Evidence map›Paper›PMID 27903584›Full record

ArticleAmerican journal of physiology. Cell physiology2017

Src-independent ERK signaling through the rat α3 isoform of Na/K-ATPase.

Namrata Madan, Yunhui Xu, Qiming Duan, Moumita Banerjee, Isabel Larre, Sandrine V Pierre, Zijian Xie

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2017. 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
2.8field-weighted citation impact, top 9% 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

21 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
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  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Synthesis and Biological Evaluation of Novel Bufalin Derivatives.International journal of molecular sciences · 2022
    Article
  10. Article
  11. Role of endogenous ouabain in the etiology of bipolar disorder.International journal of bipolar disorders · 2021
    Review
  12. Article
  13. NaInternational journal of molecular sciences · 2020
    Article
  14. Decreased NaScientific reports · 2020
    Article
  15. Ouabain Enhances Cell-Cell Adhesion Mediated by βInternational journal of molecular sciences · 2019
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

7 authors at 2 institutions in 2 countries.

Namrata MadanMarshall Institute for Interdisciplinary Research, Marshall University, Huntington, West Virginia.
Yunhui XuMarshall Institute for Interdisciplinary Research, Marshall University, Huntington, West Virginia.
Qiming DuanGladstone Institute of Cardiovascular Disease, San Francisco, California.
Moumita BanerjeeMarshall Institute for Interdisciplinary Research, Marshall University, Huntington, West Virginia.
Isabel LarreMarshall Institute for Interdisciplinary Research, Marshall University, Huntington, West Virginia.
Sandrine V PierreMarshall Institute for Interdisciplinary Research, Marshall University, Huntington, West Virginia.
Zijian XieMarshall Institute for Interdisciplinary Research, Marshall University, Huntington, West Virginia; xiez@marshall.edu.
Marshall University · USGladstone Institutes · US

Funding

Receptor Na/K-ATPase Antagonists As Novel Therapeutics For Renal/Cardiac DiseasesR01HL109015 · NHLBI · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI SHAPIRO, JOSEPH ISAAC, XIE, ZIJIAN · 2011 to 2014
$2.2M
NHLBI NIH HHS R01 HL109015
6 · The paper itself

Abstract

The Na/K-ATPase α1 polypeptide supports both ion-pumping and signaling functions. The Na/K-ATPase α3 polypeptide differs from α1 in both its primary structure and its tissue distribution. The expression of α3 seems particularly important in neurons, and recent clinical evidence supports a unique role of this isoform in normal brain function. The nature of this specific role of α3 has remained elusive, because the ubiquitous presence of α1 has hindered efforts to characterize α3-specific functions in mammalian cell systems. Using Na/K-ATPase α1 knockdown pig kidney cells (PY-17), we generated the first stable mammalian cell line expressing a ouabain-resistant form of rat Na/K-ATPase α3 in the absence of endogenous pig α1 detectable by Western blotting. In these cells, Na/K-ATPase α3 formed a functional ion-pumping enzyme and rescued the expression of Na/K-ATPase β1 and caveolin-1 to levels comparable with those observed in PY-17 cells rescued with a rat Na/K-ATPase α1 (AAC-19). The α3-containing enzymes had lower Na

Indexed as

AnimalsCell LineCell ProliferationIon Channel GatingKidneyMAP Kinase Signaling SystemProtein IsoformsRatsSodiumSodium-Potassium-Exchanging ATPasesrc-Family KinasesStem CellsAtp1a1 protein, ratProtein IsoformsSodiumSodium-Potassium-Exchanging ATPasesrc-Family Kinasescaveolinextracellular‐signal‐regulated kinase (ERK)Na+/K+-ATPasephosphatidylinositide 3‐kinase (PI 3‐kinase)signal transductionSrc

Identifiers

PMID27903584
PMCPMC5401946
OpenAlexW2559062783

What OpenQuestion holds

Textmetadata
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.