Evidence map›Paper›PMID 30068331›Full record

ArticleBMC biology2018

Species comparison of liver proteomes reveals links to naked mole-rat longevity and human aging.

Ivonne Heinze, Martin Bens, Enrico Calzia, Susanne Holtze, Oleksandr Dakhovnik, Arne Sahm, Joanna M Kirkpatrick, Karol Szafranski, Natalie Romanov, Sai Nagender Sama and 6 more

Abstract read
In one paragraph

Article in BMC biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing 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

41 citing papers in PubMed.

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  10. Chaotic aging: intrinsically disordered proteins in aging-related processes.Cellular and molecular life sciences : CMLS · 2023
    Article
  11. Biomarkers of aging.Science China. Life sciences · 2023
    Review
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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

16 authors.

Ivonne HeinzeLeibniz Institute on Aging - Fritz Lipmann Institute (FLI), Jena, Germany.
Martin BensLeibniz Institute on Aging - Fritz Lipmann Institute (FLI), Jena, Germany.
Enrico CalziaInstitute of Anesthesiological Pathophysiology and Process Engineering, University of Ulm, Ulm, Germany.
Susanne HoltzeLeibniz Institute for Zoo and Wildlife Research (IZW), Berlin, Germany.
Oleksandr DakhovnikLeibniz Institute on Aging - Fritz Lipmann Institute (FLI), Jena, Germany.
Arne SahmLeibniz Institute on Aging - Fritz Lipmann Institute (FLI), Jena, Germany.
Joanna M KirkpatrickLeibniz Institute on Aging - Fritz Lipmann Institute (FLI), Jena, Germany.
Karol SzafranskiLeibniz Institute on Aging - Fritz Lipmann Institute (FLI), Jena, Germany.
Natalie RomanovStructural and Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg, Germany.
Sai Nagender SamaLeibniz Institute on Aging - Fritz Lipmann Institute (FLI), Jena, Germany.
Kerstin HolzerInstitute of Pathology, University Medicine Greifswald, Greifswald, Germany.
Stephan SingerInstitute of Pathology, University Medicine Greifswald, Greifswald, Germany.
Maria ErmolaevaLeibniz Institute on Aging - Fritz Lipmann Institute (FLI), Jena, Germany.
Matthias PlatzerLeibniz Institute on Aging - Fritz Lipmann Institute (FLI), Jena, Germany. matthias.platzer@leibniz-fli.de.
Thomas HildebrandtLeibniz Institute for Zoo and Wildlife Research (IZW), Berlin, Germany. HILDEBRAND@izw-berlin.de.
Alessandro OriLeibniz Institute on Aging - Fritz Lipmann Institute (FLI), Jena, Germany. alessandro.ori@leibniz-fli.de.ORCID 0000-0002-3046-0871

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMammals display a wide range of variation in their lifespan. Investigating the molecular networks that distinguish long- from short-lived species has proven useful to identify determinants of longevity. Here, we compared the livers of young and old long-lived naked mole-rats (NMRs) and the phylogenetically closely related, shorter-lived, guinea pigs using an integrated omics approach.

resultsWe found that NMR livers display a unique expression pattern of mitochondrial proteins that results in distinct metabolic features of their mitochondria. For instance, we observed a generally reduced respiration rate associated with lower protein levels of respiratory chain components, particularly complex I, and increased capacity to utilize fatty acids. Interestingly, we show that the same molecular networks are affected during aging in both NMRs and humans, supporting a direct link to the extraordinary longevity of both species. Finally, we identified a novel detoxification pathway linked to longevity and validated it experimentally in the nematode Caenorhabditis elegans.

conclusionsOur work demonstrates the benefits of integrating proteomic and transcriptomic data to perform cross-species comparisons of longevity-associated networks. Using a multispecies approach, we show at the molecular level that livers of NMRs display progressive age-dependent changes that recapitulate typical signatures of aging despite the negligible senescence and extraordinary longevity of these rodents.

Indexed as

AgingLongevityProteomeAdultAgedAged, 80 and overAnimalsCaenorhabditis elegansGuinea PigsHumansLiverMaleMiddle AgedMole RatsSpecies SpecificityProteome

Identifiers

PMID30068331
PMCPMC6090990

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Registered trials

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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.