Evidence map›Paper›PMID 28557996›Full record

ArticlePLoS genetics2017

The cell non-autonomous function of ATG-18 is essential for neuroendocrine regulation of Caenorhabditis elegans lifespan.

Justin Minnerly, Jiuli Zhang, Thomas Parker, Tiffany Kaul, Kailiang Jia

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

32 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
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  15. Autophagy and the hallmarks of aging.Ageing research reviews · 2021
    Review
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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

5 authors at 1 institution in 1 country.

Justin MinnerlyDepartment of Biological Sciences, Florida Atlantic University, Jupiter, FL, United States of America.
Jiuli ZhangDepartment of Biological Sciences, Florida Atlantic University, Jupiter, FL, United States of America.
Thomas ParkerDepartment of Biological Sciences, Florida Atlantic University, Jupiter, FL, United States of America.
Tiffany KaulDepartment of Biological Sciences, Florida Atlantic University, Jupiter, FL, United States of America.ORCID http://orcid.org/0000-0001-7588-3782
Kailiang JiaDepartment of Biological Sciences, Florida Atlantic University, Jupiter, FL, United States of America.ORCID http://orcid.org/0000-0002-0005-2121
Florida Atlantic University · US

Funding

The novel role of autophagy in controlling C. elegans dauer recoveryR15HD080497 · NICHD · FLORIDA ATLANTIC UNIVERSITY · PI JIA, KAILIANG · 2014 to 2014
$357k
6 · The paper itself

Abstract

Dietary restriction (DR) and reduced insulin growth factor (IGF) signaling extend lifespan in Caenorhabditis elegans and other eukaryotic organisms. Autophagy, an evolutionarily conserved lysosomal degradation pathway, has emerged as a central pathway regulated by various longevity signals including DR and IGF signaling in promoting longevity in a variety of eukaryotic organisms. However, the mechanism remains unclear. Here we show that the autophagy protein ATG-18 acts cell non-autonomously in neuronal and intestinal tissues to maintain C. elegans wildtype lifespan and to respond to DR and IGF-mediated longevity signaling. Moreover, ATG-18 activity in chemosensory neurons that are involved in food detection sufficiently mediates the effect of these longevity pathways. Additionally, ATG-18-mediated cell non-autonomous signaling depends on the release of neurotransmitters and neuropeptides. Interestingly, our data suggest that neuronal and intestinal ATG-18 acts in parallel and converges on unidentified neurons that secrete neuropeptides to regulate C. elegans lifespan through the transcription factor DAF-16/FOXO in response to reduced IGF signaling.

Indexed as

LongevityAnimalsAutophagy-Related ProteinsCaenorhabditis elegansCaenorhabditis elegans ProteinsCaloric RestrictionForkhead Transcription FactorsInsulin-Like Growth Factor IIntestinal MucosaNeuroendocrine CellsNeuropeptidesNeurotransmitter AgentsSensory Receptor CellsAutophagy-Related ProteinsCaenorhabditis elegans Proteinsdaf-16 protein, C elegansForkhead Transcription FactorsInsulin-Like Growth Factor INeuropeptidesNeurotransmitter Agents

Identifiers

PMID28557996
PMCPMC5469504
OpenAlexW2619896194

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.