MICAG

Microbial-induced Angiogenesis in the Gut

 Coordinatore UNIVERSITATSMEDIZIN DER JOHANNES GUTENBERG-UNIVERSITAT MAINZ 

 Organization address address: Langenbeckstrasse 1
city: Mainz
postcode: 55131

contact info
Titolo: Dr.
Nome: Uta
Cognome: Veith
Email: send email
Telefono: +49 6131 179717
Fax: +49 6131 179669

 Nazionalità Coordinatore Germany [DE]
 Totale costo 45˙000 €
 EC contributo 45˙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-2009-RG
 Funding Scheme MC-ERG
 Anno di inizio 2010
 Periodo (anno-mese-giorno) 2010-07-01   -   2013-06-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITATSMEDIZIN DER JOHANNES GUTENBERG-UNIVERSITAT MAINZ

 Organization address address: Langenbeckstrasse 1
city: Mainz
postcode: 55131

contact info
Titolo: Dr.
Nome: Uta
Cognome: Veith
Email: send email
Telefono: +49 6131 179717
Fax: +49 6131 179669

DE (Mainz) coordinator 28˙750.00
2    UNIVERSITAETSKLINIKUM WUERZBURG - KLINIKUM DER BAYERISCHEN JULIUS-MAXIMILIANS-UNIVERSITAT

 Organization address address: JOSEF-SCHNEIDER-STRASSE 2
city: WUERZBURG
postcode: 97080

contact info
Titolo: Ms.
Nome: Melanie
Cognome: Bauer
Email: send email
Telefono: +49 931 201 55058
Fax: +49 931 201 61768

DE (WUERZBURG) participant 16˙250.00

Mappa


 Word cloud

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

microbial    genes    mice    host    upregulated    microvessels    bacteria    microbiota    networks    mammalian    microbes    gut    mechanisms    tf    proangiogenic    pcr    trillions    intestinal    intestine    capillary    vascularisation    qrt    gf    colonization    intricate    conv    mucosa    vascular    raised    conventional   

 Obiettivo del progetto (Objective)

'Objective: The mammalian gut is colonized by trillions of bacteria. These gut microbes (microbiota) have coevolved with the host and developed traits that affects host physiology. Interestingly, germ-free (GF) mice exhibit arrested intestinal vascularisation if compared to littermates that were raised in a non-sterile environment (CONV-R, conventional-raised). Intestinal colonization with a normal microbiota initiates massive formation of capillary networks in the intestine of ex-GF mice (CONV-D, conventional-derived). The underlying molecular mechanisms that lead to formation of intricate capillary networks are completely unknown and therefore intense research is needed to elucidate how gut microbes trigger the formation of capillary networks. In the outlined project we will dissect proangiogenic molecules that can be induced by colonization with a gut microbiota and thus regulate microvessel formation in the intestinal mucosa. Methods: To uncover proangiogenic genes upregulated in response to microbial colonization we will perform qRT-PCR-analyses on small intestinal tissues collected from GF and CONV-R mice. The vascular marker CD31 (PECAM-1) will be used to quantify villus vascularization by immunohistochemistry and qRT-PCR. Preliminary results: We found that microbial colonization of the intestine leads to formation of an intricate vascular network. This process could be efficiently blocked by administration of an antibody directed against Tissue Factor (TF), the initiator molecule of coagulation. A distinct set of proangiogenic genes was identified to be upregulated in a TF-dependent manner following microbial colonization. Significance: A detailed understanding on how microbes affect intestinal morphogenesis and in particular the formation of microvessels in the mucosa is of major interest, since a disturbed formation of microvessels is observed in inflammatory bowel disease. Moreover, this approach will lead to better knowledge of the wound healing process.'

Introduzione (Teaser)

The mammalian gut has co-evolved with trillions of colonising bacteria. A European study worked to understand the impact of these bacteria on gut vascularisation and unravel the implicated mechanisms.

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