Evidence map›Paper›PMID 31968264›Full record

ArticleCell reports2020

Transcriptional Programming of Human Mechanosensory Neuron Subtypes from Pluripotent Stem Cells.

Alec R Nickolls, Michelle M Lee, David F Espinoza, Marcin Szczot, Ruby M Lam, Qi Wang, Jeanette Beers, Jizhong Zou, Minh Q Nguyen, Hans J Solinski and 5 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Cell reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06052631 (Microneurographic Assessment of Peripheral Nerves in Healthy Volunteers and Individuals With Sensory Dysfunction Caused by Inherited Mutations in the PIEZO2 Gene), which is not on this map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
7.2field-weighted citation impact, top 2% 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.

NCT06052631 not yet recruitingnot on this mapstarted 2026, after this paper: background citation

Microneurographic Assessment of Peripheral Nerves in Healthy Volunteers and Individuals With Sensory Dysfunction Caused by Inherited Mutations in the PIEZO2 Gene

TypeobservationalSponsorNational Center for Complementary and Integrative Health (NCCIH)Ran2026 to 2026Enrolled16ConditionsPIEZO2-Deficiency Syndrome
3 · Its place in the literature

Who cites it

53 citing papers in PubMed, 87 citations in OpenAlex.

  1. Article
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  9. Review
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  11. Decoding Pain: Next-Generation In Vitro Systems for Mechanistic Insights and Drug Discovery.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Review
  12. GABAJournal of neurochemistry · 2025
    Article
  13. Article
  14. Review
  15. Accelerating Diverse Cell-Based Therapies Through Scalable Design.Annual review of chemical and biomolecular engineering · 2024
    Review
  16. Review
  17. Article
  18. PIEZO2-dependent rapid pain system in humans and mice.bioRxiv : the preprint server for biology · 2023
    Article
  19. Article
  20. Article
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

15 authors at 1 institution in 1 country.

Alec R NickollsNational Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA; Department of Neuroscience, Brown University, Providence, RI 02912, USA.
Michelle M LeeNational Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.
David F EspinozaNational Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.
Marcin SzczotNational Center for Complementary and Integrative Health, National Institutes of Health, Bethesda, MD 20892, USA.
Ruby M LamDepartment of Neuroscience, Brown University, Providence, RI 02912, USA; National Center for Complementary and Integrative Health, National Institutes of Health, Bethesda, MD 20892, USA.
Qi WangNational Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Jeanette BeersNational Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Jizhong ZouNational Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Minh Q NguyenNational Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892, USA.
Hans J SolinskiNational Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892, USA.
Aisha A AlJanahiNational Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Kory R JohnsonNational Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.
Michael E WardNational Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.
Alexander T CheslerNational Center for Complementary and Integrative Health, National Institutes of Health, Bethesda, MD 20892, USA. Electronic address: alexander.chesler@nih.gov.
Carsten G BönnemannNational Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA. Electronic address: carsten.bonnemann@nih.gov.
National Institutes of Health · US

Funding

Molecular and Clinical Manifestations of Matrix and Aggregate MyopathiesZIANS003129 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI BÖNNEMANN, CARSTEN · 2011 to 2025
$52.8M
NHLBI iPSC Core FacilityZICHL006145 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI ZOU, JIZHONG · 2012 to 2025
$23.3M
Studies on the molecular, cells, and circuit that underlie somatosensation and painZIAAT000028 · NCCIH · NATIONAL CENTER FOR COMPLEMENTARY & INTEGRATIVE HEALTH · PI CHESLER, ALEXANDER · 2014 to 2025
$12.0M
Intramural NIH HHS ZIA AT000028Intramural NIH HHS ZIA NS003129
6 · The paper itself

Abstract

Efficient and homogeneous in vitro generation of peripheral sensory neurons may provide a framework for novel drug screening platforms and disease models of touch and pain. We discover that, by overexpressing NGN2 and BRN3A, human pluripotent stem cells can be transcriptionally programmed to differentiate into a surprisingly uniform culture of cold- and mechano-sensing neurons. Although such a neuronal subtype is not found in mice, we identify molecular evidence for its existence in human sensory ganglia. Combining NGN2 and BRN3A programming with neural crest patterning, we produce two additional populations of sensory neurons, including a specialized touch receptor neuron subtype. Finally, we apply this system to model a rare inherited sensory disorder of touch and proprioception caused by inactivating mutations in PIEZO2. Together, these findings establish an approach to specify distinct sensory neuron subtypes in vitro, underscoring the utility of stem cell technology to capture human-specific features of physiology and disease.

Indexed as

Mechanotransduction, CellularTranscription, GeneticAnimalsCalciumCell LineCellular ReprogrammingCold TemperatureGene Expression ProfilingGene Expression RegulationHumansInduced Pluripotent Stem CellsIon Channel GatingIon ChannelsMiceNerve Tissue ProteinsNeural CrestCalciumIon ChannelsNerve Tissue ProteinsPIEZO2 protein, humanPOU4F1 protein, humanTranscription Factor Brn-3ATRPM8 protein, humanTRPM Cation ChannelsdifferentiationDRGhumaniPSCmechanosensationneural crestneuronPIEZO2sensoryTRPM8

Identifiers

PMID31968264
PMCPMC7059559
OpenAlexW3002843471

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.