Evidence map›Paper›PMID 31257105›Full record

ArticleNeuron2019

Non-canonical Wnt Signaling through Ryk Regulates the Generation of Somatostatin- and Parvalbumin-Expressing Cortical Interneurons.

Melissa G McKenzie, Lucy V Cobbs, Patrick D Dummer, Timothy J Petros, Michael M Halford, Steven A Stacker, Yimin Zou, Gord J Fishell, Edmund Au

Open access · bronzeAbstract read
In one paragraph

Article in Neuron, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

9 authors at 5 institutions in 2 countries.

Melissa G McKenzieDepartment of Pathology and Cell Biology, Columbia University Medical Center, New York, NY 10032, USA; NYU Neuroscience Institute, New York University Langone Medical Center, New York, NY 10016, USA.
Lucy V CobbsNYU Neuroscience Institute, New York University Langone Medical Center, New York, NY 10016, USA.
Patrick D DummerDepartment of Pathology and Cell Biology, Columbia University Medical Center, New York, NY 10032, USA.
Timothy J PetrosNYU Neuroscience Institute, New York University Langone Medical Center, New York, NY 10016, USA.
Michael M HalfordTumour Angiogenesis and Microenvironment Program, Department of Oncology, Peter MacCallum Cancer Centre, 305 Grattan St, Melbourne, Victoria 3000, Australia.
Steven A StackerTumour Angiogenesis and Microenvironment Program, Department of Oncology, Peter MacCallum Cancer Centre, 305 Grattan St, Melbourne, Victoria 3000, Australia.
Yimin ZouNeurobiology Section, Biological Sciences Division, University of California, San Diego, CA 92093, USA.
Gord J FishellNYU Neuroscience Institute, New York University Langone Medical Center, New York, NY 10016, USA; Department of Neurobiology, Harvard Medical School, Boston, MA 04115, USA; The Stanley Center at the Broad, Cambridge, MA 02142, USA.
Edmund AuDepartment of Pathology and Cell Biology, Columbia University Medical Center, New York, NY 10032, USA; NYU Neuroscience Institute, New York University Langone Medical Center, New York, NY 10016, USA; Department of Rehabilitation and Regenerative Medicine, Columbia University Medical Center, New York, NY 10032, USA; Columbia Translational Neuroscience Initiative Scholar, Columbia University Medical Center, New York, NY 10032, USA. Electronic address: ea2515@cumc.columbia.edu.
NYU Langone Health · USPeter MacCallum Cancer Centre · AUColumbia University Irving Medical Center · USHarvard University · USUniversity of California, San Diego · US

Funding

The role of genetic and activity dependent cues in the generation of 5HT3aR interneuron diversityP01NS074972 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI RUDY, BERNARDO · 2012 to 2023
$15.5M
Mechanisms regulating interneuron diversity and maturationZIAHD008962 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI PETROS, TIMOTHY · 2017 to 2025
$12.1M
Regional and Genetic Diversity of Cortical InterneuronsR01MH071679 · NIMH · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI FISHELL, GORDON J · 2005 to 2020
$8.5M
Development and validation of AAV vectors to manipulate specific neuronal subtypes and circuits involved in epilepsy and psychiatric disorders across mammalian species.UG3MH120096 · NIMH · BROAD INSTITUTE, INC. · PI DEVERMAN, BENJAMIN E, FISHELL, GORDON J · 2019 to 2021
$6.7M
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
Translational Neuroscience Training Grant.T32MH015174 · NIMH · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI DENNY, CHRISTINE ANN · 1985 to 2020
$4.0M
Developing a stem cell-based model to study MGE and CGE interneuron lineage specificationR03MH119443 · NIMH · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI AU, EDMUND · 2019 to 2020
$162k
Downstream Effectors of Shh and FGF Signaling in the Developing NeocortexF30MH087045 · NIMH · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CAMPBELL, MELISSA MCKENZIE · 2009 to 2011
$114k
NIMH NIH HHS F30 MH087045NIMH NIH HHS R01 MH071679NIMH NIH HHS R03 MH119443NIMH NIH HHS R37 MH071679NIMH NIH HHS T32 MH015174NIMH NIH HHS UG3 MH120096NINDS NIH HHS P01 NS074972NINDS NIH HHS R01 NS081297
6 · The paper itself

Abstract

GABAergic interneurons have many important functions in cortical circuitry, a reflection of their cell diversity. The developmental origins of this diversity are poorly understood. Here, we identify rostral-caudal regionality in Wnt exposure within the interneuron progenitor zone delineating the specification of the two main interneuron subclasses. Caudally situated medial ganglionic eminence (MGE) progenitors receive high levels of Wnt signaling and give rise to somatostatin (SST)-expressing cortical interneurons. By contrast, parvalbumin (PV)-expressing basket cells originate mostly from the rostral MGE, where Wnt signaling is attenuated. Interestingly, rather than canonical signaling through β-catenin, signaling via the non-canonical Wnt receptor Ryk regulates interneuron cell-fate specification in vivo and in vitro. Indeed, gain of function of Ryk intracellular domain signaling regulates SST and PV fate in a dose-dependent manner, suggesting that Ryk signaling acts in a graded fashion. These data reveal an important role for non-canonical Wnt-Ryk signaling in establishing the correct ratios of cortical interneuron subtypes.

Indexed as

Wnt Signaling PathwayAnimalsCerebral CortexGABAergic NeuronsInterneuronsMiceMouse Embryonic Stem CellsNeural Stem CellsNeurogenesisParvalbuminsReceptor Protein-Tyrosine KinasesSomatostatinWnt ProteinsParvalbuminsReceptor Protein-Tyrosine KinasesRyk protein, mouseSomatostatinWnt Proteins

Identifiers

PMID31257105
PMCPMC6728181
OpenAlexW2805053522

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.