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@ARTICLE{Methi:270707,
author = {Methi, Aditi and Islam, Rezaul and Kaurani, Lalit and
Sakib, M Sadman and Krüger, Dennis M and Pena, Tonatiuh and
Burkhardt, Susanne and Liebetanz, David and Fischer, André},
title = {{A} {S}ingle-{C}ell {T}ranscriptomic {A}nalysis of the
{M}ouse {H}ippocampus {A}fter {V}oluntary {E}xercise.},
journal = {Molecular neurobiology},
volume = {61},
number = {8},
issn = {0893-7648},
address = {Totowa, NJ},
publisher = {Humana Press},
reportid = {DZNE-2024-00879},
pages = {5628 - 5645},
year = {2024},
abstract = {Exercise has been recognized as a beneficial factor for
cognitive health, particularly in relation to the
hippocampus, a vital brain region responsible for learning
and memory. Previous research has demonstrated that
exercise-mediated improvement of learning and memory in
humans and rodents correlates with increased adult
neurogenesis and processes related to enhanced synaptic
plasticity. Nevertheless, the underlying molecular
mechanisms are not fully understood. With the aim to further
elucidate these mechanisms, we provide a comprehensive
dataset of the mouse hippocampal transcriptome at the
single-cell level after 4 weeks of voluntary wheel-running.
Our analysis provides a number of interesting observations.
For example, the results suggest that exercise affects adult
neurogenesis by accelerating the maturation of a
subpopulation of Prdm16-expressing neurons. Moreover, we
uncover the existence of an intricate crosstalk among
multiple vital signaling pathways such as NF-κB,
Wnt/β-catenin, Notch, and retinoic acid (RA) pathways
altered upon exercise in a specific cluster of excitatory
neurons within the Cornu Ammonis (CA) region of the
hippocampus. In conclusion, our study provides an important
resource dataset and sheds further light on the molecular
changes induced by exercise in the hippocampus. These
findings have implications for developing targeted
interventions aimed at optimizing cognitive health and
preventing age-related cognitive decline.},
keywords = {Animals / Hippocampus: metabolism / Physical Conditioning,
Animal: physiology / Single-Cell Analysis / Gene Expression
Profiling / Transcriptome: genetics / Mice, Inbred C57BL /
Mice / Male / Neurogenesis / Neurons: metabolism / Signal
Transduction / Volition / Aerobic exercise (Other) /
Cognitive decline (Other) / Dementia (Other) / Environmental
enrichment (Other) / Gene-expression (Other) / Hippocampus
(Other) / Learning and memory (Other) / Single-cell RNAseq
(Other)},
cin = {AG Fischer / Bioinformatics and Genome Dynamics Core ;
Bioinformatics Unit},
ddc = {570},
cid = {I:(DE-2719)1410002 / I:(DE-2719)1440016},
pnm = {352 - Disease Mechanisms (POF4-352)},
pid = {G:(DE-HGF)POF4-352},
typ = {PUB:(DE-HGF)16},
pmc = {pmc:PMC11249425},
pubmed = {pmid:38217668},
doi = {10.1007/s12035-023-03869-9},
url = {https://pub.dzne.de/record/270707},
}