期刊
JOURNAL OF CELLULAR BIOCHEMISTRY
卷 117, 期 7, 页码 1604-1612出版社
WILEY
DOI: 10.1002/jcb.25452
关键词
ANGIOGENESIS; CYTOSKELETON; POLYPHENOLS; RASPBERRY EXTRACT; VEGF SIGNALLING
资金
- FCT [EXPL/IVC-PEC/1302/2013, UID/BIM/04293/2013]
- Fundação para a Ciência e a Tecnologia [EXPL/IVC-PEC/1302/2013] Funding Source: FCT
Polyphenols are a class of natural compounds whose potential as antioxidant, anti-inflammatory, and anti-angiogenesis has been reported in many pathological conditions. Red raspberry extract, rich in polyphenols, has been reported to exert anti-inflammatory effects and prevent cell proliferation in distinct animal models. However, the signaling pathways involved remain unknown. Herein, we used human microvascular endothelial cells (HMVECs) to determine the influence of red raspberry phenolic compound extract concentrations, ranging from 10 to 250 mu g gallic acid equivalents (GAE)/mL, on endothelium viability (MTS assay), proliferation (BrdU incorporation), migration (injury assay), and capillary-like structures formation (Matrigel assay). Protein expression in cell lysates was determined by Western blot analysis. We showed that red raspberry extracts reduced cell viability (GI(50) = 87,64 +/- 6,59 mu g GAE/mL) and proliferation in a dose-dependent manner. A significant abrogation of cells ability to migrate to injured areas, even at low concentrations, was observed by injury assay. Cell assembly into capillary-like structures on Matrigel also decreased in a dose dependent-manner for higher extract concentrations, as well as the number of branching points per unit of area. Protein expression analysis showed a dose-dependent decrease in Phospho-VEGFR2 expression, implying abrogation of VEGF signaling activity. We also showed for the first time that red raspberry phenolic compounds induce the rearrangement of filamentous actin cytoskeleton, with an isotropy increase found for higher testing concentrations. Taken together, our findings corroborate the anti-angiogenic potential of red raspberry phenolic compounds and provide new insights into their mode of action upon endothelium. (C) 2015 Wiley Periodicals, Inc.
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