Evidence map›Paper›PMID 30308166›Full record

ArticleNeuron2018

Subtype Diversification and Synaptic Specificity of Stem Cell-Derived Spinal Interneurons.

Phuong T Hoang, Joshua I Chalif, Jay B Bikoff, Thomas M Jessell, George Z Mentis, Hynek Wichterle

Open access · bronzeAbstract read
In one paragraph

Article in Neuron, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Qki5 safeguards spinal motor neuron function by defining the motor neuron-specific transcriptome via pre-mRNA processing.Proceedings of the National Academy of Sciences of the United States of America · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Phuong T HoangDepartments of Pathology and Cell Biology, Neuroscience, Rehabilitation & Regenerative Medicine, and Neurology, Center for Motor Neuron Biology and Disease, Columbia Stem Cell Initiative, Columbia University Irving Medical Center, New York, NY 10032, USA.
Joshua I ChalifDepartments of Pathology and Cell Biology and Neurology, Center for Motor Neuron Biology and Disease, Columbia University Irving Medical Center, New York, NY 10032, USA.
Jay B BikoffDepartments of Neuroscience and Biochemistry and Molecular Biophysics, Columbia University Irving Medical Center, New York, NY 10032, USA; Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Thomas M JessellDepartments of Neuroscience and Biochemistry and Molecular Biophysics, Columbia University Irving Medical Center, New York, NY 10032, USA.
George Z MentisDepartments of Pathology and Cell Biology and Neurology, Center for Motor Neuron Biology and Disease, Columbia University Irving Medical Center, New York, NY 10032, USA.
Hynek WichterleDepartments of Pathology and Cell Biology, Neuroscience, Rehabilitation & Regenerative Medicine, and Neurology, Center for Motor Neuron Biology and Disease, Columbia Stem Cell Initiative, Columbia University Irving Medical Center, New York, NY 10032, USA. Electronic address: hw350@columbia.edu.
Columbia University Irving Medical Center · USColumbia University · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007367 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI REINER, STEVEN L · 1985 to 2021
$25.1M
Mechanisms of Central Synaptic Dysfunction in SMAR01NS078375 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI George Z Mentis · 2012 to 2026
$6.6M
CONTROL OF MOTOR NEURON DIFFERENTIATIONR01NS033245 · NINDS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI JESSELL, THOMAS M. · 1994 to 2009
$3.3M
ADVANCED GRADUATE TRAINING PROGRAM IN NEUROBIOLOGY & BEHAVIORT32NS064928 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI HENGST, ULRICH · 2010 to 2024
$3.0M
Motor neuron selector genes and mechanism of their actionR01NS078097 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI WICHTERLE, HYNEK · 2012 to 2016
$2.7M
CONTROL OF MOTOR NEURON DIFFERENTIATIONR37NS033245 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI JESSELL, THOMAS M. · 2010 to 2016
$2.4M
Motor neuron selector genes and mechanism of their actionR56NS078097 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI WICHTERLE, HYNEK · 2017 to 2017
$593k
Stable silencing of spinal motor neuron enhancers by transiently expressed Nkx2.2R21NS092043 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI WICHTERLE, HYNEK · 2015 to 2016
$433k
Excitatory spinal micro-circuit mechanisms involved in locomotor activityF30NS098551 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CHALIF, JOSHUA I · 2016 to 2019
$177k
Investigating V1 interneuron subtype diversity using embryonic stem cellsF30NS092262 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI HOANG, PHUONG THI · 2015 to 2017
$145k
NIGMS NIH HHS T32 GM007367NINDS NIH HHS F30 NS092262NINDS NIH HHS F30 NS098551NINDS NIH HHS R01 NS033245NINDS NIH HHS R01 NS078097NINDS NIH HHS R01 NS078375NINDS NIH HHS R21 NS092043NINDS NIH HHS R37 NS033245NINDS NIH HHS R56 NS078097NINDS NIH HHS T32 NS064928
6 · The paper itself

Abstract

Neuronal diversification is a fundamental step in the construction of functional neural circuits, but how neurons generated from single progenitor domains acquire diverse subtype identities remains poorly understood. Here we developed an embryonic stem cell (ESC)-based system to model subtype diversification of V1 interneurons, a class of spinal neurons comprising four clades collectively containing dozens of molecularly distinct neuronal subtypes. We demonstrate that V1 subtype diversity can be modified by extrinsic signals. Inhibition of Notch and activation of retinoid signaling results in a switch to MafA clade identity and enriches differentiation of Renshaw cells, a specialized MafA subtype that mediates recurrent inhibition of spinal motor neurons. We show that Renshaw cells are intrinsically programmed to migrate to species-specific laminae upon transplantation and to form subtype-specific synapses with motor neurons. Our results demonstrate that stem cell-derived neuronal subtypes can be used to investigate mechanisms underlying neuronal subtype specification and circuit assembly.

Indexed as

AnimalsCell DifferentiationEmbryonic Stem CellsInterneuronsMiceMotor NeuronsNeural Stem CellsNeurogenesisSpinal CordSynapsesdifferentiationembryonic stem cellsin vitromotor neuronneuronsRenshaw cellspinal cordsubtypesynaptic specificityV1 interneuron

Identifiers

PMID30308166
PMCPMC6590086
OpenAlexW2896423589

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.