Evidence map›Paper›PMID 19828801›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2009

Rbpj cell autonomous regulation of retinal ganglion cell and cone photoreceptor fates in the mouse retina.

Amy N Riesenberg, Zhenyi Liu, Raphael Kopan, Nadean L Brown

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

63 citing papers in PubMed, 102 citations in OpenAlex.

  1. Article
  2. Article
  3. Development of Retinal Astroglia.Annual review of vision science · 2025
    Review
  4. Expression status transition ofF1000Research · 2025
    Article
  5. Article
  6. A framework to identify functional interactors that contribute to disrupted early retinal development in Vsx2 ocular retardation J mice.Developmental dynamics : an official publication of the American Association of Anatomists · 2023
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Retinal regeneration requires dynamic Notch signaling.Neural regeneration research · 2022
    Review
  12. Review
  13. Review
  14. Article
  15. Genetic control of retinal ganglion cell genesis.Cellular and molecular life sciences : CMLS · 2021
    Review
  16. Article
  17. Article
  18. Review
  19. TheProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  20. Recapitulating developmental mechanisms for retinal regeneration.Progress in retinal and eye research · 2020
    Review

3 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 1 country.

Amy N RiesenbergDivision of Developmental Biology, Cincinnati Children's Research Foundation, University of Cincinnati College of Medicine, Cincinnati, Ohio 45229, USA.
Zhenyi Liu
Raphael Kopan
Nadean L Brown
Washington University in St. Louis · USUniversity of Cincinnati · US

Funding

BIOCHEMICAL AND GENETIC ANALYSIS OF NOTCH SIGNALINGR01GM055479 · NIGMS · WASHINGTON UNIVERSITY · PI KOPAN, RAPHAEL, WEIRAUCH, MATTHEW TYSON · 1996 to 2021
$6.4M
INVESTIGATION OF MAMMALIAN RETINAL NEURON DEVELOPMENTR01EY013612 · NEI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI BROWN, NADEAN L · 2001 to 2020
$6.0M
ROLE OF NOTCH AND KIDNEY DEVELOPMENTR01DK066408 · NIDDK · WASHINGTON UNIVERSITY · PI KOPAN, RAPHAEL · 2004 to 2012
$3.4M
Cell-Cell Signaling During Mammalian Early Eye FormationR01EY018097 · NEI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI BROWN, NADEAN L · 2008 to 2016
$2.6M
Mapping Notch 1 Activation in MiceR01HD044056 · NICHD · WASHINGTON UNIVERSITY · PI KOPAN, RAPHAEL · 2003 to 2007
$1.7M
NEI NIH HHS EY13612NEI NIH HHS EY18097NEI NIH HHS R01 EY013612NEI NIH HHS R01 EY018097NICHD NIH HHS HD44056NICHD NIH HHS R01 HD044056NIDDK NIH HHS DK66408NIDDK NIH HHS R01 DK066408NIGMS NIH HHS GM55479NIGMS NIH HHS R01 GM055479
6 · The paper itself

Abstract

Vertebrate retinal progenitor cells (RPCs) are pluripotent, but pass through competence states that progressively restrict their developmental potential (Cepko et al., 1996; Livesey and Cepko, 2001; Cayouette et al., 2006). In the rodent eye, seven retinal cell classes differentiate in overlapping waves, with RGCs, cone photoreceptors, horizontals, and amacrines forming predominantly before birth, and rod photoreceptors, bipolars, and Müller glia differentiating postnatally. Both intrinsic and extrinsic factors regulate each retinal cell type (for review, see Livesey and Cepko, 2001). Here, we conditionally deleted the transcription factor Rbpj, a critical integrator of multiple Notch signals (Jarriault et al., 1995; Honjo, 1996; Kato et al., 1997; Han et al., 2002), during prenatal mouse retinal neurogenesis. Removal of Rbpj caused reduced proliferation, premature neuronal differentiation, apoptosis, and profound mispatterning. To determine the cell autonomous requirements for Rbpj during RGC and cone formation, we marked Cre-generated retinal lineages with GFP expression, which showed that Rbpj autonomously promotes RPC mitotic activity, and suppresses RGC and cone fates. In addition, the progressive loss of Rbpj-/- RPCs resulted in a diminished progenitor pool available for rod photoreceptor formation. This circumstance, along with the overproduction of Rbpj-/- cones, revealed that photoreceptor development is under homeostatic regulation. Finally, to understand how the Notch pathway regulates the simultaneous formation of multiple cell types, we compared the RGC and cone phenotypes of Rbpj to Notch1 (Jadhav et al., 2006b; Yaron et al., 2006), Notch3, and Hes1 mutants. We found particular combinations of Notch pathway genes regulate the development of each retinal cell type.

Indexed as

AnimalsAnimals, NewbornBasic Helix-Loop-Helix ProteinsCell DifferentiationCell ProliferationDisease Models, AnimalEmbryo, MammalianEye Diseases, HereditaryGene Expression Regulation, DevelopmentalGreen Fluorescent ProteinsHomeodomain ProteinsImmunoglobulin J Recombination Signal Sequence-Binding ProteinMiceMice, TransgenicMutationNerve Tissue ProteinsAtoh7 protein, mouseBasic Helix-Loop-Helix ProteinsGreen Fluorescent ProteinsHelt protein, mouseHomeodomain ProteinsImmunoglobulin J Recombination Signal Sequence-Binding ProteinNerve Tissue ProteinsNotch3 protein, mousePou4f2 protein, mouseRbpj protein, mouseReceptor, Notch3Receptors, NotchRepressor ProteinsTranscription Factor Brn-3BTranscription FactorsVsx2 protein, mouse

Identifiers

PMID19828801
PMCPMC2788434
OpenAlexW2059678501

What OpenQuestion holds

Textmetadata
LicenceTDM
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.