Evidence map›Paper›PMID 24338818›Full record

ArticleAmerican journal of physiology. Renal physiology2014

ENaC activity is increased in isolated, split-open cortical collecting ducts from protein kinase Cα knockout mice.

Hui-Fang Bao, Tiffany L Thai, Qiang Yue, He-Ping Ma, Amity F Eaton, Hui Cai, Janet D Klein, Jeff M Sands, Douglas C Eaton

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

31 citing papers in PubMed, 39 citations in OpenAlex.

  1. Contribution of murine strain background to NabioRxiv : the preprint server for biology · 2026
    Article
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  4. PIPBiology · 2022
    Article
  5. Article
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  10. Regulating ENaC's gate.American journal of physiology. Cell physiology · 2020
    Review
  11. Article
  12. Article
  13. Article
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  15. Article
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  17. Article
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  19. Article
  20. Alveolar nonselective channels are ASIC1a/α-ENaC channels and contribute to AFC.American journal of physiology. Lung cellular and molecular physiology · 2017
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Hui-Fang BaoEmory Univ. School of Medicine, Dept. of Physiology, Whitehead Biomedical Research Bldg., 615 Michael St., Atlanta, GA 30322. deaton@emory.edu.
Tiffany L Thai
Qiang Yue
He-Ping Ma
Amity F Eaton
Hui Cai
Janet D Klein
Jeff M Sands
Douglas C Eaton
Emory University · US

Funding

REGULATION OF SODIUM IN TIGHT EPITHELIAR37DK037963 · NIDDK · EMORY UNIVERSITY · PI EATON, DOUGLAS C. · 2002 to 2011
$3.8M
Nephrology Institutional Training Grant FLSA SupplementT32DK007656 · NIDDK · EMORY UNIVERSITY · PI SANDS, JEFF M, WALL, SUSAN MARIE · 1990 to 2020
$3.5M
PATHOBIOLOGY OF MUCOSAL/EPITHELIAL DISEASET32DK007771 · NIDDK · EMORY UNIVERSITY · PI NEISH, ANDREW S · 1999 to 2015
$2.0M
Regulation of ENaC by Anionic PhospholipidsR01DK067110 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI MA, HE-PING · 2004 to 2012
$1.6M
Regulation of Urea Transport by PKC-alphaR01DK089828 · NIDDK · EMORY UNIVERSITY · PI SANDS, JEFF M · 2011 to 2014
$1.5M
NIDDK NIH HHS R01 DK067110NIDDK NIH HHS R01 DK089828NIDDK NIH HHS R01 DK89828NIDDK NIH HHS R37 DK037963NIDDK NIH HHS T32 DK007656NIDDK NIH HHS T32 DK007771NIDDK NIH HHS T32 DK07656
6 · The paper itself

Abstract

The epithelial Na channel (ENaC) is negatively regulated by protein kinase C (PKC) as shown using PKC activators in a cell culture model. To determine whether PKCα influences ENaC activity in vivo, we examined the regulation of ENaC in renal tubules from PKCα⁻/⁻ mice. Cortical collecting ducts were dissected and split open, and the exposed principal cells were subjected to cell-attached patch clamp. In the absence of PKCα, the open probability (P₀) of ENaC was increased three-fold vs. wild-type SV129 mice (0.52 ± 0.04 vs. 0.17 ± 0.02). The number of channels per patch was also increased. Using confocal microscopy, we observed an increase in membrane localization of α-, β-, and γ-subunits of ENaC in principal cells in the cortical collecting ducts of PKCα⁻/⁻ mice compared with wild-type mice. To confirm this increase, one kidney from each animal was perfused with biotin, and membrane protein was pulled down with streptavidin. The nonbiotinylated kidney was used to assess total protein. While total ENaC protein did not change in PKCα⁻/⁻ mice, membrane localization of all the ENaC subunits was increased. The increase in membrane ENaC could be explained by the observation that ERK1/2 phosphorylation was decreased in the knockout mice. These results imply a reduction in ENaC membrane accumulation and P₀ by PKCα in vivo. The PKC-mediated increase in ENaC activity was associated with an increase in blood pressure in knockout mice fed a high-salt diet.

Indexed as

AldosteroneAnimalsAquaporin 2Blood PressureEpithelial Sodium ChannelsKidney Tubules, CollectingMiceMice, KnockoutMicroscopy, ConfocalMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Patch-Clamp TechniquesPhosphorylationProtein Kinase C-alphaSodium Chloride, DietaryAldosteroneAqp2 protein, ratAquaporin 2Epithelial Sodium ChannelsMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Protein Kinase C-alphaSodium Chloride, DietaryENaChypertensionknockout miceprotein kinase Cαrenal tubulessingle channels

Identifiers

PMID24338818
PMCPMC3920049
OpenAlexW2329480915

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.