Evidence map›Paper›PMID 39356746›Full record

ArticleScience translational medicine2024

LRRK2 regulates production of reactive oxygen species in cell and animal models of Parkinson's disease.

Matthew T Keeney, Emily M Rocha, Eric K Hoffman, Kyle Farmer, Roberto Di Maio, Julie Weir, Weston G Wagner, Xiaoping Hu, Courtney L Clark, Sandra L Castro and 8 more

Abstract read
In one paragraph

Article in Science translational medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. LRRK2 as a Potential Disease-Modifying Target in Sporadic Parkinson's Disease.Movement disorders : official journal of the Movement Disorder Society · 2026
    Review
  9. Article
  10. Review
  11. bioRxiv : the preprint server for biology · 2025
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
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  20. 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

18 authors.

Matthew T KeeneyPittsburgh Institute for Neurodegenerative Diseases, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.ORCID 0000-0003-4968-3722
Emily M RochaPittsburgh Institute for Neurodegenerative Diseases, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.ORCID 0000-0003-2171-5104
Eric K HoffmanPittsburgh Institute for Neurodegenerative Diseases, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.ORCID 0000-0003-4419-2748
Kyle FarmerPittsburgh Institute for Neurodegenerative Diseases, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Roberto Di MaioPittsburgh Institute for Neurodegenerative Diseases, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.ORCID 0000-0003-2162-1781
Julie WeirPittsburgh Institute for Neurodegenerative Diseases, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Weston G WagnerPittsburgh Institute for Neurodegenerative Diseases, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Xiaoping HuPittsburgh Institute for Neurodegenerative Diseases, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Courtney L ClarkPittsburgh Institute for Neurodegenerative Diseases, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Sandra L CastroPittsburgh Institute for Neurodegenerative Diseases, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.ORCID 0009-0001-0878-6330
Abigail ScheirerPittsburgh Institute for Neurodegenerative Diseases, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.ORCID 0009-0002-5867-3657
Marco FazzariDepartment of Pharmacology and Chemical Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.ORCID 0000-0002-4051-4431
Briana R De MirandaPittsburgh Institute for Neurodegenerative Diseases, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.ORCID 0000-0001-8817-327X
Sean A PintchovskiAcurex Biosciences, San Carlos, CA, USA.ORCID 0000-0002-2345-3884
William D ShraderAcurex Biosciences, San Carlos, CA, USA.ORCID 0000-0002-5713-7636
Patrick J PaganoDepartment of Pharmacology and Chemical Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.ORCID 0000-0002-7475-808X
Teresa G HastingsPittsburgh Institute for Neurodegenerative Diseases, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
J Timothy GreenamyrePittsburgh Institute for Neurodegenerative Diseases, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.ORCID 0000-0003-3468-7878

Funding

LRRK2 and Oxidative Stress in Parkinson’s DiseaseR01NS131137 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI J Timothy Greenamyre · 2024 to 2026
$1.5M
LRRK2 and oxidative stress in Parkinson’s diseaseR56NS131137 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GREENAMYRE, J TIMOTHY · 2023 to 2023
$557k
NINDS NIH HHS R01 NS131137NINDS NIH HHS R56 NS131137
6 · The paper itself

Abstract

Oxidative stress has long been implicated in Parkinson's disease (PD) pathogenesis, although the sources and regulation of reactive oxygen species (ROS) production are poorly defined. Pathogenic mutations in the gene encoding leucine-rich repeat kinase 2 (LRRK2) are associated with increased kinase activity and a greater risk of PD. The substrates and downstream consequences of elevated LRRK2 kinase activity are still being elucidated, but overexpression of mutant LRRK2 has been associated with oxidative stress, and antioxidants reportedly mitigate LRRK2 toxicity. Here, using CRISPR-Cas9 gene-edited HEK293 cells, RAW264.7 macrophages, rat primary ventral midbrain cultures, and PD patient-derived lymphoblastoid cells, we found that elevated LRRK2 kinase activity was associated with increased ROS production and lipid peroxidation and that this was blocked by inhibitors of either LRRK2 kinase or NADPH oxidase 2 (NOX2). Oxidative stress induced by the pesticide rotenone was ameliorated by LRRK2 kinase inhibition and was absent in cells devoid of LRRK2. In a rat model of PD induced by rotenone, a LRRK2 kinase inhibitor prevented the lipid peroxidation and NOX2 activation normally seen in nigral dopaminergic neurons in this model. Mechanistically, LRRK2 kinase activity was shown to regulate phosphorylation of serine-345 in the p47

Indexed as

Disease Models, AnimalLeucine-Rich Repeat Serine-Threonine Protein Kinase-2NADPH Oxidase 2Oxidative StressParkinson DiseaseReactive Oxygen SpeciesRotenoneAnimalsHEK293 CellsHumansLipid PeroxidationMiceNADPH OxidasesPhosphorylationRatsRats, Sprague-DawleyLeucine-Rich Repeat Serine-Threonine Protein Kinase-2LRRK2 protein, humanNADPH Oxidase 2NADPH Oxidasesneutrophil cytosolic factor 1Reactive Oxygen SpeciesRotenone

Identifiers

PMID39356746
PMCPMC13280971

What Socratic holds

Textmetadata
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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 Socratic graph.