The Influence of Physicochemical Properties of Biomimetic Hydroxyapatite on the In Vitro Behavior of Endothelial Progenitor Cells and Their Interaction with Mesenchymal Stem Cells

Adv Healthc Mater. 2019 Jan;8(2):e1801138. doi: 10.1002/adhm.201801138. Epub 2018 Dec 5.

Abstract

Calcium phosphate (CaP) substrates are successfully used as bone grafts due to their osteogenic properties. However, the influence of the physicochemical features of CaPs in angiogenesis is frequently neglected despite it being a crucial process for bone regeneration. The present work focuses on analyzing the effects of textural parameters of biomimetic calcium deficient hydroxyapatite (CDHA) and sintered beta-tricalcium phosphate (β-TCP), such as specific surface area, surface roughness, and microstructure, on the behavior of rat endothelial progenitor cells (rEPCs) and their crosstalk with rat mesenchymal stem cells (rMSCs). The higher reactivity of CDHA results in low proliferation rates in monocultured and cocultured systems. This effect is especially pronounced for rMSCs alone, and for CDHA with a fine microstructure. In terms of angiogenic and osteogenic gene expressions, the upregulation of particular genes is especially enhanced for needle-like CDHA compared to plate-like CDHA and β-TCP, suggesting the importance not only of the chemistry of the substrate, but also of its textural features. Moreover, the coculture of rEPCs and rMSCs on needle-like CDHA results in early upregulation of osteogenic modulator, i.e., protein deglycase 1 might be a possible cause of overexpression of osteogenic-related genes on the same substrate.

Keywords: angiogenesis; calcium phosphates; cocultures; osteogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomimetic Materials / chemistry
  • Biomimetic Materials / pharmacology
  • Calcium / chemistry
  • Calcium Phosphates / pharmacology
  • Cell Adhesion / drug effects
  • Cell Proliferation
  • Coculture Techniques
  • Durapatite / chemistry*
  • Durapatite / pharmacology*
  • Endothelial Progenitor Cells / cytology
  • Endothelial Progenitor Cells / drug effects*
  • Endothelial Progenitor Cells / physiology
  • Gene Expression Regulation
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / drug effects
  • Mesenchymal Stem Cells / physiology
  • Neovascularization, Physiologic / genetics
  • Osteogenesis / genetics
  • Rats, Inbred Lew
  • X-Ray Diffraction

Substances

  • Calcium Phosphates
  • beta-tricalcium phosphate
  • Durapatite
  • Calcium