SALMANDNMDA

Elucidating the role of SALMs in the regulation of synapses and NMDA receptors

 Coordinatore FYZIOLOGICKY USTAV AKADEMIE VED CESKE REPUBLIKY VEREJNA VYZKUMNA INSTITUCE (VVI) 

 Organization address address: VIDENSKA 1083
city: PRAHA 4
postcode: 142 20

contact info
Titolo: Mr.
Nome: Basheer
Cognome: Suliman
Email: send email
Telefono: +420 24106 2548
Fax: +420 24106 2488

 Nazionalità Coordinatore Czech Republic [CZ]
 Totale costo 100˙000 €
 EC contributo 100˙000 €
 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-2010-RG
 Funding Scheme MC-IRG
 Anno di inizio 2011
 Periodo (anno-mese-giorno) 2011-07-01   -   2015-06-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    FYZIOLOGICKY USTAV AKADEMIE VED CESKE REPUBLIKY VEREJNA VYZKUMNA INSTITUCE (VVI)

 Organization address address: VIDENSKA 1083
city: PRAHA 4
postcode: 142 20

contact info
Titolo: Mr.
Nome: Basheer
Cognome: Suliman
Email: send email
Telefono: +420 24106 2548
Fax: +420 24106 2488

CZ (PRAHA 4) coordinator 100˙000.00

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

play    molecules    mechanisms    cells    salm    critical    receptor    family    brain    maturation    mammalian    functioning    diseases    receptors    synapses    adhesion    salms    nmda    regulate    cams       neurons    interaction    termini    excitatory    expression    regions   

 Obiettivo del progetto (Objective)

'Cell adhesion molecules (CAMs) mediate many critical processes in the mammalian brain, including formation and maturation of synapses. CAMs have been implicated in cognitive diseases, such as autism and schizophrenia, as candidate genes. These studies highlight the importance of understanding the mechanisms by which CAMs participate in normal and pathophysiological conditions. Synaptic adhesion-like molecules (SALMs) are a new family of CAMs that are expressed in the mammalian brain. The five SALM family members (SALM1-5) have conserved extracellular N-termini, but differ substantially in their intracellular C-termini. The distinct C-termini suggest the SALMs possess unique functions. In recent studies, over-expression of SALM2 increased the number of excitatory synapses and reduction of SALM5 expression decreased the number of inhibitory synapses. Furthermore, SALM1 directly interacted with the NR1 subunit of the N-methyl-D-aspartate (NMDA) receptor. NMDA receptors are key mediators of glutamatergic transmission in mammalian brains and thus a SALM/NMDA receptor interaction would have important functional consequences for excitatory synapses. The mechanisms underlying roles that SALMs play at the synapses and in the functioning of NMDA receptors remain unknown. In this proposal, we will identify regions within SALMs that regulate the formation and maturation of synapses. We will also identify regions critical for the SALM/NMDA receptor interaction, the cellular compartments where the interaction occurs and the role that SALMs play in NMDA receptor functioning. These studies will be carried out using immunocytochemistry, biochemistry and electrophysiology on heterologous cells, dissociated cultures of cerebellar granule cells and hippocampal neurons. Determination of the mechanisms by which SALMs regulate synapses and NMDA receptors is crucial for our understanding of synapse functioning as well as for discerning the etiology of diseases associated with CAMs.'

Introduzione (Teaser)

Billions of nerve cells in the brain do not touch but rely on chemical transmitters to transfer and trigger electrical impulses. EU researchers are looking at the assembly of key molecules on binding sites of neurons to understand the molecular basis of many brain disorders.

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