Evidence map›Paper›PMID 19474320›Full record

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

Distinct effects of Hedgehog signaling on neuronal fate specification and cell cycle progression in the embryonic mouse retina.

Kiyo Sakagami, Lin Gan, Xian-Jie Yang

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 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

41 citing papers in PubMed, 70 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Temporal Transcriptomic Profiling of the DevelopingbioRxiv : the preprint server for biology · 2024
    Article
  6. Review
  7. Article
  8. Genetic control of retinal ganglion cell genesis.Cellular and molecular life sciences : CMLS · 2021
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. The circadian clock geneFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  14. Retinal Ganglion Cell Replacement: Current Status and Challenges Ahead.Developmental dynamics : an official publication of the American Association of Anatomists · 2019
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

3 authors at 2 institutions in 1 country.

Kiyo SakagamiJules Stein Eye Institute and Department of Ophthalmology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California 90095, USA.
Lin Gan
Xian-Jie Yang
University of California, Los Angeles · USUniversity of Rochester · US

Funding

Math5 Regulatory Pathway in Retinal DevelopmentR01EY013426 · NEI · UNIVERSITY OF ROCHESTER · PI GAN, LIN · 2001 to 2010
$2.9M
CYTOKINE SIGNAL TRANSDUCTION IN RETINAL DEVELOPMENTR01EY012270 · NEI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI YANG, XIAN-JIE · 2000 to 2008
$2.7M
Hedgehog Signaling in Photoreceptor Differentiation and MaintenanceR01EY019052 · NEI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI YANG, XIAN-JIE · 2010 to 2013
$1.5M
NEI NIH HHS R01 EY012270NEI NIH HHS R01 EY013426NEI NIH HHS R01 EY019052
6 · The paper itself

Abstract

Cell-extrinsic signals can profoundly influence the production of various neurons from common progenitors. Yet mechanisms by which extrinsic signals coordinate progenitor cell proliferation, cell cycle exit, and cell fate choices are not well understood. Here, we address whether Hedgehog (Hh) signals independently regulate progenitor proliferation and neuronal fate decisions in the embryonic mouse retina. Conditional ablation of the essential Hh signaling component Smoothened (Smo) in proliferating progenitors, rather than in nascent postmitotic neurons, leads to a dramatic increase of retinal ganglion cells (RGCs) and a mild increase of cone photoreceptor precursors without significantly affecting other early-born neuronal cell types. In addition, Smo-deficient progenitors exhibit aberrant expression of cell cycle regulators and delayed G(1)/S transition, especially during the late embryonic stages, resulting in a reduced progenitor pool by birth. Deficiency in Smo function also causes reduced expression of the basic helix-loop-helix transcription repressor Hes1 and preferential elevation of the proneural gene Math5. In Smo and Math5 double knock-out mutants, the enhanced RGC production observed in Smo-deficient retinas is abolished, whereas defects in the G(1)/S transition persist, suggesting that Math5 mediates the Hh effect on neuronal fate specification but not on cell proliferation. These findings demonstrate that Hh signals regulate progenitor pool expansion primarily by promoting cell cycle progression and influence cell cycle exit and neuronal fates by controlling specific proneural genes. Together, these distinct cellular effects of Hh signaling in neural progenitor cells coordinate a balanced production of diverse neuronal cell types.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsCell CycleCell DifferentiationCell ProliferationEmbryo, MammalianEmbryonic Stem CellsFemaleFlow CytometryGene Expression Regulation, DevelopmentalGreen Fluorescent ProteinsHedgehog ProteinsHomeodomain ProteinsMaleMiceMice, Inbred C57BLAtoh7 protein, mouseBasic Helix-Loop-Helix ProteinsGreen Fluorescent ProteinsHedgehog ProteinsHomeodomain ProteinsNerve Tissue ProteinsReceptors, G-Protein-CoupledSmoothened ReceptorSmo protein, mouseTranscription FactorsVsx2 protein, mouse

Identifiers

PMID19474320
PMCPMC2715855
OpenAlexW1972468954

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.