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@ARTICLE{Lolansen:303082,
author = {S. D. Lolansen and E. O. Révész and S. N. Andreassen and
M. Trapp$^*$ and C. Salio and M. Sassoé-Pognetto and J. V.
Andersen and E. W. Westi and T. L. Toft-Bertelsen and J. H.
Wardman and A. M. Lundby and F. Dela and A. Patrizi$^*$ and
B. I. Aldana and N. MacAulay},
title = {{C}horoid plexus-mediated {CSF} secretion remains stable in
aging rats via high and age-resistant metabolic activity.},
journal = {Nature Communications},
volume = {16},
number = {1},
issn = {2041-1723},
address = {[London]},
publisher = {Springer Nature},
reportid = {DKFZ-2025-01507},
pages = {6778},
year = {2025},
note = {Schaller Research Group, German Cancer Research Center
(DKFZ), Heidelberg, Germany.},
abstract = {Our brain is bathed in cerebrospinal fluid (CSF) that is
produced by the choroid plexus. CSF serves as a dispersion
route for hormones and nutrients, and a conduit for waste
clearance. Age-dependent reduction in the CSF secretion rate
could influence cerebral waste clearance and thereby promote
cognitive deficits in the elderly. Here, we resolve
age-dependent modulation of CSF dynamics and choroid plexus
function by complementary in vivo determinations of
intracranial pressure (ICP) and CSF secretion/absorption
rates, combined with transcriptomic, morphological, and
metabolic analysis of choroid plexus in aging male rats. ICP
and CSF secretion rate and absorption capacity remain stable
with age, and the choroid plexus retains its morphology,
structural integrity, gene expression, and high metabolic
rate across the tested ages. This work supports the
significance of choroid plexus function for brain aging and
promotes this tissue as a future target for
neurodegenerative diseases associated with impaired waste
clearance and cognitive decline.},
keywords = {Animals / Choroid Plexus: metabolism / Choroid Plexus:
physiology / Aging: metabolism / Male / Rats / Cerebrospinal
Fluid: metabolism / Intracranial Pressure: physiology /
Brain: metabolism / Transcriptome},
cin = {B410},
ddc = {500},
cid = {I:(DE-He78)B410-20160331},
pnm = {312 - Funktionelle und strukturelle Genomforschung
(POF4-312)},
pid = {G:(DE-HGF)POF4-312},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:40701965},
doi = {10.1038/s41467-025-61889-6},
url = {https://inrepo02.dkfz.de/record/303082},
}