The Ankyrin Repeat-rich Membrane Spanning (ARMS)/Kidins220 Scaffold Protein Is Regulated by Activity-dependent Calpain Proteolysis and Modulates Synaptic Plasticity
Metadatos
Mostrar el registro completo del ítemAutor
Wu, Synphen H; Arévalo, Juan Carlos; Neubrand, Veronika Elisabeth; Zhang, Hong; Arrancio, Ottavio; Chao, Moses VEditorial
The American Society for Biochemistry and Molecular Biology
Materia
ARMS Kidins220 Synaptic plasticity Calpain proteolysis
Fecha
2010Referencia bibliográfica
J Biol Chem 285:40472-40478 [https://doi.org/10.1074/jbc.M110.171371]
Patrocinador
National Institutes of Health Grants NS21072 and HD23315 and NS049442; Medical Scientist Training Program; Marie Curie International Reintegration Grant within the 7th European Community Framework ProgrammeResumen
The expression of forms of synaptic plasticity, such as thephenomenon of long-term potentiation, requires the activity-dependent regulation of synaptic proteins and synapse composition. Here we show that ARMS (ankyrin repeat-rich membrane spanning protein)/Kidins220, a transmembrane scaffold molecule and BDNF TrkB substrate, is significantly reduced in hippocampal neurons after potassium chloride depolarization. The activity-dependent proteolysis of ARMS/Kidins220 was found to occur through calpain, a calcium-activated protease. Moreover, hippocampal long-term potentiation in ARMS/Kidins220 mice was enhanced, and inhibition of calpain in these mice reversed these effects. These results provide an ex planation for a role for the ARMS/Kidins220 protein in synap tic plasticity events and suggest that the levels of ARMS/Kidins220 can be regulated by neuronal activity and calpain action to influence synaptic function.