Evidence map›Paper›PMID 29869098›Full record

ArticlePharmaceutical research2018

Three-Dimensional Printing of Cell Exclusion Spacers (CES) for Use in Motility Assays.

Christen J Boyer, David H Ballard, Jungmi W Yun, Adam Y Xiao, Jeffery A Weisman, Mansoureh Barzegar, Jonathan Steven Alexander

Abstract read
In one paragraph

Article in Pharmaceutical research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Software for Bioprinting.International journal of bioprinting · 2020
    Review
  3. Organoids - Preclinical Models of Human Disease.The New England journal of medicine · 2019
    Article
  4. 3D Printing for Bio-Synthetic Biliary Stents.Bioengineering (Basel, Switzerland) · 2019
    Article
  5. 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

7 authors.

Christen J BoyerMolecular and Cellular Physiology, Louisiana State University Health Sciences Center, Shreveport, Louisiana, USA.
David H BallardMallinckrodt Institute of Radiology, Washington University School of Medicine, St Louis, Missouri, USA.
Jungmi W YunMolecular and Cellular Physiology, Louisiana State University Health Sciences Center, Shreveport, Louisiana, USA.
Adam Y XiaoMolecular and Cellular Physiology, Louisiana State University Health Sciences Center, Shreveport, Louisiana, USA.
Jeffery A WeismanDepartment of Anesthesiology, Washington University School of Medicine, St Louis, Missouri, USA.
Mansoureh BarzegarMolecular and Cellular Physiology, Louisiana State University Health Sciences Center, Shreveport, Louisiana, USA.
Jonathan Steven AlexanderMolecular and Cellular Physiology, Louisiana State University Health Sciences Center, Shreveport, Louisiana, USA. jalexa@lsuhsc.edu.

Funding

Training OPportunities in Translational Imaging Education and Research (TOP-TIER)T32EB021955 · NIBIB · WASHINGTON UNIVERSITY · PI Hongyu An, Joseph Edward Ippolito · 2017 to 2026
$2.4M
NIBIB NIH HHS T32 EB021955
6 · The paper itself

Abstract

purposeCell migration/invasion assays are widely used in commercial drug discovery screening. 3D printing enables the creation of diverse geometric restrictive barrier designs for use in cell motility studies, permitting on-demand assays. Here, the utility of 3D printed cell exclusion spacers (CES) was validated as a cell motility assay.

methodsA novel CES fit was fabricated using 3D printing and customized to the size and contour of 12 cell culture plates including 6 well plates of basal human brain vascular endothelial (D3) cell migration cells compared with 6 well plates with D3 cells challenged with 1uM cytochalasin D (Cyto-D), an F-actin anti-motility drug. Control and Cyto-D treated cells were monitored over 3 days under optical microscopy.

resultsDay 3 cell migration distance for untreated D3 cells was 1515.943μm ± 10.346μm compared to 356.909μm ± 38.562μm for the Cyt-D treated D3 cells (p < 0.0001). By day 3, untreated D3 cells reached confluency and completely filled the original voided spacer regions, while the Cyt-D treated D3 cells remained significantly less motile.

conclusionsCell migration distances were significantly reduced by Cyto-D, supporting the use of 3D printing for cell exclusion assays. 3D printed CES have great potential for studying cell motility, migration/invasion, and complex multi-cell interactions.

Indexed as

Printing, Three-DimensionalBrainCell Culture TechniquesCell LineCell Migration AssaysCell MovementEndothelial CellsEquipment DesignHumansTissue Culture Techniques3D printinginvasion assaysmigration assaysmotility assayspersonalized medicinethree-dimensional printing

Identifiers

PMID29869098
PMCPMC6434525

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Registered trials

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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.