Regulation of dendritic cell migration by CD74, the MHC class II-associated invariant chain

Science

Volumn 322, Issue 5908, 2008, Pages 1705-1710

  Faure André, Gabrielle ^a   Vargas, Pablo ^a,b   Yuseff, Maria Isabel ^a   Heuzé, Mélina ^a   Diaz, Jheimmy ^a   Lankar, Danielle ^a   Steri, Veronica ^a   Manry, Jeremy ^a   Hugues, Stéphanie ^a   Vascotto, Fulvia ^a   Boulanger, Jérôme ^c   Raposo, Graça ^c   Bono, Maria Rosa ^b,d   Rosemblatt, Mario ^b,d,e   Piel, Matthieu ^c   Lennon Duménil, Ana Maria ^a  

^a INSTITUT CURIE   (France)

^b UNIVERSITY OF CHILE   (Chile)

^c INSTITUT CURIE   (France)

^d Fundacion Ciencia para la Vida   (Chile)

^e UNIVERSIDAD ANDRÉS BELLO   (Chile)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIN; CD74 ANTIGEN; MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 2; MYOSIN II; UNCLASSIFIED DRUG;

ANTIGEN; CYTOLOGY; MOTILITY; PROTEIN;

ANIMAL EXPERIMENT; ARTICLE; CELL MIGRATION; CELL MOTILITY; CONTROLLED STUDY; DENDRITIC CELL; IN VIVO STUDY; MAJOR HISTOCOMPATIBILITY COMPLEX; MOUSE; NONHUMAN; PRIORITY JOURNAL;

ANIMALS; ANTIGEN PRESENTATION; ANTIGENS, DIFFERENTIATION, B-LYMPHOCYTE; CATHEPSINS; CELL MOVEMENT; DENDRITIC CELLS; ENDOCYTOSIS; HISTOCOMPATIBILITY ANTIGENS CLASS II; LIPOPOLYSACCHARIDES; LYMPH NODES; LYSOSOMES; MICE; MICE, INBRED C57BL; MYOSIN TYPE II; PHOSPHORYLATION;

EID: 58149247727     PISSN: 00368075     EISSN: 10959203     Source Type: Journal    
DOI: 10.1126/science.1159894     Document Type: Article

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23. The authors thank T. Makushok for setting up the cell migration microchannel system; A. Azicune for cell micropatterning techniques; W. Faigle and D. Lowe for proteomics analysis; C. Recchi for help with gelatin-FITC degradation experiments; H. Overkleeft for synthesizing the LHVS; J. Roger for providing magnetic nanoparticles; M. Leberre, D. Baigl, and Y. Chen for help with microfabrication; and S. Amigorena, M. Sixt, P. Benaroch, V. Soumelis, C. Hivroz, and I. Fernandez for advice on the manuscript. A.-M.L.-D. thanks Y. Bellaïche for help with manuscript redaction. G.F.-A. was supported by a fellowship from the Ministère Français de la Recherche and, together with M.H., from the Association pour la Recherche contre le Cancer (ARC). P.V. and M.-I.Y. benefited from ECOS-Comisíon Nacional de Investigacíon Científica y Technológica, Gobierno de Chile fellowship (CO3S01), Institut Curie and Inserm fellowships, respectively. V.S. was part of the Leonardo Da Vinci project (Unipharma-Graduates, Sapienza University of Rome). This work was funded in part by grants from the ARC, Fondecyt (Chile) to M.-R.B. (1060834) and M.R. (1060253); Agence Nationale pour la Recherche (ANR-06-PCVI-0010) and Human Frontiers Science Program (RGY53/2007) to M.P.