NEUROVASCULAR LINK

Neuro-vascular communication in the neural tube during development

 Coordinatore RUPRECHT-KARLS-UNIVERSITAET HEIDELBERG 

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 Nazionalità Coordinatore Germany [DE]
 Totale costo 1˙498˙419 €
 EC contributo 1˙498˙419 €
 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-2012-StG_20111109
 Funding Scheme ERC-SG
 Anno di inizio 2012
 Periodo (anno-mese-giorno) 2012-12-01   -   2017-11-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    RUPRECHT-KARLS-UNIVERSITAET HEIDELBERG

 Organization address address: SEMINARSTRASSE 2
city: HEIDELBERG
postcode: 69117

contact info
Titolo: Dr.
Nome: Carmen
Cognome: Ruiz De Almodóvar Egea
Email: send email
Telefono: +49 6221 544750
Fax: -552984

DE (HEIDELBERG) hostInstitution 1˙498˙419.00
2    RUPRECHT-KARLS-UNIVERSITAET HEIDELBERG

 Organization address address: SEMINARSTRASSE 2
city: HEIDELBERG
postcode: 69117

contact info
Titolo: Dr.
Nome: Norbert
Cognome: Huber
Email: send email
Telefono: +49 6221 54 2157
Fax: +49 6221 54 3599

DE (HEIDELBERG) hostInstitution 1˙498˙419.00

Mappa


 Word cloud

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

nt    angiogenic    primary    formed    cns    mechanisms    vessels    molecular    specialized    vascularization    identification    regions    angiogenesis    blood    tissue    tracks    cell    vascular    signals    sprouting    neuronal   

 Obiettivo del progetto (Objective)

'Despite the critical importance of a precisely formed vascular network within the central nervous system (CNS), little is known about the molecular mechanisms that specifically control CNS vascularization. While other embryonic tissues undergo primary vascularization, the CNS becomes secondarily vascularized by sprouting angiogenesis from a previously formed vascular plexus. Angiogenesis within the CNS seems to require a different code of angiogenic signals compared to other organs, as surprisingly newly formed blood vessels avoid CNS regions where the pro-angiogenic factor VEGF is expressed. Still, angiogenesis within the developing neural tube (NT) follows a highly stereotypic pattern with blood vessels sprouting always at the same locations, following the same paths and avoiding specific regions. The goal of this project is to elucidate the cellular and molecular mechanisms that control this specialized two-step CNS vascularization. The originality and innovative character of this proposal relates to the hypothesis that in contrast to primary vascularization, which happens in response to conventional angiogenic signals, NT vascularization occurs by an orchestration of neuronal-derived signals, guiding vessels into the developing CNS, thereby assuring synchrony and adaptation to the specialized CNS tissue. Two research tracks are proposed: 1: Identification of the neuronal cell populations that communicate with blood vessels during NT vascularization 2: Identification and functional characterization of the molecular players controlling vascular patterning within the NT Both tracks are designed to follow a multidisciplinary approach combining cutting edge technology in in vitro cell and 3D tissue culture, time-lapse microscopy, transcriptomics, proteomics and mouse genetics. This project will provide fundamental knowledge on the mechanisms of CNS vascularization and open new research lines for understanding and treating developmental and traumatic CNS disorders'

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