Evidence map›Paper›PMID 33893219›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2021

Continuous Monitoring of Tau-Induced Neurotoxicity in Patient-Derived iPSC-Neurons.

Derek H Oakley, Naomi Klickstein, Caitlin Commins, Mirra Chung, Simon Dujardin, Rachel E Bennett, Bradley T Hyman, Matthew P Frosch

Open access · hybridAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. A framework for translating tauopathy therapeutics: Drug discovery to clinical trials.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. All the Tau We Cannot See.Annual review of medicine · 2023
    Review
  10. Article
  11. Review
  12. 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

8 authors at 1 institution in 1 country.

Derek H OakleyHarvard Medical School, Boston, Massachusetts 02115 doakley@partners.org.ORCID 0000-0002-6998-9510
Naomi KlicksteinHarvard Medical School, Boston, Massachusetts 02115.ORCID 0000-0002-1405-4590
Caitlin ComminsHarvard Medical School, Boston, Massachusetts 02115.
Mirra ChungHarvard Medical School, Boston, Massachusetts 02115.ORCID 0000-0002-4033-7930
Simon DujardinHarvard Medical School, Boston, Massachusetts 02115.ORCID 0000-0002-5614-341X
Rachel E BennettHarvard Medical School, Boston, Massachusetts 02115.ORCID 0000-0001-9640-0575
Bradley T HymanHarvard Medical School, Boston, Massachusetts 02115.ORCID 0000-0002-7959-9401
Matthew P FroschHarvard Medical School, Boston, Massachusetts 02115.ORCID 0000-0002-3940-9861
Harvard University · US

Funding

Research Education ComponentP30AG062421 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI Christine S Ritchie · 2019 to 2026
$36.5M
Epigenomic, transcriptional and cellular dissection of Alzheimer's variantsR01AG058002 · NIA · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI HYMAN, BRADLEY T., JAENISCH, RUDOLF · 2017 to 2021
$7.9M
Are multiple tau species toxic in Alzheimer's Disease?RF1AG059789 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI HYMAN, BRADLEY T. · 2018 to 2018
$2.7M
Synergy between amyloid and tau in Alzheimer's DiseaseRF1AG058674 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI HYMAN, BRADLEY T. · 2018 to 2018
$2.6M
NIA NIH HHS P30 AG062421NIA NIH HHS R01 AG058002NIA NIH HHS RF1 AG058674NIA NIH HHS RF1 AG059789
6 · The paper itself

Abstract

Tau aggregation within neurons is a critical feature of Alzheimer's disease (AD) and related tauopathies. It is believed that soluble pathologic tau species seed the formation of tau aggregates in a prion-like manner and propagate through connected neurons during the progression of disease. Both soluble and aggregated forms of tau are thought to have neurotoxic properties. In addition, different strains of misfolded tau may cause differential neurotoxicity. In this work, we present an accelerated human neuronal model of tau-induced neurotoxicity that incorporates both soluble tau species and tau aggregation. Using patient-derived induced pluripotent stem cell (iPSC) neurons expressing a tau aggregation biosensor, we develop a cell culture system that allows continuous assessment of both induced tau aggregation and neuronal viability at single-cell resolution for periods of >1 week. We show that exogenous tau "seed" uptake, as measured by tau repeat domain (TauRD) reporter aggregation, increases the risk for subsequent neuronal death

Indexed as

Aged, 80 and overAlzheimer DiseaseAnimalsCells, CulturedCell SurvivalFemaleHumansInduced Pluripotent Stem CellsMaleMiceMiddle AgedNeurotoxicity SyndromesPresenilin-1Tauopathiestau ProteinsMAPT protein, humanPresenilin-1PSEN1 protein, humantau ProteinsAlzheimer's diseaseFTLDiPSCMAPTneurotoxicityPSEN1 L435Ftau aggregationtau seeding

Identifiers

PMID33893219
PMCPMC8143197
OpenAlexW3154765321

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.