Evidence map›Paper›PMID 26582472›Full record

ArticleAmerican journal of physiology. Cell physiology2016

Phosphorylation of rat kidney Na-K pump at Ser938 is required for rapid angiotensin II-dependent stimulation of activity and trafficking in proximal tubule cells.

Katherine J Massey, Quanwen Li, Noreen F Rossi, Susan M Keezer, Raymond R Mattingly, Douglas R Yingst

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.2field-weighted citation impact, top 42% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Stimulation of NaOxidative medicine and cellular longevity · 2019
    Article
  8. Impaired NaExperimental & molecular medicine · 2018
    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

6 authors at 3 institutions in 1 country.

Katherine J MasseyDepartment of Physiology, School of Medicine, Wayne State University, Detroit, Michigan;
Quanwen LiDepartment of Pharmacology, School of Medicine, Wayne State University, Detroit, Michigan;
Noreen F RossiDepartment of Physiology, School of Medicine, Wayne State University, Detroit, Michigan; Department of Internal Medicine, School of Medicine, Wayne State University, Detroit, Michigan; John D. Dingell Veterans Affairs Medical Center, Detroit, Michigan.
Susan M KeezerCell Signaling Technology, Danvers, Massachusetts; and.
Raymond R MattinglyDepartment of Pharmacology, School of Medicine, Wayne State University, Detroit, Michigan;
Douglas R YingstDepartment of Physiology, School of Medicine, Wayne State University, Detroit, Michigan; dyingst@med.wayne.edu.
Wayne State University · USCell Signaling Technology (United States) · USJohn D. Dingell VA Medical Center · US

Funding

Neural Control of Sodium Balance in Hypertension: ExerciseR01HL079102 · NHLBI · WAYNE STATE UNIVERSITY · PI ROSSI, NOREEN F · 2005 to 2009
$1.6M
Regulation of Ras through the Ras GRF exchange factorR01CA081150 · NCI · WAYNE STATE UNIVERSITY · PI MATTINGLY, RAYMOND R · 2001 to 2005
$1.0M
Mechanisms of Renal Na+ Pump Stimulation by AngiotensinR01DK060752 · NIDDK · WAYNE STATE UNIVERSITY · PI YINGST, DOUGLAS R · 2002 to 2005
$918k
NCI NIH HHS R01 CA-81150NHLBI NIH HHS 1R01 HL-079102NIDDK NIH HHS R01DK-60752
6 · The paper itself

Abstract

How angiotensin (ANG) II acutely stimulates the Na-K pump in proximal tubules is only partially understood, limiting insight into how ANG II increases blood pressure. First, we tested whether ANG II increases the number of pumps in plasma membranes of native rat proximal tubules under conditions of rapid activation. We found that exposure to 100 pM ANG II for 2 min, which was previously shown to increase affinity of the Na-K pump for Na and stimulate activity threefold, increased the amount of the Na-K pump in plasma membranes of native tubules by 33%. Second, we tested whether previously observed increases in phosphorylation of the Na-K pump at Ser(938) were part of the stimulatory mechanism. These experiments were carried out in opossum kidney cells, cultured proximal tubules stably coexpressing the ANG type 1 (AT1) receptor, and either wild-type or a S938A mutant of rat kidney Na-K pump under conditions found by others to stimulate activity. We found that 10 min of incubation in 10 pM ANG II stimulated activity of wild-type pumps from 2.3 to 3.5 nmol K · mg protein(-1) · min(-1) and increased the amount of the pump in the plasma membrane by 80% but had no effect on cells expressing the S938A mutant. We conclude that acute stimulation of Na-K pump activity in native rat proximal tubules includes increased trafficking to the plasma membrane and that phosphorylation at Ser(938) is part of the mechanism by which ANG II directly stimulates activity and trafficking of the rat kidney Na-K pump in opossum kidney cells.

Indexed as

Angiotensin IIAnimalsCell LineCell MembraneCyclic AMP-Dependent Protein KinasesEnzyme ActivationKidney Tubules, ProximalMaleMutationOpossumsPhosphorylationProtein Kinase CProtein TransportRats, Sprague-DawleyReceptor, Angiotensin, Type 1SerineAngiotensin IIAtp1a1 protein, ratCyclic AMP-Dependent Protein KinasesProtein Kinase CReceptor, Angiotensin, Type 1SerineSodium-Potassium-Exchanging ATPaseNa-K-ATPaseprotein kinase Aprotein kinase C

Identifiers

PMID26582472
PMCPMC4888522
OpenAlexW2287737296

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.