CORTEXSELFCONTROL

Self-Modulating Neurons in the Cerebral Cortex: From Molecular Mechanisms to Cortical Network Activities

 Coordinatore INSTITUT DU CERVEAU ET DE LA MOELLE EPINIERE FONDATION 

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 Nazionalità Coordinatore France [FR]
 Totale costo 996˙000 €
 EC contributo 996˙000 €
 Programma FP7-IDEAS-ERC
Specific programme: "Ideas" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call ERC-2007-StG
 Funding Scheme ERC-SG
 Anno di inizio 2008
 Periodo (anno-mese-giorno) 2008-10-01   -   2014-03-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    EUROPEAN BRAIN RESEARCH INSTITUTE R ITA LEVI-MONTALCINI FONDAZIONE*EBRI

 Organization address address: Via del Fosso di Fiorano 64
city: ROMA
postcode: 143

contact info
Titolo: Prof.
Nome: Giuseppe
Cognome: Nisticò
Email: send email
Telefono: +39 06 501703024
Fax: +39 06 501703335

IT (ROMA) beneficiary 0.00
2    INSTITUT DU CERVEAU ET DE LA MOELLE EPINIERE FONDATION

 Organization address address: BOULEVARD DE L'HOPITAL 47
city: PARIS
postcode: 75013

contact info
Titolo: Dr.
Nome: Alberto
Cognome: Bacci
Email: send email
Telefono: +39 06 501703123
Fax: +39 06 501703315

FR (PARIS) hostInstitution 0.00
3    INSTITUT DU CERVEAU ET DE LA MOELLE EPINIERE FONDATION

 Organization address address: BOULEVARD DE L'HOPITAL 47
city: PARIS
postcode: 75013

contact info
Titolo: Ms.
Nome: Iwona
Cognome: Jablonska
Email: send email
Telefono: +33 1 57 27 47 45

FR (PARIS) hostInstitution 0.00

Mappa


 Word cloud

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neocortical    sensory    cell    cortical    cells    self    functional    interneuron    endocannabinoid    function    fast    mechanisms    interneurons    neurons    pathological    spiking    lts    molecular    mediated    fs    microcircuits    roles    network    inhibition    gabaergic    inhibitory    autaptic   

 Obiettivo del progetto (Objective)

'In the mammalian brain, the neocortex is the site where sensory information is integrated into complex cognitive functions. This is accomplished by the activity of both principal glutamatergic neurons and locally-projecting inhibitory GABAergic interneurons, interconnected in complex networks. Inhibitory neurons play several key roles in neocortical function. For example, they shape sensory receptive fields and drive several high frequency network oscillations. On the other hand, defects in their function can lead to devastating diseases, such as epilepsy and schizophrenia. Cortical interneurons represent a highly heterogeneous cell population. Understanding the specific role of each interneuron subtype within cortical microcircuits is still a crucial open question. We have examined properties of two major functional interneuron subclasses in neocortical layer V: fast-spiking (FS) and low-threshold spiking (LTS) cells. Our previous data indicate that each group expresses a novel form of self inhibition, namely autaptic inhibitory transmission in FS cells and an endocannabinoid-mediated slow self inhibition in LTS interneurons. In this proposal we will address three major questions relevant to self-inhibition of neocortical interneurons: 1) What is the role of FS cell autapses in coordinating fast network synchrony? 2) What are the molecular mechanisms underlying autaptic asynchronous release, prolonging FS cell self-inhibition by several seconds, and what is its relevance during physiological and pathological network activities? 3) What are the induction mechanisms, the molecular players involved and the functional roles within cortical microcircuits of the endocannabinoid-mediated long-lasting self-inhibition in LTS interneurons? Results of these experiments will lead to a better understanding of GABAergic interneuron regulation of neocortical excitability, relevant to both normal and pathological cortical function.'

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