Evidence map›Paper›PMID 23104560›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2013

Mechanosensitive Cl- secretion in biliary epithelium mediated through TMEM16A.

Amal K Dutta, Kangmee Woo, Al-karim Khimji, Charles Kresge, Andrew P Feranchak

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2013. 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
1.9field-weighted citation impact, top 15% 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, 55 citations in OpenAlex.

  1. Review
  2. Purinergic Signaling in Non-Parenchymal Liver Cells.International journal of molecular sciences · 2024
    Review
  3. The role of anoctamin 1 in liver disease.Journal of cellular and molecular medicine · 2024
    Review
  4. Article
  5. Article
  6. Article
  7. Mechanisms of endothelial flow sensing.Nature cardiovascular research · 2023
    Review
  8. Article
  9. PKC regulation of ion channels: The involvement of PIPThe Journal of biological chemistry · 2022
    Review
  10. The CleLife · 2022
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. A Bile Duct-on-a-Chip With Organ-Level Functions.Hepatology (Baltimore, Md.) · 2020
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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 1 institution in 1 country.

Amal K DuttaDepartment of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX 75390-9063, USA. amal.dutta@utsouthwestern.edu
Kangmee Woo
Al-karim Khimji
Charles Kresge
Andrew P Feranchak
The University of Texas Southwestern Medical Center · US

Funding

Mechanosensitive Signaling and Cholangiocyte SecretionR01DK078587 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI FERANCHAK, ANDREW P · 2008 to 2019
$3.6M
NIDDK NIH HHS DK-078587NIDDK NIH HHS R01 DK078587
6 · The paper itself

Abstract

Bile formation by the liver is initiated by canalicular transport at the hepatocyte membrane, leading to an increase in ductular bile flow. Thus, bile duct epithelial cells (cholangiocytes), which contribute to the volume and dilution of bile through regulated Cl(-) transport, are exposed to changes in flow and shear force at the apical membrane. The aim of the present study was to determine if fluid flow, or shear stress, is a signal regulating cholangiocyte transport. The results demonstrate that, in human and mouse biliary cells, fluid flow, or shear, increases Cl(-) currents and identify TMEM16A, a Ca(2+)-activated Cl(-) channel, as the operative channel. Furthermore, activation of TMEM16A by flow is dependent on PKCα through a process involving extracellular ATP, binding purinergic P2 receptors, and increases in intracellular Ca(2+) concentration. These studies represent the initial characterization of mechanosensitive Cl(-) currents mediated by TMEM16A. Identification of this novel mechanosensitive secretory pathway provides new insight into bile formation and suggests new therapeutic targets to enhance bile formation in the treatment of cholestatic liver disorders.

Indexed as

Adenosine TriphosphateAnimalsAnoctamin-1Biliary TractCalcium SignalingCell LineCell MembraneChloride ChannelsChloridesCystic Fibrosis Transmembrane Conductance RegulatorEpitheliumGene SilencingHumansMiceNeoplasm ProteinsPerfusionAdenosine TriphosphateANO1 protein, humanANO1 protein, mouseAnoctamin-1Chloride ChannelsChloridesCystic Fibrosis Transmembrane Conductance RegulatorNeoplasm ProteinsProtein Kinase C-alphaReceptors, Purinergic P2

Identifiers

PMID23104560
PMCPMC3543635
OpenAlexW2045002854

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.