NSC) were modiﬁed with zwitterionic carboxy-betaine (CB) moieties, a compa- tible osmolyte known to regulate cellular hydration state, and used to promote the formation of β-cell spheroids using a conventional 2D cell culture technique. The NSC were synthesised by ionic gelation and surface-functionalised with CB using carbodiimide chemistry. Scanning electron microscopy (SEM), dynamic laser scattering (DLS) and Fourier transform infrared spectroscopy (FTIR) were employed as characterisation tools to conﬁrm the successful modiﬁcation of the succinylated chitosan material into spherical beads with rough surfaces and a diameter of 0.4µm. NSC with and without CB were re-suspended at con-centrations of 0.1, 0.3 and 0.6 mg/mL in saline medium and tested in vitro with MIN6 murine pancreatic β-cell line. Results showed that a concentration of 0.3 mg/mL, NSC- CB encouraged pancreatic MIN6 cells to proliferate and form spheroids via E-cadherin and Pdx-1 activation within48 h in culture. These spheroids, with a size of approxi- mately 80 µm, exhibited high cell viability and enhanced insulin protein expression and secretion when compared tocells organised by the non-modiﬁed beads.
|Journal||Journal of Materials Science: Materials in Medicine|
|Publication status||Published - 30 Dec 2017|