CBSCS

Physiology of the adult carotid body stem cell niche

 Coordinatore UNIVERSIDAD DE SEVILLA 

Spiacenti, non ci sono informazioni su questo coordinatore. Contattare Fabio per maggiori infomrazioni, grazie.

 Nazionalità Coordinatore Spain [ES]
 Totale costo 1˙476˙000 €
 EC contributo 1˙476˙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-2010-StG_20091118
 Funding Scheme ERC-SG
 Anno di inizio 2010
 Periodo (anno-mese-giorno) 2010-11-01   -   2015-10-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSIDAD DE SEVILLA

 Organization address address: CALLE S. FERNANDO 4
city: SEVILLA
postcode: 41004

contact info
Titolo: Dr.
Nome: Ricardo
Cognome: Pardal
Email: send email
Telefono: +34 955014356
Fax: +34 954617301

ES (SEVILLA) hostInstitution 1˙476˙000.00
2    UNIVERSIDAD DE SEVILLA

 Organization address address: CALLE S. FERNANDO 4
city: SEVILLA
postcode: 41004

contact info
Titolo: Ms.
Nome: Margarita
Cognome: Martínez-Pais Loscertales
Email: send email
Telefono: +34 954488129
Fax: +34 954488127

ES (SEVILLA) hostInstitution 1˙476˙000.00

Mappa


 Word cloud

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

body    carotid    cells    stem    behavior    niche    us    neural    physiology    quiescent    mechanisms    nervous    we    recently    neurogenic    organ    activate    enter    niches    nscs    exit    adult    physiological    cell    sustentacular    proliferation    cb    glomus    tissue   

 Obiettivo del progetto (Objective)

'The discovery of adult neural stem cells (NSCs) has broaden our view of the physiological plasticity of the nervous system, and has opened new perspectives on the possibility of tissue regeneration and repair in the brain. NSCs reside in specialized niches in the adult mammalian nervous system, where they are exposed to specific paracrine signals regulating their behavior. These neural progenitors are generally in a quiescent state within their niche, and they activate their proliferation depending on tissue regenerative and growth needs. Understanding the mechanisms by which NSCs enter and exit the quiescent state is crucial for the comprehension of the physiology of the adult nervous system. In this project we will study the behavior of a specific subpopulation of adult neural stem cells recently described by our group in the carotid body (CB). This small organ constitutes the most important chemosensor of the peripheral nervous system and has neuronal glomus cells responsible for the chemosensing, and glia-like sustentacular cells which were thought to have just a supportive role. We recently described that these sustentacular cells are dormant stem cells able to activate their proliferation in response to a physiological stimulus like hypoxia, and to differentiate into new glomus cells necessary for the adaptation of the organ. Due to our precise experimental control of the activation and deactivation of the CB neurogenic niche, we believe the CB is an ideal model to study fundamental questions about adult neural stem cell physiology and the interaction with the niche. We propose to study the cellular and molecular mechanisms by which these carotid body stem cells enter and exit the quiescent state, which will help us understand the physiology of adult neurogenic niches. Likewise, understanding this neurogenic process will improve the efficacy of using glomus cells for cell therapy against neurological disease, and might help us understand some neural tumors.'

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