Evidence map›Paper›PMID 36151116›Full record

ArticleScientific reports2022

Passage number affects differentiation of sensory neurons from human induced pluripotent stem cells.

Erica L Cantor, Fei Shen, Guanglong Jiang, Zhiyong Tan, Geneva M Cunningham, Xi Wu, Santosh Philips, Bryan P Schneider

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

19 citing papers in PubMed, 20 citations in OpenAlex.

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  11. A Study on iPSC-Associated Factors in the Generation of Hepatocytes.Tissue engineering and regenerative medicine · 2024
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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

8 authors at 2 institutions in 1 country.

Erica L CantorHematology/Oncology, Indiana University School of Medicine, Indianapolis, IN, USA.
Fei ShenHematology/Oncology, Indiana University School of Medicine, Indianapolis, IN, USA.
Guanglong JiangMedical & Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN, USA.
Zhiyong TanPharmacology & Toxicology, Stark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, USA.
Geneva M CunninghamMedical & Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN, USA.
Xi WuHematology/Oncology, Indiana University School of Medicine, Indianapolis, IN, USA.
Santosh PhilipsClinical Pharmacology, Indiana University School of Medicine, Indianapolis, IN, USA.
Bryan P SchneiderHematology/Oncology, Indiana University School of Medicine, Indianapolis, IN, USA. bpschnei@iu.edu.
Indiana University – Purdue University Indianapolis · USIndiana University School of Medicine

Funding

Indiana Medical Scientist/Engineer Training ProgramT32GM077229 · NIGMS · INDIANA UNIVERSITY INDIANAPOLIS · PI GASTON, BENJAMIN, HERBERT, BRITTNEY-SHEA · 2008 to 2022
$6.0M
NIGMS NIH HHS T32 GM077229Susan G. Komen
6 · The paper itself

Abstract

Induced pluripotent stem cells (iPSCs) are a valuable resource for neurological disease-modeling and drug discovery due to their ability to differentiate into neurons reflecting the genetics of the patient from which they are derived. iPSC-derived cultures, however, are highly variable due to heterogeneity in culture conditions. We investigated the effect of passage number on iPSC differentiation to optimize the generation of sensory neurons (iPSC-dSNs). Three iPSC lines reprogrammed from the peripheral blood of three donors were differentiated into iPSC-dSNs at passage numbers within each of the following ranges: low (5-10), intermediate (20-26), and high (30-38). Morphology and pluripotency of the parent iPSCs were assessed prior to differentiation. iPSC-dSNs were evaluated based on electrophysiological properties and expression of key neuronal markers. All iPSC lines displayed similar morphology and were similarly pluripotent across passage numbers. However, the expression levels of neuronal markers and sodium channel function analyses indicated that iPSC-dSNs differentiated from low passage numbers better recapitulated the sensory neuron phenotype than those differentiated from intermediate or high passage numbers. Our results demonstrate that lower passage numbers may be better suited for differentiation into peripheral sensory neurons.

Indexed as

Induced Pluripotent Stem CellsCell DifferentiationElectrophysiological PhenomenaHumansSensory Receptor Cells

Identifiers

PMID36151116
PMCPMC9508090
OpenAlexW4297009461

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.