Evidence map›Paper›PMID 21536028›Full record

ArticleExperimental cell research2011

Migration of connective tissue-derived cells is mediated by ultra-low concentration gradient fields of EGF.

Qingjun Kong, Robert J Majeska, Maribel Vazquez

Open access · greenAbstract read
In one paragraph

Article in Experimental cell research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed, 38 citations in OpenAlex.

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  16. EGF as a New Therapeutic Target for Medulloblastoma Metastasis.Cellular and molecular bioengineering · 2015
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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 1 institution in 1 country.

Qingjun KongNew York Center for Biomedical Engineering, Department of Biomedical Engineering, The City College of The City University of New York, USA.
Robert J Majeska
Maribel Vazquez
City College of New York · US

Funding

A mu Migration Assay for Temporal Protein LocalizationR21CA118255 · NCI · CITY COLLEGE OF NEW YORK · PI VAZQUEZ, MARIBEL · 2005 to 2006
$358k
Microsystems to Manipulate Fibroblast ChemotaxisR21GM071703 · NIGMS · CITY COLLEGE OF NEW YORK · PI VAZQUEZ, MARIBEL · 2005 to 2006
$322k
NCI NIH HHS R21 CA118255NIGMS NIH HHS R21 GM071703
6 · The paper itself

Abstract

The directed migration of cells towards chemical stimuli incorporates simultaneous changes in both the concentration of a chemotactic agent and its concentration gradient, each of which may influence cell migratory response. In this study, we utilized a microfluidic system to examine the interactions between epidermal growth factor (EGF) concentration and EGF gradient in stimulating the chemotaxis of connective tissue-derived fibroblast cells. Cells seeded within microfluidic devices were exposed to concentration gradients established by EGF concentrations that matched or exceeded those required for maximum chemotactic responses seen in transfilter migration assays. The migration of individual cells within the device was measured optically after steady-state gradients had been experimentally established. Results illustrate that motility was maximal at EGF concentration gradients between .01- and 0.1-ng/(mL.mm) for all concentrations used. In contrast, the number of motile cells continually increased with increasing gradient steepness for all concentrations examined. Microfluidics-based experiments exposed cells to minute changes in EGF concentration and gradient that were in line with the acute EGFR phosphorylation measured. Correlation of experimental data with established mathematical models illustrated that the fibroblasts studied exhibit an unreported chemosensitivity to minute changes in EGF concentration, similar to that reported for highly motile cells, such as macrophages. Our results demonstrate that shallow chemotactic gradients, while previously unexplored, are necessary to induce the rate of directed cellular migration and the number of motile cells in the connective tissue-derived cells examined.

Indexed as

AnimalsBlotting, WesternCattleCell Migration AssaysCell MovementCell ProliferationCells, CulturedChemotaxisConnective Tissue CellsEpidermal Growth FactorFibroblastsMicrofluidic Analytical TechniquesMicrofluidicsEpidermal Growth Factor

Identifiers

PMID21536028
PMCPMC3118560
OpenAlexW2057700419

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.