RENALSTEM

Developing a stem cell based therapy to replace nephrons lost through reflux nephropathy

 Coordinatore THE UNIVERSITY OF LIVERPOOL 

 Organization address address: Brownlow Hill, Foundation Building 765
city: LIVERPOOL
postcode: L69 7ZX

contact info
Titolo: Dr.
Nome: Patricia
Cognome: Murray
Email: send email
Telefono: +44 151 795 4456
Fax: +44 151 795 4410

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 167˙689 €
 EC contributo 167˙689 €
 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-2007-4-2-IIF
 Funding Scheme MC-IIF
 Anno di inizio 2008
 Periodo (anno-mese-giorno) 2008-08-01   -   2010-07-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    THE UNIVERSITY OF LIVERPOOL

 Organization address address: Brownlow Hill, Foundation Building 765
city: LIVERPOOL
postcode: L69 7ZX

contact info
Titolo: Dr.
Nome: Patricia
Cognome: Murray
Email: send email
Telefono: +44 151 795 4456
Fax: +44 151 795 4410

UK (LIVERPOOL) coordinator 0.00

Mappa


 Word cloud

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

vivo    reflux    tested    children    kidney    therapies    tissue    transplantation    esrd    stem    magnetic    disease    cells    mouse    resident    cell    renal    vur   

 Obiettivo del progetto (Objective)

'The prevalence of end stage renal disease (ESRD) continues to grow worldwide. Current treatment options for ESRD are peritoneal dialysis, haemodialysis, or renal transplantation, all of which have significant drawbacks both in terms of quality and quantity of life. In children and young adults, the most common cause of ESRD is vesicoureteric reflux (VUR), a condition where urine from the bladder re-enters the kidney. VUR creates an increased risk of urinary tract infection, predisposing to pyelonephritis, renal scarring, and in the most severe cases, ESRD. However, there is usually a time-window of several years from initial diagnosis of VUR to the development of ESRD, which presents an opportunity to design therapies aimed at preventing disease progression by repairing renal tissue before it becomes non functional. Recent advances in stem cell science and tissue engineering suggests that stem cell based therapies for reflux nephropathy could be feasible. The long-term aim is to explore the potential of resident kidney stem cells for renal replacement therapy in order to prevent susceptible children from developing ESRD. In this project, the potential of resident kidney stem cells will be tested by transplantation into mouse embryonic kidneys ex vivo. To devise a suitable scaffold to, a range of biocompatible polymeric substrates will be fabricated and tested for their ability to support nephrogenesis from disaggregated mouse kidney rudiments in vitro. Finally, we will develop a magnetic nanoparticle-based cell tracking technique that will enable the transplanted cells to be monitored in vivo using magnetic resonance imaging. Results generated by the project will establish if kidney stem cells have potential for future use in regenerative medicine. Should the results prove positive, further work will determine if the isolated kidney stem are capable of generating nephrons in animal models in vivo.'

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