Extracellular Protease Inhibition Alters the Phenotype of Chondrogenically Differentiating Human Mesenchymal Stem Cells (MSCs) in 3D Collagen Microspheres

PLoS One. 2016 Jan 13;11(1):e0146928. doi: 10.1371/journal.pone.0146928. eCollection 2016.

Abstract

Matrix remodeling of cells is highly regulated by proteases and their inhibitors. Nevertheless, how would the chondrogenesis of mesenchymal stem cells (MSCs) be affected, when the balance of the matrix remodeling is disturbed by inhibiting matrix proteases, is incompletely known. Using a previously developed collagen microencapsulation platform, we investigated whether exposing chondrogenically differentiating MSCs to intracellular and extracellular protease inhibitors will affect the extracellular matrix remodeling and hence the outcomes of chondrogenesis. Results showed that inhibition of matrix proteases particularly the extracellular ones favors the phenotype of fibrocartilage rather than hyaline cartilage in chondrogenically differentiating hMSCs by upregulating type I collagen protein deposition and type II collagen gene expression without significantly altering the hypertrophic markers at gene level. This study suggests the potential of manipulating extracellular proteases to alter the outcomes of hMSC chondrogenesis, contributing to future development of differentiation protocols for fibrocartilage tissues for intervertebral disc and meniscus tissue engineering.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cartilage / metabolism
  • Cell Differentiation
  • Chondrocytes / cytology
  • Chondrogenesis
  • Collagen / chemistry*
  • Collagen Type I / chemistry
  • Collagen Type II / chemistry
  • Extracellular Matrix / metabolism
  • Fibrocartilage / metabolism
  • Humans
  • Hydroxyproline / chemistry
  • Immunohistochemistry
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / enzymology
  • Microscopy, Fluorescence
  • Microspheres*
  • Phenotype
  • Protease Inhibitors / chemistry*
  • Real-Time Polymerase Chain Reaction
  • Tissue Engineering / methods
  • Tissue Scaffolds / chemistry

Substances

  • Collagen Type I
  • Collagen Type II
  • Protease Inhibitors
  • Collagen
  • Hydroxyproline

Grants and funding

This work was supported by a grant from The University of Hong Kong Small Project Funding (201109176132), a Hong Kong Research Grants Council General Research Fund award (17100714) and a Hong Kong Innovation and Technology Commission Grant (ITS/081/14FP). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.