Evidence map›Paper›PMID 31940260›Full record

ArticleMolecular biology of the cell2020

Angiomotin links ROCK and YAP signaling in mechanosensitive differentiation of neural stem cells.

Phillip H Kang, David V Schaffer, Sanjay Kumar

Open access · bronzeAbstract read
In one paragraph

Article in Molecular biology of the cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.0field-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

28 citing papers in PubMed, 38 citations in OpenAlex.

  1. Evidence for Drop-Like Nuclear Deformation in Sheared Endothelial Monolayers.Small (Weinheim an der Bergstrasse, Germany) · 2026
    Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Role of angiomotin family members in human diseases (Review).Experimental and therapeutic medicine · 2024
    Review
  11. Article
  12. Review
  13. Implications of Cellular Mechanical Memory in Bioengineering.ACS biomaterials science & engineering · 2023
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Rho Kinases in Embryonic Development and Stem Cell Research.Archivum immunologiae et therapiae experimentalis · 2022
    Review
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 2 countries.

Phillip H KangGraduate Program in Bioengineering, University of California, Berkeley-University of California, San Francisco.
David V SchafferGraduate Program in Bioengineering, University of California, Berkeley-University of California, San Francisco.
Sanjay KumarGraduate Program in Bioengineering, University of California, Berkeley-University of California, San Francisco.
University of California, San Francisco · USLawrence Berkeley National Laboratory · US

Funding

Mechanisms of Neural Stem Cell MechanoregulationR01NS074831 · NINDS · UNIVERSITY OF CALIFORNIA BERKELEY · PI Sanjay Kumar, DAVID V SCHAFFER · 2012 to 2026
$5.9M
NINDS NIH HHS R01 NS074831
6 · The paper itself

Abstract

Mechanical cues regulate the function of a broad range of stem cells in culture and in tissue. For example, soft substrates promote the neuronal differentiation of neural stem cells (NSCs) by suppressing cytoskeletal contractility. However, the mechanisms that link cytoskeletal signaling to the transcriptional regulatory processes that ultimately govern stiffness-dependent NSC fate commitment are not fully understood. Here, we show that Angiomotin (AMOT), which can bind both F-actin and the neurosuppressive transcriptional coactivator Yes-associated protein (YAP), is critical for mechanotransduction in NSCs. On soft substrates, loss of AMOT substantially reduces neurogenesis, whereas on stiff substrates, loss of AMOT negates the rescue of neurogenesis normally induced by pharmacologic inhibition of myosin activity. Furthermore, overexpression of a phospho-mimetic S175E AMOT mutant, which has been established to enhance AMOT-YAP binding, increases β-catenin activity and rescues neurogenesis on stiff substrates. Together, our data identify AMOT as an important intermediate signal transducer that allows NSCs to sense and respond to extracellular stiffness cues.

Indexed as

Cell DifferentiationMechanotransduction, CellularActinsAngiomotinsAnimalsApoptosis Regulatory Proteinsbeta CateninFemaleIntercellular Signaling Peptides and ProteinsMembrane ProteinsModels, BiologicalNeural Stem CellsNeurogenesisPhosphorylationProtein BindingRats, Inbred F344ActinsAmot protein, ratAngiomotinsApoptosis Regulatory Proteinsbeta CateninIntercellular Signaling Peptides and ProteinsMembrane Proteinsrho-Associated Kinasesrho GTP-Binding ProteinsYap1 protein, ratYAP-Signaling Proteins

Identifiers

PMID31940260
PMCPMC7183791
OpenAlexW2999475563

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.