Evidence map›Paper›PMID 30133321›Full record

ArticleAmerican journal of physiology. Cell physiology2018

Nonselective autophagy reduces mitochondrial content during starvation in Caenorhabditis elegans.

Jonathan D Hibshman, Tess C Leuthner, Chelsea Shoben, Danielle F Mello, David R Sherwood, Joel N Meyer, L Ryan Baugh

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

21 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
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.

Jonathan D HibshmanDepartment of Biology, Duke University , Durham, North Carolina.ORCID 0000-0001-7324-9382
Tess C LeuthnerNicholas School of the Environment, Duke University , Durham, North Carolina.
Chelsea ShobenDepartment of Biology, Duke University , Durham, North Carolina.
Danielle F MelloNicholas School of the Environment, Duke University , Durham, North Carolina.
David R SherwoodDepartment of Biology, Duke University , Durham, North Carolina.
Joel N MeyerNicholas School of the Environment, Duke University , Durham, North Carolina.
L Ryan BaughDepartment of Biology, Duke University , Durham, North Carolina.
Duke University · USUniversity of North Carolina at Chapel Hill · US

Funding

Zebrafish as a Detector of Organophosphate ExposureP42ES010356 · NIEHS · DUKE UNIVERSITY · PI EDWARD D LEVIN · 2000 to 2026
$56.2M
Genetics Training Grant-Year 26T32GM007754 · NIGMS · DUKE UNIVERSITY · PI HAASE, STEVEN B · 1985 to 2019
$8.3M
Duke University Program in Environmental HealthT32ES021432 · NIEHS · DUKE UNIVERSITY · PI Akhenaton-Andrew Dhafir Jones, Joel Newman Meyer · 2013 to 2026
$4.0M
Systemic, maternal and transgenerational effects of nutrient stressR01GM117408 · NIGMS · DUKE UNIVERSITY · PI BAUGH, LARRY RYAN · 2015 to 2022
$2.5M
Does exposure to mitochondrial toxicants during germ cell development result in lifelong alterations in mitochondrial function mediated by epigenetic changes?R01ES028218 · NIEHS · DUKE UNIVERSITY · PI MEYER, JOEL NEWMAN · 2017 to 2021
$1.5M
NIEHS NIH HHS P42 ES010356NIEHS NIH HHS R01 ES028218NIEHS NIH HHS T32 ES021432NIGMS NIH HHS R01 GM117408NIGMS NIH HHS T32 GM007754
6 · The paper itself

Abstract

Starvation significantly alters cellular physiology, and signs of aging have been reported to occur during starvation. Mitochondria are essential to the regulation of cellular energetics and aging. We sought to determine whether mitochondria exhibit signs of aging during starvation and whether quality control mechanisms regulate mitochondrial physiology during starvation. We describe effects of starvation on mitochondria in the first and third larval stages of the nematode Caenorhabditis elegans. When starved, C. elegans larvae enter developmental arrest. We observed fragmentation of the mitochondrial network, a reduction in mitochondrial DNA (mtDNA) copy number, and accumulation of DNA damage during starvation-induced developmental arrest. Mitochondrial function was also compromised by starvation. Starved worms had lower basal, maximal, and ATP-linked respiration. These observations are consistent with reduced mitochondrial quality, similar to mitochondrial phenotypes during aging. Using pharmacological and genetic approaches, we found that worms deficient for autophagy were short-lived during starvation and recovered poorly from extended starvation, indicating sensitivity to nutrient stress. Autophagy mutants unc-51/Atg1 and atg-18/Atg18 maintained greater mtDNA content than wild-type worms during starvation, suggesting that autophagy promotes mitochondrial degradation during starvation. unc-51 mutants also had a proportionally smaller reduction in oxygen consumption rate during starvation, suggesting that autophagy also contributes to reduced mitochondrial function. Surprisingly, mutations in genes involved in mitochondrial fission and fusion as well as selective mitophagy of damaged mitochondria did not affect mitochondrial content during starvation. Our results demonstrate the profound influence of starvation on mitochondrial physiology with organismal consequences, and they show that these physiological effects are influenced by autophagy.

Indexed as

AnimalsAutophagyAutophagy-Related Protein-1 HomologAutophagy-Related ProteinsCaenorhabditis elegansCaenorhabditis elegans ProteinsDNA DamageDNA, MitochondrialLarvaLongevityMembrane ProteinsMitochondriaMitochondrial DynamicsMitophagyStarvationatg -18 protein, C elegansAutophagy-Related Protein-1 HomologAutophagy-Related ProteinsCaenorhabditis elegans ProteinsDNA, MitochondrialMembrane Proteinsagingautophagymitochondriastarvation

Identifiers

PMID30133321
PMCPMC6336938
OpenAlexW2888539854

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.