Evidence map›Paper›PMID 17257591›Full record

ArticleDevelopmental biology2007

Insulin signaling in Caenorhabditis elegans regulates both endocrine-like and cell-autonomous outputs.

Wendy B Iser, Minaxi S Gami, Catherine A Wolkow

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
0.8field-weighted citation impact, top 35% 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

30 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
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  8. Gene-diet interactions and aging in C. elegans.Experimental gerontology · 2016
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  16. Neurite sprouting and synapse deterioration in the aging Caenorhabditis elegans nervous system.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2012
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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

3 authors at 1 institution in 1 country.

Wendy B IserLaboratory of Neurosciences, National Institute on Aging-IRP, 5600 Nathan Shock Drive, Baltimore, MD 21224, USA.
Minaxi S Gami
Catherine A Wolkow
National Institute on Aging · US

Funding

Genetic and environmental factors that regulate aging and longevityZIAAG000320 · NIA · NATIONAL INSTITUTE ON AGING · PI WOLKOW, CATHERINE A · 2009 to 2010
$2.1M
Genetic and environmental factors that regulate aging and longevityZ01AG000320 · NIA · NATIONAL INSTITUTE ON AGING · PI WOLKOW, CATHERINE A · 2002 to 2008
$1.9M
Intramural NIH HHS Z01 AG000320
6 · The paper itself

Abstract

In C. elegans, insulin signaling affects development, lifespan and stress resistance. Several studies have shown that insulin signaling affects lifespan in an endocrine-like manner from different cells, while the major downstream target of insulin, the FOXO transcription factor encoded by daf-16, may act preferentially in intestinal cells to prolong lifespan. This discrepancy raised the possibility that insulin may have both endocrine and cell-intrinsic outputs. Here, we further investigated the types of cells capable of producing endocrine outputs of insulin and also identified a new cell-intrinsic insulin output. We found that insulin signaling within groups of neurons promoted wildtype lifespan, showing that the endocrine outputs of insulin were not restricted to specific cells. In contrast, DAF-16 appeared to have a greater effect on lifespan when expressed in a combination of tissues. These results suggest that insulin signaling may regulate DAF-16 through cell-intrinsic and endocrine pathways. We also found that an insulin-dependent response to fasting in intestinal cells was preferentially regulated by intestinal insulin signaling and was less responsive to insulin signaling from non-intestinal cells. Together, these results show that C. elegans insulin signaling has endocrine as well as tissue-specific outputs which could influence lifespan in a combinatorial fashion.

Indexed as

AgingAnimalsAnimals, Genetically ModifiedCaenorhabditis elegansCaenorhabditis elegans ProteinsFastingForkhead Transcription FactorsGenes, HelminthInsulinLongevityModels, BiologicalMutationNeuronsPhosphatidylinositol 3-KinasesSignal TransductionTranscription FactorsAGE-1 protein, C elegansCaenorhabditis elegans Proteinsdaf-16 protein, C elegansForkhead Transcription FactorsInsulinPhosphatidylinositol 3-KinasesTranscription Factors

Identifiers

PMID17257591
PMCPMC2262836
OpenAlexW2070586322

What OpenQuestion holds

Textmetadata
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.