Evidence map›Paper›PMID 20652960›Full record

ArticleStem cells (Dayton, Ohio)2010

FRS2α regulates Erk levels to control a self-renewal target Hes1 and proliferation of FGF-responsive neural stem/progenitor cells.

Takuya Sato, Takuya Shimazaki, Hayato Naka, Shin-Ichi Fukami, Yasushi Satoh, Hideyuki Okano, Irit Lax, Joseph Schlessinger, Noriko Gotoh

Open access · bronzeAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

17 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Transcriptional profiling of β-2MStem cell reports · 2022
    Article
  4. Review
  5. The doublesex-related Dmrta2 safeguards neural progenitor maintenance involving transcriptional regulation of Hes1.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  6. Article
  7. Hes1: the maestro in neurogenesis.Cellular and molecular life sciences : CMLS · 2016
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. 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

9 authors at 4 institutions in 2 countries.

Takuya SatoDivision of Systems Biomedical Technology, Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Takuya Shimazaki
Hayato Naka
Shin-Ichi Fukami
Yasushi Satoh
Hideyuki Okano
Irit Lax
Joseph Schlessinger
Noriko Gotoh
Keio University · JPThe University of Tokyo · JPYale University · USNational Defense Medical College · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fibroblast growth factor (FGF) is among the most common growth factors used in cultures to maintain self-renewal and proliferative capabilities of a variety of stem cells, including neural stem cells (NSCs). However, the molecular mechanisms underlying the control by FGF have remained elusive. Studies on mutant mice of FGF receptor substrate 2α (FRS2α), a central mediator for FGF signaling, combined with FRS2α knockdown or gain-of-function experiments, allowed us to dissect the role of FGF signaling for the self-renewal and proliferation of NSCs and to provide novel molecular mechanisms for them. We identified Hes1 as a novel self-renewal target of FGF-signaling. Quantitatively different levels of Erk activation mediated by FRS2α may regulate self-renewal of NSCs and proliferation of neural stem/progenitor cells (NSPCs); low levels of Erk activation are sufficient for the former, however, higher levels are required for maximum activity of the latter. Thus, FRS2α fine-tunes the FGF-signaling to control qualitatively different biological activities, self-renewal at least partly through Hes1 versus proliferation of NSPCs.

Indexed as

Cell ProliferationSignal TransductionAnimalsBasic Helix-Loop-Helix ProteinsBinding SitesCell DifferentiationEnzyme ActivationExtracellular Signal-Regulated MAP KinasesFibroblast Growth Factor 2GRB2 Adaptor ProteinHomeodomain ProteinsMembrane ProteinsMiceMice, Inbred ICRMice, TransgenicMutationBasic Helix-Loop-Helix ProteinsExtracellular Signal-Regulated MAP KinasesFibroblast Growth Factor 2FRS2alpha protein, mouseGRB2 Adaptor ProteinGrb2 protein, mouseHes1 protein, mouseHomeodomain ProteinsMembrane ProteinsProtein Kinase InhibitorsTranscription Factor HES-1

Identifiers

PMID20652960
PMCPMC2996081
OpenAlexW1996013055

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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.