Evidence map›Paper›PMID 41324576›Full record

ArticleeLife2025

Cerebellar Purkinje cell stripe patterns reveal a differential vulnerability and resistance to cell loss during normal aging in mice.

Sarah G Donofrio, Cheryl Brandenburg, Amanda M Brown, Tao Lin, Hsiang-Chih Lu, Roy V Sillitoe

Abstract read
In one paragraph

Article in eLife, 2025. 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
–field-weighted citation impact
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.

  1. Cerebellar Purkinje cell firing reduction contributes to aging-related declining motor coordination in mice.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. Article
  4. Tremor pathophysiology.Clinical parkinsonism & related disorders · 2026
    Review
  5. Glial Cells and Aging: From the CNS to the Cerebellum.International journal of molecular sciences · 2025
    Review
  6. Axonal pathology differentially affects human Purkinje cell subpopulations in the essential tremor cerebellum.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Sarah G DonofrioDepartment of Pathology and Immunology, Baylor College of Medicine, Houston, United States.ORCID https://orcid.org/0000-0003-1680-3302
Cheryl BrandenburgDepartment of Pathology and Immunology, Baylor College of Medicine, Houston, United States.ORCID https://orcid.org/0000-0002-9370-2313
Amanda M BrownDepartment of Pathology and Immunology, Baylor College of Medicine, Houston, United States.ORCID https://orcid.org/0000-0002-1484-8972
Tao LinDepartment of Pathology and Immunology, Baylor College of Medicine, Houston, United States.
Hsiang-Chih LuDepartment of Pathology and Immunology, Baylor College of Medicine, Houston, United States.
Roy V SillitoeDepartment of Pathology and Immunology, Baylor College of Medicine, Houston, United States.ORCID https://orcid.org/0000-0002-6177-6190

Funding

Preclinical and Clincial OutcomesP50HD103555 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI Sandesh Chakravarthy Sreenath Nagamani, David Loren Nelson · 2020 to 2026
$9.9M
Steps towards a paternal gene activation therapy for Angelman syndromeU54HD083092 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI NELSON, DAVID LOREN, NEUL, JEFFREY L · 2014 to 2019
$7.8M
Cerebellar Deep Brain StimulationR01NS119301 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI SILLITOE, ROY VINCENT · 2020 to 2024
$2.0M
Spatial and temporal pathophysiology of developmental dystoniaR01NS127435 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI Roy Vincent Sillitoe · 2022 to 2026
$2.0M
Adult-onset Purkinje cell loss in cerebellar dysfunctionF31NS129279 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI DONOFRIO, SARAH · 2022 to 2024
$146k
Eunice Kennedy Shriver National Institute of Child Health and Human Development P50HD103555NICHD NIH HHS P50 HD103555NICHD NIH HHS U54 HD083092NINDS NIH HHS F31 NS129279NINDS NIH HHS F31NS129279NINDS NIH HHS R01 NS119301NINDS NIH HHS R01NS119301NINDS NIH HHS R01 NS127435NINDS NIH HHS R01NS127435
6 · The paper itself

Abstract

Age-related neurodegenerative diseases involve reduced cell numbers and impaired behavioral capacity. Neurodegeneration and behavioral deficits also occur during aging, and notably in the absence of disease. The cerebellum, which modulates movement and cognition, is susceptible to cell loss in both aging and disease. Here, we demonstrate that cerebellar Purkinje cell loss in aged mice is not spatially random but rather occurs in a pattern of parasagittal stripes. We also find that aged mice exhibit impaired motor coordination and more severe tremor compared to younger mice. However, the relationship between patterned Purkinje cell loss and motor dysfunction is not straightforward. Examination of postmortem samples of human cerebella from neurologically typical individuals supports the presence of selective loss of Purkinje cells during aging. These data reveal a spatiotemporal cellular substrate for aging in the cerebellum that may inform how neuronal vulnerability leads to neurodegeneration and the ensuing deterioration of behavior.

Indexed as

AgingCerebellumPurkinje CellsAnimalsFemaleHumansMaleMiceMice, Inbred C57BLagingcerebellumhuman pathologymousemovementneurosciencePurkinje cell losszones

Identifiers

PMID41324576
PMCPMC12668675

What Socratic 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 Socratic graph.