Telomerized human microvasculature is functional in vivo

Nat Biotechnol. 2001 Mar;19(3):219-24. doi: 10.1038/85655.

Abstract

Previously we showed the superior in vitro survival of human telomerase reverse transcriptase (hTERT)-transduced human endothelial cells (EC). Here we show that retroviral-mediated transduction of hTERT in human dermal microvascular EC (HDMEC) results in cell lines that form microvascular structures when subcutaneously implanted in severe combined immunodeficiency (SCID) mice. Anti-human type IV collagen basement membrane immunoreactivity and visualization of enhanced green fluorescent protein (eGFP)-labeled microvessels confirmed the human origin of these capillaries. No human vasculature was observed after implantation of HT1080 fibrosarcoma cells, 293 human embryonic kidney cells, or human skin fibroblasts. Intravascular red fluorescent microspheres injected into host circulation were found within green "telomerized" microvessels, indicating functional murine-human vessel anastamoses. Whereas primary HDMEC-derived vessel density decreased with time, telomerized HDMEC maintained durable vessels six weeks after xenografting. Modulation of implant vessel density by exposure to different angiogenic and angiostatic factors demonstrated the utility of this system for the study of human microvascular remodeling in vivo.

Publication types

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

MeSH terms

  • Angiogenesis Inhibitors / pharmacology
  • Animals
  • Basement Membrane / chemistry
  • Capillaries / drug effects
  • Capillaries / growth & development
  • Cells, Cultured
  • Chimera
  • Collagen / analysis
  • Collagen / pharmacology
  • Collagen Type XVIII
  • Dermis / blood supply
  • Endostatins
  • Endothelium, Vascular / drug effects
  • Endothelium, Vascular / enzymology*
  • Endothelium, Vascular / metabolism
  • Endothelium, Vascular / transplantation*
  • Fibroblasts
  • Humans
  • Mice
  • Mice, SCID
  • Microcirculation* / drug effects
  • Microcirculation* / growth & development
  • Microspheres
  • Models, Animal*
  • Neovascularization, Physiologic / drug effects
  • Peptide Fragments / pharmacology
  • Telomerase / genetics
  • Telomerase / metabolism*
  • Telomere / genetics
  • Transduction, Genetic
  • Transplantation, Heterologous
  • Tumor Cells, Cultured

Substances

  • Angiogenesis Inhibitors
  • Collagen Type XVIII
  • Endostatins
  • Peptide Fragments
  • Collagen
  • Telomerase