Responsable: Ricardo Pardal Redondo
Tipo de Proyecto/Ayuda: 7º Programa Marco de la U.E.
Referencia: 260964
Web: http://cordis.europa.eu/projects/rcn/96660_en.html
Fecha de Inicio: 01-11-2010
Fecha de Finalización: 31-10-2015

Empresa/Organismo financiador/es:

• Comisión Europea

Contratados:

• Investigadores:
  • Diana Aguilar Morante
  • Valentina Annese
  • Verónica Sobrino Cabello
  • Francisco Manuel Vega Moreno
• Técnicos/Personal Administrativo:
  • Lourdes Maite García Quintanilla
  • Ismael Rodríguez Prieto

Resumen del proyecto:

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 tumours.