Evidence map›Paper›PMID 28582422›Full record

ArticlePloS one2017

Role of LRRK2 in the regulation of dopamine receptor trafficking.

Mauro Rassu, Maria Grazia Del Giudice, Simona Sanna, Jean Marc Taymans, Michele Morari, Alberto Brugnoli, Martina Frassineti, Alessandra Masala, Sonia Esposito, Manuela Galioto and 6 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
5.6field-weighted citation impact, top 4% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 81 citations in OpenAlex.

  1. Pooled it
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  10. Leucine-rich repeat kinase 2 limits dopamine D1 receptor signaling in striatum and biases against heavy persistent alcohol drinking.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
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  17. Inhibition of the Exocyst Complex Attenuates the LRRK2 Pathological Effects.International journal of molecular sciences · 2023
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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

16 authors at 6 institutions in 2 countries.

Mauro RassuDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Maria Grazia Del GiudiceDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Simona SannaDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Jean Marc TaymansUMR-S1172, Jean-Pierre Aubert Research Center (Inserm - Université de Lille - CHRU de Lille), Lille, France.
Michele MorariDepartment of Medical Sciences, University of Ferrara, Ferrara, Italy and National Institute for Neuroscience, Ferrara, Italy.
Alberto BrugnoliDepartment of Medical Sciences, University of Ferrara, Ferrara, Italy and National Institute for Neuroscience, Ferrara, Italy.
Martina FrassinetiDepartment of Medical Sciences, University of Ferrara, Ferrara, Italy and National Institute for Neuroscience, Ferrara, Italy.
Alessandra MasalaDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Sonia EspositoDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Manuela GaliotoDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Cristiana ValleFondazione Santa Lucia, IRCCS, Rome, Italy.
Maria Teresa CarriFondazione Santa Lucia, IRCCS, Rome, Italy.
Alice BiosaDepartment of Biology, University of Padova, Padova, Italy.
Elisa GreggioDepartment of Biology, University of Padova, Padova, Italy.
Claudia CrosioDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Ciro IaccarinoDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.ORCID http://orcid.org/0000-0003-1619-7146
University of Sassari · ITUniversity of Ferrara · ITUniversity of Padua · ITFondazione Santa Lucia · ITInserm · FRUniversity of Rome Tor Vergata · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutations in LRRK2 play a critical role in both familial and sporadic Parkinson's disease (PD). Up to date, the role of LRRK2 in PD onset and progression remains largely unknown. However, experimental evidence highlights a critical role of LRRK2 in the control of vesicle trafficking that in turn may regulate different aspects of neuronal physiology. We have analyzed the role of LRRK2 in regulating dopamine receptor D1 (DRD1) and D2 (DRD2) trafficking. DRD1 and DRD2 are the most abundant dopamine receptors in the brain. They differ in structural, pharmacological and biochemical properties, as well as in localization and internalization mechanisms. Our results indicate that disease-associated mutant G2019S LRRK2 impairs DRD1 internalization, leading to an alteration in signal transduction. Moreover, the mutant forms of LRRK2 affect receptor turnover by decreasing the rate of DRD2 trafficking from the Golgi complex to the cell membrane. Collectively, our findings are consistent with the conclusion that LRRK2 influences the motility of neuronal vesicles and the neuronal receptor trafficking. These findings have important implications for the complex role that LRRK2 plays in neuronal physiology and the possible pathological mechanisms that may lead to neuronal death in PD.

Indexed as

AnimalsCell Line, TumorCell MembraneDisease Models, AnimalGene Expression RegulationGene Knock-In TechniquesGolgi ApparatusHumansLeucine-Rich Repeat Serine-Threonine Protein Kinase-2MaleMiceMice, Inbred C57BLMutationNeuronsParkinson DiseaseProtein TransportDrd1 protein, mouseDRD2 protein, mouseLeucine-Rich Repeat Serine-Threonine Protein Kinase-2Lrrk2 protein, mouseReceptors, Dopamine D1Receptors, Dopamine D2

Identifiers

PMID28582422
PMCPMC5459500
OpenAlexW2623680887

What OpenQuestion holds

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LicenceCC BY
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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.