4.8 Article

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

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NATURE COMMUNICATIONS
卷 6, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/ncomms8526

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资金

  1. Fondation pour la Recherche Medicale
  2. Association pour la Recherche contre le Cancer
  3. City of Paris
  4. European Research Council [Strapacemi 243103]
  5. Association Nationale pour la Recherche [ANR-09-PIRI-0027-PCVI]
  6. InnaBiosante foundation (Micemico)
  7. DCBIOL Labex from the French Government [ANR-10-IDEX-0001-02-PSL*, ANR-11-LABX-0043]
  8. ERC Advanced Investigator Grant (Institut Curie) [250367, CNRS UMR3215/Inserm U934]
  9. Agence Nationale de la Recherche (ANR) [ANR-09-PIRI-0027] Funding Source: Agence Nationale de la Recherche (ANR)

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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.

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