Evidence map›Paper›PMID 22770513›Full record

ArticleNeural development2012

Layer 6 cortical neurons require Reelin-Dab1 signaling for cellular orientation, Golgi deployment, and directed neurite growth into the marginal zone.

Ryan S O'Dell, Candida J M Ustine, David A Cameron, Sean M Lawless, Rebecca M Williams, Warren R Zipfel, Eric C Olson

Open access · goldAbstract read
In one paragraph

Article in Neural development, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

28 citing papers in PubMed, 39 citations in OpenAlex.

  1. MTCL2 Is Essential for the Bipolar-to-Multipolar Transition in the Dendrite Extension of Cerebellar Granule Neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
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  14. Beyond Axon Guidance: Roles of Slit-Robo Signaling in Neocortical Formation.Frontiers in cell and developmental biology · 2020
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  20. Reelin Prevents Apical Neurite Retraction during Terminal Translocation and Dendrite Initiation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    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

7 authors at 2 institutions in 1 country.

Ryan S O'DellDepartment of Neuroscience and Physiology, SUNY Upstate Medical University, 750 E. Adams St, Syracuse, NY 13210, USA.
Candida J M Ustine
David A Cameron
Sean M Lawless
Rebecca M Williams
Warren R Zipfel
Eric C Olson
SUNY Upstate Medical University · USCornell University · US

Funding

YIELD SINGLE MOLECULE IN FCS COLLECTION VOLUME BY NUMERICAL SIMULATIONP41RR004224 · NCRR · CORNELL UNIVERSITY ITHACA · PI WEBB, WATT W · 1988 to 2002
$3.1M
Cellular and Molecular Mechanisms of Early Cortical DevelopmentR01NS066071 · NINDS · UPSTATE MEDICAL UNIVERSITY · PI OLSON, ERIC CHRISTOPHER · 2009 to 2013
$1.2M
NCRR NIH HHS P41-RR04224NINDS NIH HHS NS066071NINDS NIH HHS R01 NS066071
6 · The paper itself

Abstract

backgroundThe secreted ligand Reelin is believed to regulate the translocation of prospective layer 6 (L6) neocortical neurons into the preplate, a loose layer of pioneer neurons that overlies the ventricular zone. Recent studies have also suggested that Reelin controls neuronal orientation and polarized dendritic growth during this period of early cortical development. To explicitly characterize and quantify how Reelin controls this critical aspect of neurite initiation and growth we used a new ex utero explant model of early cortical development to selectively label a subset of L6 cortical neurons for complete 3-D reconstruction.

resultsThe total neurite arbor sizes of neurons in Reelin-deficient (reeler mutant) and Dab1-deficient (Reelin-non-responsive scrambler mutant) cortices were quantified and unexpectedly were not different than control arbor lengths (p = 0.51). For each mutant, however, arbor organization was markedly different: mutant neurons manifested more primary processes (neurites emitted directly from the soma) than wild type, and these neurites were longer and displayed less branching. Reeler and scrambler mutant neurites extended tangentially rather than radially, and the Golgi apparatus that normally invests the apical neurite was compact in both reeler and scrambler mutants. Mutant cortices also exhibited a neurite "exclusion zone" which was relatively devoid of L6 neuron neurites and extended at least 15 μm beneath the pial surface, an area corresponding to the marginal zone (MZ) in the wild type explants. The presence of an exclusion zone was also indicated in the orientation of mutant primary neurite and neuronal somata, which failed to adopt angles within ~20˚ of the radial line to the pial surface. Injection of recombinant Reelin to reeler, but not scrambler, mutant cortices fully rescued soma orientation, Golgi organization, and dendritic projection defects within four hrs.

conclusionsThese findings indicate Reelin promotes directional dendritic growth into the MZ, an otherwise exclusionary zone for L6 neurites.

Indexed as

AnimalsCell Adhesion Molecules, NeuronalExtracellular Matrix ProteinsFemaleHEK293 CellsHumansMaleMiceMice, KnockoutMice, Neurologic MutantsMice, TransgenicNeocortexNerve Tissue ProteinsNeuritesNeuronsOrgan Culture TechniquesCell Adhesion Molecules, NeuronalDab1 protein, mouseExtracellular Matrix ProteinsNerve Tissue ProteinsReelin ProteinRELN protein, humanReln protein, mouseSerine Endopeptidases

Identifiers

PMID22770513
PMCPMC3466444
OpenAlexW2108867585

What OpenQuestion holds

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LicenceCC BY
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.