Evidence map›Paper›PMID 31397930›Full record

ArticleBrain pathology (Zurich, Switzerland)2020

Relevance of host tau in tau seeding and spreading in tauopathies.

Isidro Ferrer, Maria Victoria Zelaya, Meritxell Aguiló García, Margarita Carmona, Irene López-González, Pol Andrés-Benito, Laia Lidón, Rosalina Gavín, Paula Garcia-Esparcia, José Antonio Del Rio

Open access · greenAbstract read
In one paragraph

Article in Brain pathology (Zurich, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

25 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Astroglial activation: Current concepts and future directions.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024
    Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Differences in Tau Seeding in Newborn and Adult Wild-Type Mice.International journal of molecular sciences · 2022
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Tau Seeding Mouse Models with Patient Brain-Derived Aggregates.International journal of molecular sciences · 2021
    Review
  20. 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

10 authors at 4 institutions in 1 country.

Isidro FerrerDepartment of Pathology and Experimental Therapeutics, University of Barcelona, Hospitalet de Llobregat, Spain.ORCID 0000-0001-9888-8754
Maria Victoria ZelayaPathological Anatomy Department, Hospital of Navarra, Instituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain.
Meritxell Aguiló GarcíaDepartment of Pathology and Experimental Therapeutics, University of Barcelona, Hospitalet de Llobregat, Spain.
Margarita CarmonaDepartment of Pathology and Experimental Therapeutics, University of Barcelona, Hospitalet de Llobregat, Spain.
Irene López-GonzálezDepartment of Pathology and Experimental Therapeutics, University of Barcelona, Hospitalet de Llobregat, Spain.
Pol Andrés-BenitoDepartment of Pathology and Experimental Therapeutics, University of Barcelona, Hospitalet de Llobregat, Spain.ORCID 0000-0003-3000-0338
Laia LidónMolecular and Cellular Neurobiotechnology, Institute of Bioengineering of Catalonia (IBEC), Barcelona Institute for Science and Technology, Parc Científic de Barcelona, Barcelona, Spain.
Rosalina GavínMolecular and Cellular Neurobiotechnology, Institute of Bioengineering of Catalonia (IBEC), Barcelona Institute for Science and Technology, Parc Científic de Barcelona, Barcelona, Spain.
Paula Garcia-EsparciaDepartment of Pathology and Experimental Therapeutics, University of Barcelona, Hospitalet de Llobregat, Spain.
José Antonio Del RioCIBERNED (Network Centre of Biomedical Research of Neurodegenerative Diseases), Institute of Health Carlos III, Ministry of Economy and Competitiveness, Madrid, Spain.
Instituto de Salud Carlos III · ESBarcelona Institute of Science and Technology · ESNavarre Institute of Health Research · ESUniversitat de Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human tau seeding and spreading occur following intracerebral inoculation of brain homogenates obtained from tauopathies in transgenic mice expressing natural or mutant tau, and in wild-type (WT) mice. The present study was geared to learning about the patterns of tau seeding, the cells involved and the characteristics of tau following intracerebral inoculation of homogenates from primary age-related tauopathy (PART: neuronal 4Rtau and 3Rtau), aging-related tau astrogliopathy (ARTAG: astrocytic 4Rtau) and globular glial tauopathy (GGT: 4Rtau with neuronal deposits and specific tau inclusions in astrocytes and oligodendrocytes). For this purpose, young and adult WT mice were inoculated unilaterally in the hippocampus or in the lateral corpus callosum with sarkosyl-insoluble fractions from PART, ARTAG and GGT cases, and were killed at variable periods of three to seven months. Brains were processed for immunohistochemistry in paraffin sections. Tau seeding occurred in the ipsilateral hippocampus and corpus callosum and spread to the septal nuclei, periventricular hypothalamus and contralateral corpus callosum, respectively. Tau deposits were mainly found in neurons, oligodendrocytes and threads; the deposits were diffuse or granular, composed of phosphorylated tau, tau with abnormal conformation and 3Rtau and 4Rtau independently of the type of tauopathy. Truncated tau at the aspartic acid 421 and ubiquitination were absent. Tau deposits had the characteristics of pre-tangles. A percentage of intracellular tau deposits co-localized with active (phosphorylated) tau kinases p38 and ERK 1/2. Present study shows that seeding and spreading of human tau into the brain of WT mice involves neurons and glial cells, mainly oligodendrocytes, thereby supporting the idea of a primary role of oligodendrogliopathy, together with neuronopathy, in the progression of tauopathies. In addition, it suggests that human tau inoculation modifies murine tau metabolism with the production and deposition of 3Rtau and 4Rtau, and by activation of specific tau kinases in affected cells.

Indexed as

AnimalsBrainHumansMiceMice, Inbred C57BLMice, TransgenicTauopathiestau Proteinstau Proteinsaging-related tau astrogliopathyglobular glial tauopathyprimary age-related tauopathyseedingspreadingtautauopathies

Identifiers

PMID31397930
PMCPMC8018022
OpenAlexW2968517106

What OpenQuestion holds

Textmetadata
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.