Evidence map›Paper›PMID 28165006›Full record

ArticleNature communications2017

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

Tsai-Yi Lu, Jennifer M MacDonald, Lukas J Neukomm, Amy E Sheehan, Rachel Bradshaw, Mary A Logan, Marc R Freeman

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.7field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

43 citing papers in PubMed, 86 citations in OpenAlex.

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  8. Glial Regulation of Circuit Wiring, Firing, and Expiring in theCold Spring Harbor perspectives in biology · 2024
    Review
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  18. A nerve-wracking buzz: lessons fromFrontiers in aging neuroscience · 2023
    Review
  19. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Tsai-Yi LuDepartment of Neurobiology, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA.
Jennifer M MacDonaldDepartment of Neurobiology, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA.
Lukas J NeukommDepartment of Neurobiology, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA.
Amy E SheehanDepartment of Neurobiology, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA.
Rachel BradshawDepartment of Neurobiology, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA.
Mary A LoganDepartment of Neurobiology, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA.
Marc R FreemanDepartment of Neurobiology, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA.
University of Massachusetts Chan Medical School · USOregon Health & Science University · US

Funding

The Draper signaling pathway in Drosophila glial immune functionsR01NS053538 · NINDS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Marc R Freeman · 2006 to 2026
$5.3M
Astrocyte control of neural circuits and behaviorR37NS053538 · NINDS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI FREEMAN, MARC R · 2016 to 2022
$2.9M
NINDS NIH HHS R01 NS053538NINDS NIH HHS R37 NS053538
6 · The paper itself

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.

Indexed as

AnimalsAnimals, Genetically ModifiedAxonsCell MembraneDrosophila melanogasterDrosophila ProteinsFemaleJNK Mitogen-Activated Protein KinasesMaleMembrane ProteinsNerve DegenerationNeurogliaPhagocytosisSignal TransductionSTAT Transcription FactorsTNF Receptor-Associated Factor 4Drosophila Proteinsdrpr protein, DrosophilaJNK Mitogen-Activated Protein KinasesMembrane ProteinsStat92E protein, DrosophilaSTAT Transcription FactorsTNF Receptor-Associated Factor 4Transcription Factor AP-1

Identifiers

PMID28165006
PMCPMC5303877
OpenAlexW2586939872

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.