Evidence map›Paper›PMID 24030149›Full record

ArticleCell death & disease2013

Loss of Pde6 reduces cell body Ca(2+) transients within photoreceptors.

E Y Ma, A Lewis, P Barabas, G Stearns, S Suzuki, D Krizaj, S E Brockerhoff

Abstract read
In one paragraph

Article in Cell death & disease, 2013. 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
–field-weighted citation impact
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.

  1. Article
  2. Biochemistry and physiology of zebrafish photoreceptors.Pflugers Archiv : European journal of physiology · 2021
    Review
  3. Metabolism in the Zebrafish Retina.Journal of developmental biology · 2021
    Review
  4. Review
  5. Increasing CaCell death and differentiation · 2020
    Article
  6. Review
  7. Article
  8. Article
  9. Endoplasmic reticulum (ER) CaThe Journal of biological chemistry · 2017
    Article
  10. Mitochondria Maintain Distinct CaThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  11. Review
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

7 authors.

E Y MaDepartment of Biochemistry, University of Washington, Seattle, WA 98195, USA.
A Lewis
P Barabas
G Stearns
S Suzuki
D Krizaj
S E Brockerhoff

Funding

Vision Research CoreP30EY001730 · NEI · UNIVERSITY OF WASHINGTON · PI MAUREEN E NEITZ · 1985 to 2026
$23.5M
University of Utah, Core Vision Research GrantP30EY014800 · NEI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI PAUL STEVEN BERNSTEIN · 2005 to 2026
$14.6M
In Vivo Analysis of the Developing Vertebrate RetinaR01EY014358 · NEI · WASHINGTON UNIVERSITY · PI WONG, RACHEL O · 2003 to 2016
$4.3M
REGULATION OF NEUROTRANSMISSION IN THE RETINAR01EY013870 · NEI · UNIVERSITY OF UTAH · PI KRIZAJ, DAVID · 2002 to 2011
$2.7M
Photoreceptor degeneration and rescue in zebrafishR01EY018814 · NEI · UNIVERSITY OF WASHINGTON · PI BROCKERHOFF, SUSAN E · 2009 to 2012
$1.9M
The role of mechanosensation in the vertebrate retinaR01EY022076 · NEI · UNIVERSITY OF UTAH · PI KRIZAJ, DAVID · 2013 to 2017
$1.9M
NEI NIH HHS EY014800NEI NIH HHS EY022076NEI NIH HHS P30 EY001730NEI NIH HHS P30EY001730NEI NIH HHS P30 EY014800NEI NIH HHS R01 EY013870NEI NIH HHS R01 EY014358NEI NIH HHS R01 EY018814NEI NIH HHS R01 EY022076NEI NIH HHS R01 EY13870NEI NIH HHS R01 EY14358
6 · The paper itself

Abstract

Modulation of Ca(2+) within cells is tightly regulated through complex and dynamic interactions between the plasma membrane and internal compartments. In this study, we exploit in vivo imaging strategies based on genetically encoded Ca(2+) indicators to define changes in perikaryal Ca(2+) concentration of intact photoreceptors. We developed double-transgenic zebrafish larvae expressing GCaMP3 in all cones and tdTomato in long-wavelength cones to test the hypothesis that photoreceptor degeneration induced by mutations in the phosphodiesterase-6 (Pde6) gene is driven by excessive [Ca(2+)]i levels within the cell body. Arguing against Ca(2+) overload in Pde6 mutant photoreceptors, simultaneous analysis of cone photoreceptor morphology and Ca(2+) fluxes revealed that degeneration of pde6c(w59) mutant cones, which lack the cone-specific cGMP phosphodiesterase, is not associated with sustained increases in perikaryal [Ca(2+)]i. Analysis of [Ca(2+)]i in dissociated Pde6β(rd1)mouse rods shows conservation of this finding across vertebrates. In vivo, transient and Pde6-independent Ca(2+) elevations ('flashes') were detected throughout the inner segment and the synapse. As the mutant cells proceeded to degenerate, these Ca(2+) fluxes diminished. This study thus provides insight into Ca(2+) dynamics in a common form of inherited blindness and uncovers a dramatic, light-independent modulation of [Ca(2+)]i that occurs in normal cones.

Indexed as

Calcium SignalingAnimalsAnimals, Genetically ModifiedCell DeathCyclic Nucleotide Phosphodiesterases, Type 6ElectroretinographyLightMiceMutationRetinal Cone Photoreceptor CellsRetinal Rod Photoreceptor CellsZebrafishZebrafish ProteinsCyclic Nucleotide Phosphodiesterases, Type 6Pde6b protein, mousePde6c protein, zebrafishZebrafish Proteins

Identifiers

PMID24030149
PMCPMC3789190

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.