Evidence map›Paper›PMID 36399251›Full record

ArticleMolecular neurobiology2023

Direct and Indirect Effects of Filamin A on Tau Pathology in Neuronal Cells.

Stéphanie Levert, Julie Pilliod, Étienne Aumont, Sandrine Armanville, Cyntia Tremblay, Frédéric Calon, Nicole Leclerc

Open access · hybridAbstract read
In one paragraph

Article in Molecular neurobiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
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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

7 authors at 3 institutions in 1 country.

Stéphanie Levert *Centre de Recherche du Centre Hospitalier de L'Université de Montréal, Montreal, Canada.
Julie Pilliod *Centre de Recherche du Centre Hospitalier de L'Université de Montréal, Montreal, Canada.
Étienne AumontDépartement de Psychologie de L'Université du Québec À Montréal, Montreal, Canada.
Sandrine ArmanvilleCentre de Recherche du Centre Hospitalier de L'Université de Montréal, Montreal, Canada.
Cyntia TremblayCentre de Recherche du Centre Hospitalier Universitaire de Québec-Université Laval, Québec City, Canada.
Frédéric CalonCentre de Recherche du Centre Hospitalier Universitaire de Québec-Université Laval, Québec City, Canada.
Nicole LeclercCentre de Recherche du Centre Hospitalier de L'Université de Montréal, Montreal, Canada. Nicole.leclerc@umontreal.ca.ORCID http://orcid.org/0000-0002-2678-0020
Centre Hospitalier de l’Université de Montréal · CACentre hospitalier universitaire de Québec · CAMontreal Neurological Institute and Hospital · CA

Funding

CIHR PJT-155993CIHR PJT 168927
6 · The paper itself

Abstract

In Alzheimer disease (AD), Tau, an axonal microtubule-associated protein, becomes hyperphosphorylated, detaches from microtubules, accumulates, and self-aggregates in the somatodendritic (SD) compartment. The accumulation of hyperphosphorylated and aggregated Tau is also seen in other neurodegenerative diseases such as frontotemporal lobar degeneration (FTLD-Tau). Previous studies reported a link between filamin A (FLNA), an actin-binding protein found in the SD compartment, and Tau pathology. In the present study, we further explored this link. We confirmed the interaction of Tau with FLNA in neuroblastoma 2a (N2a) cells. This interaction was mediated by a domain located between the 157 and 383 amino acids (a.a.) of Tau. Our results also revealed that the overexpression of FLNA resulted in an intracellular accumulation of wild-type Tau and Tau mutants (P301L, V337M, and R406W) in N2a cells. Tau phosphorylation and cleavage by caspase-3 but not its aggregation were increased upon FLNA overexpression in N2a cells. In the parietal cortex of AD brain, insoluble FLNA was increased compared to control brain, but it did not correlate with Tau pathology. Interestingly, Tau binding to microtubules and F-actin was preserved upon FLNA overexpression in N2a cells. Lastly, our results revealed that FLNA also induced the accumulation of annexin A2, a Tau interacting partner involved in its axonal localization. Collectively, our data indicated that in Tauopathies, FLNA could contribute to Tau pathology by acting on Tau and annexin A2.

Indexed as

Alzheimer DiseaseAnnexin A2Frontotemporal Lobar DegenerationTauopathiesAnimalsFilaminsMiceNeuronsPhosphorylationtau ProteinsAnnexin A2FilaminsFlnA protein, mousetau ProteinsAnnexin A2F-actinFLNAMicrotubulesTau protein

Identifiers

PMID36399251
PMCPMC9849303
OpenAlexW4309281484

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.