Functionality of decellularized matrix in cartilage regeneration: A comparison of tissue versus cell sources

Acta Biomater. 2018 Jul 1:74:56-73. doi: 10.1016/j.actbio.2018.04.048. Epub 2018 Apr 24.

Abstract

Increasing evidence indicates that decellularized extracellular matrices (dECMs) derived from cartilage tissues (T-dECMs) or chondrocytes/stem cells (C-dECMs) can support proliferation and chondrogenic differentiation of cartilage-forming cells. However, few review papers compare the differences between these dECMs when they serve as substrates for cartilage regeneration. In this review, after an introduction of cartilage immunogenicity and decellularization methods to prepare T-dECMs and C-dECMs, a comprehensive comparison focuses on the effects of T-dECMs and C-dECMs on proliferation and chondrogenic differentiation of chondrocytes/stem cells in vitro and in vivo. Key factors within dECMs, consisting of microarchitecture characteristics and micromechanical properties as well as retained insoluble and soluble matrix components, are discussed in-depth for potential mechanisms underlying the functionality of these dECMs in regulating chondrogenesis. With this information, we hope to benefit dECM based cartilage engineering and tissue regeneration for future clinical application.

Statement of significance: The use of decellularized extracellular matrix (dECM) is becoming a promising approach for tissue engineering and regeneration. Compared to dECM derived from cartilage tissue, recently reported dECM from cell sources exhibits a distinct role in cell based cartilage regeneration. In this review paper, for the first time, tissue and cell based dECMs are comprehensively compared for their functionality in cartilage regeneration. This information is expected to provide an update for dECM based cartilage regeneration.

Keywords: Cartilage regeneration; Chondrocyte; Chondrogenic differentiation; Decellularized matrix; Extracellular matrix; Proliferation; Stem cell.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Cartilage / physiology*
  • Chondrocytes / metabolism*
  • Chondrogenesis*
  • Extracellular Matrix / chemistry*
  • Humans
  • Regeneration*
  • Stem Cells / metabolism*
  • Tissue Engineering / methods