Extracellular Matrix (ECM) Multilayer Membrane as a Sustained Releasing Growth Factor Delivery System for rhTGF-β3 in Articular Cartilage Repair

PLoS One. 2016 Jun 3;11(6):e0156292. doi: 10.1371/journal.pone.0156292. eCollection 2016.

Abstract

Recombinant human transforming growth factor beta-3 (rhTGF-β3) is a key regulator of chondrogenesis in stem cells and cartilage formation. We have developed a novel drug delivery system that continuously releases rhTGF-β3 using a multilayered extracellular matrix (ECM) membrane. We hypothesize that the sustained release of rhTGF-β3 could activate stem cells and result in enhanced repair of cartilage defects. The properties and efficacy of the ECM multilayer-based delivery system (EMLDS) are investigated using rhTGF-β3 as a candidate drug. The bioactivity of the released rhTGF-ß3 was evaluated through chondrogenic differentiation of mesenchymal stem cells (MSCs) using western blot and circular dichroism (CD) analyses in vitro. The cartilage reparability was evaluated through implanting EMLDS with endogenous and exogenous MSC in both in vivo and ex vivo models, respectively. In the results, the sustained release of rhTGF-ß3 was clearly observed over a prolonged period of time in vitro and the released rhTGF-β3 maintained its structural stability and biological activity. Successful cartilage repair was also demonstrated when rabbit MSCs were treated with rhTGF-β3-loaded EMLDS ((+) rhTGF-β3 EMLDS) in an in vivo model and when rabbit chondrocytes and MSCs were treated in ex vivo models. Therefore, the multilayer ECM membrane could be a useful drug delivery system for cartilage repair.

MeSH terms

  • Animals
  • Biological Assay
  • Cartilage, Articular / metabolism*
  • Cells, Cultured
  • Chondrocytes / cytology
  • Chondrocytes / metabolism
  • Chondrogenesis / physiology
  • Circular Dichroism
  • Extracellular Matrix / metabolism*
  • Mesenchymal Stem Cells / metabolism*
  • Rabbits
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism*
  • Swine
  • Transforming Growth Factor beta3 / genetics
  • Transforming Growth Factor beta3 / metabolism*

Substances

  • Recombinant Proteins
  • TGFB3 protein, human
  • Transforming Growth Factor beta3

Grants and funding

This study was supported by a grant from the Ministry of Science, ICT & Future Planning (NRF-2013R1A1A1011040), Republic of Korea. There is no other potential conflict of interest relevant to this article.