Evidence map›Paper›PMID 24314726›Full record

ArticleNeuron2013

A modular gain-of-function approach to generate cortical interneuron subtypes from ES cells.

Edmund Au, Tanzeel Ahmed, Theofanis Karayannis, Shiona Biswas, Lin Gan, Gord Fishell

Abstract read
In one paragraph

Article in Neuron, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
–field-weighted citation impact
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

31 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Interneuron Types as Attractors and Controllers.Annual review of neuroscience · 2020
    Review
  11. Article
  12. Review
  13. Article
  14. Characterization of Glcci1 expression in a subpopulation of lateral ganglionic eminence progenitors in the mouse telencephalon.Developmental dynamics : an official publication of the American Association of Anatomists · 2018
    Article
  15. Article
  16. Cortical interneuron development: a tale of time and space.Development (Cambridge, England) · 2017
    Review
  17. Review
  18. Development (Cambridge, England) · 2017
    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

6 authors.

Edmund AuNYU Neuroscience Institute, NYU Langone Medical Center, 522 First Avenue, New York, NY 10016, USA; New York University School of Medicine, NYU Langone Medical Center, 522 First Avenue, New York, NY 10016, USA.
Tanzeel Ahmed
Theofanis Karayannis
Shiona Biswas
Lin Gan
Gord Fishell

Funding

The role of genetic and activity dependent cues in the generation of 5HT3aR interneuron diversityP01NS074972 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI MACHOLD, ROBERT P · 2012 to 2023
$15.5M
Regional and Genetic Diversity of Cortical InterneuronsR01MH071679 · NIMH · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI FISHELL, GORDON J · 2005 to 2020
$8.5M
The Development and Integration of Early Born SST-Expressing Interneurons in the CortexR01NS081297 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI GORDON J FISHELL · 2012 to 2026
$6.6M
The molecular and cellular basis of cortical interneuron divergenceR37MH071679 · NIMH · HARVARD MEDICAL SCHOOL · PI GORDON J FISHELL · 2022 to 2026
$4.1M
FoxG1 in the Development of Cerebral Cortex and the Adult Neural Niche.R01MH095147 · NIMH · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI FISHELL, GORDON J · 2012 to 2013
$1.2M
CIHRNIMH NIH HHS MH071679NIMH NIH HHS MH095147NIMH NIH HHS R01 MH071679NIMH NIH HHS R37 MH071679NINDS NIH HHS NS074972NINDS NIH HHS NS081297
6 · The paper itself

Abstract

Whereas past work indicates that cortical interneurons (cINs) can be generically produced from stem cells, generating large numbers of specific subtypes of this population has remained elusive. This reflects an information gap in our understanding of the transcriptional programs required for different interneuron subtypes. Here, we have utilized the directed differentiation of stem cells into specific subpopulations of cortical interneurons as a means to identify some of these missing factors. To establish this approach, we utilized two factors known to be required for the generation of cINs, Nkx2-1 and Dlx2. As predicted, their regulated transient expression greatly improved the differentiation efficiency and specificity over baseline. We extended upon this "cIN-primed" model in order to establish a modular system whereby a third transcription factor could be systematically introduced. Using this approach, we identified Lmo3 and Pou3f4 as genes that can augment the differentiation and/or subtype specificity of cINs in vitro.

Indexed as

Action PotentialsAnimalsAnimals, NewbornCell DifferentiationCell LineageCerebral CortexEmbryo, MammalianEmbryonic Stem CellsGene Expression Regulation, DevelopmentalGreen Fluorescent ProteinsHomeodomain ProteinsInterneuronsIn Vitro TechniquesLIM Domain ProteinsMiceMice, TransgenicDistal-less homeobox proteinsGreen Fluorescent ProteinsHomeodomain ProteinsLIM Domain ProteinsNerve Tissue ProteinsNkx2-1 protein, mouseNuclear ProteinsThyroid Nuclear Factor 1Transcription Factors

Identifiers

PMID24314726
PMCPMC5085060

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.