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Kidins220/ARMS mediates the integration of the neurotrophin and VEGF pathways in the vascular and nervous systems

Item Type:Article
Title:Kidins220/ARMS mediates the integration of the neurotrophin and VEGF pathways in the vascular and nervous systems
Creators Name:Cesca, F., Yabe, A., Spencer-Dene, B., Scholz-Starke, J., Medrihan, L., Maden, C.H., Gerhardt, H., Orriss, I.R., Baldelli, P., Al-Qatari, M., Koltzenburg, M., Adams, R.H., Benfenati, F. and Schiavo, G.
Abstract:Signaling downstream of receptor tyrosine kinases controls cell differentiation and survival. How signals from different receptors are integrated is, however, still poorly understood. In this work, we have identified Kidins220 (Kinase D interacting substrate of 220 kDa)/ARMS (Ankyrin repeat-rich membrane spanning) as a main player in the modulation of neurotrophin and vascular endothelial growth factor (VEGF) signaling in vivo, and a primary determinant for neuronal and cardiovascular development. Kidins220(-/-) embryos die at late stages of gestation, and show extensive cell death in the central and peripheral nervous systems. Primary neurons from Kidins220(-/-) mice exhibit reduced responsiveness to brain-derived neurotrophic factor, in terms of activation of mitogen-activated protein kinase signaling, neurite outgrowth and potentiation of excitatory postsynaptic currents. In addition, mice lacking Kidins220 display striking cardiovascular abnormalities, possibly due to impaired VEGF signaling. In support of this hypothesis, we demonstrate that Kidins220 constitutively interacts with VEGFR2. These findings, together with the data presented in the accompanying paper, indicate that Kidins220 mediates the integration of several growth factor receptor pathways during development, and mediates the activation of distinct downstream cascades according to the location and timing of stimulation.
Keywords:Kidins220/ARMS, Neurotrophin Signaling, Synaptic Plasticity, VEGF Receptor, Animals, Mice
Source:Cell Death and Differentiation
Publisher:Nature Publishing Group
Page Range:194-208
Date:February 2012
Official Publication:https://doi.org/10.1038/cddis.2011.108
PubMed:View item in PubMed

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