LEUKOSELECTIN

Tailoring the tail of L-selectin

Coordinatore	MAX PLANCK GESELLSCHAFT ZUR FOERDERUNG DER WISSENSCHAFTEN E.V.    more  Organization address address: Hofgartenstrasse 8 city: MUENCHEN postcode: 80539 contact info Titolo: Dr. Nome: Anne Katrin Cognome: Werenskiold Email: send email Telefono: 498986000000 Fax: 498986000000
Nazionalità Coordinatore	Germany [DE]
Totale costo	223˙778 €
EC contributo	223˙778 €
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-2012-IEF
Funding Scheme	MC-IEF
Anno di inizio	2013
Periodo (anno-mese-giorno)	2013-05-01   -   2015-04-30

 Partecipanti

#	participant	country	role	EC contrib. [€]
1	MAX PLANCK GESELLSCHAFT ZUR FOERDERUNG DER WISSENSCHAFTEN E.V.  Organization address address: Hofgartenstrasse 8 city: MUENCHEN postcode: 80539 contact info Titolo: Dr. Nome: Anne Katrin Cognome: Werenskiold Email: send email Telefono: 498986000000 Fax: 498986000000	DE (MUENCHEN)	coordinator	223˙778.40

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 Obiettivo del progetto (Objective)

'Leukocytes protect humans from pathogens. During episodes of infection, leukocytes leave the blood circulation and migrate to sites in the body where they mount a response against pathogens. In order for leukocytes to migrate, they must adhere to endothelial cells which cover blood vessels. Such adhesion allows them to migrate along the endothelial layer, pass though endothelial junctions, and reach tissues. Excessive migration of leukocytes is a characteristic of inflammatory and auto-immune diseases, and leads to tissue damage as leukocytes have destructive capacities. L-selectin is an adhesion receptor expressed in leukocytes. This receptor plays a critical role in the adhesion of leukocytes to endothelial cells. Interaction of proteins with the cytoplasmic tail of L-selectin controls the functions of L-selectin. As L-selectin tail contains only one serine residue at position 364, it was proposed but not proven that such phosphorylation may be essential for the recruitment of proteins to L-selectin tail and regulation of L-selectin functions. By using sophisticated proteomics, and by generating mice harbouring nonphosphorylatable serine-to-alanine knock-In substitution at position 364 of the L-selectin tail, we will get insights into the mechanisms by which L-selectin functions are regulated. Our objectives are: 1- To identify new proteins interacting with L-selectin tail and identify which one are important for L-selectin functions 2- To investigate whether serine phosphorylation of L-selectin tail regulates interaction with binding partners and L-selectin functions in vitro 3- To investigate whether leukocytes from L-selectin tail serine-to-alanine knock-In mice exhibit impaired adhesion and migration in vivo Identification of new proteins binding to L-selectin tail and understanding the mechanisms controlling this interaction is essential for the design of new therapeutic strategies for the treatment of inflammatory and auto-immune diseases.'