Evidence map›Paper›PMID 36251631›Full record

ArticlePloS one2022

Accumulation of senescence observed in spinocerebellar ataxia type 7 mouse model.

William Miller, Charles Lewis Humphrey Pruett, William Stone, Cindy Eide, Megan Riddle, Courtney Popp, Matthew Yousefzadeh, Christopher Lees, Davis Seelig, Elizabeth Thompson and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 81% 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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. 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

13 authors at 2 institutions in 1 country.

William MillerDepartment of Pediatrics, Medical School, University of Minnesota, Minneapolis, MN, United States of America.
Charles Lewis Humphrey PruettDepartment of Pediatrics, Medical School, University of Minnesota, Minneapolis, MN, United States of America.
William StoneDepartment of Pediatrics, Medical School, University of Minnesota, Minneapolis, MN, United States of America.
Cindy EideDepartment of Pediatrics, Medical School, University of Minnesota, Minneapolis, MN, United States of America.
Megan RiddleDepartment of Pediatrics, Medical School, University of Minnesota, Minneapolis, MN, United States of America.ORCID 0000-0002-9557-217X
Courtney PoppDepartment of Pediatrics, Medical School, University of Minnesota, Minneapolis, MN, United States of America.
Matthew YousefzadehInstitute on the Biology of Aging and Metabolism, University of Minnesota, Minneapolis, MN, United States of America.ORCID 0000-0003-2869-1029
Christopher LeesDepartment of Pediatrics, Medical School, University of Minnesota, Minneapolis, MN, United States of America.
Davis SeeligComparative Pathology Shared Resource, College of Veterinary Medicine, University of Minnesota, Minneapolis, MN, United States of America.
Elizabeth ThompsonInstitute on the Biology of Aging and Metabolism, University of Minnesota, Minneapolis, MN, United States of America.
Harry OrrInstitute for Translational Neuroscience, University of Minnesota, Minneapolis, MN, United States of America.
Laura NiedernhoferInstitute on the Biology of Aging and Metabolism, University of Minnesota, Minneapolis, MN, United States of America.
Jakub TolarDepartment of Pediatrics, Medical School, University of Minnesota, Minneapolis, MN, United States of America.ORCID 0000-0002-0957-4380
University of Minnesota Medical Center · USUniversity of Minnesota · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spinocerebellar ataxia type 7 (SCA7) is a neurodegenerative disease caused by a trinucleotide CAG repeat. SCA7 predominantly causes a loss of photoreceptors in the retina and Purkinje cells of the cerebellum. Severe infantile-onset SCA7 also causes renal and cardiac irregularities. Previous reports have shown that SCA7 results in increased susceptibility to DNA damage. Since DNA damage can lead to accumulation of senescent cells, we hypothesized that SCA7 causes an accumulation of senescent cells over the course of disease. A 140-CAG repeat SCA7 mouse model was evaluated for signs of disease-specific involvement in the kidney, heart, and cerebellum, tissues that are commonly affected in the infantile form. We found evidence of significant renal abnormality that coincided with an accumulation of senescent cells in the kidneys of SCA7140Q/5Q mice, based on histology findings in addition to RT-qPCR for the cell cycle inhibitors p16Ink4a and p21Cip1 and senescence-associated ß-galactosidase (SA-ßgal) staining, respectively. The Purkinje layer in the cerebellum of SCA7140Q/5Q mice also displayed SA-ßgal+ cells. These novel findings offer evidence that senescent cells accumulate in affected tissues and may possibly contribute to SCA7's specific phenotype.

Indexed as

Nerve Tissue ProteinsSpinocerebellar AtaxiasAnimalsAtaxin-7Disease Models, AnimalGalactosidasesMiceTrinucleotide RepeatsAtaxin-7GalactosidasesNerve Tissue Proteins

Identifiers

PMID36251631
PMCPMC9576077
OpenAlexW4306630449

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.