CACCINNP

Microglia and Neuropathic Pain: The role of calcium activated chloride channels

 Coordinatore EUROPEAN MOLECULAR BIOLOGY LABORATORY 

 Organization address address: Meyerhofstrasse 1
city: HEIDELBERG
postcode: 69117

contact info
Titolo: Ms.
Nome: Genevieve
Cognome: Reinke
Email: send email
Telefono: +49 6221 3878153
Fax: +49 6221 3878575

 Nazionalità Coordinatore Germany [DE]
 Totale costo 181˙084 €
 EC contributo 181˙084 €
 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-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2011
 Periodo (anno-mese-giorno) 2011-04-01   -   2013-03-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    EUROPEAN MOLECULAR BIOLOGY LABORATORY

 Organization address address: Meyerhofstrasse 1
city: HEIDELBERG
postcode: 69117

contact info
Titolo: Ms.
Nome: Genevieve
Cognome: Reinke
Email: send email
Telefono: +49 6221 3878153
Fax: +49 6221 3878575

DE (HEIDELBERG) coordinator 181˙084.00

Mappa


 Word cloud

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

ano    damage    molecular    embl    activation    mouse    pain    spinal    vivo    model    expression    independent    anoctamin    possibility    skills    currents    chloride    me    profiling    microglial    neuropathic    microglia    cells   

 Obiettivo del progetto (Objective)

'Neuropathic pain is a significant worldwide health problem that is poorly understood and often untreatable. A major factor in the pathogenesis of neuropathic pain is an activation of microglial cells in the spinal cord. Following damage to peripheral nerves, these activated cells release factors that increase excitability in spinal pain circuitry. Using expression profiling studies of microglial cells the host laboratory discovered a putative chloride channel transcript that is highly upregulated in these cells: Anoctamin-6 (Ano6). Although the functions of chloride currents in microglia are already known the underlying molecular entity of these currents is not known. The aims of this project are twofold. Firstly I will continue with expression profiling of microglia in a mouse model of neuropathic pain. Secondly I will perform a full characterization of Ano6. Initially I will analyze its activation mechanisms and pore properties in heterologous cells. Subsequently, I will examine its function in vivo using a mouse knockout model, determining its involvement in microglial physiology and in neuropathic pain. Results originated in this study will contribute to a better understanding of neuron-microglia communication in neuropathic states with the possibility to further uncover novel targets for treating human neuropathic pain. EMBL Monterotondo would offer me the possibility to gain specific skills in molecular biology, electrophysiology and in vivo mouse genetics thanks to the on-site Core Facilities and to the collaboration with EMBL Heidelberg and La Sapienza Rome. The skills acquired will greatly benefit my scientific career leading to maturity and independence, allowing me to interact with many research fields and to use powerful tools. Collaborations with other research groups will also improve my independent thinking. Finally, such a research experience would facilitate the ultimate achievement of an independent leading position in the Neuroimmunology research'

Introduzione (Teaser)

Neuropathic pain is caused by damage to the body's sensory system and affects the five senses. European research has investigated the role of one particularly protein, anoctamin-6 in this debilitating disease.

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