| Literature DB >> 26051280 |
Yi-Yong Baek1, Dong-Keon Lee1, Ju-Hoon So2, Cheol-Hee Kim2, Dooil Jeoung3, Hansoo Lee4, Jongseon Choe5, Moo-Ho Won6, Kwon-Soo Ha1, Young-Guen Kwon7, Young-Myeong Kim8.
Abstract
Kringle 5, derived from plasminogen, is highly capable of inhibiting angiogenesis. Here, we have designed and synthesized 10 tetrapeptides, based on the amino acid properties of the core tetrapeptide Lys-Leu-Tyr-Asp (KLYD) originating from anti-angiogenic kringle 5 of human plasminogen. Of these, Arg-Leu-Tyr-Glu (RLYE) effectively inhibited vascular endothelial growth factor (VEGF)-induced endothelial cell proliferation, migration and tube formation, with an IC50 of 0.06-0.08 nM, which was about ten-fold lower than that of the control peptide KLYD (0.79 nM), as well as suppressed developmental angiogenesis in a zebrafish model. Furthermore, this peptide effectively inhibited the cellular events that precede angiogenesis, such as ERK and eNOS phosphorylation and nitric oxide production, in endothelial cells stimulated with VEGF. Collectively, these data demonstrate that RLYE is a potent anti-angiogenic peptide that targets the VEGF signaling pathway.Entities:
Keywords: Angiogenesis; ERK; Endothelial cells; Tetrapeptide; eNOS
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Year: 2015 PMID: 26051280 DOI: 10.1016/j.bbrc.2015.05.073
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575