CELLCYCLEGROWTHSIZE

Cell Growth and Size Homeostasis in Proliferating Mammalian Cells

 Coordinatore BAR ILAN UNIVERSITY 

 Organization address address: BAR ILAN UNIVERSITY CAMPUS
city: RAMAT GAN
postcode: 52900

contact info
Titolo: Ms.
Nome: Estelle
Cognome: Waise
Email: send email
Telefono: 97235317439
Fax: 97236353277

 Nazionalità Coordinatore Israel [IL]
 Totale costo 100˙000 €
 EC contributo 100˙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-2010-RG
 Funding Scheme MC-IRG
 Anno di inizio 2011
 Periodo (anno-mese-giorno) 2011-08-01   -   2015-07-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    BAR ILAN UNIVERSITY

 Organization address address: BAR ILAN UNIVERSITY CAMPUS
city: RAMAT GAN
postcode: 52900

contact info
Titolo: Ms.
Nome: Estelle
Cognome: Waise
Email: send email
Telefono: 97235317439
Fax: 97236353277

IL (RAMAT GAN) coordinator 100˙000.00

Mappa


 Word cloud

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

division    biology    yeast    intrinsic    proliferating    mechanism    coordinates    mammalian    sensing    cells    size    time    cycle    cell   

 Obiettivo del progetto (Objective)

'Cell size is central to cell function and ultimately to tissue architecture. Size reflects a balance between cell growth - steadily increase of size, and cytokinesis which halves the cell’s size on each division. How cells attain and maintain their size is a fundamental question that has fascinated generations of biologists, but the answer remains obscure. For proliferating cells growing in unvarying conditions, cell size is basically time-invariant, suggesting that the growth cycle and the cell cycle are coupled. In yeast, an intrinsic size-sensing mechanism coordinates cell cycle with cell growth. Whether such a mechanism is restricted to single-celled organisms is a long-lasting debate. These problems pioneered by Mitchison, Nurse and Zetterberg, captivated the scientific community in the past. But the real challenge of monitoring growth of objects as minute as cells, left these questions neglected for decades. In order to meet the challenge, I have combined cell biology approaches with engineering and mathematics, and was able to overcome long-standing experimental limitations, and, for the first time, to accurately describe the growth (size over time) of a proliferating mammalian cell. These studies suggested that at least some mammalian cells must have an intrinsic size control mechanism that, like in yeast, coordinates cell size with cell division. My work, performed in Marc Kirschner lab at Harvard, was published as a full article in Science. Here I propose to study the physiology and the molecular basis of size homeostasis in proliferating mammalian cells. Using advanced methodologies to monitor cell growth, cell cycle and cell size, and by applying cell and systems biology approaches to cell growth and cell cycle regulation, I aim to elucidate i) whether size-sensing mechanism typically exist in animal cells and ii) the underlying mechanism linking cell growth to cell cycle in mammalian systems with relevance to cancer, differentiation and regeneration'

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