Evidence map›Paper›PMID 22750882›Full record

ArticleNature biotechnology2012

Combined small-molecule inhibition accelerates developmental timing and converts human pluripotent stem cells into nociceptors.

Stuart M Chambers, Yuchen Qi, Yvonne Mica, Gabsang Lee, Xin-Jun Zhang, Lei Niu, James Bilsland, Lishuang Cao, Edward Stevens, Paul Whiting and 2 more

Open access · greenAbstract read
In one paragraph

Article in Nature biotechnology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 369 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
369citing papers in PubMed, 2 pooled it
14.1field-weighted citation impact, top 1% 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

369 citing papers in PubMed, 2 syntheses or guidelines pooled it, 613 citations in OpenAlex.

  1. Pooled it
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  7. The Role of the Nervous System in Lung Disease.Current neurology and neuroscience reports · 2026
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309 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

12 authors at 2 institutions in 2 countries.

Stuart M ChambersCenter for Stem Cell Biology, Sloan-Kettering Institute, New York, New York, USA. chambers@mskcc.org
Yuchen Qi
Yvonne Mica
Gabsang Lee
Xin-Jun Zhang
Lei Niu
James Bilsland
Lishuang Cao
Edward Stevens
Paul Whiting
Song-Hai Shi
Lorenz Studer
Kettering University · USPfizer (United Kingdom) · GB

Funding

The Regulation of MGE Proliferation and Cortical Interneuron Fate DeterminationP01NS048120 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI ANDERSON, STEWART A · 2006 to 2015
$12.9M
Molecular Control of Progenitor Cell Polarity and Cortical NeurogenesisR01DA024681 · NIDA · SLOAN-KETTERING INST CAN RESEARCH · PI JOYNER, ALEXANDRA L. · 2008 to 2020
$5.7M
Defining fate potential in human ESC derived neural stem cellsR01NS066390 · NINDS · SLOAN-KETTERING INST CAN RESEARCH · PI STUDER, LORENZ P. · 2009 to 2010
$1.0M
NIDA NIH HHS R01DA024681NINDS NIH HHS NS066390NINDS NIH HHS P01NS048120NINDS NIH HHS R01 NS066390
6 · The paper itself

Abstract

Considerable progress has been made in identifying signaling pathways that direct the differentiation of human pluripotent stem cells (hPSCs) into specialized cell types, including neurons. However, differentiation of hPSCs with extrinsic factors is a slow, step-wise process, mimicking the protracted timing of human development. Using a small-molecule screen, we identified a combination of five small-molecule pathway inhibitors that yield hPSC-derived neurons at >75% efficiency within 10 d of differentiation. The resulting neurons express canonical markers and functional properties of human nociceptors, including tetrodotoxin (TTX)-resistant, SCN10A-dependent sodium currents and response to nociceptive stimuli such as ATP and capsaicin. Neuronal fate acquisition occurs about threefold faster than during in vivo development, suggesting that use of small-molecule pathway inhibitors could become a general strategy for accelerating developmental timing in vitro. The quick and high-efficiency derivation of nociceptors offers unprecedented access to this medically relevant cell type for studies of human pain.

Indexed as

Cell DifferentiationNociceptorsPluripotent Stem CellsSmall Molecule LibrariesAcetanilidesCaffeic AcidsCell Culture TechniquesCell LineGene Expression Regulation, DevelopmentalHumansMolecular Sequence DataNAV1.8 Voltage-Gated Sodium ChannelPainPyridinesPyrimidinesPyrrolesAcetanilidesCaffeic AcidsChir 99021N-(4-(3-(3,4-dihydroxyphenyl)acryloyl)phenyl)-2-(thiophen-2-yl)acetamideNAV1.8 Voltage-Gated Sodium ChannelPyridinesPyrimidinesPyrrolesSCN10A protein, humanSmall Molecule LibrariesSU 5402Tetrodotoxin

Identifiers

PMID22750882
PMCPMC3516136
OpenAlexW2082682623

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.