Evidence map›Paper›PMID 40076730›Full record

ReviewInternational journal of molecular sciences2025

LRRK2 in Drosophila Melanogaster Model: Insights into Cellular Dysfunction and Neuroinflammation in Parkinson's Disease.

Cristina Ciampelli, Grazia Galleri, Manuela Galioto, Paolo Mereu, Monica Pirastru, Roberto Bernardoni, Diego Albani, Claudia Crosio, Ciro Iaccarino

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Cristina CiampelliDepartment of Biomedical Sciences, University of Sassari, via Francesco Muroni 25, 07100 Sassari, Italy.ORCID 0000-0002-1761-3124
Grazia GalleriDepartment of Biomedical Sciences, University of Sassari, via Francesco Muroni 25, 07100 Sassari, Italy.ORCID 0000-0001-5379-9387
Manuela GaliotoDepartment of Biomedical Sciences, University of Sassari, via Francesco Muroni 25, 07100 Sassari, Italy.
Paolo MereuDepartment of Biomedical Sciences, University of Sassari, via Francesco Muroni 25, 07100 Sassari, Italy.ORCID 0000-0001-6615-4828
Monica PirastruDepartment of Biomedical Sciences, University of Sassari, via Francesco Muroni 25, 07100 Sassari, Italy.ORCID 0000-0002-0847-1128
Roberto BernardoniDepartment Pharmacy and Biotechnology, University of Bologna, 40126 Bologna, Italy.ORCID 0000-0001-8677-4151
Diego AlbaniDepartment of Agricultural Sciences, University of Sassari, 07100 Sassari, Italy.ORCID 0000-0002-1793-9212
Claudia CrosioDepartment of Biomedical Sciences, University of Sassari, via Francesco Muroni 25, 07100 Sassari, Italy.ORCID 0000-0003-2452-1145
Ciro IaccarinoDepartment of Biomedical Sciences, University of Sassari, via Francesco Muroni 25, 07100 Sassari, Italy.ORCID 0000-0003-1619-7146

Funding

DM 737/2021 FormatoDM 737/2021 Galleri
6 · The paper itself

Abstract

Parkinson's disease (PD) is a fatal neurodegenerative disease for which there are no still effective treatments able to stop or slow down neurodegeneration. To date, pathological mutations in the leucine-rich repeat kinase 2 (LRRK2) gene have been identified as the major genetic cause of PD, although the molecular mechanism responsible for the loss of dopaminergic neurons is still cryptic. In this review, we explore the contribution of Drosophila models to the elucidation of LRRK2 function in different cellular pathways in either neurons or glial cells. Importantly, recent studies have shown that LRRK2 is highly expressed in immunocompetent cells, including astrocytes and microglia in the brain, compared to neuronal expression. LRRK2 mutations are also strongly associated with the development of inflammatory diseases and the production of inflammatory molecules. Using Drosophila models, this paper shows that a genetic reduction of the inflammatory response protects flies from the neurodegeneration induced by LRRK2 pathological mutant expression.

Indexed as

Drosophila melanogasterDrosophila ProteinsLeucine-Rich Repeat Serine-Threonine Protein Kinase-2Neuroinflammatory DiseasesParkinson DiseaseAnimalsDisease Models, AnimalDopaminergic NeuronsHumansMutationProtein Serine-Threonine KinasesDrosophila ProteinsLeucine-Rich Repeat Serine-Threonine Protein Kinase-2LRRK protein, DrosophilaProtein Serine-Threonine KinasesAttacin-ADrosophilaLRRK2Parkinson’s disease

Identifiers

PMID40076730
PMCPMC11900240

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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.