Cell migration and antigen capture are antagonistic processes coupled by myosin II in dendritic cells

M. Chabaud , M.L. Heuze , M. Bretou , P. Vargas , P. Maiuri , P. Solanes , M. Maurin , E. Terriac , M. Le Berre , D. Lankar , T. Piolot , R.S. Adelstein , Y. Zhang , M. Sixt , J. Jacobelli , O. Benichou , R. Voituriez , M. Piel , A.M. Lennon-Dumenil

Bibtex , URL
NATURE COMMUNICATIONS, 6, 7526
Published 01 Jun. 2015
DOI: 10.1038/ncomms8526
ISSN: 2041-1723

Abstract

The immune response relies on the migration of leukocytes and on their ability to stop in precise anatomical locations to fulfil their task. How leukocyte migration and function are coordinated is unknown. Here we show that in immature dendritic cells, which patrol their environment by engulfing extracellular material, cell migration and antigen capture are antagonistic. This antagonism results from transient enrichment of myosin IIA at the cell front, which disrupts the back-to-front gradient of the motor protein, slowing down locomotion but promoting antigen capture. We further highlight that myosin IIA enrichment at the cell front requires the MHC class II-associated invariant chain (Ii). Thus, by controlling myosin IIA localization, Ii imposes on dendritic cells an intermittent antigen capture behaviour that might facilitate environment patrolling. We propose that the requirement for myosin II in both cell migration and specific cell functions may provide a general mechanism for their coordination in time and space.

Cette publication est associée à :

Dynamique stochastique des systèmes réactifs et vivants