CD34+/CD45-dim stem cell mobilization by hyperbaric oxygen - changes with oxygen dosage

Stem Cell Res. 2014 May;12(3):638-45. doi: 10.1016/j.scr.2014.02.005. Epub 2014 Feb 28.

Abstract

Because hyperbaric oxygen treatment mobilizes bone marrow derived-stem/progenitor cells by a free radical mediated mechanism, we hypothesized that there may be differences in mobilization efficiency based on exposure to different oxygen partial pressures. Blood from twenty consecutive patients was obtained before and after the 1st, 10th and 20th treatment at two clinical centers using protocols involving exposures to oxygen at either 2.0 or 2.5 atmospheres absolute (ATA). Post-treatment values of CD34+, CD45-dim leukocytes were always 2-fold greater than the pre-treatment values for both protocols. Values for those treated at 2.5 ATA were significantly greater than those treated at 2.0 ATA by factors of 1.9 to 3-fold after the 10th and before and after the 20th treatments. Intracellular content of hypoxia inducible factors -1, -2, and -3, thioredoxin-1 and poly-ADP-ribose polymerase assessed in permeabilized CD34+ cells with fluorophore-conjugated antibodies were twice as high in all post- versus pre-treatment samples with no significant differences between 2.0 and 2.5 ATA protocols. We conclude that putative progenitor cell mobilization is higher with 2.5 versus 2.0 ATA treatments, and all newly mobilized cells exhibit higher concentrations of an array of regulatory proteins.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Antigens, CD34 / metabolism*
  • Cells, Cultured
  • Female
  • Hematopoietic Stem Cell Mobilization
  • Humans
  • Hyperbaric Oxygenation*
  • Leukocyte Common Antigens / metabolism*
  • Male
  • Middle Aged
  • Neoplasms / metabolism
  • Neoplasms / physiopathology
  • Neoplasms / therapy*
  • Oxygen / metabolism*
  • Poly(ADP-ribose) Polymerases / genetics
  • Poly(ADP-ribose) Polymerases / metabolism
  • Stem Cells / cytology*
  • Stem Cells / metabolism
  • Thioredoxins / genetics
  • Thioredoxins / metabolism

Substances

  • Antigens, CD34
  • Thioredoxins
  • Poly(ADP-ribose) Polymerases
  • Leukocyte Common Antigens
  • Oxygen