Evidence map›Paper›PMID 27336410›Full record

ArticleCellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology2016

STIM1fl/fl Ksp-Cre Mouse has Impaired Renal Water Balance.

Liudmila Cebotaru, Valeriu Cebotaru, Hua Wang, Lois J Arend, William B Guggino

Open access · goldAbstract read
In one paragraph

Article in Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Store-operated calcium entry: Pivotal roles in renal physiology and pathophysiology.Experimental biology and medicine (Maywood, N.J.) · 2021
    Review
  4. 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

5 authors at 2 institutions in 1 country.

Liudmila CebotaruDivision of Gastroenterology, Department of Medicine, Division of Nephrology, University of Maryland, Baltimore, USA.
Valeriu Cebotaru
Hua Wang
Lois J Arend
William B Guggino
Johns Hopkins University · USUniversity of Maryland, Baltimore · US

Funding

Research BaseP30DK090868 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI WATNICK, TERRY J · 2010 to 2019
$11.1M
MECHANISMS OF TRANSPORT IN PROXIMAL AND DISTAL TUBULESR01DK032753 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI GUGGINO, WILLIAM B. · 1986 to 2011
$3.7M
Role of PC1, Pc2 and HDAC6 in cyst formation in ADPKDK08DK103078 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI CEBOTARU, VALERIU · 2014 to 2018
$779k
NIDDK NIH HHS K08 DK103078NIDDK NIH HHS P30 DK090868NIDDK NIH HHS R01 DK032753
6 · The paper itself

Abstract

BACKGROUND/

aimSTIM1 is as an essential component in store operated Ca2+ entry. However give the paucity of information on the role of STIM1 in kidney, the aim was to study the function of STIM1 in the medulla of the kidney.

methodswe crossed a Ksp-cre mouse with another mouse containing two loxP sites flanking Exon 6 of STIM1. The Ksp-cre mouse is based upon the Ksp-cadherin gene promoter which expresses cre recombinase in developing nephrons, collecting ducts (SD) and thick ascending limbs (TAL) of the loop of Henle.

resultsThe offspring of these mice are viable without gross morphological changes, however, we noticed that the STIM1 Ksp-cre knockout mice produced more urine compared to control. To examine this more carefully, we fed mice low (LP) and high protein (HP) diets respectively. When mice were fed HP diet STIM1 ko mice had significantly increased urinary volume and lower specific gravity compared to wt mice. In STIM1 ko mice fed HP diet urine creatinine and urea were significantly lower compared to wt mice fed HP diet, however the fractional excretion was the same.

conclusionThese data support the idea that STIM1 ko mice have impaired urinary concentrating ability when challenged with HP diet is most likely caused by impaired Ca2+-dependent signal transduction through the vasopressin receptor cascade.

Indexed as

AnimalsCalciumCreatinineDietary ProteinsKidneyKidney Concentrating AbilityKinesinsMice, KnockoutMice, TransgenicRenal InsufficiencyStromal Interaction Molecule 1UreaUrinationWaterWater-Electrolyte BalanceCalciumCreatinineDietary ProteinsKif11 protein, mouseKinesinsStim1 protein, mouseStromal Interaction Molecule 1UreaWater

Identifiers

PMID27336410
PMCPMC4938254
OpenAlexW2462464620

What OpenQuestion holds

Textmetadata
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.