Evidence map›Paper›PMID 18652824›Full record

ArticleExperimental cell research2008

Engineering amount of cell-cell contact demonstrates biphasic proliferative regulation through RhoA and the actin cytoskeleton.

Darren S Gray, Wendy F Liu, Colette J Shen, Kiran Bhadriraju, Celeste M Nelson, Christopher S Chen

Open access · greenAbstract read
In one paragraph

Article in Experimental cell research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 63 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Engineering extracellular matrix through nanotechnology.Journal of the Royal Society, Interface · 2010
    Review
  15. Article
  16. Article
  17. Article
  18. Tunable interplay between epidermal growth factor and cell-cell contact governs the spatial dynamics of epithelial growth.Proceedings of the National Academy of Sciences of the United States of America · 2009
    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

6 authors at 3 institutions in 1 country.

Darren S GrayDepartment of Biomedical Engineering, Johns Hopkins University School of Medicine, 720 Rutland Avenue, Baltimore, MD 21205, USA.
Wendy F Liu
Colette J Shen
Kiran Bhadriraju
Celeste M Nelson
Christopher S Chen
University of Pennsylvania · USJohns Hopkins Medicine · USJohns Hopkins University · US

Funding

REGULATION OF ANGIOGENESIS BY MICROENVIRONMENTAL CUESR01EB000262 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI CHEN, CHRISTOPHER S · 2002 to 2023
$6.2M
Cadherins, integrins, and mechanochemical signalingR01HL073305 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI CHEN, CHRISTOPHER S · 2003 to 2011
$3.4M
NHLBI NIH HHS HL 073305NHLBI NIH HHS R01 HL073305NIBIB NIH HHS EB00262NIBIB NIH HHS R01 EB000262
6 · The paper itself

Abstract

Endothelial cell-cell contact via VE-cadherin plays an important role in regulating numerous cell functions, including proliferation. However, using different experimental approaches to manipulate cell-cell contact, investigators have observed both inhibition and stimulation of proliferation depending on the adhesive context. In this study, we used micropatterned wells combined with active positioning of cells by dielectrophoresis in order to investigate whether the number of contacting neighbors affected the proliferative response. Varying cell-cell contact resulted in a biphasic effect on proliferation; one contacting neighbor increased proliferation, while two or more neighboring cells partially inhibited this increase. We also observed that cell-cell contact increased the formation of actin stress fibers, and that expression of dominant negative RhoA (RhoN19) blocked the contact-mediated increase in stress fibers and proliferation. Furthermore, examination of heterotypic pairs of untreated cells in contact with RhoN19-expressing cells revealed that intracellular, but not intercellular, tension is required for the contact-mediated stimulation of proliferation. Moreover, engagement of VE-cadherin with cadherin-coated beads was sufficient to stimulate proliferation in the absence of actual cell-cell contact. In all, these results demonstrate that cell-cell contact signals through VE-cadherin, RhoA, and intracellular tension in the actin cytoskeleton to regulate proliferation.

Indexed as

Cell ProliferationActinsAnimalsAntigens, CDBiomedical EngineeringCadherin 5CadherinsCattleCell AdhesionCell CommunicationCell MembraneCells, CulturedCytoskeletonElectrophoresisEndothelial CellsIntercellular JunctionsActinsAntigens, CDCadherin 5CadherinsrhoA GTP-Binding Protein

Identifiers

PMID18652824
PMCPMC2601564
OpenAlexW2163491624

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.