Evidence map›Paper›PMID 26989485›Full record

ArticleRSC advances2015

Establishment of a Long-Term Chick Forebrain Neuronal Culture on a Microelectrode Array Platform.

Serena Y Kuang, Ting Huang, Zhonghai Wang, Yongliang Lin, Mark Kindy, Tingfei Xi, Bruce Z Gao

Open access · greenAbstract read
In one paragraph

Article in RSC advances, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 42% 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

1 citing paper in PubMed, 7 citations in OpenAlex.

  1. 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 at 5 institutions in 3 countries.

Serena Y KuangWilliam Beaumont School of Medicine, Oakland University, Rochester, MI 49309, USA.
Ting HuangAcademy for Advanced Interdisciplinary Studies, Center for Biomedical Materials and Tissue Engineering, Peking University, Beijing, 100871, China.
Zhonghai WangDepartment of Bioengineering, Clemson University, 201-5 Rhodes Research Hall, Clemson, SC 29634, USA.
Yongliang LinNational Engineering Laboratory for Regenerative Implantable Medical Devices, Guangzhou, Guangdong 510530, China.
Mark KindyDepartments of Neuroscience and Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, SC 29466, USA.
Tingfei XiAcademy for Advanced Interdisciplinary Studies, Center for Biomedical Materials and Tissue Engineering, Peking University, Beijing, 100871, China.
Bruce Z GaoDepartment of Bioengineering, Clemson University, 201-5 Rhodes Research Hall, Clemson, SC 29634, USA.
Center for Life Sciences · CNClemson University · USBeaumont Hospital, Troy · USCenter for Neuroscience and Regenerative Medicine · USUniversity of Charleston · US

Funding

Targeted Nano-therapeutics for Neural RegenerationP20GM103444 · NIGMS · CLEMSON UNIVERSITY · PI MARKWALD, ROGER R, VYAVAHARE, NAREN R · 2012 to 2018
$14.9M
UNDERSTANDING AND CONTROLLING TISSUE-SPECIFIC VASCULAR PATTERNINGP20RR021949 · NCRR · CLEMSON UNIVERSITY · PI MARKWALD, ROGER R · 2009 to 2011
$5.2M
Microfabricated coculture model: Myocyte rescue by TNT-transferred mitochondriaR01HL124782 · NHLBI · CLEMSON UNIVERSITY · PI GAO, BRUCE Z, RUNYAN, RAYMOND BRUCE · 2014 to 2017
$1.5M
NCRR NIH HHS P20 RR021949NHLBI NIH HHS R01 HL124782NIGMS NIH HHS P20 GM103444
6 · The paper itself

Abstract

The biosensor system formed by culturing primary animal neurons on a microelectrode array (MEA) platform is drawing an increasing research interest for its power as a rapid, sensitive, functional neurotoxicity assessment, as well as for many other electrophysiological related research purposes. In this paper, we established a long-term chick forebrain neuron culture (C-FBN-C) on MEAs with a more than 5 month long lifespan and up to 5 month long stability in morphology and physiological function; characterized the C-FBN-C morphologically, functionally, and developmentally; partially compared its functional features with rodent counterpart; and discussed its pros and cons as a novel biosensor system in comparison to rodent counterpart and human induced pluripotent stem cells (hiPSCs). Our results show that C-FBN-C on MEA platform 1) can be used as a biosensor of its own type in a wide spectrum of basic biomedical research; 2) is of value in comparative physiology in cross-species studies; and 3) may have potential to be used as an alternative, cost-effective approach to rodent counterpart within shared common functional domains (such as specific types of ligand-gated ion channel receptors and subtypes expressed in the cortical tissues of both species) in large-scale environmental neurotoxicant screening that would otherwise require millions of animals.

Indexed as

biosensorchick forebrain neuronlong-term culturemicroelectrode array

Identifiers

PMID26989485
PMCPMC4792308
OpenAlexW2147600025

What OpenQuestion holds

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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.