Evidence map›Paper›PMID 26415569›Full record

ArticleThe Journal of general physiology2015

A novel Ca2+-feedback mechanism extends the operating range of mammalian rods to brighter light.

Frans Vinberg, Teemu T Turunen, Hanna Heikkinen, Marja Pitkänen, Ari Koskelainen

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of general physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Investigating the CaScientific reports · 2018
    Article
  5. Article
  6. Article
  7. The Binding Properties and Physiological Functions of Recoverin.Frontiers in molecular neuroscience · 2018
    Review
  8. 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.

Frans VinbergDepartment of Neuroscience and Biomedical Engineering, Aalto University School of Science, FI-00076 Aalto, Finland Department of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, MO 63110 ari.koskelainen@aalto.fi frans.vinberg@gmail.com.
Teemu T TurunenDepartment of Neuroscience and Biomedical Engineering, Aalto University School of Science, FI-00076 Aalto, Finland.
Hanna HeikkinenDepartment of Neuroscience and Biomedical Engineering, Aalto University School of Science, FI-00076 Aalto, Finland.
Marja PitkänenDepartment of Neuroscience and Biomedical Engineering, Aalto University School of Science, FI-00076 Aalto, Finland.
Ari KoskelainenDepartment of Neuroscience and Biomedical Engineering, Aalto University School of Science, FI-00076 Aalto, Finland ari.koskelainen@aalto.fi frans.vinberg@gmail.com.
Aalto University · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sensory cells adjust their sensitivity to incoming signals, such as odor or light, in response to changes in background stimulation, thereby extending the range over which they operate. For instance, rod photoreceptors are extremely sensitive in darkness, so that they are able to detect individual photons, but remain responsive to visual stimuli under conditions of bright ambient light, which would be expected to saturate their response given the high gain of the rod transduction cascade in darkness. These photoreceptors regulate their sensitivity to light rapidly and reversibly in response to changes in ambient illumination, thereby avoiding saturation. Calcium ions (Ca2+) play a major role in mediating the rapid, subsecond adaptation to light, and the Ca2+-binding proteins GCAP1 and GCAP2 (or guanylyl cyclase-activating proteins [GCAPs]) have been identified as important mediators of the photoreceptor response to changes in intracellular Ca2+. However, mouse rods lacking both GCAP1 and GCAP2 (GCAP-/-) still show substantial light adaptation. Here, we determined the Ca2+ dependency of this residual light adaptation and, by combining pharmacological, genetic, and electrophysiological tools, showed that an unknown Ca2+-dependent mechanism contributes to light adaptation in GCAP-/- mouse rods. We found that mimicking the light-induced decrease in intracellular [Ca2+] accelerated recovery of the response to visual stimuli and caused a fourfold decrease of sensitivity in GCAP-/- rods. About half of this Ca2+-dependent regulation of sensitivity could be attributed to the recoverin-mediated pathway, whereas half of it was caused by the unknown mechanism. Furthermore, our data demonstrate that the feedback mechanisms regulating the sensitivity of mammalian rods on the second and subsecond time scales are all Ca2+ dependent and that, unlike salamander rods, Ca2+-independent background-induced acceleration of flash response kinetics is rather weak in mouse rods.

Indexed as

Calcium SignalingFeedback, PhysiologicalAnimalsCells, CulturedGuanylate Cyclase-Activating ProteinsMiceMice, Inbred C57BLRetinal Rod Photoreceptor CellsGuanylate Cyclase-Activating ProteinsGuca1a protein, mouseGuca1b protein, mouse

Identifiers

PMID26415569
PMCPMC4586592
OpenAlexW2132882339

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.