Evidence map›Paper›PMID 34728600›Full record

ArticleNature communications2021

Extracellular LGALS3BP regulates neural progenitor position and relates to human cortical complexity.

Christina Kyrousi, Adam C O'Neill, Agnieska Brazovskaja, Zhisong He, Pavel Kielkowski, Laure Coquand, Rossella Di Giaimo, Pierpaolo D' Andrea, Alexander Belka, Andrea Forero Echeverry and 14 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
8.4field-weighted citation impact, top 2% 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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 61 citations in OpenAlex.

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  20. The Control of Cortical Folding: Multiple Mechanisms, Multiple Models.The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry · 2024
    Review
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

24 authors at 11 institutions in 8 countries.

Christina KyrousiMax Planck Institute of Psychiatry, 80804, Munich, Germany.
Adam C O'NeillDepartment of Women's and Children's Health, University of Otago, 9054, Dunedin, New Zealand.
Agnieska BrazovskajaMax Planck Institute for Evolutionary Anthropology, 04103, Leipzig, Germany.
Zhisong HeMax Planck Institute for Evolutionary Anthropology, 04103, Leipzig, Germany.ORCID http://orcid.org/0000-0002-1502-4801
Pavel KielkowskiDepartment of Chemistry, Chair of Organic Chemistry II, Center for Integrated Protein Science (CIPSM), Technische Universität München, Garching, Germany.
Laure CoquandInstitut Curie, PSL Research University, CNRS, UMR 144, 26 rue d'Ulm, F-75005, Paris, France.
Rossella Di GiaimoMax Planck Institute of Psychiatry, 80804, Munich, Germany.ORCID http://orcid.org/0000-0003-3604-3697
Pierpaolo D' AndreaMax Planck Institute of Psychiatry, 80804, Munich, Germany.
Alexander BelkaMax Planck Institute of Psychiatry, 80804, Munich, Germany.ORCID http://orcid.org/0000-0001-8051-683X
Andrea Forero EcheverryMax Planck Institute of Psychiatry, 80804, Munich, Germany.
Davide MeiNeuroscience Department, Children's Hospital A. Meyer-University of Florence, 50139, Florence, Italy.
Matteo LengeNeuroscience Department, Children's Hospital A. Meyer-University of Florence, 50139, Florence, Italy.ORCID http://orcid.org/0000-0003-2848-621X
Cristiana CruceanuDepartment of Translational Research in Psychiatry, Max Planck Institute of Psychiatry, 80804, Munich, Germany.
Isabel Y BuchsbaumMax Planck Institute of Psychiatry, 80804, Munich, Germany.
Shahryar KhattakDFG-Research Center and Cluster of Excellence for Regenerative Therapies (CRTD), School of Medicine, Technical University Dresden, 01307, Dresden, Germany.ORCID http://orcid.org/0000-0003-0580-190X
Guimiot FabienUnité de Foetopathologie, Assistance Publique-Hôpitaux de Paris, CHU Robert Debré, F-75019, Paris, France.
Elisabeth BinderDepartment of Translational Research in Psychiatry, Max Planck Institute of Psychiatry, 80804, Munich, Germany.ORCID http://orcid.org/0000-0001-7088-6618
Frances ElmslieSouth West Thames Regional Genetics Service, St George's, University of London, London, SW17 0RE, UK.
Renzo GuerriniNeuroscience Department, Children's Hospital A. Meyer-University of Florence, 50139, Florence, Italy.
Alexandre D BaffetInstitut Curie, PSL Research University, CNRS, UMR 144, 26 rue d'Ulm, F-75005, Paris, France.ORCID http://orcid.org/0000-0001-9194-4258
Stephan A SieberDepartment of Chemistry, Chair of Organic Chemistry II, Center for Integrated Protein Science (CIPSM), Technische Universität München, Garching, Germany.ORCID http://orcid.org/0000-0002-9400-906X
Barbara TreutleinMax Planck Institute for Evolutionary Anthropology, 04103, Leipzig, Germany.ORCID http://orcid.org/0000-0002-3299-5597
Stephen P RobertsonDepartment of Women's and Children's Health, University of Otago, 9054, Dunedin, New Zealand. stephen.robertson@otago.ac.nz.ORCID http://orcid.org/0000-0002-5181-7809
Silvia CappelloMax Planck Institute of Psychiatry, 80804, Munich, Germany. silvia_cappello@psych.mpg.de.ORCID http://orcid.org/0000-0003-1553-6775
Max Planck Institute of Psychiatry · DEMeyer Children's Hospital · ITCenter for Integrated Protein Science Munich · DECentre National de la Recherche Scientifique · FRETH Zurich · CHUniversity of Otago · NZAssistance Publique – Hôpitaux de Paris · FRMax Planck Institute for Evolutionary Anthropology · DENational and Kapodistrian University of Athens · GRRoyal College of Surgeons in Ireland - Bahrain · BHSt George's, University of London · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

Basal progenitors (BPs), including intermediate progenitors and basal radial glia, are generated from apical radial glia and are enriched in gyrencephalic species like humans, contributing to neuronal expansion. Shortly after generation, BPs delaminate towards the subventricular zone, where they further proliferate before differentiation. Gene expression alterations involved in BP delamination and function in humans are poorly understood. Here, we study the role of LGALS3BP, so far known as a cancer biomarker, which is a secreted protein enriched in human neural progenitors (NPCs). We show that individuals with LGALS3BP de novo variants exhibit altered local gyrification, sulcal depth, surface area and thickness in their cortex. Additionally, using cerebral organoids, human fetal tissues and mice, we show that LGALS3BP regulates the position of NPCs. Single-cell RNA-sequencing and proteomics reveal that LGALS3BP-mediated mechanisms involve the extracellular matrix in NPCs' anchoring and migration within the human brain. We propose that its temporal expression influences NPCs' delamination, corticogenesis and gyrification extrinsically.

Indexed as

AnimalsAntigens, NeoplasmBiomarkers, TumorCell DifferentiationCerebral CortexExtracellular Matrix ProteinsExtracellular VesiclesFemaleHumansInduced Pluripotent Stem CellsLateral VentriclesMiceMice, Inbred C57BLModels, AnimalNeocortexNeural Stem CellsAntigens, NeoplasmBiomarkers, TumorExtracellular Matrix ProteinsLGALS3BP protein, human

Identifiers

PMID34728600
PMCPMC8564519
OpenAlexW3210544435

What OpenQuestion holds

Textmetadata
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.