Evidence map›Paper›PMID 34515684›Full record

ArticleJournal of visualized experiments : JoVE2021

Establishment of an Electrophysiological Platform for Modeling ALS with Regionally-Specific Human Pluripotent Stem Cell-Derived Astrocytes and Neurons.

Arens Taga, Christa W Habela, Alexandra Johns, Shiyu Liu, Mollie O'Brien, Nicholas J Maragakis

Open access · greenAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2021. 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
0.8field-weighted citation impact, top 29% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  3. Review
  4. Article
  5. In Vitro Models of Amyotrophic Lateral Sclerosis.Cellular and molecular neurobiology · 2023
    Review
  6. Article
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  9. Review
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

6 authors at 1 institution in 1 country.

Arens Taga *Department of Neurology, Johns Hopkins University.
Christa W Habela *Department of Neurology, Johns Hopkins University.
Alexandra JohnsDepartment of Neurology, Johns Hopkins University.
Shiyu LiuDepartment of Neurology, Johns Hopkins University.
Mollie O'BrienDepartment of Neurology, Johns Hopkins University.
Nicholas J MaragakisDepartment of Neurology, Johns Hopkins University; nmaragak@jhmi.edu.
Johns Hopkins University · US

Funding

Modulating an Astrocyte Hemichannel to Delay Spatial and Temporal Progression in ALS.R01NS117604 · NINDS · JOHNS HOPKINS UNIVERSITY · PI MARAGAKIS, NICHOLAS J · 2020 to 2024
$1.9M
Modeling genetic risk for epilepsy using IPSC and animal models.K08NS102526 · NINDS · JOHNS HOPKINS UNIVERSITY · PI HABELA, CHRISTA · 2020 to 2024
$996k
NINDS NIH HHS K08 NS102526NINDS NIH HHS R01 NS117604
6 · The paper itself

Abstract

Human pluripotent stem cell-derived astrocytes (hiPSC-A) and neurons (hiPSC-N) provide a powerful tool for modeling Amyotrophic Lateral Sclerosis (ALS) pathophysiology in vitro. Multi-electrode array (MEA) recordings are a means to record electrical field potentials from large populations of neurons and analyze network activity over time. It was previously demonstrated that the presence of hiPSC-A that are differentiated using techniques to promote a spinal cord astrocyte phenotype improved maturation and electrophysiological activity of regionally specific spinal cord hiPSC-motor neurons (MN) when compared to those cultured without hiPSC-A or in the presence of rodent astrocytes. Described here is a method to co-culture spinal cord hiPSC-A with hiPSC-MN and record electrophysiological activity using MEA recordings. While the differentiation protocols described here are particular to astrocytes and neurons that are regionally specific to the spinal cord, the co-culturing platform can be applied to astrocytes and neurons differentiated with techniques specific to other fates, including cortical hiPSC-A and hiPSC-N. These protocols aim to provide an electrophysiological assay to inform about glia-neuron interactions and provide a platform for testing drugs with therapeutic potential in ALS.

Indexed as

Amyotrophic Lateral SclerosisInduced Pluripotent Stem CellsPluripotent Stem CellsAstrocytesCell DifferentiationCells, CulturedHumansMotor Neurons

Identifiers

PMID34515684
PMCPMC9169687
OpenAlexW3198323703

What OpenQuestion holds

Textmetadata
LicenceTDM
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.