Evidence map›Paper›PMID 35613261›Full record

ArticleScience advances2022

Actin-binding protein filamin-A drives tau aggregation and contributes to progressive supranuclear palsy pathology.

Koyo Tsujikawa, Kohei Hamanaka, Yuichi Riku, Yuki Hattori, Norikazu Hara, Yohei Iguchi, Shinsuke Ishigaki, Atsushi Hashizume, Satoko Miyatake, Satomi Mitsuhashi and 23 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.4field-weighted citation impact, top 6% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

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  16. Neurodegenerative Disorder Risk in Krabbe Disease Carriers.International journal of molecular sciences · 2022
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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

33 authors at 12 institutions in 1 country.

Koyo TsujikawaDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID 0000-0002-9316-2476
Kohei HamanakaDepartment of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Yuichi RikuDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID 0000-0002-6493-8976
Yuki HattoriDepartment of Anatomy and Cell Biology, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID 0000-0001-6576-0121
Norikazu HaraDepartment of Molecular Genetics, Brain Research Institute, Niigata University, Niigata, Japan.ORCID 0000-0001-8525-3469
Yohei IguchiDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Shinsuke IshigakiDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID 0000-0002-9555-0659
Atsushi HashizumeDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID 0000-0002-3098-7390
Satoko MiyatakeDepartment of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.ORCID 0000-0001-7587-5168
Satomi MitsuhashiDepartment of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.ORCID 0000-0003-4769-5922
Yu MiyazakiDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Mayumi KataokaDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Li JiayiDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Keizo YasuiDepartment of Neurology, Japanese Red Cross Aichi Medical Center Nagoya Daini Hospital, Nagoya, Japan.
Satoshi KuruDepartment of Neurology , National Hospital Organization Suzuka National Hospital, Suzuka, Japan.
Haruki KoikeDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID 0000-0002-4612-3183
Kenta KobayashiSection of Viral Vector Development, National Institute for Physiological Sciences, Okazaki, Japan.ORCID 0000-0002-7389-3693
Naruhiko SaharaDepartment of Functional Brain Imaging, National Institutes for Quantum and Radiological Science and Technology, Chiba, Japan.
Norio OzakiDepartment of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Mari YoshidaDepartment of Neuropathology, Institute for Medical Science of Aging, Aichi Medical University, Nagakute, Japan.
Akiyoshi KakitaDepartment of Pathology, Brain Research Institute, Niigata University, Niigata, Japan.
Yuko SaitoDepartment of Neurology and Neuropathology (The Brain Bank for Aging Research), Tokyo Metropolitan Geriatric Hospital and Institute of Gerontology, Tokyo, Japan.
Yasushi IwasakiDepartment of Neuropathology, Institute for Medical Science of Aging, Aichi Medical University, Nagakute, Japan.ORCID 0000-0002-0059-3104
Akinori MiyashitaDepartment of Molecular Genetics, Brain Research Institute, Niigata University, Niigata, Japan.
Takeshi IwatsuboDepartment of Neuropathology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Japanese Alzheimer’s Disease Neuroimaging Initiative (J-ADNI)
Takeshi IkeuchiDepartment of Molecular Genetics, Brain Research Institute, Niigata University, Niigata, Japan.ORCID 0000-0001-8828-8085
Japanese Longitudinal Biomarker Study in PSP and CBD (JALPAC) Consortium
Takaki MiyataDepartment of Anatomy and Cell Biology, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID 0000-0002-5952-0241
Gen SobueResearch Division of Dementia and Neurodegenerative Disease, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Naomichi MatsumotoDepartment of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.ORCID 0000-0001-9846-6500
Kentaro SahashiDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID 0000-0003-3256-9659
Masahisa KatsunoDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID 0000-0001-9453-9311
Nagoya University · JPNiigata University · JPAichi Medical University · JPNational Institute of Technology, Suzuka College · JPJapanese Red Cross Nagoya Daini Hospital · JPNational Institute for Physiological Sciences · JPNational Institutes for Quantum Science and Technology · JPThe University of Tokyo · JPTokyo Medical and Dental University · JPTokyo Metropolitan Geriatric Hospital · JPYokohama City University · JPYokohama City University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While amyloid-β lies upstream of tau pathology in Alzheimer's disease, key drivers for other tauopathies, including progressive supranuclear palsy (PSP), are largely unknown. Various tau mutations are known to facilitate tau aggregation, but how the nonmutated tau, which most cases with PSP share, increases its propensity to aggregate in neurons and glial cells has remained elusive. Here, we identified genetic variations and protein abundance of filamin-A in the PSP brains without tau mutations. We provided in vivo biochemical evidence that increased filamin-A levels enhance the phosphorylation and insolubility of tau through interacting actin filaments. In addition, reduction of filamin-A corrected aberrant tau levels in the culture cells from PSP cases. Moreover, transgenic mice carrying human filamin-A recapitulated tau pathology in the neurons. Our data highlight that filamin-A promotes tau aggregation, providing a potential mechanism by which filamin-A contributes to PSP pathology.

Identifiers

PMID35613261
PMCPMC9132466
OpenAlexW4281476900

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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.