Evidence map›Paper›PMID 11479341›Full record

ArticleThe Journal of general physiology2001

The relationship between cAMP, Ca(2)+, and transport of CFTR to the plasma membrane.

P Chen, T C Hwang, K D Gillis

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of general physiology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Molecular motors and apical CFTR traffic in epithelia.International journal of molecular sciences · 2013
    Review
  3. Differential effects of lysophospholipids on exocytosis in rat PC12 cells.Journal of neural transmission (Vienna, Austria : 1996) · 2010
    Article
  4. PKC epsilon facilitates recovery of exocytosis after an exhausting stimulation.Pflugers Archiv : European journal of physiology · 2009
    Article
  5. Article
  6. Article
  7. Twenty odd years of stretch-sensitive channels.Pflugers Archiv : European journal of physiology · 2006
    Review
  8. Article
  9. CFTR chloride channels are regulated by a SNAP-23/syntaxin 1A complex.Proceedings of the National Academy of Sciences of the United States of America · 2002
    Article
  10. The number of K(+) channels in the plasma membrane of guard cell protoplasts changes in parallel with the surface area.Proceedings of the National Academy of Sciences of the United States of America · 2002
    Article
  11. 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

3 authors at 1 institution in 1 country.

P ChenDepartment of Electrical Engineering, University of Missouri-Columbia, Columbia, MO 65211, USA.
T C Hwang
K D Gillis
University of Missouri · US

Funding

MOLECULAR PATHOPHYSIOLOGY OF CYSTIC FIBROSISR01DK055835 · NIDDK · UNIVERSITY OF MISSOURI-COLUMBIA · PI HWANG, TZYH-CHANG · 1999 to 2022
$6.1M
NIDDK NIH HHS R01 DK055835NIDDK NIH HHS R01 DK55835
6 · The paper itself

Abstract

The mechanism whereby cAMP stimulates Cl(-) flux through CFTR ion channels in secretory epithelia remains controversial. It is generally accepted that phosphorylation by cAMP-dependent protein kinase increases the open probability of the CFTR channel. A more controversial hypothesis is that cAMP triggers the translocation of CFTR from an intracellular pool to the cell surface. We have monitored membrane turnover in Calu-3 cells, a cell line derived from human airway submucosal glands that expresses high levels of CFTR using membrane capacitance and FM1-43 fluorescence measurements. Using a conventional capacitance measurement technique, we observe an apparent increase in membrane capacitance in most cells that exhibit an increase in Cl(-) current. However, after we carefully correct our recordings for changes in membrane conductance, the apparent changes in capacitance are eliminated. Measurements using the fluorescent membrane marker FM1-43 also indicate that no changes in membrane turnover accompany the activation of CFTR. Robust membrane insertion can be triggered with photorelease of caged Ca(2)+ in Calu-3 cells. However, no increase in Cl(-) current accompanies Ca(2)+-evoked membrane fusion. We conclude that neither increases in cAMP or Ca(2)+ lead to transport of CFTR to the plasma membrane in Calu-3 cells. In addition, we conclude that membrane capacitance measurements must be interpreted with caution when large changes in membrane conductance occur.

Indexed as

Biological TransportCalciumCell LineCell MembraneCyclic AMPCystic Fibrosis Transmembrane Conductance RegulatorElectric ConductivityExocytosisFluorescent DyesHumansPatch-Clamp TechniquesPhotic StimulationPhotolysisPyridinium CompoundsQuaternary Ammonium CompoundsRespiratory Mucosa(2-nitrophenyl)ethyl-cyclic adenosine monophosphateCalciumCFTR protein, humanCyclic AMPCystic Fibrosis Transmembrane Conductance RegulatorFluorescent DyesFM1 43Pyridinium CompoundsQuaternary Ammonium Compounds

Identifiers

PMID11479341
PMCPMC2233831
OpenAlexW2116657787

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.