Journal
FREE RADICAL BIOLOGY AND MEDICINE
Volume 44, Issue 2, Pages 180-192Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.freeradbiomed.2007.01.025
Keywords
free radicals
Funding
- NHLBI NIH HHS [HL073087] Funding Source: Medline
- NIGMS NIH HHS [GM069589, GM077185] Funding Source: Medline
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Vascularization, under physiological or pathophysiological conditions, typically takes place by one or more of the following processes: angiogenesis, vasculogenesis, arteriogenesis, and lymphangiogenesis. Although all of these mechanisms of vascularization have sufficient contrasting features to warrant consideration under separate cover, one common feature shared by all is their sensitivity to the VEGF signaling pathway. Conditions such as wound healing and physical exercise result in increased production of reactive oxygen species such as H2O2, and both are associated with increased tissue vasculatization. Understanding these two scenarios of adult tissue vascularization in tandem offers the potential to unlock the significance of redox regulation of the VEGF signaling pathway. Does H2O2 support tissue vascularization? H2O2 induces the expression of the most angiogenic form of VEGF, VEGF-A, by a HIF-indeperident and Sp1-dependent mechanism. Ligation of VEGF-A to VEGFR2 results in signal transduction leading to tissue vascularization. Such ligation generates H2O2 via an NADPH oxidase-dependent mechanism. Disruption of VEGF-VEGFR2 ligation-dependent H2O2 production or decomposition of such H2O2 stalls VEGFR2 signaling. Numerous antioxidants exhibit antiangiogenic properties. Current evidence lends firm credence to the hypothesis that low-level endogenous H2O2 supports vascular growth. (C) 2007 Elsevier Inc. All rights reserved.
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