Evidence map›Paper›PMID 28112163›Full record

ArticleScientific reports2017

Developmental Expression of 4-Repeat-Tau Induces Neuronal Aneuploidy in Drosophila Tauopathy Models.

Nicolas Malmanche, Pierre Dourlen, Marc Gistelinck, Florie Demiautte, Nichole Link, Cloé Dupont, Lies Vanden Broeck, Elisabeth Werkmeister, Philippe Amouyel, Antonino Bongiovanni and 8 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. IncreasediScience · 2022
    Article
  6. Article
  7. Article
  8. Phospho-Tau and Chromatin Landscapes in Early and Late Alzheimer's Disease.International journal of molecular sciences · 2021
    Review
  9. Tau oligomers accumulation sensitizes prostate cancer cells to docetaxel treatment.Journal of cancer research and clinical oncology · 2021
    Article
  10. Tau Oligomers Neurotoxicity.Life (Basel, Switzerland) · 2021
    Review
  11. Review
  12. Developmental Pathogenicity of 4-Repeat Human Tau Is Lost with the P301L Mutation in Genetically Matched Tau-Transgenic Mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  13. Article
  14. Article
  15. Article
  16. Article
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  18. Review
  19. 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 at 6 institutions in 3 countries.

Nicolas MalmancheInserm UMR1167, Laboratoire d'Excellence Distalz, Lille, F59000, France.
Pierre DourlenInserm UMR1167, Laboratoire d'Excellence Distalz, Lille, F59000, France.
Marc GistelinckLaboratory of Behavioral and Developmental Genetics, Center for Human Genetics, KU Leuven, Leuven, 3000, Belgium.
Florie DemiautteInserm UMR1167, Laboratoire d'Excellence Distalz, Lille, F59000, France.
Nichole LinkDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Cloé DupontInserm UMR1167, Laboratoire d'Excellence Distalz, Lille, F59000, France.
Lies Vanden BroeckLaboratory of Behavioral and Developmental Genetics, Center for Human Genetics, KU Leuven, Leuven, 3000, Belgium.
Elisabeth WerkmeisterInstitut Pasteur de Lille, Longevity Research Center, Lille, F59000, France.
Philippe AmouyelInserm UMR1167, Laboratoire d'Excellence Distalz, Lille, F59000, France.
Antonino BongiovanniInstitut Pasteur de Lille, Longevity Research Center, Lille, F59000, France.
Hélène BauderliqueInstitut Pasteur de Lille, Longevity Research Center, Lille, F59000, France.
Dieder MoecharsNeuroscience Department, Janssen Research and Development, a Division of Janssen Pharmaceutica NV, Beerse, 2340, Belgium.
Anne RoyouCNRS UMR5095, Pessac, 33607, France.
Hugo J BellenDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Frank LafontCenter for Infection and Immunity of Lille, 59019, France.
Patrick CallaertsLaboratory of Behavioral and Developmental Genetics, Center for Human Genetics, KU Leuven, Leuven, 3000, Belgium.
Jean-Charles LambertInserm UMR1167, Laboratoire d'Excellence Distalz, Lille, F59000, France.
Bart DermautInserm UMR1167, Laboratoire d'Excellence Distalz, Lille, F59000, France.
Inserm · FRCentre National de la Recherche Scientifique · FRVIB-KU Leuven Center for Cancer Biology · BEBaylor College of Medicine · USHoward Hughes Medical Institute · USJanssen (Belgium) · BE

Funding

Functional analysis of ANKLE2 in microcephaly using a genetic model systemF32NS092270 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI LINK, NICHOLE L · 2015 to 2017
$136k
Howard Hughes Medical InstituteMedical Research CouncilNINDS NIH HHS F32 NS092270
6 · The paper itself

Abstract

Tau-mediated neurodegeneration in Alzheimer's disease and tauopathies is generally assumed to start in a normally developed brain. However, several lines of evidence suggest that impaired Tau isoform expression during development could affect mitosis and ploidy in post-mitotic differentiated tissue. Interestingly, the relative expression levels of Tau isoforms containing either 3 (3R-Tau) or 4 repeats (4R-Tau) play an important role both during brain development and neurodegeneration. Here, we used genetic and cellular tools to study the link between 3R and 4R-Tau isoform expression, mitotic progression in neuronal progenitors and post-mitotic neuronal survival. Our results illustrated that the severity of Tau-induced adult phenotypes depends on 4R-Tau isoform expression during development. As recently described, we observed a mitotic delay in 4R-Tau expressing cells of larval eye discs and brains. Live imaging revealed that the spindle undergoes a cycle of collapse and recovery before proceeding to anaphase. Furthermore, we found a high level of aneuploidy in post-mitotic differentiated tissue. Finally, we showed that overexpression of wild type and mutant 4R-Tau isoform in neuroblastoma SH-SY5Y cell lines is sufficient to induce monopolar spindles. Taken together, our results suggested that neurodegeneration could be in part linked to neuronal aneuploidy caused by 4R-Tau expression during brain development.

Indexed as

AneuploidyGene Expression Regulation, DevelopmentalAnimalsCell LineCell SurvivalHumansMitosisMutationNeural Stem CellsNeuronsPhenotypePhotoreceptor CellsProtein IsoformsTauopathiestau ProteinsProtein Isoformstau Proteins

Identifiers

PMID28112163
PMCPMC5256094
OpenAlexW2580395304

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.