2010
DOI: 10.1152/ajpheart.00921.2009
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Circulating endothelial progenitor cells are not affected by acute systemic inflammation

Abstract: Vascular injury causes acute systemic inflammation and mobilizes endothelial progenitor cells (EPCs) and endothelial cell (EC) colony-forming units (EC-CFUs). Whether such mobilization occurs as part of a nonspecific acute phase response or is a phenomenon specific to vascular injury remains unclear. We aimed to determine the effect of acute systemic inflammation on EPCs and EC-CFU mobilization in the absence of vascular injury. Salmonella typhus vaccination was used as a model of acute systemic inflammation. … Show more

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Cited by 38 publications
(40 citation statements)
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“…Our results are consistent with recent reports that acute injuries induced by S. typhus vaccination injection (28) or acute hypoxia (29) do not cause immediate mobilization of vascular progenitors.…”
supporting
confidence: 94%
“…Our results are consistent with recent reports that acute injuries induced by S. typhus vaccination injection (28) or acute hypoxia (29) do not cause immediate mobilization of vascular progenitors.…”
supporting
confidence: 94%
“…This rare presence of circulating BM-derived EC-CFUs is also consistent with existing literature. 13,[32][33][34] To evaluate BM chimerism and provide a control for further transplantationinduced side effects, we decided to perform the assessment of the inflammatory response in parallel. Many BM-derived inflammatory cells (macrophages, neutrophils, DCs, B cells and T cells) were recruited to the kidney and this could be found to the same extent in all chimeric mice, demonstrating that the BM and BM originating cells were functional.…”
Section: Discussionmentioning
confidence: 99%
“…Putative EPC and angiogenic monocytes were identified by flow cytometry and analysed as described previously17 using the following preconjugated antihuman monoclonal antibodies: anti-CD45-PercP (Becton Dickinson, UK), anti-CD34-FITC, anti-VEGFR-2-PE, anti-Tie-2-APC (R&D systems, USA), anti-CD-133-PE (Miltenyi Biotec, UK) and anti-CD14-FITC (Caltag Systems, UK) (figure 1). A total of 500 000 events were acquired in the leukocyte gate for each sample using a FACS-Calibur flow-cytometer (Becton Dickinson, UK).…”
Section: Methodsmentioning
confidence: 99%