Evidence map›Paper›PMID 23524265›Full record

ArticleBiochemical and biophysical research communications2013

Rac1 and Cdc42 GTPases regulate shear stress-driven β-catenin signaling in osteoblasts.

Qiaoqiao Wan, Eunhye Cho, Hiroki Yokota, Sungsoo Na

Open access · greenAbstract read
In one paragraph

Article in Biochemical and biophysical research communications, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.5field-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

22 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. A biomechanical view of epigenetic tumor regulation.Journal of biological physics · 2023
    Review
  5. Review
  6. Review
  7. Article
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  9. Article
  10. AnJBMR plus · 2021
    Article
  11. Article
  12. Article
  13. Article
  14. The Rho GTPase RAC1 in Osteoblasts Controls Their Function.International journal of molecular sciences · 2020
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

4 authors at 2 institutions in 1 country.

Qiaoqiao WanDepartment of Biomedical Engineering, Indiana University-Purdue University Indianapolis, Indianapolis, IN 46202, USA.
Eunhye Cho
Hiroki Yokota
Sungsoo Na
Indiana University – Purdue University Indianapolis · USUniversity of Indianapolis · US

Funding

MECHANICAL LOADING AND BONER01AR052144 · NIAMS · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI YOKOTA, HIROKI · 2006 to 2018
$4.2M
NIAMS NIH HHS AR052144NIAMS NIH HHS R01 AR052144
6 · The paper itself

Abstract

Beta-catenin-dependent TCF/LEF (T-cell factor/lymphocyte enhancing factor) is known to be mechanosensitive and an important regulator for promoting bone formation. However, the functional connection between TCF/LEF activity and Rho family GTPases is not well understood in osteoblasts. Herein we investigated the molecular mechanisms underlying oscillatory shear stress-induced TCF/LEF activity in MC3T3-E1 osteoblast cells using live cell imaging. We employed fluorescence resonance energy transfer (FRET)-based and green fluorescent protein (GFP)-based biosensors, which allowed us to monitor signal transduction in living cells in real time. Oscillatory (1Hz) shear stress (10 dynes/cm2) increased TCF/LEF activity and stimulated translocation of β-catenin to the nucleus with the distinct activity patterns of Rac1 and Cdc42. The shear stress-induced TCF/LEF activity was blocked by the inhibition of Rac1 and Cdc42 with their dominant negative mutants or selective drugs, but not by a dominant negative mutant of RhoA. In contrast, constitutively active Rac1 and Cdc42 mutants caused a significant enhancement of TCF/LEF activity. Moreover, activation of Rac1 and Cdc42 increased the basal level of TCF/LEF activity, while their inhibition decreased the basal level. Interestingly, disruption of cytoskeletal structures or inhibition of myosin activity did not significantly affect shear stress-induced TCF/LEF activity. Although Rac1 is reported to be involved in β-catenin in cancer cells, the involvement of Cdc42 in β-catenin signaling in osteoblasts has not been identified. Our findings in this study demonstrate that both Rac1 and Cdc42 GTPases are critical regulators in shear stress-driven β-catenin signaling in osteoblasts.

Indexed as

Signal TransductionStress, Mechanical3T3 CellsActive Transport, Cell NucleusAminoquinolinesAnimalsbeta CateninCytoskeletonEnzyme ActivationFluorescence Resonance Energy TransferGenes, ReporterGreen Fluorescent ProteinsGTPase-Activating ProteinsMechanotransduction, CellularMiceNeuropeptidesAminoquinolinesArhgap31 protein, mousebeta CateninCTNNB1 protein, mouseGreen Fluorescent ProteinsGTPase-Activating ProteinsNeuropeptidesNSC 23766Pyrimidinesrac1 GTP-Binding ProteinRac1 protein, mouserac GTP-Binding ProteinsrhoA GTP-Binding ProteinRhoA protein, mouserho GTP-Binding ProteinsT Cell Transcription Factor 1

Identifiers

PMID23524265
PMCPMC3648988
OpenAlexW1995244622

What OpenQuestion holds

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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.