Evidence map›Paper›PMID 18509662›Full record

ArticleActa neuropathologica2008

Close association of water channel AQP1 with amyloid-beta deposition in Alzheimer disease brains.

Tamako Misawa, Kunimasa Arima, Hidehiro Mizusawa, Jun-ichi Satoh

Open access · hybridAbstract read
In one paragraph

Article in Acta neuropathologica, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 14% 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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 89 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Multifaceted Roles of Aquaporins in the Pathogenesis of Alzheimer's Disease.International journal of molecular sciences · 2023
    Review
  11. Article
  12. Non-Transport Functions of Aquaporins.Advances in experimental medicine and biology · 2023
    Article
  13. Methods for studying mammalian aquaporin biology.Biology methods & protocols · 2023
    Review
  14. Aquaporins in Nervous System.Advances in experimental medicine and biology · 2023
    Article
  15. Article
  16. Insight into the Mammalian Aquaporin Interactome.International journal of molecular sciences · 2022
    Review
  17. Review
  18. Article
  19. Article
  20. Water exchange rate across the blood-brain barrier is associated with CSF amyloid-β 42 in healthy older adults.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2021
    Article
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

4 authors at 3 institutions in 1 country.

Tamako MisawaDepartment of Bioinformatics and Molecular Neuropathology, Meiji Pharmaceutical University, 2-522-1 Noshio, Kiyose, Tokyo, 204-8588, Japan.
Kunimasa Arima
Hidehiro Mizusawa
Jun-ichi Satoh
Meiji Pharmaceutical University · JPNational Center of Neurology and Psychiatry · JPTokyo Medical and Dental University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aquaporin-1 (AQP1), a membrane water channel protein, is expressed exclusively in the choroid plexus epithelium in the central nervous system under physiological conditions. However, AQP1 expression is enhanced in reactive astrocytes, accumulating in brain lesions of Creutzfeldt-Jakob disease and multiple sclerosis, suggesting a role of AQP1-expressing astrocytes in brain water homeostasis under pathological conditions. To clarify a pathological implication of AQP1 in Alzheimer disease (AD), we investigated the possible relationship between amyloid-beta (Abeta) deposition and astrocytic AQP1 expression in the motor cortex and hippocampus of 11 AD patients and 16 age-matched other neurological disease cases. In all cases, AQP1 was expressed exclusively in a subpopulation of multipolar fibrillary astrocytes. The great majority of AQP1-expressing astrocytes were located either on the top of or in close proximity to Abeta plaques in AD brains but not in non-AD cases, whereas those independent of Abeta deposition were found predominantly in non-AD brains. By Western blot, cultured human astrocytes constitutively expressed AQP1, and the levels of AQP1 protein expression were not affected by exposure to Abeta(1-42) peptide, but were elevated by hypertonic sodium chloride. By immunoprecipitation, the C-terminal fragment-beta (CTFbeta) of amyloid precursor protein interacted with the N-terminal half of AQP1 spanning the transmembrane helices H1, H2 and H3. These observations suggest the possible association of astrocytic AQP1 with Abeta deposition in AD brains.

Indexed as

AgedAlzheimer DiseaseAmyloid beta-PeptidesAquaporin 1AstrocytesBlotting, WesternCells, CulturedFemaleFluorescent Antibody Technique, IndirectHippocampusHumansImmunoprecipitationMaleMotor CortexWaterAmyloid beta-PeptidesAQP1 protein, humanAquaporin 1Water

Identifiers

PMID18509662
PMCPMC2516196
OpenAlexW2109163351

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.