Inflammatory Responses and Barrier Function of Endothelial Cells Derived from Human Induced Pluripotent Stem Cells

Stem Cell Reports. 2018 May 8;10(5):1642-1656. doi: 10.1016/j.stemcr.2018.03.012. Epub 2018 Apr 12.

Abstract

Several studies have reported endothelial cell (EC) derivation from human induced pluripotent stem cells (hiPSCs). However, few have explored their functional properties in depth with respect to line-to-line and batch-to-batch variability and how they relate to primary ECs. We therefore carried out accurate characterization of hiPSC-derived ECs (hiPSC-ECs) from multiple (non-integrating) hiPSC lines and compared them with primary ECs in various functional assays, which included barrier function using real-time impedance spectroscopy with an integrated assay of electric wound healing, endothelia-leukocyte interaction under physiological flow to mimic inflammation and angiogenic responses in in vitro and in vivo assays. Overall, we found many similarities but also some important differences between hiPSC-derived and primary ECs. Assessment of vasculogenic responses in vivo showed little difference between primary ECs and hiPSC-ECs with regard to functional blood vessel formation, which may be important in future regenerative medicine applications requiring vascularization.

Keywords: Matrigel plug assay; electric cell-substrate impedance sensing (ECIS); endothelial cell barrier function; hiPSC-derived endothelial cells (hiPSC-ECs); human induced pluripotent stem cells (hiPSC); inflammatory responses; junctional integrity; leukocyte adhesion under flow; two-dimensional vasculogenesis assay.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD34 / metabolism
  • Biological Assay
  • Cell Differentiation
  • Cell Line
  • Cell Movement
  • Cells, Cultured
  • Human Umbilical Vein Endothelial Cells / metabolism
  • Human Umbilical Vein Endothelial Cells / pathology*
  • Humans
  • Induced Pluripotent Stem Cells / metabolism
  • Induced Pluripotent Stem Cells / pathology*
  • Inflammation / pathology*
  • Intercellular Junctions / metabolism
  • Neovascularization, Physiologic
  • Platelet Endothelial Cell Adhesion Molecule-1 / metabolism

Substances

  • Antigens, CD34
  • Platelet Endothelial Cell Adhesion Molecule-1