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@ARTICLE{Hetzer:281363,
author = {Hetzer, Martin W and Toda, Tomohisa},
title = {{L}ong-lived cellular molecules in the brain.},
journal = {Trends in neurosciences},
volume = {48},
number = {9},
issn = {0378-5912},
address = {Amsterdam [u.a.]},
publisher = {Elsevier Science},
reportid = {DZNE-2025-01110},
pages = {645 - 654},
year = {2025},
abstract = {In long-lived mammals, including humans, brain cell
homeostasis is critical for maintaining brain function
throughout life. Most neurons are generated during
development and must maintain their cellular identity and
plasticity to preserve brain function. Although extensive
studies indicate the importance of recycling and
regenerating cellular molecules to maintain cellular
homeostasis, recent evidence has shown that some proteins
and RNAs do not turn over for months and even years. We
propose that these long-lived cellular molecules may be the
basis for maintaining brain function in the long term, but
also a potential convergent target of brain aging. We
highlight key discoveries and challenges, and propose
potential directions to unravel the mystery of brain cell
longevity.},
subtyp = {Review Article},
keywords = {Humans / Animals / Brain: cytology / Brain: metabolism /
Brain: physiology / Neurons: physiology / Neurons:
metabolism / Homeostasis: physiology / Aging: physiology /
brain aging (Other) / epigenetic regulation (Other) /
long-lived RNA (Other) / long-lived proteins (Other) /
long-term memory (Other) / longevity (Other)},
cin = {AG Toda},
ddc = {610},
cid = {I:(DE-2719)1710014},
pnm = {352 - Disease Mechanisms (POF4-352)},
pid = {G:(DE-HGF)POF4-352},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:40744775},
doi = {10.1016/j.tins.2025.07.004},
url = {https://pub.dzne.de/record/281363},
}