Evidence map›Paper›PMID 21617644›Full record

ArticleNature2011

Induction of human neuronal cells by defined transcription factors.

Zhiping P Pang, Nan Yang, Thomas Vierbuchen, Austin Ostermeier, Daniel R Fuentes, Troy Q Yang, Ami Citri, Vittorio Sebastiano, Samuele Marro, Thomas C Südhof and 1 more

Registry-linked trialAbstract read
In one paragraph

Article in Nature, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02980302 (Development of the Tool " iPSC "), which is not on this map. Cited by 735 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
735citing papers in PubMed, 2 pooled it
50.0field-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.

NCT02980302 nacompletednot on this mapstarted 2015, after this paper: background citation

Development of the Tool " iPSC " (Induced Pluripotent Stem Cells) for the Functional Study of Mutations Responsible for Mental Retardation - Application to Familial Study of MYT1L Gene Mutations

TypeinterventionalSponsorUniversity Hospital, GrenobleRan2015 to 2017Enrolled4ConditionsIntellectual Deficiency, Asymptomatic Carrier of the Mutation of the Gene MYT1L, Healthy VolunteersArmsCutaneous biopsy
3 · Its place in the literature

Who cites it

735 citing papers in PubMed, 2 syntheses or guidelines pooled it, 1,262 citations in OpenAlex.

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  19. Reprogramming of neuronal genome function and phenotype by astrocytes.bioRxiv : the preprint server for biology · 2026
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675 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Zhiping P PangDepartment of Molecular and Cellular Physiology, Stanford University School of Medicine, 265 Campus Drive, Stanford, California 94305, USA.
Nan Yang
Thomas Vierbuchen
Austin Ostermeier
Daniel R Fuentes
Troy Q Yang
Ami Citri
Vittorio Sebastiano
Samuele Marro
Thomas C Südhof
Marius Wernig
Stanford University · USHoward Hughes Medical Institute · US

Funding

Leveraging innovative technologies in basic and clinical cancer researchT32CA009302 · NCI · STANFORD UNIVERSITY · PI LAURA D ATTARDI, Aaron M Newman · 1985 to 2026
$19.1M
Induced neuronal cells: A novel tool to study neuropsychiatric diseasesR01MH092931 · NIMH · STANFORD UNIVERSITY · PI Thomas C. Sudhof, Marius Wernig · 2010 to 2026
$9.7M
Dissecting the mechanism of direct neural induction through genomic interrogationRC4NS073015 · NINDS · STANFORD UNIVERSITY · PI CHANG, HOWARD Y, QUAKE, STEPHEN R · 2010 to 2010
$2.9M
Howard Hughes Medical InstituteNCI NIH HHS T32 CA009302NIMH NIH HHS 1R01MH092931NIMH NIH HHS R01 MH092931NINDS NIH HHS RC4 NS073015NINDS NIH HHS RC4NS073015
6 · The paper itself

Abstract

Somatic cell nuclear transfer, cell fusion, or expression of lineage-specific factors have been shown to induce cell-fate changes in diverse somatic cell types. We recently observed that forced expression of a combination of three transcription factors, Brn2 (also known as Pou3f2), Ascl1 and Myt1l, can efficiently convert mouse fibroblasts into functional induced neuronal (iN) cells. Here we show that the same three factors can generate functional neurons from human pluripotent stem cells as early as 6 days after transgene activation. When combined with the basic helix-loop-helix transcription factor NeuroD1, these factors could also convert fetal and postnatal human fibroblasts into iN cells showing typical neuronal morphologies and expressing multiple neuronal markers, even after downregulation of the exogenous transcription factors. Importantly, the vast majority of human iN cells were able to generate action potentials and many matured to receive synaptic contacts when co-cultured with primary mouse cortical neurons. Our data demonstrate that non-neural human somatic cells, as well as pluripotent stem cells, can be converted directly into neurons by lineage-determining transcription factors. These methods may facilitate robust generation of patient-specific human neurons for in vitro disease modelling or future applications in regenerative medicine.

Indexed as

Cell DifferentiationCellular ReprogrammingAnimalsBasic Helix-Loop-Helix ProteinsCell LineCells, CulturedCerebral CortexCoculture TechniquesDNA-Binding ProteinsElectric ConductivityFibroblastsHumansMembrane PotentialsMiceNerve Tissue ProteinsNeuronsAscl1 protein, mouseBasic Helix-Loop-Helix ProteinsDNA-Binding ProteinsMyt1l protein, mouseMyt1 protein, mouseNerve Tissue ProteinsNeurod1 protein, mousePou3f2 protein, mousePOU Domain FactorsTranscription Factors

Identifiers

PMID21617644
PMCPMC3159048
OpenAlexW2095546080

What OpenQuestion holds

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LicenceTDM
Read underepoch 390

Registered trials

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.