Evidence map›Paper›PMID 25804737›Full record

ArticleDevelopment (Cambridge, England)2015

Duration of culture and sonic hedgehog signaling differentially specify PV versus SST cortical interneuron fates from embryonic stem cells.

Jennifer A Tyson, Ethan M Goldberg, Asif M Maroof, Qing Xu, Timothy J Petros, Stewart A Anderson

Open access · greenAbstract read
In one paragraph

Article in Development (Cambridge, England), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

27 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Development, Diversity, and Death of MGE-Derived Cortical Interneurons.International journal of molecular sciences · 2021
    Review
  9. Article
  10. Direct reprogramming into interneurons: potential for brain repair.Cellular and molecular life sciences : CMLS · 2019
    Review
  11. Article
  12. Review
  13. Embryonic stem cell transplants as a therapeutic strategy in a rodent model of autism.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2018
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  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 at 5 institutions in 2 countries.

Jennifer A TysonDepartment of Psychiatry, Children's Hospital of Philadelphia, University of Pennsylvania School of Medicine ARC 517, Philadelphia, PA 19104-5127, USA Department of Psychiatry, Weill Medical College of Cornell University, New York, NY 10021, USA.
Ethan M GoldbergDivision of Neurology, The Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia, PA 19083, USA Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19083, USA.
Asif M MaroofHarvard University Department of Stem Cell and Regenerative Biology, Cambridge, MA 02138, USA.
Qing XuCenter for Genomics and Systems Biology, New York University Abu Dhabi, Abu Dhabi, United Arab Emirates.
Timothy J PetrosDepartment of Neuroscience, NYU Langone Medical Center, New York, NY 10016, USA.
Stewart A AndersonDepartment of Psychiatry, Children's Hospital of Philadelphia, University of Pennsylvania School of Medicine ARC 517, Philadelphia, PA 19104-5127, USA sande@mail.med.upenn.edu.
Philadelphia University · USChildren's Hospital of Philadelphia · USHarvard Stem Cell Institute · USNew York University Abu Dhabi · AENYU Langone Health · US

Funding

Specification of Interneurons of the Cerebral CortexR01MH066912 · NIMH · WEILL MEDICAL COLL OF CORNELL UNIV · PI ANDERSON, STEWART A · 2003 to 2020
$5.7M
NSADA Training Grant for Child NeurologistsK12NS049453 · NINDS · CHILDREN'S HOSP OF PHILADELPHIA · PI TENNEKOON, GIHAN I · 2006 to 2015
$4.4M
Training Program in Developmental BiologyT32HD060600 · NICHD · WEILL MEDICAL COLL OF CORNELL UNIV · PI BAO, ZHIRONG, STUHLMANN, HEIDI · 2010 to 2024
$3.5M
Specification of Cortical InterneuronsK02MH070031 · NIMH · WEILL MEDICAL COLL OF CORNELL UNIV · PI ANDERSON, STEWART A · 2004 to 2013
$1.2M
Investigation into the mechanisms for generating interneuron diversityK99MH104595 · NIMH · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI PETROS, TIMOTHY J · 2014 to 2015
$180k
Generation of interneurons derived from ES cells using inducible expression of trF32NS074742 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI PETROS, TIMOTHY J · 2011 to 2013
$153k
NICHD NIH HHS T32 1T32HD060600NICHD NIH HHS T32 HD060600NIMH NIH HHS K02 MH070031NIMH NIH HHS K99 MH104595NIMH NIH HHS R01 MH066912NIMH NIH HHS R01 MH066912-01NINDS NIH HHS F32 NS074742NINDS NIH HHS K12 NS049453PHS HHS NSADA K12NS049453
6 · The paper itself

Abstract

Medial ganglionic eminence (MGE)-derived GABAergic cortical interneurons (cINs) consist of multiple subtypes that are involved in many cortical functions. They also have a remarkable capacity to migrate, survive and integrate into cortical circuitry after transplantation into postnatal cortex. These features have engendered considerable interest in generating distinct subgroups of interneurons from pluripotent stem cells (PSCs) for the study of interneuron fate and function, and for the development of cell-based therapies. Although advances have been made, the capacity to generate highly enriched pools of subgroup fate-committed interneuron progenitors from PSCs has remained elusive. Previous studies have suggested that the two main MGE-derived interneuron subgroups--those expressing somatostatin (SST) and those expressing parvalbumin (PV)--are specified in the MGE from Nkx2.1-expressing progenitors at higher or lower levels of sonic hedgehog (Shh) signaling, respectively. To further explore the role of Shh and other factors in cIN fate determination, we generated a reporter line such that Nkx2.1-expressing progenitors express mCherry and postmitotic Lhx6-expressing MGE-derived interneurons express GFP. Manipulations of Shh exposure and time in culture influenced the subgroup fates of ESC-derived interneurons. Exposure to higher Shh levels, and collecting GFP-expressing precursors at 12 days in culture, resulted in the strongest enrichment for SST interneurons over those expressing PV, whereas the strongest enrichment for PV interneurons was produced by lower Shh and by collecting mCherry-expressing cells after 17 days in culture. These findings confirm that fate determination of cIN subgroups is crucially influenced by Shh signaling, and provide a system for the further study of interneuron fate and function.

Indexed as

Cell LineageSignal TransductionAction PotentialsAnimalsBody PatterningCell LineCell SeparationCerebral CortexEmbryonic Stem CellsGABAergic NeuronsGenes, ReporterGreen Fluorescent ProteinsHedgehog ProteinsInterneuronsMedian EminenceMiceGreen Fluorescent ProteinsHedgehog ProteinsParvalbuminsShh protein, mouseSomatostatinCortical interneuronsEmbryonic stem cellsFate specificationMouseParvalbuminSomatostatinSonic hedgehog

Identifiers

PMID25804737
PMCPMC4378243
OpenAlexW2095335071

What OpenQuestion holds

Textmetadata
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.