Evidence map›Paper›PMID 29235973›Full record

ArticleBioTechniques2017

Linear array of multi-substrate tracts for simultaneous assessment of cell adhesion, migration, and differentiation.

Ricardo A Moreno-Rodriguez, Edward L Krug, Leticia Reyes, Roger R Markwald

Abstract read
In one paragraph

Article in BioTechniques, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Ricardo A Moreno-RodriguezDepartment of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, SC.
Edward L KrugDepartment of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, SC.
Leticia ReyesDepartment of Pharmacology, Medical University of South Carolina, Charleston, SC.
Roger R MarkwaldDepartment of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, SC.

Funding

UBIQUITIN CARBOXYL TERMINAL HYDROLASE L1 (UCH-L1) AND VASCULAR LESION FORMATIONP20RR016434 · NCRR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MARKWALD, ROGER R · 2001 to 2011
$24.8M
VASCULAR SIGNALS AND RECEPTORS IN ENDOCARDIAL MORPHOGENESISP01HL052813 · NHLBI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MARKWALD, ROGER R · 1994 to 2004
$8.3M
SC COBRE for Developmentally Based Cardiovascular DiseasesP30GM103342 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MARKWALD, ROGER R · 2012 to 2016
$5.5M
MUCOPOLYSACCHRIDE METABOLISM IN CARDIAC ANOMALIESR01HL033756 · NHLBI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MARKWALD, ROGER R · 1985 to 2015
$4.8M
NCRR NIH HHS P20 RR016434NHLBI NIH HHS P01 HL052813NHLBI NIH HHS R01 HL033756NIGMS NIH HHS P30 GM103342
6 · The paper itself

Abstract

Cell migration, which is central to a wide variety of life processes, involves integration of the extracellular matrix (ECM) with the internal cytoskeleton and motor proteins via receptors spanning the plasma membrane. Cell migration can be induced by a variety of signals, including gradients of external soluble molecules, differences in ECM composition, or electrical gradients. Current in vitro methods to study cell migration only test one substrate at a time. Here, we present a method for assessing cell adhesion, migration, and differentiation in up to 20 different test conditions simultaneously, using only minute amounts of target substrate. Our system, which we call the linear array of multi-substrate cell migration assay (LAMA), has two configurations for direct comparison of one or two cell types in response to an array of ECM constituents under the same culture conditions. This culture model utilizes only nanogram amounts of test substrates and a minimal number of cells, which maximizes the use of limited and expensive test reagents. Moreover, LAMA can also be used for high-throughput screening of potential pharmaceuticals that target ECM-dependent cell behavior and differentiation.

Indexed as

AnimalsCell LineCell Physiological PhenomenaChick EmbryoCytological TechniquesEmbryonic Stem CellsExtracellular MatrixPC12 CellsRatscell migrationdifferentiation assaygap closure assayswound healing

Identifiers

PMID29235973
PMCPMC5884634

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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.