Evidence map›Paper›PMID 27466368›Full record

ArticleThe Journal of biological chemistry2016

Aldosterone Upregulates Transient Receptor Potential Melastatin 7 (TRPM7).

William C Valinsky, Anna Jolly, Perrine Miquel, Rhian M Touyz, Alvin Shrier

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Observational
  3. Review
  4. Article
  5. Review
  6. Article
  7. Steroids and TRP Channels: A Close Relationship.International journal of molecular sciences · 2020
    Review
  8. Article
  9. Article
  10. TRPM7, Magnesium, and Signaling.International journal of molecular sciences · 2019
    Review
  11. Magnesium-sensitive upstream ORF controls PRL phosphatase expression to mediate energy metabolism.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  12. Article
  13. Aldosterone, SGK1, and ion channels in the kidney.Clinical science (London, England : 1979) · 2018
    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

5 authors at 2 institutions in 2 countries.

William C ValinskyFrom the Department of Physiology, McGill University, Montreal, Quebec H3G 0B1, Canada and.
Anna JollyFrom the Department of Physiology, McGill University, Montreal, Quebec H3G 0B1, Canada and.
Perrine MiquelFrom the Department of Physiology, McGill University, Montreal, Quebec H3G 0B1, Canada and.
Rhian M Touyzthe Institute of Cardiovascular and Medical Sciences, University of Glasgow, BHF GCRC, 126 University Place, Glasgow G12 8TA, United Kingdom.ORCID 0000-0003-0670-0887
Alvin ShrierFrom the Department of Physiology, McGill University, Montreal, Quebec H3G 0B1, Canada and alvin.shrier@mcgill.ca.ORCID 0000-0002-6133-4931
McGill University · CAUniversity of Glasgow · GB

Funding

British Heart Foundation RG/13/7/30099
6 · The paper itself

Abstract

Transient receptor potential melastatin 7 (TRPM7) is a ubiquitously expressed Mg(2+)-permeable ion channel fused to a C-terminal α-kinase domain. Recently, aldosterone was shown to increase intracellular Mg(2+) levels and alter inflammatory signaling in TRPM7-expressing HEK293 cells. This study was undertaken to assess whether these effects were related to an aldosterone-mediated increase of TRPM7 current and/or plasma membrane localization. Using HEK293 cells stably expressing WT-TRPM7, we found that 18-h application of aldosterone significantly increased TRPM7 current and TRPM7 plasma membrane protein expression by 48% and 34%, respectively. The aldosterone-mediated increase of TRPM7 current was inhibited by eplerenone, a mineralocorticoid receptor (MR) blocker, and GSK-650394, an inhibitor of the serum- and glucocorticoid-regulated kinase 1 (SGK1). SGK1 blockade also prevented the aldosterone-induced increase of TRPM7 plasma membrane protein. It was further determined that K1648R-TRPM7, the phosphotransferase-inactive TRPM7 mutant, was unresponsive to aldosterone. Therefore, chronic aldosterone treatment increases the plasma membrane expression of TRPM7, which is associated with an increase of TRPM7 current. This process occurs via an MR-dependent, genomic signaling cascade involving SGK1 and a functioning TRPM7 α-kinase domain. We suggest that this mechanism may be of general relevance when interpreting the effects of aldosterone because the MR receptor is found in multiple tissues, and TRPM7 and SGK1 are ubiquitously expressed.

Indexed as

AldosteroneBenzoatesBridged Bicyclo Compounds, HeterocyclicEplerenoneHEK293 CellsHumansImmediate-Early ProteinsProtein DomainsProtein Serine-Threonine KinasesReceptors, MineralocorticoidSerum-Glucocorticoid Regulated KinasesSignal TransductionSpironolactoneTRPM Cation ChannelsUp-Regulation2-cyclopentyl-4-(5-phenyl-1H-pyrrolo(2,3-b)pyridin-3-yl)-benzoic acidAldosteroneBenzoatesBridged Bicyclo Compounds, HeterocyclicEplerenoneImmediate-Early ProteinsProtein Serine-Threonine KinasesReceptors, MineralocorticoidSerum-Glucocorticoid Regulated KinasesSpironolactoneTRPM7 protein, humanTRPM Cation Channelsaldosteroneelectrophysiologymineralocorticoid receptorplasma membraneSGK1transient receptor potential channels (TRP channels)α-kinase

Identifiers

PMID27466368
PMCPMC5025699
OpenAlexW2481786269

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.