3D HMEC-MT-TIP

Regulation of mammary epithelial morphogenesis by microtubule plus-end tracking proteins

 Coordinatore UNIVERSITEIT UTRECHT 

 Organization address address: Heidelberglaan 8
city: UTRECHT
postcode: 3584 CS

contact info
Titolo: Ms.
Nome: Astrid
Cognome: Haijma
Email: send email
Telefono: 31302539227

 Nazionalità Coordinatore Netherlands [NL]
 Totale costo 176˙685 €
 EC contributo 176˙685 €
 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-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2012
 Periodo (anno-mese-giorno) 2012-04-01   -   2014-03-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITEIT UTRECHT

 Organization address address: Heidelberglaan 8
city: UTRECHT
postcode: 3584 CS

contact info
Titolo: Ms.
Nome: Astrid
Cognome: Haijma
Email: send email
Telefono: 31302539227

NL (UTRECHT) coordinator 176˙685.60

Mappa


 Word cloud

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

morphogenesis    tips    network    mammary    dimensional    behavior    architecture    grown    model    acinar    microtubule    functions    components    microtubules    epithelial    cells   

 Obiettivo del progetto (Objective)

'The mammary gland functional unit develops as a result of a complex morphogenetic process organizing polarized epithelial cells into a branched network of ducts terminating in acini. Most of human breast cancers originate from transformation of epithelial cells and induce breakdown of this structure. Studies in cells grown in two-dimensional (2D) cultures have shown that microtubules target and regulate actin network and adhesion complexes, which are also known to be essential components of three-dimensional (3D) tissue architecture. Here, I propose to address microtubule functions and behavior in a more relevant system to model physiological morphogenesis. For this purpose, I intend to investigate mechanisms underlying the regulation of microtubule dynamics and their biological impact in an in vitro reconstituted acinar model of untransformed mammary epithelial cells grown in 3D. My project aims at addressing the role of the growing family of microtubule plus-end tracking proteins (TIPs) in the control of microtubule functions during 3D mammary epithelial morphogenesis. Special focus will be given to TIP-dependent microtubule cross-talk with key structural components of acinar architecture. Imaging of microtubules in 3D mammary epithelial culture will be used to analyze microtubule behavior during epithelial-mesenchymal transition and the role of TIPs in this process.'

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