IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v8y2017i1d10.1038_ncomms14355.html
   My bibliography  Save this article

Axon degeneration induces glial responses through Draper-TRAF4-JNK signalling

Author

Listed:
  • Tsai-Yi Lu

    (University of Massachusetts Medical School
    Present address: Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, 725 N. Wolfe St., WBSB 1001, Baltimore, Maryland 21205, USA)

  • Jennifer M. MacDonald

    (University of Massachusetts Medical School)

  • Lukas J. Neukomm

    (University of Massachusetts Medical School)

  • Amy E. Sheehan

    (University of Massachusetts Medical School)

  • Rachel Bradshaw

    (University of Massachusetts Medical School)

  • Mary A. Logan

    (University of Massachusetts Medical School
    Present address: Junger’s Center for Neurosciences Research, Oregon Health and Science University, 3181 SW Sam Jackson Park Rd., Portland, Oregon 97239, USA)

  • Marc R. Freeman

    (University of Massachusetts Medical School
    Present address: Vollum Institute, Oregon Health and Science University, 3181 SW Sam Jackson Park Rd., Portland, Oregon 97239, USA)

Abstract

Draper/Ced-1/MEGF-10 is an engulfment receptor that promotes clearance of cellular debris in C. elegans, Drosophila and mammals. Draper signals through an evolutionarily conserved Src family kinase cascade to drive cytoskeletal rearrangements and target engulfment through Rac1. Glia also alter gene expression patterns in response to axonal injury but pathways mediating these responses are poorly defined. We show Draper is cell autonomously required for glial activation of transcriptional reporters after axonal injury. We identify TNF receptor associated factor 4 (TRAF4) as a novel Draper binding partner that is required for reporter activation and phagocytosis of axonal debris. TRAF4 and misshapen (MSN) act downstream of Draper to activate c-Jun N-terminal kinase (JNK) signalling in glia, resulting in changes in transcriptional reporters that are dependent on Drosophila AP-1 (dAP-1) and STAT92E. Our data argue injury signals received by Draper at the membrane are important regulators of downstream transcriptional responses in reactive glia.

Suggested Citation

  • Tsai-Yi Lu & Jennifer M. MacDonald & Lukas J. Neukomm & Amy E. Sheehan & Rachel Bradshaw & Mary A. Logan & Marc R. Freeman, 2017. "Axon degeneration induces glial responses through Draper-TRAF4-JNK signalling," Nature Communications, Nature, vol. 8(1), pages 1-9, April.
  • Handle: RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_ncomms14355
    DOI: 10.1038/ncomms14355
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/ncomms14355
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/ncomms14355?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    Citations

    Citations are extracted by the CitEc Project, subscribe to its RSS feed for this item.
    as


    Cited by:

    1. Yupu Wang & Ruiling Zhang & Sihao Huang & Parisa Tajalli Tehrani Valverde & Meike Lobb-Rabe & James Ashley & Lalanti Venkatasubramanian & Robert A. Carrillo, 2023. "Glial Draper signaling triggers cross-neuron plasticity in bystander neurons after neuronal cell death in Drosophila," Nature Communications, Nature, vol. 14(1), pages 1-15, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_ncomms14355. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.