Transient Extremity Ischemia Augments CD34+ Progenitor Cell Availability

David Czeiger, Oleg Dukhno, Amos Douvdevani, Yael Porat, Daphna Shimoni, Valentin Fulga, Jared D. Ament, Gad Shaked

Research output: Contribution to journalArticlepeer-review

12 Scopus citations


Peripheral blood is an easily accessed source for stem cell production; however, the number of cells produced is relatively low. We hypothesized that ischemic preconditioning may serve as a safe method to increase the number of CD34+ cells that can be harvested and cultured in a short period. This study was conducted to test this hypothesis by examining the safety and efficacy of brief, transient ischemia of the lower limbs to augment the number of cells that can be produced from blood of healthy volunteers. Following induction of ischemia, blood samples were withdrawn at baseline, 30 min, 12 h and 24 h. The number of progenitor cells was determined by flow cytometry after the harvested cells were cultured for 5 days. We also analyzed the blood samples to determine IL-8 and VEGF concentrations. No serious adverse events were observed. The total number of cells increased from 0.46 ± 0.1 × 106 cells/ml in the pretreatment blood samples to 0.7 ± 0.1 × 106 cells/ml in blood taken 12 h after the conclusion of transient ischemia, p = 0.0029. The number of CD34+ cells increased from 4.23 ± 0.8 × 104 cells/ml in the pretreatment samples to 7.17 ± 1.34 × 104 cells/ml in blood taken 12 h after ischemia, p = 0.0001. The harvested stem cells maintained their ability to construct tubular structures. The augmentation in the number of CD34+ cells was positively correlated with the increase of IL-8, but not with VEGF concentrations. Ischemic preconditioning is a safe and effective technique to increase the availability of stem cells for therapeutic purposes.

Original languageEnglish
Pages (from-to)639-645
Number of pages7
JournalStem Cell Reviews and Reports
Issue number3
StatePublished - 1 Sep 2011


  • Endothelial progenitor cells
  • Ischemic preconditioning
  • Stem cells

ASJC Scopus subject areas

  • Cell Biology
  • Cancer Research


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