Kidins220/ARMS as a functional mediator of multiple receptor signalling pathways

An increasing body of evidence suggests that several membrane receptors – in addition to activating distinct signalling cascades – also engage in substantial crosstalk with each other, thereby adjusting their signalling outcome as a function of specific input information. However, little is known about the molecular mechanisms that control their coordination and integration of downstream signalling. A protein that is likely to have a role in this process is kinase-D-interacting substrate of 220 kDa [Kidins220, also known as ankyrin repeat-rich membrane spanning (ARMS), hereafter referred to as Kidins220/ARMS]. Kidins220/ARMS is a conserved membrane protein that is preferentially expressed in the nervous system and interacts with the microtubule and actin cytoskeleton. It interacts with neurotrophin, ephrin, vascular endothelial growth factor (VEGF) and glutamate receptors, and is a common downstream target of several trophic stimuli. Kidins220/ARMS is required for neuronal differentiation and survival, and its expression levels modulate synaptic plasticity. Kidins220/ARMS knockout mice show developmental defects mainly in the nervous and cardiovascular systems, suggesting a crucial role for this protein in modulating the cross talk between different signalling pathways. In this Commentary, we summarise existing knowledge regarding the physiological functions of Kidins220/ARMS, and highlight some interesting directions for future studies on the role of this protein in health and disease.
This study was supported by research grants from: Cancer Research UK (to G.S.); the Italian Institute of Technology (to F.C. and F.B.); the Italian Ministry of University and Research [2008T4ZCNL grant number 2008T4ZCNL to F.B.]; the Compagnia di San Paolo, Torino (to F.B.); Telethon-Italy [grant number GGP09134 to F.B.] and the Spanish Ministry of Science and Innovation [grant number JCI-2008-01843 to V.N.].