Evidence map›Paper›PMID 23312517›Full record

ArticleNeuron2013

Directed migration of cortical interneurons depends on the cell-autonomous action of Sip1.

Veronique van den Berghe, Elke Stappers, Bram Vandesande, Jordane Dimidschstein, Roel Kroes, Annick Francis, Andrea Conidi, Flore Lesage, Ruben Dries, Silvia Cazzola and 12 more

Open access · bronzeAbstract read
PubMed Publisher
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 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
7.2field-weighted citation impact, top 3% 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

77 citing papers in PubMed, 128 citations in OpenAlex.

  1. Article
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  7. Developmental trajectories of GABAergic cortical interneurons are sequentially modulated by dynamicProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
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  11. Review
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  16. Transcriptional regulation of neuronal identity.The European journal of neuroscience · 2022
    Review
  17. Article
  18. Article
  19. Article
  20. FLRT2 and FLRT3 Cooperate in Maintaining the Tangential Migratory Streams of Cortical Interneurons during Development.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article

17 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 8 institutions in 4 countries.

Veronique van den BergheLaboratory of Molecular Biology (Celgen), Department of Development and Regeneration, University of Leuven, 3000 Leuven, Belgium.
Elke Stappers
Bram Vandesande
Jordane Dimidschstein
Roel Kroes
Annick Francis
Andrea Conidi
Flore Lesage
Ruben Dries
Silvia Cazzola
Geert Berx
Nicoletta Kessaris
Pierre Vanderhaeghen
Wilfred van Ijcken
Frank G Grosveld
Steven Goossens
Jody J Haigh
Gord Fishell
André Goffinet
Stein Aerts
Danny Huylebroeck
Eve Seuntjens
KU Leuven · BEGhent University · BEUniversité Libre de Bruxelles · BEErasmus MC · NLErasmus University Rotterdam · NLNYU Langone Health · USUCLouvain · BEUniversity College London · GB

Funding

European Research Council 207807Medical Research Council G0501173Wellcome Trust
6 · The paper itself

Abstract

GABAergic interneurons mainly originate in the medial ganglionic eminence (MGE) of the embryonic ventral telencephalon (VT) and migrate tangentially to the cortex, guided by membrane-bound and secreted factors. We found that Sip1 (Zfhx1b, Zeb2), a transcription factor enriched in migrating cortical interneurons, is required for their proper differentiation and correct guidance. The majority of Sip1 knockout interneurons fail to migrate to the neocortex and stall in the VT. RNA sequencing reveals that Sip1 knockout interneurons do not acquire a fully mature cortical interneuron identity and contain increased levels of the repulsive receptor Unc5b. Focal electroporation of Unc5b-encoding vectors in the MGE of wild-type brain slices disturbs migration to the neocortex, whereas reducing Unc5b levels in Sip1 knockout slices and brains rescues the migration defect. Our results reveal that Sip1, through tuning of Unc5b levels, is essential for cortical interneuron guidance.

Indexed as

AnimalsCell MovementCerebral CortexGene Knockout TechniquesInterneuronsMiceMice, TransgenicNeocortexNerve Tissue ProteinsNetrin ReceptorsOrgan Culture TechniquesReceptors, Cell SurfaceTelencephalonNerve Tissue ProteinsNetrin ReceptorsReceptors, Cell SurfaceSip1 protein, mouse

Identifiers

PMID23312517
OpenAlexW2144628304

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.