Neuropilin-1 Modulates p53/Caspases Axis to Promote Endothelial Cell Survival

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Neuropilin-1 Modulates p53/Caspases Axis to Promote Endothelial Cell Survival

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Title: Neuropilin-1 Modulates p53/Caspases Axis to Promote Endothelial Cell Survival
Author: Dutta, Shamit K.; Kojima, Tatsuyoshi; Xu, Xiaolei; Ekker, Stephen C.; Mukhopadhyay, Debabrata; Wang, Ling; Khosravi-Far, Roya

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Citation: Wang, Ling, Shamit K. Dutta, Tatsuyoshi Kojima, Xiaolei Xu, Roya Khosravi-Far, Stephen C. Ekker, and Debabrata Mukhopadhyay. 2007. Neuropilin-1 modulates p53/caspases axis to promote endothelial cell survival. PLoS ONE 2(11): e1161.
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Abstract: Vascular permeability factor/vascular endothelial growth factor (VPF/VEGF), one of the crucial pro-angiogenic factors, functions as a potent inhibitor of endothelial cell (EC) apoptosis. Previous progress has been made towards delineating the VPF/VEGF survival signaling downstream of the activation of VEGFR-2. Here, we seek to define the function of NRP-1 in VPF/VEGF-induced survival signaling in EC and to elucidate the concomitant molecular signaling events that are pivotal for our understanding of the signaling of VPF/VEGF. Utilizing two different in vitro cell culture systems and an in vivo zebrafish model, we demonstrate that NRP-1 mediates VPF/VEGF-induced EC survival independent of VEGFR-2. Furthermore, we show here a novel mechanism for NRP-1-specific control of the anti-apoptotic pathway in EC through involvement of the NRP-1-interacting protein (NIP/GIPC) in the activation of PI-3K/Akt and subsequent inactivation of p53 pathways and FoxOs, as well as activation of p21. This study, by elucidating the mechanisms that govern VPF/VEGF-induced EC survival signaling via NRP-1, contributes to a better understanding of molecular mechanisms of cardiovascular development and disease and widens the possibilities for better therapeutic targets.
Published Version: doi:10.1371/journal.pone.0001161
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2048754/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:4774195

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