Evidence map›Paper›PMID 24419539›Full record

ArticlePflugers Archiv : European journal of physiology2014

Anoctamin 6 differs from VRAC and VSOAC but is involved in apoptosis and supports volume regulation in the presence of Ca2+.

C A Juul, S Grubb, K A Poulsen, T Kyed, N Hashem, I H Lambert, E H Larsen, E K Hoffmann

Open access · hybridAbstract read
In one paragraph

Article in Pflugers Archiv : European journal of 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
4.6field-weighted citation impact, top 4% 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. Article
  3. ANO10 Function in Health and Disease.Cerebellum (London, England) · 2023
    Review
  4. Review
  5. Article
  6. Structure-Function of TMEM16 Ion Channels and Lipid Scramblases.Advances in experimental medicine and biology · 2021
    Article
  7. Article
  8. CaFrontiers in cell and developmental biology · 2020
    Article
  9. Review
  10. Article
  11. CFTR supports cell death through ROS-dependent activation of TMEM16F (anoctamin 6).Pflugers Archiv : European journal of physiology · 2018
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Regulatory Roles of Anoctamin-6 in Human Trabecular Meshwork Cells.Investigative ophthalmology & visual science · 2017
    Article
  17. Relationship between TMEM16A/anoctamin 1 and LRRC8A.Pflugers Archiv : European journal of physiology · 2016
    Article
  18. ClEuropean biophysics journal : EBJ · 2016
    Article
  19. Ion channels in regulated cell death.Cellular and molecular life sciences : CMLS · 2016
    Review
  20. Non-essential contribution of LRRC8A to volume regulation.Pflugers Archiv : European journal of physiology · 2016
    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

8 authors at 1 institution in 1 country.

C A JuulDepartment of Biology, August Krogh Building, 13 Universitetsparken, 2100, Copenhagen Ø, Denmark.
S Grubb
K A Poulsen
T Kyed
N Hashem
I H Lambert
E H Larsen
E K Hoffmann
University of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anoctamin 6 (ANO6), also known as TMEM16F, has been shown to be a calcium-activated anion channel with delayed calcium activation. The cellular function of ANO6 is under debate, and different groups have come to different conclusions about ANO6's physiological role. Although it is now quite well established that ANO6 is distinct from the volume-regulated anion channel, it is still unclear whether ANO6 or other anoctamins can be activated by cell swelling. In this study, we suggest that ANO1, ANO6, and ANO10 do not contribute to the volume-activated current in ANO-overexpressing HEK293 cells. Furthermore, knock-down of ANO6 in Ehrlich ascites tumor cells (EATC) and Ehrlich-Lettre ascites (ELA) did not decrease but instead significantly increased swelling-activated membrane currents. Knock-down of ANO6 in EATC did not reduce regulatory volume decrease (RVD) in the absence of extracellular calcium, whereas it significantly reduced RVD in the presence of calcium. Interestingly, we found that knock-down of ANO6 in ELA cells resulted in a decrease in cisplatin-induced caspase-3 activity, confirming earlier findings that ANO6 is involved in apoptosis. Finally, knock-down of ANO1 and ANO6 did not affect the volume-sensitive release of taurine in ELA cells. Thus, our data provide evidence that ANO6 cannot be activated directly by cell swelling unless Ca(2+) is present. We also conclude that ANO6 carries a current during RVD, provided extracellular calcium is present. Thus, swelling activation of ANO6 requires the presence of free calcium.

Indexed as

ApoptosisCell SizeAnimalsAnoctamin-1AnoctaminsCalciumCaspase 3Cell Line, TumorChloride ChannelsHEK293 CellsHumansMicePhospholipid Transfer ProteinsTaurineANO1 protein, mouseANO6 protein, mouseAnoctamin-1AnoctaminsCalciumCaspase 3Chloride ChannelsPhospholipid Transfer ProteinsTaurine

Identifiers

PMID24419539
PMCPMC4159566
OpenAlexW2166080840

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.