Protection of esophageal multi-lineage progenitors of squamous epithelium (stem cells) from ionizing irradiation by manganese superoxide dismutase-plasmid/liposome (MnSOD-PL) gene therapy

In Vivo. 2005 Nov-Dec;19(6):965-74.

Abstract

Background: Intraesophageal manganese superoxide dismutase plasmid liposome (MnSOD-PL) gene therapy protects against irradiation damage.

Materials and methods: To determine whether esophageal side population (SP) stem cells were protected, epitope-tagged (hemagglutinin) (HA) MnSOD-PL was administered to C57BL/6J mice 24 hours prior to 30 Gy esophageal irradiation. SP cells were isolated, and apoptosis and multi-lineage vimentin/endothelin/F4/80 (macrophage) colonies in vitro were quantitated.

Results: The number and percent of SP cells, apoptotic cells, or numbers of multi-lineage vimentin/endothelin/F4/80-positive in vitro colonies isolated from non-irradiated HA-MnSOD-PL-treated or 30 Gy-irradiated esophagus did not differ between groups. Irradiation in vitro significantly increased apoptosis in explanted non-SP cells from control (p = 0.021) compared to MnSOD-PL-treated mice. Irradiation-induced cell division was significantly increased in SP cells from control-irradiated mice (p = 0.001), but not MnSOD-PL-treated mice. Irradiation-induced apoptosis detected in vivo at 5 days was decreased by MnSOD-PL.

Conclusion: MnSOD-PL gene therapy protects esophageal SP cells from irradiation in vitro and in vivo.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Annexin A5 / metabolism
  • Antigens, Differentiation / metabolism
  • Apoptosis / radiation effects
  • Biomarkers / metabolism
  • Cell Culture Techniques
  • Cell Division / radiation effects
  • Cell Lineage
  • Cells, Cultured
  • Endothelins / metabolism
  • Esophagus / enzymology
  • Esophagus / pathology
  • Esophagus / radiation effects*
  • Fluorescein-5-isothiocyanate
  • Fluorescent Dyes
  • Genetic Therapy*
  • Liposomes
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Plasmids
  • Proliferating Cell Nuclear Antigen / metabolism
  • Radiation Injuries, Experimental / pathology*
  • Radiation Injuries, Experimental / prevention & control
  • Radiation Protection*
  • Radiation, Ionizing
  • Stem Cells / cytology
  • Stem Cells / radiation effects*
  • Superoxide Dismutase / administration & dosage*
  • Superoxide Dismutase / genetics
  • Vimentin / metabolism

Substances

  • Annexin A5
  • Antigens, Differentiation
  • Biomarkers
  • Endothelins
  • Fluorescent Dyes
  • Liposomes
  • Proliferating Cell Nuclear Antigen
  • Vimentin
  • monocyte-macrophage differentiation antigen
  • Superoxide Dismutase
  • Fluorescein-5-isothiocyanate