Temporally degradable collagen-mimetic hydrogels tuned to chondrogenesis of human mesenchymal stem cells

Biomaterials. 2016 Aug;99:56-71. doi: 10.1016/j.biomaterials.2016.05.011. Epub 2016 May 10.

Abstract

Tissue engineering strategies for repairing and regenerating articular cartilage face critical challenges to recapitulate the dynamic and complex biochemical microenvironment of native tissues. One approach to mimic the biochemical complexity of articular cartilage is through the use of recombinant bacterial collagens as they provide a well-defined biological 'blank template' that can be modified to incorporate bioactive and biodegradable peptide sequences within a precisely defined three-dimensional system. We customized the backbone of a Streptococcal collagen-like 2 (Scl2) protein with heparin-binding, integrin-binding, and hyaluronic acid-binding peptide sequences previously shown to modulate chondrogenesis and then cross-linked the recombinant Scl2 protein with a combination of matrix metalloproteinase 7 (MMP7)- and aggrecanase (ADAMTS4)-cleavable peptides at varying ratios to form biodegradable hydrogels with degradation characteristics matching the temporal expression pattern of these enzymes in human mesenchymal stem cells (hMSCs) during chondrogenesis. hMSCs encapsulated within the hydrogels cross-linked with both degradable peptides exhibited enhanced chondrogenic characteristics as demonstrated by gene expression and extracellular matrix deposition compared to the hydrogels cross-linked with a single peptide. Additionally, these combined peptide hydrogels displayed increased MMP7 and ADAMTS4 activities and yet increased compression moduli after 6 weeks, suggesting a positive correlation between the degradation of the hydrogels and the accumulation of matrix by hMSCs undergoing chondrogenesis. Our results suggest that including dual degradation motifs designed to respond to enzymatic activity of hMSCs going through chondrogenic differentiation led to improvements in chondrogenesis. Our hydrogel system demonstrates a bimodal enzymatically degradable biological platform that can mimic native cellular processes in a temporal manner. As such, this novel collagen-mimetic protein, cross-linked via multiple enzymatically degradable peptides, provides a highly adaptable and well defined platform to recapitulate a high degree of biological complexity, which could be applicable to numerous tissue engineering and regenerative medicine applications.

Keywords: Bacterial collagen; Biodegradation; Biomimetic material; Cartilage tissue engineering; Hydrogel; Mesenchymal stem cell.

MeSH terms

  • ADAMTS4 Protein / chemistry
  • Bacterial Proteins / chemistry*
  • Bacterial Proteins / genetics
  • Biomimetic Materials / chemistry*
  • Biomimetic Materials / metabolism
  • Cartilage, Articular / cytology
  • Cell Differentiation
  • Cells, Cultured
  • Chondrogenesis*
  • Collagen / chemistry*
  • Collagen / genetics
  • Collagen / metabolism
  • Cross-Linking Reagents / chemistry
  • Endopeptidases / chemistry
  • Extracellular Matrix / ultrastructure
  • Humans
  • Hydrogel, Polyethylene Glycol Dimethacrylate / chemistry*
  • Matrix Metalloproteinase 7 / chemistry
  • Mesenchymal Stem Cells / cytology*
  • Peptides / chemistry
  • Proteolysis
  • Streptococcus
  • Tissue Engineering / methods

Substances

  • Bacterial Proteins
  • Cross-Linking Reagents
  • Peptides
  • Scl2 protein, Streptococcus
  • Hydrogel, Polyethylene Glycol Dimethacrylate
  • Collagen
  • Endopeptidases
  • Matrix Metalloproteinase 7
  • ADAMTS4 Protein
  • aggrecanase