Evidence map›Paper›PMID 17280659›Full record

ArticleDevelopmental biology2007

Transient inactivation of Notch signaling synchronizes differentiation of neural progenitor cells.

Branden R Nelson, Byron H Hartman, Sean A Georgi, Michael S Lan, Thomas A Reh

Abstract read
In one paragraph

Article in Developmental biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers.

0numbers the graph read from it
0cells of the map it votes in
89citing 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

89 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Stimulating the regenerative capacity of the human retina with proneural transcription factors in 3D cultures.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Multiple Cell Lineages Give Rise to a Cell Type.Results and problems in cell differentiation · 2024
    Article
  11. Article
  12. Article
  13. Cell-Based Therapies: Strategies for Regeneration.Cold Spring Harbor perspectives in medicine · 2023
    Review
  14. 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
  15. Review
  16. Article
  17. Transcriptomics of CD29Scientific reports · 2023
    Article
  18. Review
  19. Article
  20. Article

29 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

5 authors.

Branden R NelsonDepartment of Biological Structure, Box 357420, University of Washington, Seattle, WA 98195, and The Research Institute for Children, Children's Hospital, New Orleans, LA 70118, USA.
Byron H Hartman
Sean A Georgi
Michael S Lan
Thomas A Reh

Funding

INTERDISCIPLINARY TRAINING IN DEVELOPMENTAL BIOLOGYT32HD007183 · NICHD · UNIVERSITY OF WASHINGTON · PI RAIBLE, DAVID W · 1985 to 2015
$5.7M
Stem Cells in the RetinaR01EY013475 · NEI · UNIVERSITY OF WASHINGTON · PI REH, THOMAS A · 2002 to 2010
$3.5M
REGULATION OF NEURONAL PROLIFERATION AND DIFFERENTIATIONR01NS028308 · NINDS · UNIVERSITY OF WASHINGTON · PI REH, THOMAS A · 1989 to 2005
$2.1M
Mechanisms of Retinal Ganglion Cell PatterningF32EY015631 · NEI · UNIVERSITY OF WASHINGTON · PI NELSON, BRANDEN R · 2004 to 2007
$142k
NEI NIH HHS EY13475NEI NIH HHS F32 EY015631NEI NIH HHS F32 EY15631-01A1NEI NIH HHS R01 EY013475NICHD NIH HHS T32 HD007183NINDS NIH HHS R01 NS028308NINDS NIH HHS R01 NS28308
6 · The paper itself

Abstract

In the developing nervous system, the balance between proliferation and differentiation is critical to generate the appropriate numbers and types of neurons and glia. Notch signaling maintains the progenitor pool throughout this process. While many components of the Notch pathway have been identified, the downstream molecular events leading to neural differentiation are not well understood. We have taken advantage of a small molecule inhibitor, DAPT, to block Notch activity in retinal progenitor cells, and analyzed the resulting molecular and cellular changes over time. DAPT treatment causes a massive, coordinated differentiation of progenitors that produces cell types appropriate for their developmental stage. Transient exposure of retina to DAPT for specific time periods allowed us to define the period of Notch inactivation that is required for a permanent commitment to differentiate. Inactivation of Notch signaling revealed a cascade of proneural bHLH transcription factor gene expression that correlates with stages in progenitor cell differentiation. Microarray/QPCR analysis confirms the changes in Notch signaling components, and reveals new molecular targets for investigating neuronal differentiation. Thus, transient inactivation of Notch signaling synchronizes progenitor cell differentiation, and allows for a systematic analysis of key steps in this process.

Indexed as

Amyloid Precursor Protein SecretasesAnimalsBasic Helix-Loop-Helix ProteinsCell DifferentiationChick Embryogamma-Aminobutyric AcidGene Expression Regulation, DevelopmentalNeurogliaNeuronsOligonucleotide Array Sequence AnalysisReceptors, NotchRetinaSignal TransductionStem CellsTriglycerides1,2-dilinolenoyl-3-(4-aminobutyryl)propane-1,2,3-triolAmyloid Precursor Protein SecretasesBasic Helix-Loop-Helix Proteinsgamma-Aminobutyric AcidReceptors, NotchTriglycerides

Identifiers

PMID17280659
PMCPMC1979095

What OpenQuestion holds

Textmetadata
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.