Microtubule plus-end dynamics link wound repair to the innate immune response

Author:

Taffoni Clara1ORCID,Omi Shizue1ORCID,Huber Caroline1ORCID,Mailfert Sébastien1ORCID,Fallet Mathieu1ORCID,Rupprecht Jean-François2ORCID,Ewbank Jonathan J1ORCID,Pujol Nathalie1ORCID

Affiliation:

1. CIML, Centre d’Immunologie de Marseille-Luminy, Turing Centre for Living Systems, Aix Marseille Univ, INSERM, CNRS, Marseille, France

2. CPT, Turing Centre for Living Systems, Aix Marseille Univ, CNRS, Marseille, France

Abstract

The skin protects animals from infection and physical damage. In Caenorhabditis elegans, wounding the epidermis triggers an immune reaction and a repair response, but it is not clear how these are coordinated. Previous work implicated the microtubule cytoskeleton in the maintenance of epidermal integrity (Chuang et al., 2016). Here, by establishing a simple wounding system, we show that wounding provokes a reorganisation of plasma membrane subdomains. This is followed by recruitment of the microtubule plus end-binding protein EB1/EBP-2 around the wound and actin ring formation, dependent on ARP2/3 branched actin polymerisation. We show that microtubule dynamics are required for the recruitment and closure of the actin ring, and for the trafficking of the key signalling protein SLC6/SNF-12 toward the injury site. Without SNF-12 recruitment, there is an abrogation of the immune response. Our results suggest that microtubule dynamics coordinate the cytoskeletal changes required for wound repair and the concomitant activation of innate immunity.

Funder

Agence Nationale de la Recherche

Institut National de la Santé et de la Recherche Médicale

Centre National de la Recherche Scientifique

Aix-Marseille Université

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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