NOVEXPAND

Identification of novel factors to expand hematopoietic stem cells in vitro

 Coordinatore LUNDS UNIVERSITET 

 Organization address address: Paradisgatan 5c
city: LUND
postcode: 22100

contact info
Titolo: Dr.
Nome: Jens
Cognome: Forsberg
Email: send email
Telefono: +46 (0)46 222 0575
Fax: +46 (0)46 222 0568

 Nazionalità Coordinatore Sweden [SE]
 Totale costo 180˙669 €
 EC contributo 180˙669 €
 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-IIF
 Funding Scheme MC-IIF
 Anno di inizio 2011
 Periodo (anno-mese-giorno) 2011-01-01   -   2012-12-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    LUNDS UNIVERSITET

 Organization address address: Paradisgatan 5c
city: LUND
postcode: 22100

contact info
Titolo: Dr.
Nome: Jens
Cognome: Forsberg
Email: send email
Telefono: +46 (0)46 222 0575
Fax: +46 (0)46 222 0568

SE (LUND) coordinator 180˙669.40

Mappa


 Word cloud

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

samples    hscs    proliferation    prior    stem    assay    patients    marrow    engraftment    culture    donor    cells    genes    suitable    es    blood    pluripotent    ips    lack    transplantation    cell    immature    expressed    molecules    hsc    successful    bmt    cb    adults    expansion    transduced   

 Obiettivo del progetto (Objective)

'Blood and marrow transplantation (BMT) has been used successfully to treat malignant blood disorders and genetic diseases. Although BMT has been effective, problems remain, for example lack of suitable donors and engraftment failure. Cord blood (CB) contains hematopoietic stem cells (HSC) that can be used to transplant children. However, there are too few HSC in most CB samples to reliably engraft adult patients following BMT. Development of HSC expansion prior to transplantation would allow successful engraftment in patients that cannot be transplanted today due to a lack of a suitable donor. While some classical cytokines can maintain the number of HSC in culture, expansion of HSC in vitro will require discovery of novel factors that can increase more symmetrical divisions of HSC. In this project we will identify new factors that can expand HSCs by increasing the proliferation of immature HSC, using recent findings from embryonic stem (ES) cells and induced pluripotent stem (iPS) cells. ES/iPS cells are cell lines that have strong proliferation ability and are pluripotent in the presence of defined factors. Several genes expressed in ES/iPS cells have been identified as stem cell regulators, but a comprehensive analysis of all possible genes is essential to find additional factors that may be important for expansion of HSC. The screening will be done by using microarray analysis, subtraction assay, and over expression using cDNA libraries. Genes that are differentially expressed in immature ES cells and differentiated cells will be inserted into lentiviral vectors and transduced to HSC. The transduced HSCs will be analyzed with respect to inceased stem cell function using a transplantation assay in vivo. Findings from the project are expected to discover several novel regulatory molecules that will allow HSC expansion prior to transplantation. Successful HSC expansion will make most CB donor samples useful for adults requiring HSC transplantation therapy.'

Introduzione (Teaser)

Bone marrow transplantation (BMT) is a well-established procedure for treating blood cancers including leukaemia. Identification of molecules that could increase numbers of blood cell stem cells in culture is expected to improve the overall outcome of transplantation in adults.

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