Replicative senescent human cells possess altered circadian clocks with a prolonged period and delayed peak-time.
TIG-3 cells
aging
cellular senescence
circadian clock
primary fibroblast
Journal
Aging
ISSN: 1945-4589
Titre abrégé: Aging (Albany NY)
Pays: United States
ID NLM: 101508617
Informations de publication
Date de publication:
09 02 2019
09 02 2019
Historique:
received:
09
09
2018
accepted:
24
01
2019
pubmed:
10
2
2019
medline:
16
4
2020
entrez:
10
2
2019
Statut:
ppublish
Résumé
Over the last decade, a wide array of evidence has been accumulated that disruption of circadian clock is prone to cause age-related diseases and premature aging. On the other hand, aging has been identified as one of the risk factors linked to the alteration of circadian clock. These evidences suggest that the processes of aging and circadian clock feedback on each other at the animal level. However, at the cellular level, we recently revealed that the primary fibroblast cells derived from
Identifiants
pubmed: 30738414
doi: 10.18632/aging.101794
pii: 101794
pmc: PMC6382424
doi:
Substances chimiques
PER1 protein, human
0
PER2 protein, human
0
Period Circadian Proteins
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
950-973Références
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