Optimizing mesoderm progenitor selection and three-dimensional microniche culture allows highly efficient endothelial differentiation and ischemic tissue repair from human pluripotent stem cells

Stem Cell Res Ther. 2017 Jan 23;8(1):6. doi: 10.1186/s13287-016-0455-4.

Abstract

Background: Generation of large quantities of endothelial cells is highly desirable for vascular research, for the treatment of ischemia diseases, and for tissue regeneration. To achieve this goal, we developed a simple, chemically defined culture system to efficiently and rapidly differentiate endothelial cells from human pluripotent stem cells by going through an MESP1 mesoderm progenitor stage.

Methods: Mesp1 is a key transcription factor that regulates the development of early cardiovascular tissue. Using an MESP1-mTomato knock-in reporter human embryonic stem cell line, we compared the gene expression profiles of MESP1+ and MESP1- cells and identified new signaling pathways that may promote endothelial differentiation. We also used a 3D scaffold to mimic the in vivo microenvironment to further improve the efficiency of endothelial cell generation. Finally, we performed cell transplantation into a critical limb ischemia mouse model to test the repairing potential of endothelial-primed MESP1+ cells.

Results: MESP1+ mesoderm progenitors, but not MESP1- cells, have strong endothelial differentiation potential. Global gene expression analysis revealed that transcription factors essential for early endothelial differentiation were enriched in MESP1+ cells. Interestingly, MESP1 cells highly expressed Sphingosine-1-phosphate (S1P) receptor and the addition of S1P significantly increased the endothelial differentiation efficiency. Upon seeding in a novel 3D microniche and priming with VEGF and bFGF, MESP1+ cells markedly upregulated genes related to vessel development and regeneration. 3D microniches also enabled long-term endothelial differentiation and proliferation from MESP1+ cells with minimal medium supplements. Finally, we showed that transplanting a small number of endothelial-primed MESP1+ cells in 3D microniches was sufficient to mediate rapid repair of a mouse model of critical limb ischemia.

Conclusions: Our study demonstrates that combining MESP1+ mesoderm progenitor cells with tissue-engineered 3D microniche and a chemically defined endothelial induction medium is a promising route to maximizing the production of endothelial cells in vitro and augment their regenerative power in vivo.

Keywords: 3D culture; Endothelial cells; Human pluripotent stem cells; MESP1; Vascularization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Cell Culture Techniques*
  • Cell Differentiation / physiology*
  • Cell Line
  • Cell Proliferation / drug effects
  • Disease Models, Animal
  • Endothelial Cells / cytology*
  • Endothelial Cells / metabolism
  • Endothelial Cells / transplantation
  • Extremities / pathology
  • Female
  • Fibroblast Growth Factor 2 / pharmacology
  • Gene Expression / drug effects
  • Gene Knock-In Techniques
  • Human Embryonic Stem Cells / cytology
  • Human Embryonic Stem Cells / metabolism
  • Humans
  • Ischemia / pathology
  • Ischemia / therapy*
  • Ischemia / veterinary
  • Mesoderm / cytology*
  • Mice
  • Mice, Inbred BALB C
  • Neovascularization, Physiologic / drug effects
  • Receptors, Lysosphingolipid / genetics
  • Receptors, Lysosphingolipid / metabolism
  • Signal Transduction
  • Vascular Endothelial Growth Factor A / pharmacology

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • MESP1 protein, human
  • Receptors, Lysosphingolipid
  • Vascular Endothelial Growth Factor A
  • Fibroblast Growth Factor 2