Evidence map›Paper›PMID 23048038›Full record

ArticleThe Journal of biological chemistry2012

Regulation of Na(+)/K(+)-ATPase by nuclear respiratory factor 1: implication in the tight coupling of neuronal activity, energy generation, and energy consumption.

Kaid Johar, Anusha Priya, Margaret T T Wong-Riley

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. CytochromeFrontiers in physiology · 2019
    Review
  8. Article
  9. Metabolic reprogramming during neuronal differentiation.Cell death and differentiation · 2016
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Transcriptional regulators of Na,K-ATPase subunits.Frontiers in cell and developmental biology · 2015
    Review
  16. Article
  17. 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

3 authors at 1 institution in 1 country.

Kaid JoharDepartment of Cell Biology, Neurobiology, and Anatomy, Medical College of Wisconsin, Milwaukee, WI 53226, USA.
Anusha Priya
Margaret T T Wong-Riley
Medical College of Wisconsin · US

Funding

Rresearch Training Program in Vision ScienceT32EY014537 · NEI · MEDICAL COLLEGE OF WISCONSIN · PI Elena V Semina · 2002 to 2026
$4.2M
Neurochemical and Metabolic Regulation in the Visual CortexR01EY018441 · NEI · MEDICAL COLLEGE OF WISCONSIN · PI WONG-RILEY, MARGARET TT · 2007 to 2013
$2.4M
NEI NIH HHS R01 EY018441NEI NIH HHS R01EY018441NEI NIH HHS T32 EY014537NEI NIH HHS T32-EY14537
6 · The paper itself

Abstract

backgroundNRF-1 regulates mediators of neuronal activity and energy generation.

resultsNRF-1 transcriptionally regulates Na(+)/K(+)-ATPase subunits α1 and β1.

conclusionNRF-1 functionally regulates mediators of energy consumption in neurons. SIGNIFICANCE: NRF-1 mediates the tight coupling of neuronal activity, energy generation, and energy consumption at the molecular level. Energy generation and energy consumption are tightly coupled to neuronal activity at the cellular level. Na(+)/K(+)-ATPase, a major energy-consuming enzyme, is well expressed in neurons rich in cytochrome c oxidase, an important enzyme of the energy-generating machinery, and glutamatergic receptors that are mediators of neuronal activity. The present study sought to test our hypothesis that the coupling extends to the molecular level, whereby Na(+)/K(+)-ATPase subunits are regulated by the same transcription factor, nuclear respiratory factor 1 (NRF-1), found recently by our laboratory to regulate all cytochrome c oxidase subunit genes and some NMDA and AMPA receptor subunit genes. By means of multiple approaches, including in silico analysis, electrophoretic mobility shift and supershift assays, in vivo chromatin immunoprecipitation, promoter mutational analysis, and real-time quantitative PCR, NRF-1 was found to functionally bind to the promoters of Atp1a1 and Atp1b1 genes but not of the Atp1a3 gene in neurons. The transcripts of Atp1a1 and Atp1b1 subunit genes were up-regulated by KCl and down-regulated by tetrodotoxin. Atp1b1 is positively regulated by NRF-1, and silencing of NRF-1 with small interference RNA blocked the up-regulation of Atp1b1 induced by KCl, whereas overexpression of NRF-1 rescued these transcripts from being suppressed by tetrodotoxin. On the other hand, Atp1a1 is negatively regulated by NRF-1. The binding sites of NRF-1 on Atp1a1 and Atp1b1 are conserved among mice, rats, and humans. Thus, NRF-1 regulates key Na(+)/K(+)-ATPase subunits and plays an important role in mediating the tight coupling between energy consumption, energy generation, and neuronal activity at the molecular level.

Indexed as

Energy MetabolismGene Expression Regulation, EnzymologicAnimalsBase SequenceBinding SitesCell Line, TumorHeLa CellsHumansMiceMolecular Sequence DataNeuronsNuclear Respiratory Factor 1Promoter Regions, GeneticProtein BindingRatsSodium-Potassium-Exchanging ATPaseAtp1a1 protein, mouseAtp1b1 protein, mouseNuclear Respiratory Factor 1Sodium-Potassium-Exchanging ATPase

Identifiers

PMID23048038
PMCPMC3504753
OpenAlexW2008402547

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.