Evidence map›Paper›PMID 36482070›Full record

ArticleNature communications2022

Neural precursor cells tune striatal connectivity through the release of IGFBPL1.

Erica Butti, Stefano Cattaneo, Marco Bacigaluppi, Marco Cambiaghi, Giulia Maria Scotti, Elena Brambilla, Francesca Ruffini, Giacomo Sferruzza, Maddalena Ripamonti, Fabio Simeoni and 12 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 18 citations in OpenAlex.

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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

22 authors at 4 institutions in 1 country.

Erica ButtiNeuroimmunology Unit, Division of Neuroscience, Institute of Experimental Neurology (INSPE), IRCCS San Raffaele Hospital, Milan, Italy.ORCID 0000-0003-0362-273X
Stefano Cattaneo *Neuroimmunology Unit, Division of Neuroscience, Institute of Experimental Neurology (INSPE), IRCCS San Raffaele Hospital, Milan, Italy.ORCID 0000-0002-4287-692X
Marco Bacigaluppi *Neuroimmunology Unit, Division of Neuroscience, Institute of Experimental Neurology (INSPE), IRCCS San Raffaele Hospital, Milan, Italy.ORCID 0000-0002-0213-2328
Marco CambiaghiDepartment of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.
Giulia Maria ScottiOmics Sciences Center, IRCCS San Raffaele Hospital, Milan, Italy.ORCID 0000-0002-6929-4858
Elena BrambillaNeuroimmunology Unit, Division of Neuroscience, Institute of Experimental Neurology (INSPE), IRCCS San Raffaele Hospital, Milan, Italy.ORCID 0000-0003-1399-2128
Francesca RuffiniNeuroimmunology Unit, Division of Neuroscience, Institute of Experimental Neurology (INSPE), IRCCS San Raffaele Hospital, Milan, Italy.ORCID 0000-0002-2226-6366
Giacomo SferruzzaNeuroimmunology Unit, Division of Neuroscience, Institute of Experimental Neurology (INSPE), IRCCS San Raffaele Hospital, Milan, Italy.ORCID 0000-0003-2360-4803
Maddalena RipamontiNeuroimmunology Unit, Division of Neuroscience, Institute of Experimental Neurology (INSPE), IRCCS San Raffaele Hospital, Milan, Italy.ORCID 0000-0002-2664-8898
Fabio SimeoniOmics Sciences Center, IRCCS San Raffaele Hospital, Milan, Italy.ORCID 0000-0003-2475-1311
Laura CacciaguerraNeuroimaging Research Unit, Institute of Experimental Neurology (INSPE), Division of Neuroscience, IRCCS San Raffaele Hospital, Milan, Italy.ORCID 0000-0001-9342-2410
Aurora ZanghìNeuroimaging Research Unit, Institute of Experimental Neurology (INSPE), Division of Neuroscience, IRCCS San Raffaele Hospital, Milan, Italy.
Angelo QuattriniNeuropathology Unit, Institute of Experimental Neurology (INSPE), Division of Neuroscience, IRCCS San Raffaele Hospital, Milan, Italy.
Riccardo FesceDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy.ORCID 0000-0001-9473-896X
Paola Panina-BordignonNeuroimmunology Unit, Division of Neuroscience, Institute of Experimental Neurology (INSPE), IRCCS San Raffaele Hospital, Milan, Italy.ORCID 0000-0001-9913-8568
Francesca GianneseOmics Sciences Center, IRCCS San Raffaele Hospital, Milan, Italy.ORCID 0000-0001-8695-649X
Davide CittaroOmics Sciences Center, IRCCS San Raffaele Hospital, Milan, Italy.ORCID 0000-0003-0384-3700
Tanja KuhlmannInstitute of Neuropathology, University Hospital Muster, Muster, Germany.ORCID 0000-0002-0174-5042
Patrizia D'AdamoMolecular genetics of Intellectual Disability, Division of Neuroscience, IRCCS San Raffaele Hospital, Milan, Italy.ORCID 0000-0002-0312-5541
Maria Assunta RoccaVita-Salute San Raffaele University, Milan, Italy.
Stefano TavernaNeuroimmunology Unit, Division of Neuroscience, Institute of Experimental Neurology (INSPE), IRCCS San Raffaele Hospital, Milan, Italy.ORCID 0000-0003-1871-8662
Gianvito MartinoNeuroimmunology Unit, Division of Neuroscience, Institute of Experimental Neurology (INSPE), IRCCS San Raffaele Hospital, Milan, Italy. martino.gianvito@hsr.it.ORCID 0000-0003-1295-9131
Vita-Salute San Raffaele University · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITHumanitas University · ITUniversity of Verona · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The adult brain retains over life endogenous neural stem/precursor cells (eNPCs) within the subventricular zone (SVZ). Whether or not these cells exert physiological functions is still unclear. In the present work, we provide evidence that SVZ-eNPCs tune structural, electrophysiological, and behavioural aspects of striatal function via secretion of insulin-like growth factor binding protein-like 1 (IGFBPL1). In mice, selective ablation of SVZ-eNPCs or selective abrogation of IGFBPL1 determined an impairment of striatal medium spiny neuron morphology, a higher failure rate in GABAergic transmission mediated by fast-spiking interneurons, and striatum-related behavioural dysfunctions. We also found IGFBPL1 expression in the human SVZ, foetal and induced-pluripotent stem cell-derived NPCs. Finally, we found a significant correlation between SVZ damage, reduction of striatum volume, and impairment of information processing speed in neurological patients. Our results highlight the physiological role of adult SVZ-eNPCs in supporting cognitive functions by regulating striatal neuronal activity.

Indexed as

Insulin-Like Growth Factor Binding ProteinsLateral VentriclesNeural Stem CellsTumor Suppressor ProteinsAnimalsCardiac ElectrophysiologyHumansInsulin-Like Growth Factor Binding Protein 1MiceIGFBPL1 protein, humanIGFBPL-1 protein, mouseInsulin-Like Growth Factor Binding Protein 1Insulin-Like Growth Factor Binding ProteinsTumor Suppressor Proteins

Identifiers

PMID36482070
PMCPMC9731988
OpenAlexW4311583541

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Registered trials

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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.