CHANNELRHODOPSIN

Information processing in distal dendrites of neocortical layer 5 pyramidal neurons

 Coordinatore MEDICAL RESEARCH COUNCIL 

 Organization address address: NORTH STAR AVENUE POLARIS HOUSE
city: SWINDON
postcode: SN2 1FL

contact info
Titolo: Ms.
Nome: Elizabeth
Cognome: Cutler
Email: send email
Telefono: + 44 (0)1223 402357
Fax: + 44 (0)1223 412515

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 0 €
 EC contributo 180˙216 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-IEF-2008
 Funding Scheme MC-IEF
 Anno di inizio 2009
 Periodo (anno-mese-giorno) 2009-03-01   -   2011-02-28

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    MEDICAL RESEARCH COUNCIL

 Organization address address: NORTH STAR AVENUE POLARIS HOUSE
city: SWINDON
postcode: SN2 1FL

contact info
Titolo: Ms.
Nome: Elizabeth
Cognome: Cutler
Email: send email
Telefono: + 44 (0)1223 402357
Fax: + 44 (0)1223 412515

UK (SWINDON) coordinator 180˙216.73

Mappa


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synaptic    branches    dendritic    plan    light    individual    apical    distal    neurons    output    inputs    activated    layer    electrical    tree    neocortical    central    excite    sites    dendrites    pyramidal    channels   

 Obiettivo del progetto (Objective)

'The aim of the current proposal is to investigate how synaptic inputs that innervate the distal dendrites of central neurons are integrated to form a neuronal output. The distal dendritic tree is the dendritic compartment furthest away from the action potential initiation zone. In the neocortex ascending afferent and intra-cortical information converges in neocortical layer 1 suggesting a prominent functional role, however only the most distal apical dendrites of layer 5 pyramidal neurons enter layer 1. We hypothesise that synaptic inputs are locally integrated at distal dendritic sites, perhaps in individual dendritic branches, leading to the generation of dendritic spikes as an output of compartmentalised integration. This hypothesis has until now been difficult to test experimentally as such distal dendrites are not amenable to direct electrical recording techniques. We plan to explore if these structures are capable of generating regenerative spike activity by remotely exciting individual branches of the distal apical dendritic tree using light-activated ion channels expressed in neocortical pyramidal neurons and measuring electrical activity at accessible nearby large calibre apical dendritic trunk sites and the soma. The use of light-activated channels to excite neurons is at the cutting edge of neuroscience research. Our plan is to use these channels to excite individual dendritic elements; a proposal that will require a multidisciplinary approach utilizing molecular, microscopy and electrophysiological approaches in an attempt to unravel the integrative operations of central neurons.'

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