Evidence map›Paper›PMID 30181589›Full record

ArticleScientific reports2018

Single-neuronal cell culture and monitoring platform using a fully transparent microfluidic DEP device.

Hyungsoo Kim, In-Kyu Lee, Kendra Taylor, Karl Richters, Dong-Hyun Baek, Jae Ha Ryu, Sang June Cho, Yei Hwan Jung, Dong-Wook Park, Joseph Novello and 7 more

Abstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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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

17 authors.

Hyungsoo KimDepartment of Electrical and Computer Engineering, University of Wisconsin-Madison, Madison, WI, 53706, USA.
In-Kyu LeeDepartment of Electrical and Computer Engineering, University of Wisconsin-Madison, Madison, WI, 53706, USA.
Kendra TaylorNeuroscience Training Program, University of Wisconsin-Madison, Madison, WI, 53705, USA.
Karl RichtersDepartment of Neuroscience, University of Wisconsin-Madison, Madison, WI, 53706, USA.
Dong-Hyun BaekDepartment of Biomedical Engineering, University of Wisconsin-Madison, Madison, WI, 53706, USA.
Jae Ha RyuDepartment of Electrical and Computer Engineering, University of Wisconsin-Madison, Madison, WI, 53706, USA.
Sang June ChoDepartment of Electrical and Computer Engineering, University of Wisconsin-Madison, Madison, WI, 53706, USA.ORCID 0000-0002-7784-2498
Yei Hwan JungDepartment of Electrical and Computer Engineering, University of Wisconsin-Madison, Madison, WI, 53706, USA.
Dong-Wook ParkDepartment of Electrical and Computer Engineering, University of Wisconsin-Madison, Madison, WI, 53706, USA.
Joseph NovelloDepartment of Biomedical Engineering, University of Wisconsin-Madison, Madison, WI, 53706, USA.
Jihye BongDepartment of Electrical and Computer Engineering, University of Wisconsin-Madison, Madison, WI, 53706, USA.
Aaron J SuminskiDepartment of Biomedical Engineering, University of Wisconsin-Madison, Madison, WI, 53706, USA.
Aaron M DingleDepartment of Surgery, University of Wisconsin-Madison, Madison, WI, 53706, USA.
Robert H BlickDepartment of Electrical and Computer Engineering, University of Wisconsin-Madison, Madison, WI, 53706, USA.
Justin C WilliamsDepartment of Biomedical Engineering, University of Wisconsin-Madison, Madison, WI, 53706, USA. jwilliams@engr.wisc.edu.ORCID 0000-0002-8710-7497
Erik W DentDepartment of Neuroscience, University of Wisconsin-Madison, Madison, WI, 53706, USA. ewdent@wisc.edu.
Zhenqiang MaDepartment of Electrical and Computer Engineering, University of Wisconsin-Madison, Madison, WI, 53706, USA. mazq@engr.wisc.edu.

Funding

Role of F-BAR proteins in neuronal developmentR01NS080928 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI DENT, ERIK W · 2013 to 2017
$1.6M
NINDS NIH HHS R01 NS080928
6 · The paper itself

Abstract

Dielectrophoresis using multi-electrode arrays allows a non-invasive interface with biological cells for long-term monitoring of electrophysiological parameters as well as a label-free and non-destructive technique for neuronal cell manipulation. However, experiments for neuronal cell manipulation utilizing dielectrophoresis have been constrained because dielectrophoresis devices generally function outside of the controlled environment (i.e. incubator) during the cell manipulation process, which is problematic because neurons are highly susceptible to the properties of the physiochemical environment. Furthermore, the conventional multi-electrode arrays designed to generate dielectrophoretic force are often fabricated with non-transparent materials that confound live-cell imaging. Here we present an advanced single-neuronal cell culture and monitoring platform using a fully transparent microfluidic dielectrophoresis device for the unabated monitoring of neuronal cell development and function. The device is mounted inside a sealed incubation chamber to ensure improved homeostatic conditions and reduced contamination risk. Consequently, we successfully trap and culture single neurons on a desired location and monitor their growth process over a week. The proposed single-neuronal cell culture and monitoring platform not only has significant potential to realize an in vitro ordered neuronal network, but also offers a useful tool for a wide range of neurological research and electrophysiological studies of neuronal networks.

Indexed as

Lab-On-A-Chip DevicesAnimalsCell Culture TechniquesCells, CulturedEquipment DesignMicrofluidic Analytical TechniquesNeuronsOptical ImagingRats, Sprague-DawleySingle-Cell Analysis

Identifiers

PMID30181589
PMCPMC6123457

What OpenQuestion holds

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LicenceCC BY
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.