The mechanism of a chitosan-collagen composite film used as biomaterial support for MC3T3-E1 cell differentiation

Sci Rep. 2016 Dec 21:6:39322. doi: 10.1038/srep39322.

Abstract

Natural composite biomaterials are good structural supports for bone cells to regenerate lost bone. Here, we report that a chitosan-collagen composite film accelerated osteoblast proliferation, differentiation and matrix mineralization in MC3T3-E1 cells. Intriguingly, we observed that the film enhanced the phosphorylation of Erk1/2. We showed that the chitosan-collagen composite film increased the transcriptional activity of Runx2, which is an important factor regulating osteoblast differentiation downstream of phosphorylated Erk1/2. Consistent with this observation, we found that the chitosan-collagen composite film increased the expression of osteoblastic marker genes, including Type I Collagen and Runx2 in MC3T3-E1 cells. We conclude that this film promoted osteoblast differentiation and matrix mineralization through an Erk1/2-activated Runx2 pathway. Our findings provide new evidence that chitosan-collagen composites are promising biomaterials for bone tissue engineering in bone defect-related diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biocompatible Materials / metabolism*
  • Cell Culture Techniques
  • Cell Differentiation*
  • Cell Line
  • Chitosan / metabolism*
  • Collagen / metabolism*
  • Core Binding Factor Alpha 1 Subunit / metabolism
  • Gene Expression Profiling
  • MAP Kinase Signaling System
  • Mice
  • Osteoblasts / physiology*
  • Phosphorylation
  • Protein Processing, Post-Translational
  • Signal Transduction

Substances

  • Biocompatible Materials
  • Core Binding Factor Alpha 1 Subunit
  • Collagen
  • Chitosan