Evidence map›Paper›PMID 31074077›Full record

ArticlePhysiological reports2019

A bell-shaped pattern of urinary aquaporin-2-bearing extracellular vesicle release in an experimental model of nephronophthisis.

Nobuyuki Mikoda, Hiroko Sonoda, Sayaka Oshikawa, Yuya Hoshino, Toshiyuki Matsuzaki, Masahiro Ikeda

Open access · goldAbstract read
In one paragraph

Article in Physiological reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 22% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Emerging roles for AQP in mammalian extracellular vesicles.Biochimica et biophysica acta. Biomembranes · 2022
    Review
  4. Article
  5. Article
  6. 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

6 authors at 2 institutions in 1 country.

Nobuyuki MikodaDepartment of Veterinary Pharmacology, University of Miyazaki, Miyazaki, Japan.
Hiroko SonodaDepartment of Veterinary Pharmacology, University of Miyazaki, Miyazaki, Japan.
Sayaka OshikawaDepartment of Veterinary Pharmacology, University of Miyazaki, Miyazaki, Japan.
Yuya HoshinoDepartment of Veterinary Pharmacology, University of Miyazaki, Miyazaki, Japan.
Toshiyuki MatsuzakiDepartment of Anatomy and Cell Biology, Gunma University Graduate School of Medicine, Maebashi, Japan.
Masahiro IkedaDepartment of Veterinary Pharmacology, University of Miyazaki, Miyazaki, Japan.ORCID 0000-0003-2539-8812
University of Miyazaki · JPGunma University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The DBA/2-FG pcy (pcy) mouse is a model of human nephronophthisis, a recessive cystic kidney disease. Renal expression of aquaporin-2 (AQP2), a water channel protein, has been shown to be altered in pcy mice. However, the relationship between the renal expression and its release in urinary extracellular vesicles (uEV-AQP2), which account for most urinary AQP2, in pcy mice has remained largely unknown. In this study, we examined age-related alterations of this relationship in pcy mice. In comparison with control mice, pcy mice after the age of 14 weeks showed defective urinary concentration ability with an increase in urinary volume. Interestingly, the release of uEV-AQP2 increased progressively up to the age of 16 weeks, but at 21 weeks the release did not significantly differ from that in control mice (i.e., a bell-shaped pattern was evident). Similar results were obtained for uEV marker proteins, including tumor susceptibility gene 101 (TSG101) protein and apoptosis-linked gene 2-interacting protein X (Alix). Immunoblot analysis revealed that renal AQP2 expression increased progressively from 11 weeks, and immunohistochemistry showed that this increase was possibly due to an increase in the number of AQP2-positive cells. Analysis of mRNAs for seven types of AQP expressed in the kidney supported this notion. These data suggest that the level of uEV-AQP2 does not simply mirror the renal expression of AQP2 and that the altered release of uEV-AQP2 in pcy mice depends on the numbers of both renal AQP2-positive cells and EVs released into the urine.

Indexed as

AgingAnimalsAquaporin 2Calcium-Binding ProteinsDisease Models, AnimalDNA-Binding ProteinsEndosomal Sorting Complexes Required for TransportExtracellular VesiclesGene Expression RegulationKidneyKidney Diseases, CysticMice, Inbred DBAMice, Mutant StrainsRNA, MessengerTranscription FactorsTsg101 ProteinAquaporin 2Calcium-Binding ProteinsDNA-Binding ProteinsEndosomal Sorting Complexes Required for TransportPdcd6ip protein, mouseRNA, MessengerTranscription FactorsTsg101 ProteinAquaporin-2pcy micepolycystic kidney diseaseurinary extracellular vesicles (exosomes)

Identifiers

PMID31074077
PMCPMC6509436
OpenAlexW2944235653

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.