Evidence map›Paper›PMID 26656270›Full record

ArticlePLoS genetics2015

Reproductive Aging Drives Protein Accumulation in the Uterus and Limits Lifespan in C. elegans.

Stephanie M Zimmerman, Izumi V Hinkson, Joshua E Elias, Stuart K Kim

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.4field-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

22 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. A hierarchy of causes of death in senescentbioRxiv : the preprint server for biology · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. AdvancingPhilosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
    Review
  8. Article
  9. Review
  10. Article
  11. Aging Hallmarks and the Role of Oxidative Stress.Antioxidants (Basel, Switzerland) · 2023
    Review
  12. Article
  13. AbioRxiv : the preprint server for biology · 2023
    Article
  14. Molecular basis of reproductive senescence: insights from model organisms.Journal of assisted reproduction and genetics · 2021
    Review
  15. Journal of developmental biology · 2020
    Review
  16. The proteostasis network and its decline in ageing.Nature reviews. Molecular cell biology · 2019
    Review
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Stephanie M ZimmermanDepartment of Genetics, Stanford University, Stanford, California, United States of America.
Izumi V HinksonDepartment of Chemical and Systems Biology, Stanford University, Stanford, California, United States of America.
Joshua E EliasDepartment of Chemical and Systems Biology, Stanford University, Stanford, California, United States of America.
Stuart K KimDepartment of Genetics, Stanford University, Stanford, California, United States of America.
Stanford University · US

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
Mechanisms of Aging in C. elegansR01AG025941 · NIA · STANFORD UNIVERSITY · PI DAVIS, RONALD WAYNE · 2007 to 2017
$3.1M
NIA NIH HHS R01 AG025941NIA NIH HHS R01AG025941NIH HHS ISI0OD01068001A1NIH HHS P40 OD010440
6 · The paper itself

Abstract

Aging in Caenorhabditis elegans is characterized by widespread physiological and molecular changes, but the mechanisms that determine the rate at which these changes occur are not well understood. In this study, we identify a novel link between reproductive aging and somatic aging in C. elegans. By measuring global age-related changes in the proteome, we identify a previously uncharacterized group of secreted proteins in the adult uterus that dramatically increase in abundance with age. This accumulation is blunted in animals with an extended reproductive period and accelerated in sterile animals lacking a germline. Uterine proteins are not removed in old post-reproductive animals or in young vulvaless worms, indicating that egg-laying is necessary for their rapid removal in wild-type young animals. Together, these results suggest that age-induced infertility contributes to extracellular protein accumulation in the uterus with age. Finally, we show that knocking down multiple age-increased proteins simultaneously extends lifespan. These results provide a mechanistic example of how the cessation of reproduction contributes to detrimental changes in the soma, and demonstrate how the timing of reproductive decline can influence the rate of aging.

Indexed as

AgingAnimalsCaenorhabditis elegansFemaleGerm CellsHumansLongevityReproductionUterus

Identifiers

PMID26656270
PMCPMC4676719
OpenAlexW2218106415

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.