Evidence map›Paper›PMID 29658935›Full record

ArticleJournal of visualized experiments : JoVE2018

Fabrication of Custom Agarose Wells for Cell Seeding and Tissue Ring Self-assembly Using 3D-Printed Molds.

Hannah A Strobel, Elizabeth L Calamari, Brittany Alphonse, Tracy A Hookway, Marsha W Rolle

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2018. 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
1.6field-weighted citation impact, top 18% 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, 27 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Hannah A StrobelBiomedical Engineering, Worcester Polytechnic Institute.
Elizabeth L CalamariBiomedical Engineering, Worcester Polytechnic Institute.
Brittany AlphonseBiomedical Engineering, Worcester Polytechnic Institute.
Tracy A HookwayBiomedical Engineering, Worcester Polytechnic Institute; Gladstone Institute for Cardiovascular Disease.
Marsha W RolleBiomedical Engineering, Worcester Polytechnic Institute; mrolle@wpi.edu.
Worcester Polytechnic Institute · USGladstone Institutes · US

Funding

Engineering a Self-assembled, multi-tissue Tracheal ReplacementR01EB023907 · NIBIB · UNIVERSITY OF ILLINOIS AT CHICAGO · PI ALSBERG, EBEN, ROLLE, MARSHA W · 2017 to 2020
$1.9M
Engineering a functional human intimal hyperplasia modelR15HL137197 · NHLBI · WORCESTER POLYTECHNIC INSTITUTE · PI ROLLE, MARSHA W · 2018 to 2018
$438k
Rapid Fabrication of Cell-Derived Tissue RingsR15HL097332 · NHLBI · WORCESTER POLYTECHNIC INSTITUTE · PI ROLLE, MARSHA W · 2009 to 2009
$216k
NHLBI NIH HHS R15 HL097332NHLBI NIH HHS R15 HL137197NIBIB NIH HHS R01 EB023907
6 · The paper itself

Abstract

Engineered tissues are being used clinically for tissue repair and replacement, and are being developed as tools for drug screening and human disease modeling. Self-assembled tissues offer advantages over scaffold-based tissue engineering, such as enhanced matrix deposition, strength, and function. However, there are few available methods for fabricating 3D tissues without seeding cells on or within a supporting scaffold. Previously, we developed a system for fabricating self-assembled tissue rings by seeding cells into non-adhesive agarose wells. A polydimethylsiloxane (PDMS) negative was first cast in a machined polycarbonate mold, and then agarose was gelled in the PDMS negative to create ring-shaped cell seeding wells. However, the versatility of this approach was limited by the resolution of the tools available for machining the polycarbonate mold. Here, we demonstrate that 3D-printed plastic can be used as an alternative to machined polycarbonate for fabricating PDMS negatives. The 3D-printed mold and revised mold design is simpler to use, inexpensive to produce, and requires significantly less agarose and PDMS per cell seeding well. We have demonstrated that the resulting agarose wells can be used to create self-assembled tissue rings with customized diameters from a variety of different cell types. Rings can then be used for mechanical, functional, and histological analysis, or for fabricating larger and more complex tubular tissues.

Indexed as

Printing, Three-DimensionalCells, CulturedHumansSepharoseTissue EngineeringSepharose

Identifiers

PMID29658935
PMCPMC5933294
OpenAlexW2796159826

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.