Evidence map›Paper›PMID 24522391›Full record

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

Fibroblasts from long-lived rodent species exclude cadmium.

Lubomír Dostál, William M Kohler, James E Penner-Hahn, Richard A Miller, Carol A Fierke

Open access · bronzeAbstract 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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.8field-weighted citation impact, top 18% 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

5 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Fibroblasts From Longer-Lived Species of Primates, Rodents, Bats, Carnivores, and Birds Resist Protein Damage.The journals of gerontology. Series A, Biological sciences and medical sciences · 2015
    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 at 1 institution in 1 country.

Lubomír DostálDepartment of Chemistry, University of Michigan, Ann Arbor. Department of Pathology, University of Michigan, Ann Arbor.
William M KohlerDepartment of Pathology, University of Michigan, Ann Arbor.
James E Penner-HahnDepartment of Chemistry, University of Michigan, Ann Arbor. Department of Biophysics, University of Michigan, Ann Arbor.
Richard A MillerDepartment of Pathology, University of Michigan, Ann Arbor. Geriatrics Center, University of Michigan, Ann Arbor.
Carol A FierkeDepartment of Chemistry, University of Michigan, Ann Arbor. Department of Biological Chemistry, University of Michigan, Ann Arbor. fierke@umich.edu.
University of Michigan–Ann Arbor · US

Funding

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
STRUCTURE/FUNCTION OF ZINC METALLOPROTEINSR01GM040602 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI FIERKE, CAROL A · 1993 to 2017
$6.0M
Disruption of transition metal homeostasis by Cd: Implications for agingR21ES018993 · NIEHS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI FIERKE, CAROL A · 2010 to 2011
$417k
MUTAGENESIS TO PROBE CATALYSIS BY CARBONIC ANHYDRASE IIR29GM040602 · NIGMS · DUKE UNIVERSITY · PI FIERKE, CAROL A · 1988 to 1992
–
NIA NIH HHS AG000114NIA NIH HHS AG013283NIA NIH HHS AG023122NIA NIH HHS P30 AG013283NIA NIH HHS T32 AG000114NIA NIH HHS U19 AG023122NIEHS NIH HHS ES018993NIEHS NIH HHS R21 ES018993NIGMS NIH HHS GM40602NIGMS NIH HHS R01 GM040602
6 · The paper itself

Abstract

Resistance to the lethal effects of cellular stressors, including the toxic heavy metal cadmium (Cd), is characteristic of fibroblast cell lines derived from long-lived bird and rodent species, as well as cell lines from several varieties of long-lived mutant mice. To explore the mechanism of resistance to Cd, we used inductively coupled plasma mass spectroscopy to measure the rate of Cd uptake into primary fibroblasts of 15 rodent species. These data indicate that fibroblasts from long-lived rodent species have slower rates of Cd uptake from the extracellular medium than those from short-lived species. In addition, fibroblasts from short-lived species export more zinc after exposure to extracellular Cd than cells from long-lived species. Lastly, fibroblasts from long-lived rodent species have lower baseline concentrations of two redox-active metals, iron and copper. Our results suggest that evolution of longevity among rodents required adjustment of cellular properties to alter metal homeostasis and to reduce the toxic effects of heavy metals that accumulate over the course of a longer life span.

Indexed as

AnimalsBiological Transport, ActiveCadmiumCell LineCopperCricetinaeDrug ResistanceFibroblastsGuinea PigsHeavy Metal PoisoningIronLongevityMass SpectrometryMetals, HeavyMicePoisoningCadmiumCopperIronMetals, HeavyCadmiumIron.LongevityRodentsZinc

Identifiers

PMID24522391
PMCPMC4296162
OpenAlexW2100334756

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.