Evidence map›Paper›PMID 33323945›Full record

ArticleCell death and differentiation2021

Gender biased neuroprotective effect of Transferrin Receptor 2 deletion in multiple models of Parkinson's disease.

Chiara Milanese, Sylvia Gabriels, Sander Barnhoorn, Silvia Cerri, Ayse Ulusoy, S V Gornati, Daniel F Wallace, Fabio Blandini, Donato A Di Monte, V Nathan Subramaniam and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Cell death and differentiation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.5field-weighted citation impact, top 28% 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

10 citing papers in PubMed, 11 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

11 authors at 7 institutions in 4 countries.

Chiara MilaneseDepartment of Molecular Genetics, Rotterdam, the Netherlands.ORCID http://orcid.org/0000-0001-8696-2603
Sylvia GabrielsDepartment of Molecular Genetics, Rotterdam, the Netherlands.
Sander BarnhoornDepartment of Molecular Genetics, Rotterdam, the Netherlands.
Silvia CerriIRCCS Mondino Foundation, 27100, Pavia, Italy.
Ayse UlusoyGerman Centre for Neurodegenerative Diseases (DZNE), 53175, Bonn, Germany.ORCID http://orcid.org/0000-0003-2840-3429
S V GornatiDepartment of Neuroscience Erasmus MC, Rotterdam, the Netherlands.
Daniel F WallaceSchool of Biomedical Sciences, Institute of Health and Biomedical Innovation, Queensland University of Technology (QUT), Brisbane, QLD, Australia.ORCID http://orcid.org/0000-0002-6019-9424
Fabio BlandiniIRCCS Mondino Foundation, 27100, Pavia, Italy.
Donato A Di MonteGerman Centre for Neurodegenerative Diseases (DZNE), 53175, Bonn, Germany.
V Nathan SubramaniamSchool of Biomedical Sciences, Institute of Health and Biomedical Innovation, Queensland University of Technology (QUT), Brisbane, QLD, Australia.ORCID http://orcid.org/0000-0002-4583-7790
Pier G MastroberardinoDepartment of Molecular Genetics, Rotterdam, the Netherlands. p.g.mastroberardino@erasmusmc.nl.ORCID http://orcid.org/0000-0003-2364-4258
German Center for Neurodegenerative Diseases · DEQueensland University of Technology · AURotterdam University of Applied Sciences · NLErasmus MC · NLIFOM · ITUniversity of L'Aquila · ITUniversity of Pavia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alterations in the metabolism of iron and its accumulation in the substantia nigra pars compacta accompany the pathogenesis of Parkinson's disease (PD). Changes in iron homeostasis also occur during aging, which constitutes a PD major risk factor. As such, mitigation of iron overload via chelation strategies has been considered a plausible disease modifying approach. Iron chelation, however, is imperfect because of general undesired side effects and lack of specificity; more effective approaches would rely on targeting distinctive pathways responsible for iron overload in brain regions relevant to PD and, in particular, the substantia nigra. We have previously demonstrated that the Transferrin/Transferrin Receptor 2 (TfR2) iron import mechanism functions in nigral dopaminergic neurons, is perturbed in PD models and patients, and therefore constitutes a potential therapeutic target to halt iron accumulation. To validate this hypothesis, we generated mice with targeted deletion of TfR2 in dopaminergic neurons. In these animals, we modeled PD with multiple approaches, based either on neurotoxin exposure or alpha-synuclein proteotoxic mechanisms. We found that TfR2 deletion can provide neuroprotection against dopaminergic degeneration, and against PD- and aging-related iron overload. The effects, however, were significantly more pronounced in females rather than in males. Our data indicate that the TfR2 iron import pathway represents an amenable strategy to hamper PD progression. Data also suggest, however, that therapeutic strategies targeting TfR2 should consider a potential sexual dimorphism in neuroprotective response.

Indexed as

AnimalsDisease Models, AnimalFemaleGender IdentityHumansMiceNeuroprotective AgentsParkinson DiseaseReceptors, TransferrinNeuroprotective AgentsReceptors, TransferrinTFR2 protein, mouse

Identifiers

PMID33323945
PMCPMC8166951
OpenAlexW3110946485

What OpenQuestion holds

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LicenceCC BY
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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.