Evidence map›Paper›PMID 29304346›Full record

ArticleNeurobiology of aging2018

Nrf2 mediates the expression of BAG3 and autophagy cargo adaptor proteins and tau clearance in an age-dependent manner.

Maoping Tang, Changyi Ji, Susanne Pallo, Irfan Rahman, Gail V W Johnson

Abstract read
In one paragraph

Article in Neurobiology of aging, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 2 pooled it
2.2field-weighted citation impact, top 11% 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, 2 syntheses or guidelines pooled it, 60 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  5. Review
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  8. Article
  9. Article
  10. Aging, NRF2, and TAU: A Perfect Match for Neurodegeneration?Antioxidants (Basel, Switzerland) · 2023
    Review
  11. Article
  12. Review
  13. Review
  14. Insulin and aging - a disappointing relationship.Frontiers in endocrinology · 2023
    Review
  15. Article
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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

5 authors at 1 institution in 1 country.

Maoping TangDepartment of Anesthesiology, University of Rochester Medical Center, University of Rochester, Rochester, NY, USA.
Changyi JiDepartment of Anesthesiology, University of Rochester Medical Center, University of Rochester, Rochester, NY, USA.
Susanne PalloDepartment of Anesthesiology, University of Rochester Medical Center, University of Rochester, Rochester, NY, USA.
Irfan RahmanDepartment of Environmental Medicine, Lung Biology and Disease Program, University of Rochester Medical Center, University of Rochester, Rochester, NY, USA.
Gail V W JohnsonDepartment of Anesthesiology, University of Rochester Medical Center, University of Rochester, Rochester, NY, USA. Electronic address: gail_johnsonvoll@urmc.rochester.edu.
University of Rochester Medical Center · US

Funding

The degradation of tau by selective autophagyR01NS098769 · NINDS · UNIVERSITY OF ROCHESTER · PI JOHNSON, GAIL V. W. · 2017 to 2020
$1.8M
NINDS NIH HHS R01 NS098769
6 · The paper itself

Abstract

During aging, decreased efficiency of nuclear factor (erythroid-derived 2)-like 2 (Nrf2) activation and autophagic processes in the brain may be a contributing factor in the pathogenesis of neurodegenerative diseases such as Alzheimer's disease. Therefore, we analyzed the expression of Bcl-2-associated athanogene 3, a cochaperone that mediates autophagy, and the autophagy adaptors NBR1, NDP52, and sequestosome 1/p62 in the brains of 4-, 8-, and 12-month-old wild-type and Nrf2 knockout (-/-) mice. We also analyzed the levels of total tau and phospho-tau species. There were minimal differences in the expression of autophagy-related genes or tau species in 4-month-old animals; however, by 12 months, all of these autophagy-associated genes were expressed at significantly lower levels in the Nrf2 (-/-) mice. The decreases in the autophagy-associated genes were accompanied by significantly elevated levels of phospho-tau species in the 12-month-old Nrf2 (-/-) brains. These findings indicate that Nrf2 regulation of autophagy-related genes likely plays a greater role in mediating the clearance of tau as an organism ages.

Indexed as

Adaptor Proteins, Signal TransducingAgingAlzheimer DiseaseAnimalsApoptosis Regulatory ProteinsAutophagyAutophagy-Related ProteinsBrainGene ExpressionMice, Inbred C57BLMice, KnockoutNeurodegenerative DiseasesNF-E2-Related Factor 2tau ProteinsAdaptor Proteins, Signal TransducingApoptosis Regulatory ProteinsAutophagy-Related ProteinsBag3 protein, mouseNfe2l2 protein, mouseNF-E2-Related Factor 2tau ProteinsAutophagy adaptorsBAG3Nrf2Tau

Identifiers

PMID29304346
PMCPMC5801049
OpenAlexW2775143558

What OpenQuestion holds

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LicenceTDM
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.