Evidence map›Paper›PMID 24637580›Full record

ArticleJournal of visualized experiments : JoVE2014

Cell patterning on photolithographically defined parylene-C: SiO2 substrates.

Mark A Hughes, Paul M Brennan, Andrew S Bunting, Mike J Shipston, Alan F Murray

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

5 authors.

Mark A HughesCentre for Integrative Physiology, School of Biomedical Sciences, The University of Edinburgh; mhughes4@staffmail.ed.ac.uk.
Paul M BrennanEdinburgh Cancer Research Centre, Institute of Genetics and Molecular Medicine, Western General Hospital.
Andrew S BuntingSchool of Engineering, Institute for Integrated Micro and Nano Systems, The University of Edinburgh.
Mike J ShipstonCentre for Integrative Physiology, School of Biomedical Sciences, The University of Edinburgh.
Alan F MurraySchool of Engineering, Institute for Integrated Micro and Nano Systems, The University of Edinburgh.

Funding

Wellcome Trust
6 · The paper itself

Abstract

Cell patterning platforms support broad research goals, such as construction of predefined in vitro neuronal networks and the exploration of certain central aspects of cellular physiology. To easily combine cell patterning with Multi-Electrode Arrays (MEAs) and silicon-based 'lab on a chip' technologies, a microfabrication-compatible protocol is required. We describe a method that utilizes deposition of the polymer parylene-C on SiO2 wafers. Photolithography enables accurate and reliable patterning of parylene-C at micron-level resolution. Subsequent activation by immersion in fetal bovine serum (or another specific activation solution) results in a substrate in which cultured cells adhere to, or are repulsed by, parylene or SiO2 regions respectively. This technique has allowed patterning of a broad range of cell types (including primary murine hippocampal cells, HEK 293 cell line, human neuron-like teratocarcinoma cell line, primary murine cerebellar granule cells, and primary human glioma-derived stem-like cells). Interestingly, however, the platform is not universal; reflecting the importance of cell-specific adhesion molecules. This cell patterning process is cost effective, reliable, and importantly can be incorporated into standard microfabrication (chip manufacturing) protocols, paving the way for integration of microelectronic technology.

Indexed as

AnimalsCattleElectrophoresis, MicrochipHEK293 CellsHumansMicrotechnologyPolymersSilicon DioxideXylenesparylenePolymersSilicon DioxideXylenes

Identifiers

PMID24637580
PMCPMC4143168

What OpenQuestion holds

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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.