Chondrogenesis-inductive nanofibrous substrate using both biological fluids and mesenchymal stem cells from an autologous source

Mater Sci Eng C Mater Biol Appl. 2019 May:98:1169-1178. doi: 10.1016/j.msec.2019.01.069. Epub 2019 Jan 16.

Abstract

During the last decade, many cartilage tissue engineering strategies have been developed, being the stem cell-based approach one of the most promising. Transforming Growth Factor-β3 (TGF-β3) and Insulin-like Growth Factor-I (IGF-I) are key proteins involved in the regulation of chondrogenic differentiation. Therefore, these two growth factors (GFs) were immobilized at the surface of a single electrospun nanofibrous mesh (NFM) aiming to differentiate human Bone Marrow-derived Mesenchymal Stem Cells (hBM-MSCs). The immobilization of defined antibodies (i.e. anti-TGF-β3 and anti-IGF-I) allows the selective retrieval of the abovementioned GFs from human platelet lysates (PL). Biochemical assays, involving hBM-MSCs cultured on biofunctional nanofibrous substrates under basal culture medium during 28 days, confirm the biological activity of bound TGF-β3 and IGF-I. Specifically, the typical spherical morphology of chondrocytes and the immunolocalization of collagen type II confirmed the formation of a cartilaginous ECM. Therefore, the proposed biofunctional nanofibrous substrate is able to promote chondrogenesis.

Keywords: Chondrogenic differentiation; Electrospun nanofibrous meshes; Insulin-like growth factor-I (IGF-I); Platelet lysates; Transforming growth factor-β3 (TGF-β3).

MeSH terms

  • Aged, 80 and over
  • Blood Platelets / metabolism
  • Cartilage / drug effects
  • Cartilage / metabolism
  • Cell Culture Techniques / methods
  • Cell Differentiation / drug effects
  • Cells, Cultured
  • Chondrocytes / cytology
  • Chondrocytes / drug effects
  • Chondrocytes / metabolism
  • Chondrogenesis / drug effects*
  • Chondrogenesis / physiology*
  • Collagen Type II / metabolism
  • Female
  • Humans
  • Insulin-Like Growth Factor I / metabolism
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / metabolism
  • Nanofibers / chemistry*
  • Tissue Engineering / methods
  • Transforming Growth Factor beta3 / metabolism

Substances

  • Collagen Type II
  • Transforming Growth Factor beta3
  • Insulin-Like Growth Factor I