Evidence map›Paper›PMID 28617242›Full record

ArticleeLife2017

A subset of ipRGCs regulates both maturation of the circadian clock and segregation of retinogeniculate projections in mice.

Kylie S Chew, Jordan M Renna, David S McNeill, Diego C Fernandez, William T Keenan, Michael B Thomsen, Jennifer L Ecker, Gideon S Loevinsohn, Cassandra VanDunk, Daniel C Vicarel and 8 more

Abstract read
In one paragraph

Article in eLife, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 1 pooled it
–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

55 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Prolonged Light Exposure Induces Long-Lasting Retinal Wave Plasticity via Retrograde Melanopsin-Dopamine Signaling.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
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  14. Article
  15. Flp-recombinase mouse line for genetic manipulation of ipRGCs.bioRxiv : the preprint server for biology · 2024
    Article
  16. A newbioRxiv : the preprint server for biology · 2024
    Article
  17. Article
  18. Review
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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

18 authors.

Kylie S ChewDepartment of Biology, Johns Hopkins University, Baltimore, United States.ORCID 0000-0003-4752-009X
Jordan M RennaDepartment of Biology, Program in Integrated Bioscience, The University of Akron, Akron, United States.
David S McNeillDepartment of Biology, Johns Hopkins University, Baltimore, United States.
Diego C FernandezDepartment of Biology, Johns Hopkins University, Baltimore, United States.
William T KeenanDepartment of Biology, Johns Hopkins University, Baltimore, United States.ORCID 0000-0003-3381-744X
Michael B ThomsenDepartment of Biology, Johns Hopkins University, Baltimore, United States.
Jennifer L EckerDepartment of Biology, Johns Hopkins University, Baltimore, United States.
Gideon S LoevinsohnDepartment of Neuroscience, Brown University, Providence, United States.
Cassandra VanDunkDepartment of Anatomy and Neurobiology, Washington University, St. Louis, United States.
Daniel C VicarelDepartment of Biology, Program in Integrated Bioscience, The University of Akron, Akron, United States.
Adele TuffordCellular Neurobiology Research Unit, Institut De Recherches Cliniques De Montréal, Montreal, Canada.
Shijun WengDepartment of Neuroscience, Brown University, Providence, United States.
Paul A GrayDepartment of Anatomy and Neurobiology, Washington University, St. Louis, United States.
Michel CayouetteCellular Neurobiology Research Unit, Institut De Recherches Cliniques De Montréal, Montreal, Canada.
Erik D HerzogDepartment of Biology, Washington University, St. Louis, United States.
Haiqing ZhaoDepartment of Biology, Johns Hopkins University, Baltimore, United States.
David M BersonDepartment of Neuroscience, Brown University, Providence, United States.
Samer HattarDepartment of Biology, Johns Hopkins University, Baltimore, United States.ORCID 0000-0002-3124-9525

Funding

Section on Light and Circadian RhythmsZIAMH002964 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI HATTAR, SAMER · 2017 to 2025
$24.1M
CELLULAR AND MOLECULAR BIOLOGYT32GM007231 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI VAN DOREN, MARK B · 1985 to 2020
$18.4M
STRUCTURE AND FUNCTION OF MAMMALIAN GANGLION CELLSR01EY012793 · NEI · BROWN UNIVERSITY · PI BERSON, DAVID M. · 2000 to 2022
$9.3M
Role of mammalian retinal photoreceptors in non-image-forming visual functionsR01GM076430 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI ZHAO, HAIQING · 2005 to 2018
$4.8M
Regulation of Olfactory Signal TransductionR01DC007395 · NIDCD · JOHNS HOPKINS UNIVERSITY · PI ZHAO, HAIQING · 2008 to 2016
$3.5M
Biology of Photosensitive Ganglion CellsR01EY017137 · NEI · BROWN UNIVERSITY · PI BERSON, DAVID M. · 2006 to 2014
$2.9M
GENETIC ORGANIZATION OF RESPIRATORY CIRCUITS IN MOUSE BRAINSTEMR01HL089742 · NHLBI · WASHINGTON UNIVERSITY · PI GRAY, PAUL ANDREW · 2009 to 2013
$2.1M
NEURONAL EXCITABILITY IN THE REGULATION OF CIRCADIAN RHYTHMSR01GM104991 · NIGMS · WASHINGTON UNIVERSITY · PI HERZOG, ERIK, NERBONNE, JEANNE M. · 2013 to 2016
$1.2M
Molecular characterization of mouse melanopsin and second messenger pathway.R01EY019053 · NEI · UNIVERSITY OF MARYLAND BALTIMORE COUNTY · PI ROBINSON, PHYLLIS R · 2009 to 2012
$1.2M
Melanopsin Ganglion Cell DevelopmentR15EY026255 · NEI · UNIVERSITY OF AKRON · PI RENNA, JORDAN MICHAEL · 2016 to 2016
$456k
ipRGC participation and modulation of retinal wave activityF32EY020108 · NEI · BROWN UNIVERSITY · PI RENNA, JORDAN MICHAEL · 2010 to 2012
$159k
CIHR MOP-77570NEI NIH HHS F32 EY020108NEI NIH HHS R01 EY012793NEI NIH HHS R01 EY017137NEI NIH HHS R01 EY019053NEI NIH HHS R15 EY026255NHLBI NIH HHS R01 HL089742NIDCD NIH HHS R01 DC007395NIGMS NIH HHS R01 GM076430NIGMS NIH HHS R01 GM104991NIGMS NIH HHS T32 GM007231
6 · The paper itself

Abstract

The visual system consists of two major subsystems, image-forming circuits that drive conscious vision and non-image-forming circuits for behaviors such as circadian photoentrainment. While historically considered non-overlapping, recent evidence has uncovered crosstalk between these subsystems. Here, we investigated shared developmental mechanisms. We revealed an unprecedented role for light in the maturation of the circadian clock and discovered that intrinsically photosensitive retinal ganglion cells (ipRGCs) are critical for this refinement process. In addition, ipRGCs regulate retinal waves independent of light, and developmental ablation of a subset of ipRGCs disrupts eye-specific segregation of retinogeniculate projections. Specifically, a subset of ipRGCs, comprising ~200 cells and which project intraretinally and to circadian centers in the brain, are sufficient to mediate both of these developmental processes. Thus, this subset of ipRGCs constitute a shared node in the neural networks that mediate light-dependent maturation of the circadian clock and light-independent refinement of retinogeniculate projections.

Indexed as

Circadian ClocksLightAnimalsMiceMice, KnockoutRetinaRetinal Ganglion CellsVisual Pathwaysaxonal refinementcircadianipRGClateral geniculate nucleusmelanopsinmouseneurosciencesuprachiasmatic nucleus

Identifiers

PMID28617242
PMCPMC5513697

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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.