Proliferation and differentiation of human dental pulp stem cells on phosphorylated cellulose nanofiber scaffolds

Carbohydr Polym. 2025 Jul 1:359:123593. doi: 10.1016/j.carbpol.2025.123593. Epub 2025 Apr 9.

Abstract

Human dental pulp stem cells (hDPSCs) are a promising cell source for tooth regeneration therapies. However, conventional culture scaffold materials are often animal-derived, leading to immunogenicity concerns and limited availability. In this study, we explored phosphorylated cellulose nanofibers (P-CNFs), which have a fine fiber morphology and phosphate groups, as a novel scaffold material for cell culture. Immortalized hDPSCs were cultured on P-CNF scaffolds with different phosphate contents (0-1.42 mmol g-1) prepared by varying the molar ratio of urea and diammonium hydrogen phosphate and the reaction time. Cells cultured on unmodified CNFs exhibited poor adhesion and formed spheroids, indicating low bioadaptability. In contrast, P-CNF scaffolds with moderate phosphate content (0.54-0.78 mmol g-1) significantly improved cell adhesion; further increases in phosphate content decreased cell adhesion, indicating a strong dependence on phosphate content. Intriguingly, even in the absence of differentiation inducers, hDPSCs on P-CNF scaffolds with an optimal phosphate content of 0.78 mmol g-1 showed equal or higher expression of hard tissue marker genes compared to collagen scaffolds with differentiation inducers, suggesting that P-CNFs can directly promote hard tissue differentiation. These findings highlight plant-derived, animal-free P-CNFs as a promising biomaterial for advanced dental tissue engineering.

Keywords: Animal-free scaffold; Dental stem cell culture; Hard tissue differentiation.

MeSH terms

  • Biocompatible Materials / chemistry
  • Cell Adhesion / drug effects
  • Cell Differentiation* / drug effects
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Cellulose* / chemistry
  • Dental Pulp* / cytology
  • Humans
  • Nanofibers* / chemistry
  • Phosphorylation
  • Stem Cells* / cytology
  • Stem Cells* / drug effects
  • Tissue Engineering / methods
  • Tissue Scaffolds* / chemistry

Substances

  • Cellulose
  • Biocompatible Materials