Evidence map›Paper›PMID 25070662›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2015

Fibroblasts From Longer-Lived Species of Primates, Rodents, Bats, Carnivores, and Birds Resist Protein Damage.

Andrew M Pickering, Marcus Lehr, William J Kohler, Melissa L Han, Richard A Miller

Abstract read
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–field-weighted citation impact
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

23 citing papers in PubMed.

  1. Review
  2. Bats as instructive animal models for studying longevity and aging.Annals of the New York Academy of Sciences · 2024
    Review
  3. Review
  4. Review
  5. Article
  6. A new approach method for characterizing inter-species toxicodynamic variability.Journal of toxicology and environmental health. Part A · 2021
    Article
  7. Article
  8. Review
  9. Growth hormone and aging.Reviews in endocrine & metabolic disorders · 2021
    Review
  10. Article
  11. Aggresome-Like Formation Promotes Resistance to Proteotoxicity in Cells from Long-Lived Species.The journals of gerontology. Series A, Biological sciences and medical sciences · 2020
    Article
  12. Review
  13. Article
  14. Cause or casualty: The role of mitochondrial DNA in aging and age-associated disease.Biochimica et biophysica acta. Molecular basis of disease · 2019
    Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  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

5 authors.

Andrew M PickeringDepartment of Pathology and Geriatrics Center, University of Michigan, Ann Arbor.
Marcus LehrDepartment of Pathology and Geriatrics Center, University of Michigan, Ann Arbor.
William J KohlerDepartment of Pathology and Geriatrics Center, University of Michigan, Ann Arbor.
Melissa L HanDepartment of Pathology and Geriatrics Center, University of Michigan, Ann Arbor.
Richard A MillerDepartment of Pathology and Geriatrics Center, University of Michigan, Ann Arbor. millerr@umich.edu.

Funding

The Southwest National Primate Research Center Supplement- Infrastructure improvements of ABSL2 holding areasP51OD011133 · OD · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI Larry S. Schlesinger · 2012 to 2026
$129.7M
Systems BiologyU19AG023122 · NIA · TRANSLATIONAL GENOMICS RESEARCH INST · PI Thomas Girke, NICHOLAS Joseph SCHORK · 2004 to 2026
$102.6M
Research Training in BiogerontologyT32AG000114 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SCOTT PLETCHER · 1985 to 2026
$12.4M
Research DevelopmentP30AG013283 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MILLER, RICHARD A · 1995 to 2014
$12.3M
Comparative Cell Biology of Aging: Proteostasis Control in Long- and Short-Lived SpeciesF32AG049555 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PICKERING, ANDREW MICHAEL · 2015 to 2016
$75k
NIA NIH HHS AG013283NIA NIH HHS AG023122NIA NIH HHS F32 AG049555NIA NIH HHS P30 AG013283NIA NIH HHS T32 AG000114NIA NIH HHS U19 AG023122NIH HHS P51 OD011133
6 · The paper itself

Abstract

Species differ greatly in their rates of aging. Among mammalian species life span ranges from 2 to over 60 years. Here, we test the hypothesis that skin-derived fibroblasts from long-lived species of animals differ from those of short-lived animals in their defenses against protein damage. In parallel studies of rodents, nonhuman primates, birds, and species from the Laurasiatheria superorder (bats, carnivores, shrews, and ungulates), we find associations between species longevity and resistance of proteins to oxidative stress after exposure to H(2)O(2) or paraquat. In addition, baseline levels of protein carbonyl appear to be higher in cells from shorter-lived mammals compared with longer-lived mammals. Thus, resistance to protein oxidation is associated with species maximal life span in independent clades of mammals, suggesting that this cellular property may be required for evolution of longevity. Evaluation of the properties of primary fibroblast cell lines can provide insights into the factors that regulate the pace of aging across species of mammals.

Indexed as

AnimalsBirdsCarnivoraCell Culture TechniquesChiropteraFibroblastsHydrogen PeroxideLongevityOxidantsOxidative StressPrimatesProteolysisRodentiaSpecies SpecificityHydrogen PeroxideOxidantsAgingComparative biologyKey Words:Oxidative stress.

Identifiers

PMID25070662
PMCPMC4481684

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.