Evidence map›Paper›PMID 20157567›Full record

ArticleAging2009

Dermal fibroblasts from long-lived Ames dwarf mice maintain their in vivo resistance to mitochondrial generated reactive oxygen species (ROS).

Ching-Chyuan Hsieh, John Papaconstantinou

Abstract read
In one paragraph

Article in Aging, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Healthspan and longevity can be extended by suppression of growth hormone signaling.Mammalian genome : official journal of the International Mammalian Genome Society · 2016
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Therapeutic targets in the ASK1-dependent stress signaling pathways.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2012
    Review
  15. Article
  16. Article
  17. Hepatic response to oxidative injury in long-lived Ames dwarf mice.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2011
    Article
  18. p66Shc aging protein in control of fibroblasts cell fate.International journal of molecular sciences · 2011
    Review
  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

2 authors.

Ching-Chyuan HsiehDepartment of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, Texas 77555, USA.
John Papaconstantinou

Funding

UTMB OAIC Research Education Component (REC)P30AG024832 · NIA · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI JAMES S. GOODWIN, MD, MELISSA M. MORROW · 2005 to 2026
$26.7M
OXIDATIVE STRESS,REPAIR OF OXIDIZED GUANINES IN AGED CELLSP01AG021830 · NIA · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI PAPACONSTANTINOU, JOHN NMN · 2004 to 2010
$6.4M
NIA NIH HHS 1P01 AG 021830NIA NIH HHS 1 P30 AG024832NIA NIH HHS P01 AG021830NIA NIH HHS P30 AG024832
6 · The paper itself

Abstract

Activation of p38 MAPK by ROS involves dissociation of an inactive, reduced thioredoxin-ASK1 complex [(SH)(2)Trx-ASK1]. Release of ASK1 activates its kinase activity thus stimulating the p38 MAPK pathway. The level of p38 MAPK activity is, therefore, regulated by the balance of free vs. bound ASK1. Longevity of Ames dwarf mice is attributed to their resistance to oxidative stress. The levels of (SH)(2) Trx-ASK1 are more abundant in young and old dwarf mice compared to their age-matched controls suggesting that the levels of this complex may play a role in their resistance to oxidative stress. In these studies we demonstrate that dermal fibroblasts from these long-lived mice exhibit (a) higher levels of (SH)(2)Trx-ASK1 that correlate with their resistance to ROS generated by inhibitors of electron transport chain complexes CI (rotenone), CII (3-nitropropionic acid), CIII, (antimycin A), and H(2)O(2)-mediated activation of p38 MAPK, and (b) maintain their in vivo resistance to ROS generated by 3NPA. We propose that elevated levels of (SH)(2)Trx-ASK1 play a role in conferring resistance to mitochondrial generated oxidative stress and decreased endogenous ROS which are characteristics of longevity determination.

Indexed as

AcetylcysteineActivating Transcription Factor 2AgingAnimalsAntimycin ACell ProliferationElectron Transport Chain Complex ProteinsEnzyme InhibitorsFibroblastsHydrogen PeroxideLongevityMaleMAP Kinase Kinase Kinase 5MiceMice, Inbred StrainsMice, Mutant Strains3-nitropropionic acidAcetylcysteineActivating Transcription Factor 2Antimycin AAtf2 protein, mouseElectron Transport Chain Complex ProteinsEnzyme InhibitorsHydrogen PeroxideMap3k5 protein, mouseMAP Kinase Kinase Kinase 5Nitro Compoundsp38 Mitogen-Activated Protein KinasesPropionatesReactive Oxygen SpeciesRotenoneThioredoxins3-nitropropionic acidagingAmes dwarf mouseantimycin AASK1dermal fibroblastsmitochondrial ROSp38 MAPKresistance to ROSrotenonethioredoxin

Identifiers

PMID20157567
PMCPMC2815737

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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.