| Literature DB >> 29079589 |
Marine Bretou1, Pablo J Sáez2,3,4, Doriane Sanséau2, Mathieu Maurin2, Danielle Lankar2, Melanie Chabaud2, Carmine Spampanato5, Odile Malbec2, Lucie Barbier3,4,6, Shmuel Muallem7, Paolo Maiuri3,4,8,9, Andrea Ballabio5,10,11, Julie Helft2, Matthieu Piel3,4, Pablo Vargas1,3,4, Ana-Maria Lennon-Duménil1.
Abstract
Dendritic cells (DCs) patrol their environment by linking antigen acquisition by macropinocytosis to cell locomotion. DC activation upon bacterial sensing inhibits macropinocytosis and increases DC migration, thus promoting the arrival of DCs to lymph nodes for antigen presentation to T cells. The signaling events that trigger such changes are not fully understood. We show that lysosome signaling plays a critical role in this process. Upon bacterial sensing, lysosomal calcium is released by the ionic channel TRPML1 (transient receptor potential cation channel, mucolipin subfamily, member 1), which activates the actin-based motor protein myosin II at the cell rear, promoting fast and directional migration. Lysosomal calcium further induces the activation of the transcription factor EB (TFEB), which translocates to the nucleus to maintain TRPML1 expression. We found that the TRPML1-TFEB axis results from the down-regulation of macropinocytosis after bacterial sensing by DCs. Lysosomal signaling therefore emerges as a hitherto unexpected link between macropinocytosis, actomyosin cytoskeleton organization, and DC migration.Entities:
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Year: 2017 PMID: 29079589 DOI: 10.1126/sciimmunol.aak9573
Source DB: PubMed Journal: Sci Immunol ISSN: 2470-9468