Evidence map›Paper›PMID 23395376›Full record

ArticleNeuron2013

Apoptosis regulates ipRGC spacing necessary for rods and cones to drive circadian photoentrainment.

Shih-Kuo Chen, Kylie S Chew, David S McNeill, Patrick W Keeley, Jennifer L Ecker, Buqing Q Mao, Johan Pahlberg, Bright Kim, Sammy C S Lee, Michael A Fox and 6 more

Abstract read
In one paragraph

Article in Neuron, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

  1. Article
  2. Article
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  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Complement Targets Newborn Retinal Ganglion Cells for Phagocytic Elimination by Microglia.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  15. Ocular Clocks: Adapting Mechanisms for Eye Functions and Health.Investigative ophthalmology & visual science · 2018
    Review
  16. External light activates hair follicle stem cells through eyes via an ipRGC-SCN-sympathetic neural pathway.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Shih-Kuo ChenDepartment of Biology, Johns Hopkins University, Baltimore, MD 21218, USA.
Kylie S Chew
David S McNeill
Patrick W Keeley
Jennifer L Ecker
Buqing Q Mao
Johan Pahlberg
Bright Kim
Sammy C S Lee
Michael A Fox
William Guido
Kwoon Y Wong
Alapakkam P Sampath
Benjamin E Reese
Rejji Kuruvilla
Samer Hattar

Funding

VIVARIUM MODULEP30EY007003 · NEI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Peter F Hitchcock · 1987 to 2026
$17.6M
FUNCTIONAL STATE OF DEVELOPING RETINOGENICULATE SYNAPSER01EY012716 · NEI · VIRGINIA COMMONWEALTH UNIVERSITY · PI GUIDO, WILLIAM · 2001 to 2021
$6.9M
Development of Retinal Bipolar CellsR01EY019968 · NEI · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI REESE, BENJAMIN E · 2010 to 2023
$4.9M
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 nuclei-specific retinogeniculate targetingR01EY021222 · NEI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI FOX, MICHAEL A · 2011 to 2021
$3.8M
Functional characteristics of rod pathways in the retinaR01EY017606 · NEI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI SAMPATH, ALAPAKKAM P · 2006 to 2015
$3.7M
Neurotrophin mechanisms in neural development and diseaseR01NS073751 · NINDS · JOHNS HOPKINS UNIVERSITY · PI KURUVILLA, REJJI · 2011 to 2015
$1.7M
Crosstalk between neurotrophin and Wnt signaling pathways in neuronal developmentR01MH080738 · NIMH · JOHNS HOPKINS UNIVERSITY · PI KURUVILLA, REJJI · 2007 to 2011
$1.5M
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
Cross-talk between ganglion-cell photoreceptors and other neurons in the retinaR00EY018863 · NEI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WONG, KWOON Y. · 2010 to 2012
$700k
NEI NIH HHS EY012716NEI NIH HHS P30 EY007003NEI NIH HHS P30-EY007003NEI NIH HHS R00 EY018863NEI NIH HHS R00-EY18863NEI NIH HHS R01 EY012716NEI NIH HHS R01 EY017606NEI NIH HHS R01 EY019053NEI NIH HHS R01-EY019053NEI NIH HHS R01 EY019968NEI NIH HHS R01-EY019968NEI NIH HHS R01 EY021222NEI NIH HHS R01-EY021222NEI NIH HHS R01-EY17606NIGMS NIH HHS R01 GM076430NIGMS NIH HHS R01-GM076430NIMH NIH HHS R01 MH080738NIMH NIH HHS R01-MH080738NINDS NIH HHS R01 NS073751
6 · The paper itself

Abstract

The retina consists of ordered arrays of individual types of neurons for processing vision. Here, we show that such order is necessary for intrinsically photosensitive retinal ganglion cells (ipRGCs) to function as irradiance detectors. We found that during development, ipRGCs undergo proximity-dependent Bax-mediated apoptosis. Bax mutant mice exhibit disrupted ipRGC spacing and dendritic stratification with an increase in abnormally localized synapses. ipRGCs are the sole conduit for light input to circadian photoentrainment, and either their melanopsin-based photosensitivity or ability to relay rod/cone input is sufficient for circadian photoentrainment. Remarkably, the disrupted ipRGC spacing does not affect melanopsin-based circadian photoentrainment but severely impairs rod/cone-driven photoentrainment. We demonstrate reduced rod/cone-driven cFos activation and electrophysiological responses in ipRGCs, suggesting that impaired synaptic input to ipRGCs underlies the photoentrainment deficits. Thus, for irradiance detection, developmental apoptosis is necessary for the spacing and connectivity of ipRGCs that underlie their functioning within a neural network.

Indexed as

Action PotentialsAlcohol OxidoreductasesAnimalsApoptosisBasic Helix-Loop-Helix Proteinsbcl-2-Associated X Proteinbcl-2 Homologous Antagonist-Killer ProteinBiophysical PhenomenaCircadian RhythmCo-Repressor ProteinsDNA-Binding ProteinsFemaleGene Expression RegulationGreen Fluorescent ProteinsIn Situ Nick-End LabelingIn Vitro TechniquesAlcohol OxidoreductasesAtoh7 protein, mouseBak1 protein, mouseBasic Helix-Loop-Helix ProteinsBax protein, mousebcl-2-Associated X Proteinbcl-2 Homologous Antagonist-Killer ProteinBsn protein, mouseCo-Repressor ProteinsCtbp2 protein, mouseDNA-Binding ProteinsGreen Fluorescent ProteinsMelanopsinNerve Tissue ProteinsPhosphoproteinsProto-Oncogene Proteins c-fosRod OpsinsTyrosine 3-Monooxygenase

Identifiers

PMID23395376
PMCPMC3569737

What OpenQuestion holds

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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.