Evidence map›Paper›PMID 25072157›Full record

ArticlePloS one2014

A time course analysis of the electrophysiological properties of neurons differentiated from human induced pluripotent stem cells (iPSCs).

Deborah Prè, Michael W Nestor, Andrew A Sproul, Samson Jacob, Peter Koppensteiner, Vorapin Chinchalongporn, Matthew Zimmer, Ai Yamamoto, Scott A Noggle, Ottavio Arancio

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed, 1 pooled it
5.5field-weighted citation impact, top 3% 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

75 citing papers in PubMed, 1 synthesis or guideline pooled it, 123 citations in OpenAlex.

  1. Pooled it
  2. Temporal Interference Stimulation Enhances Neural Regeneration.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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  15. ZCCHC17 Modulates Neuronal RNA Splicing and Supports Cognitive Resilience in Alzheimer's Disease.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
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15 more citing papers are in PubMed but not listed here.

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

10 authors at 2 institutions in 2 countries.

Deborah PrèDepartment of Pathology & Cell Biology, Columbia University, New York, New York, United States of America; The Taub Institute for Research on Alzheimer's Disease and the Aging Brain, Columbia University, New York, New York, United States of America; Columbia Stem Cell Initiative, Columbia University, New York, New York, United States of America.
Michael W NestorThe New York Stem Cell Foundation Research Institute, New York, New York, United States of America.
Andrew A SproulThe New York Stem Cell Foundation Research Institute, New York, New York, United States of America.
Samson JacobThe New York Stem Cell Foundation Research Institute, New York, New York, United States of America.
Peter KoppensteinerDepartment of Pathology & Cell Biology, Columbia University, New York, New York, United States of America; The Taub Institute for Research on Alzheimer's Disease and the Aging Brain, Columbia University, New York, New York, United States of America; Columbia Stem Cell Initiative, Columbia University, New York, New York, United States of America.
Vorapin ChinchalongpornDepartment of Pathology & Cell Biology, Columbia University, New York, New York, United States of America; The Taub Institute for Research on Alzheimer's Disease and the Aging Brain, Columbia University, New York, New York, United States of America; Columbia Stem Cell Initiative, Columbia University, New York, New York, United States of America; Research Center for Neuroscience, Institute of Molecular Biosciences, Mahidol University, Salaya, Nakhonpathom, Thailand.
Matthew ZimmerThe New York Stem Cell Foundation Research Institute, New York, New York, United States of America.
Ai YamamotoDepartment of Pathology & Cell Biology, Columbia University, New York, New York, United States of America; Department of Neurology, Columbia University, New York, New York, United States of America.
Scott A NoggleThe New York Stem Cell Foundation Research Institute, New York, New York, United States of America.
Ottavio ArancioDepartment of Pathology & Cell Biology, Columbia University, New York, New York, United States of America; The Taub Institute for Research on Alzheimer's Disease and the Aging Brain, Columbia University, New York, New York, United States of America; Columbia Stem Cell Initiative, Columbia University, New York, New York, United States of America.
Columbia University · USNew York Stem Cell Foundation · US

Funding

Modulating selective autophagy to modify Huntington's diseaseR01NS077111 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Ai Yamamoto · 2012 to 2026
$4.3M
SUMOylation and Amyloid-beta elevationR01NS049442 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI ARANCIO, OTTAVIO · 2005 to 2015
$4.1M
Generation and Characterization of Alzheimer Brain CellsRF1AG042965 · NIA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI GANDY, SAMUEL E., NOGGLE, SCOTT ALLEN · 2012 to 2012
$516k
NIA NIH HHS R21AG042965NIA NIH HHS RF1 AG042965NINDS NIH HHS NS049442NINDS NIH HHS R01 NS049442NINDS NIH HHS R01 NS077111
6 · The paper itself

Abstract

Many protocols have been designed to differentiate human embryonic stem cells (ESCs) and human induced pluripotent stem cells (iPSCs) into neurons. Despite the relevance of electrophysiological properties for proper neuronal function, little is known about the evolution over time of important neuronal electrophysiological parameters in iPSC-derived neurons. Yet, understanding the development of basic electrophysiological characteristics of iPSC-derived neurons is critical for evaluating their usefulness in basic and translational research. Therefore, we analyzed the basic electrophysiological parameters of forebrain neurons differentiated from human iPSCs, from day 31 to day 55 after the initiation of neuronal differentiation. We assayed the developmental progression of various properties, including resting membrane potential, action potential, sodium and potassium channel currents, somatic calcium transients and synaptic activity. During the maturation of iPSC-derived neurons, the resting membrane potential became more negative, the expression of voltage-gated sodium channels increased, the membrane became capable of generating action potentials following adequate depolarization and, at day 48-55, 50% of the cells were capable of firing action potentials in response to a prolonged depolarizing current step, of which 30% produced multiple action potentials. The percentage of cells exhibiting miniature excitatory post-synaptic currents increased over time with a significant increase in their frequency and amplitude. These changes were associated with an increase of Ca2+ transient frequency. Co-culturing iPSC-derived neurons with mouse glial cells enhanced the development of electrophysiological parameters as compared to pure iPSC-derived neuronal cultures. This study demonstrates the importance of properly evaluating the electrophysiological status of the newly generated neurons when using stem cell technology, as electrophysiological properties of iPSC-derived neurons mature over time.

Indexed as

Cell DifferentiationAnimalsCalciumCoculture TechniquesElectrophysiological PhenomenaHumansImmunophenotypingInduced Pluripotent Stem CellsMiceNeurogliaNeuronsPatch-Clamp TechniquesSynaptic PotentialsSynaptic TransmissionTime FactorsCalcium

Identifiers

PMID25072157
PMCPMC4114788
OpenAlexW2053798951

What OpenQuestion holds

Textmetadata
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.