Cited by 116Telomeres, Telomerase, and SenescenceGenetics, Aging, and Longevity in Model OrganismsNeuroinflammation and Neurodegeneration Mechanisms

The DOI matches its Crossref record; 191 of the 191 references it cites were found in a registry or an index.

Are there roles for brain cell senescence in aging and neurodegenerative disorders?

Open access

Abstract

The term cellular senescence was introduced more than five decades ago to describe the state of growth arrest observed in aging cells. Since this initial discovery, the phenotypes associated with cellular senescence have expanded beyond growth arrest to include alterations in cellular metabolism, secreted cytokines, epigenetic regulation and protein expression. Recently, senescence has been shown to play an important role in vivo not only in relation to aging, but also during embryonic development. Thus, cellular senescence serves different purposes and comprises a wide range of distinct phenotypes across multiple cell types. Whether all cell types, including post-mitotic neurons, are capable of entering into a senescent state remains unclear. In this review we examine recent data that suggest that cellular senescence plays a role in brain aging and, notably, may not be limited to glia but also neurons. We suggest that there is a high level of similarity between some of the pathological changes that occur in the brain in Alzheimer's and Parkinson's diseases and those phenotypes observed in cellular senescence, leading us to propose that neurons and glia can exhibit hallmarks of senescence previously documented in peripheral tissues.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1007/s10522-014-9532-1

Cites

191 of 191 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

2 retracted

Show all 191 references

Cited by

Sorted by citations

Metadata

Authors
Tan, F. C. C., Hutchison, E. R., Eitan, E., & Mattson, M. P.
Affiliations
National Institute on Aging (US)
Corresponding author
  • Hutchison, Emmette R.
  • Eitan, Erez
Venue
Biogerontology
Published
2014-10-11
Volume
15
Issue
6
Pages
643-660
ISSN
  • 1389-5729 (ISSN-L)
  • 1573-6768
OpenAlex
W1977085416
Cited by
116
References
191
Citations by year
2026: 3 · 2025: 6 · 2024: 4 · 2023: 8 · 2022: 14 · 2021: 12 · 2020: 15 · 2019: 16 · 2018: 19 · 2017: 10 · 2016: 4 · 2015: 2 · 2014: 2
FWCI
0.70
Type
journal article
Language
en
Open access
Locations
  • Biogerontology (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
National Institutes of Health (Z99 AG999999)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Telomeres, Telomerase, and Senescence
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
  • Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
Keywords
cellular senescence, brain aging, neurodegenerative diseases, Alzheimer's disease, Parkinson's disease, neuronal senescence, senescence-associated secretory phenotype, epigenetic regulation, postmitotic neurons, embryonic development
MeSH terms
Aged, Aging, Animals, Brain, Humans, Neuroglia, Neurons, Cellular Senescence, Neurodegenerative Diseases, Epigenesis, Genetic, Mice

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review