Evidence map›Paper›PMID 30822304›Full record

ArticlePLoS biology2019

Rods contribute to the light-induced phase shift of the retinal clock in mammals.

Hugo Calligaro, Christine Coutanson, Raymond P Najjar, Nadia Mazzaro, Howard M Cooper, Nasser Haddjeri, Marie-Paule Felder-Schmittbuhl, Ouria Dkhissi-Benyahya

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

27 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
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  10. The physiological role of TRP channels in sleep and circadian rhythm.Journal of cellular and molecular medicine · 2024
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  15. IMI 2023 Digest.Investigative ophthalmology & visual science · 2023
    Article
  16. Review
  17. Article
  18. The Role of GJD2(Cx36) in Refractive Error Development.Investigative ophthalmology & visual science · 2022
    Review
  19. Review
  20. Photoreceptor Degeneration in Homozygous Male Per2Journal of biological rhythms · 2021
    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 6 institutions in 2 countries.

Hugo CalligaroUniv Lyon, Université Claude Bernard Lyon 1, Inserm, Stem Cell and Brain Research Institute, Bron, France.
Christine CoutansonUniv Lyon, Université Claude Bernard Lyon 1, Inserm, Stem Cell and Brain Research Institute, Bron, France.
Raymond P NajjarVisual Neurosciences Research Group, Singapore Eye Research Institute, Singapore.
Nadia MazzaroCNRS UPR3212, Institut des Neurosciences Cellulaires et Intégratives, Université de Strasbourg, Strasbourg, France.
Howard M CooperUniv Lyon, Université Claude Bernard Lyon 1, Inserm, Stem Cell and Brain Research Institute, Bron, France.
Nasser HaddjeriUniv Lyon, Université Claude Bernard Lyon 1, Inserm, Stem Cell and Brain Research Institute, Bron, France.
Marie-Paule Felder-SchmittbuhlCNRS UPR3212, Institut des Neurosciences Cellulaires et Intégratives, Université de Strasbourg, Strasbourg, France.
Ouria Dkhissi-BenyahyaUniv Lyon, Université Claude Bernard Lyon 1, Inserm, Stem Cell and Brain Research Institute, Bron, France.
Institut Cellule Souche et Cerveau · FRUniversité Claude Bernard Lyon 1 · FRDuke-NUS Medical School · SGInserm · FRInstitut des Neurosciences Cellulaires et Intégratives · FRUniversité de Strasbourg · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While rods, cones, and intrinsically photosensitive melanopsin-containing ganglion cells (ipRGCs) all drive light entrainment of the master circadian pacemaker of the suprachiasmatic nucleus, recent studies have proposed that entrainment of the mouse retinal clock is exclusively mediated by a UV-sensitive photopigment, neuropsin (OPN5). Here, we report that the retinal circadian clock can be phase shifted by short duration and relatively low-irradiance monochromatic light in the visible part of the spectrum, up to 520 nm. Phase shifts exhibit a classical photon dose-response curve. Comparing the response of mouse models that specifically lack middle-wavelength (MW) cones, melanopsin, and/or rods, we found that only the absence of rods prevented light-induced phase shifts of the retinal clock, whereas light-induced phase shifts of locomotor activity are normal. In a "rod-only" mouse model, phase shifting response of the retinal clock to light is conserved. At shorter UV wavelengths, our results also reveal additional recruitment of short-wavelength (SW) cones and/or OPN5. These findings suggest a primary role of rod photoreceptors in the light response of the retinal clock in mammals.

Indexed as

LightAnimalsCircadian ClocksCircadian RhythmFemaleMaleMammalsMembrane ProteinsMiceOpsinsRetinaRetinal Cone Photoreceptor CellsReverse Transcriptase Polymerase Chain ReactionTemperatureMembrane ProteinsOPN5 protein, mouseOpsins

Identifiers

PMID30822304
PMCPMC6415865
OpenAlexW2918699434

What OpenQuestion holds

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LicenceCC BY
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.