Synergistic effect of sustained release of growth factors and dynamic culture on osteoblastic differentiation of mesenchymal stem cells

J Biomed Mater Res A. 2015 Jun;103(6):2161-71. doi: 10.1002/jbm.a.35354. Epub 2014 Nov 5.

Abstract

Microparticles have been utilized as delivery vehicles of soluble factors to modify cellular behavior and therefore enhance tissue engineering regeneration. When incorporated into three-dimensional systems, microparticles can provide geometrical and temporal controlled release of bioactive agents, such as growth factors (GFs) to surrounding cells. This study investigates the effect of GFs release from biopolymer microparticles on osteoblastic differentiation of human mesenchymal stem cells (hMSCs) encapsulated in calcium (Ca)-alginate scaffolds while cultured in a tubular perfusion system bioreactor system. Empirical and deterministic models were used to demonstrate that poly(D,L-lactic-co-glycolic acid)-encapsulated GFs would result in a delayed release profile compared to GFs encapsulated into scaffolds directly. We hypothesized that the dual delivery of human bone-morphogenetic protein 2 (hBMP2) and human vascular endothelial growth factor to cells in dynamic culture would provide molecular and physical cues to promote differentiation. Results indicated that the exposures of hBMP2 and dynamic flow are sufficient in enhancing the osteoblastic differentiation pathway compared to no GF addition and static culture. The GF delivery system in a dynamic flow environment resulted in a synergistic effect on osteoblastic differentiation of hMSCs.

Keywords: PLGA microparticles; growth factors; hMSCs; osteoblastic differentiation; perfusion.

Publication types

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

MeSH terms

  • Alginates / pharmacology
  • Biomarkers / metabolism
  • Bioreactors
  • Bone Morphogenetic Protein 2 / pharmacology*
  • Calcification, Physiologic / drug effects
  • Cell Culture Techniques / methods*
  • Cell Differentiation / drug effects*
  • Delayed-Action Preparations / pharmacology
  • Drug Synergism
  • Emulsions
  • Gene Expression Regulation / drug effects
  • Glucuronic Acid / pharmacology
  • Hexuronic Acids / pharmacology
  • Humans
  • Immunoassay
  • Lactic Acid / chemistry
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / drug effects
  • Mesenchymal Stem Cells / metabolism
  • Osteoblasts / cytology*
  • Osteoblasts / drug effects
  • Osteoblasts / metabolism
  • Particle Size
  • Perfusion
  • Polyglycolic Acid / chemistry
  • Polylactic Acid-Polyglycolic Acid Copolymer
  • Serum Albumin / pharmacology
  • Tissue Engineering
  • Tissue Scaffolds / chemistry
  • Vascular Endothelial Growth Factor A / pharmacology*

Substances

  • Alginates
  • BMP2 protein, human
  • Biomarkers
  • Bone Morphogenetic Protein 2
  • Delayed-Action Preparations
  • Emulsions
  • Hexuronic Acids
  • Serum Albumin
  • VEGFA protein, human
  • Vascular Endothelial Growth Factor A
  • Polylactic Acid-Polyglycolic Acid Copolymer
  • Polyglycolic Acid
  • Lactic Acid
  • Glucuronic Acid