Evidence map›Paper›PMID 26248058›Full record

ArticleBiochimica et biophysica acta2015

Age-related changes in the proteostasis network in the brain of the naked mole-rat: Implications promoting healthy longevity.

Judy C Triplett, Antonella Tramutola, Aaron Swomley, Jessime Kirk, Kelly Grimes, Kaitilyn Lewis, Miranda Orr, Karl Rodriguez, Jian Cai, Jon B Klein and 3 more

Open access · greenAbstract read
In one paragraph

Article in Biochimica et biophysica acta, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

37 citing papers in PubMed, 76 citations in OpenAlex.

  1. Eusocial reproduction selects for longevity.bioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. Review
  4. Heavy metal-induced disruption of the autophagy-lysosomal pathway: implications for aging and neurodegenerative disorders.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2025
    Review
  5. Review
  6. The Critical Role of Autophagy and Phagocytosis in the Aging Brain.International journal of molecular sciences · 2024
    Review
  7. Article
  8. Review
  9. Article
  10. Mechanisms of DNA Damage Response in Mammalian Oocytes.Advances in anatomy, embryology, and cell biology · 2024
    Review
  11. Proteostasis in T cell aging.Seminars in immunology · 2023
    Review
  12. The mTOR signaling pathway in cardiac aging.The journal of cardiovascular aging · 2023
    Article
  13. Review
  14. Article
  15. Mitophagy in the aging nervous system.Frontiers in cell and developmental biology · 2022
    Review
  16. Review
  17. Review
  18. Molecular and cellular pathways contributing to brain aging.Behavioral and brain functions : BBF · 2021
    Review
  19. DNA Homeostasis and Senescence: Lessons from the Naked Mole Rat.International journal of molecular sciences · 2021
    Review
  20. Regulation of Age-Related Protein Toxicity.Frontiers in cell and developmental biology · 2021
    Review
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

13 authors at 4 institutions in 2 countries.

Judy C TriplettDepartment of Chemistry, University of Kentucky, Lexington, KY 40506, United States.
Antonella TramutolaDepartment of Biochemical Sciences, Sapienza University of Rome, Piazzale Aldo Moro 5, 00185 Rome, Italy.
Aaron SwomleyDepartment of Chemistry, University of Kentucky, Lexington, KY 40506, United States.
Jessime KirkDepartment of Chemistry, University of Kentucky, Lexington, KY 40506, United States.
Kelly GrimesSam and Ann Barshop Institute for Longevity and Aging Studies, University of Texas Health Science Center, San Antonio, TX 78245, United States; Department of Physiology, University of Texas Health Science Center, San Antonio, TX 78245, United States.
Kaitilyn LewisSam and Ann Barshop Institute for Longevity and Aging Studies, University of Texas Health Science Center, San Antonio, TX 78245, United States; Department of Cellular and Structural Biology, University of Texas Health Science Center, San Antonio, TX 78245, United States.
Miranda OrrSam and Ann Barshop Institute for Longevity and Aging Studies, University of Texas Health Science Center, San Antonio, TX 78245, United States; Department of Physiology, University of Texas Health Science Center, San Antonio, TX 78245, United States.
Karl RodriguezSam and Ann Barshop Institute for Longevity and Aging Studies, University of Texas Health Science Center, San Antonio, TX 78245, United States; Department of Physiology, University of Texas Health Science Center, San Antonio, TX 78245, United States.
Jian CaiDepartment of Nephrology and Proteomics Center, University of Louisville, Louisville, KY 40202, United States.
Jon B KleinDepartment of Nephrology and Proteomics Center, University of Louisville, Louisville, KY 40202, United States.
Marzia PerluigiDepartment of Biochemical Sciences, Sapienza University of Rome, Piazzale Aldo Moro 5, 00185 Rome, Italy.
Rochelle BuffensteinSam and Ann Barshop Institute for Longevity and Aging Studies, University of Texas Health Science Center, San Antonio, TX 78245, United States; Department of Physiology, University of Texas Health Science Center, San Antonio, TX 78245, United States. Electronic address: Buffenstein@UTHSCSA.edu.
D Allan ButterfieldDepartment of Chemistry, University of Kentucky, Lexington, KY 40506, United States; Sanders-Brown Center on Aging, University of Kentucky, Lexington, KY 40506, United States. Electronic address: dabcns@uky.edu.
The University of Texas Health Science Center at San Antonio · USUniversity of Kentucky · USSapienza University of Rome · ITUniversity of Louisville · US

Funding

TRAINING GRANT ON THE BIOLOGY OF AGINGT32AG021890 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Erzsebet Kokovay, JAMES FLOYD NELSON · 2003 to 2026
$11.4M
The role of the small molecular chaperone HSP25 in longevity and healthy agingK99AG049940 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI RODRIGUEZ, KARL A · 2015 to 2016
$194k
NIA NIH HHS K99 AG049940NIA NIH HHS T32 AG021890
6 · The paper itself

Abstract

The naked mole-rat (NMR) is the longest-lived rodent and possesses several exceptional traits: marked cancer resistance, negligible senescence, prolonged genomic integrity, pronounced proteostasis, and a sustained health span. The underlying molecular mechanisms that contribute to these extraordinary attributes are currently under investigation to gain insights that may conceivably promote and extend human health span and lifespan. The ubiquitin-proteasome and autophagy-lysosomal systems play a vital role in eliminating cellular detritus to maintain proteostasis and have been previously shown to be more robust in NMRs when compared with shorter-lived rodents. Using a 2-D PAGE proteomics approach, differential expression and phosphorylation levels of proteins involved in proteostasis networks were evaluated in the brains of NMRs in an age-dependent manner. We identified 9 proteins with significantly altered levels and/or phosphorylation states that have key roles involved in proteostasis networks. To further investigate the possible role that autophagy may play in maintaining cellular proteostasis, we examined aspects of the PI3K/Akt/mammalian target of rapamycin (mTOR) axis as well as levels of Beclin-1, LC3-I, and LC3-II in the brain of the NMR as a function of age. Together, these results show that NMRs maintain high levels of autophagy throughout the majority of their lifespan and may contribute to the extraordinary health span of these rodents. The potential of augmenting human health span via activating the proteostasis network will require further studies.

Indexed as

AgingmTORNaked mole-ratPhosphoproteomicsProteomicsProteostasis networks

Identifiers

PMID26248058
PMCPMC4845741
OpenAlexW1104912482

What OpenQuestion holds

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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.