Evidence map›Paper›PMID 31363062›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2019

GPRIN3 Controls Neuronal Excitability, Morphology, and Striatal-Dependent Behaviors in the Indirect Pathway of the Striatum.

Deniz Karadurmus, Daniel Rial, Jean-François De Backer, David Communi, Alban de Kerchove d'Exaerde, Serge N Schiffmann

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

18 citing papers in PubMed, 33 citations in OpenAlex.

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  7. Unsupervised pattern identification in spatial gene expression atlas reveals mouse brain regions beyond established ontology.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  8. Article
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  13. Genetic Elements at the Alpha-Synuclein Locus.Frontiers in neuroscience · 2022
    Review
  14. Article
  15. Article
  16. Drug addiction: from bench to bedside.Translational psychiatry · 2021
    Review
  17. Article
  18. 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

6 authors at 1 institution in 2 countries.

Deniz KaradurmusLaboratory of Neurophysiology, ULB-Neuroscience Institute, Université Libre de Bruxelles.ORCID 0000-0001-8663-6357
Daniel RialLaboratory of Neurophysiology, ULB-Neuroscience Institute, Université Libre de Bruxelles.ORCID 0000-0002-2079-7331
Jean-François De BackerLaboratory of Neurophysiology, ULB-Neuroscience Institute, Université Libre de Bruxelles.
David CommuniInstitut de Recherche Interdisciplinaire en Biologie Humaine et Moléculaire, Université Libre de Bruxelles, Brussels, B-1070, Belgium, and.
Alban de Kerchove d'ExaerdeLaboratory of Neurophysiology, ULB-Neuroscience Institute, Université Libre de Bruxelles, adekerch@ulb.ac.be sschiffm@ulb.ac.be.ORCID 0000-0002-0682-5877
Serge N SchiffmannLaboratory of Neurophysiology, ULB-Neuroscience Institute, Université Libre de Bruxelles, adekerch@ulb.ac.be sschiffm@ulb.ac.be.ORCID 0000-0002-0118-9816
Université Libre de Bruxelles · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The regulation of the striatum by the GPCR signaling through neuromodulators is essential for its physiology and physiopathology, so it is necessary to know all the compounds of these pathways. In this study, we identified a new important partner of the dopaminergic pathway: GPRIN3 (a member of the GPRIN family). GPRIN3 is highly expressed in the striatum but with undefined function. Cell sorting of medium spiny neurons (MSNs) in indirect MSNs and direct MSNs indicated the presence of the GPRIN3 gene in both populations with a preferential expression in indirect MSNs. This led us to generate GPRIN3 KO mice by CRISPR/Cas9 and test male animals to access possible alterations in morphological, electrophysiological, and behavioral parameters following its absence. 3D reconstruction analysis of MSNs revealed increased neuronal arborization in GPRIN3 KO and modified passive and active electrophysiological properties. These cellular alterations were coupled with increased motivation and cocaine-induced hyperlocomotion. Additionally, using a specific indirect MSN knockdown, we showed a preferential role for GPRIN3 in indirect MSNs related to the D

Indexed as

AnimalsCorpus StriatumMaleMiceMice, KnockoutNerve Tissue ProteinsNeuronsReceptors, Dopamine D2Signal TransductionGprin3 protein, mouseNerve Tissue ProteinsReceptors, Dopamine D2Crispr/Cas9D2 receptorsGPRIN3iMSNsstriatum

Identifiers

PMID31363062
PMCPMC6750934
OpenAlexW2965899752

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.