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@ARTICLE{Nebli:1028714,
author = {Nebli, Ahmed and Schiffer, Christian and Niu, Meiqi and
Palomero-Gallagher, Nicola and Amunts, Katrin and
Dickscheid, Timo},
title = {{G}enerative {M}odelling of {C}ortical {R}eceptor
{D}istributions from {C}ytoarchitectonic {I}mages in the
{M}acaque {B}rain},
journal = {Neuroinformatics},
volume = {22},
issn = {1539-2791},
address = {New York, NY},
publisher = {Springer},
reportid = {FZJ-2024-04771},
pages = {389-402},
year = {2024},
abstract = {Neurotransmitter receptor densities are relevant for
understanding the molecular architecture of brain regions.
Quantitative in vitro receptor autoradiography, has been
introduced to map neurotransmitter receptor distributions of
brain areas. However, it is very time and cost-intensive,
which makes it challenging to obtain whole-brain
distributions. At the same time, high-throughput light
microscopy and 3D reconstructions have enabled
high-resolution brain maps capturing measures of cell
density across the whole human brain. Aiming to bridge gaps
in receptor measurements for building detailed whole-brain
atlases, we study the feasibility of predicting realistic
neurotransmitter density distributions from cell-body
stainings. Specifically, we utilize conditional Generative
Adversarial Networks (cGANs) to predict the density
distributions of the M2 receptor of acetylcholine and the
kainate receptor for glutamate in the macaque monkey’s
primary visual (V1) and motor cortex (M1), based on light
microscopic scans of cell-body stained sections. Our model
is trained on corresponding patches from aligned consecutive
sections that display cell-body and receptor distributions,
ensuring a mapping between the two modalities. Evaluations
of our cGANs, both qualitative and quantitative, show their
capability to predict receptor densities from cell-body
stained sections while maintaining cortical features such as
laminar thickness and curvature. Our work underscores the
feasibility of cross-modality image translation problems to
address data gaps in multi-modal brain atlases.},
cin = {INM-1},
ddc = {540},
cid = {I:(DE-Juel1)INM-1-20090406},
pnm = {5251 - Multilevel Brain Organization and Variability
(POF4-525) / 5254 - Neuroscientific Data Analytics and AI
(POF4-525) / HIBALL - Helmholtz International BigBrain
Analytics and Learning Laboratory (HIBALL) (InterLabs-0015)
/ Helmholtz AI - Helmholtz Artificial Intelligence
Coordination Unit – Local Unit FZJ (E.40401.62) / HBP SGA3
- Human Brain Project Specific Grant Agreement 3 (945539) /
EBRAINS 2.0 - EBRAINS 2.0: A Research Infrastructure to
Advance Neuroscience and Brain Health (101147319)},
pid = {G:(DE-HGF)POF4-5251 / G:(DE-HGF)POF4-5254 /
G:(DE-HGF)InterLabs-0015 / G:(DE-Juel-1)E.40401.62 /
G:(EU-Grant)945539 / G:(EU-Grant)101147319},
typ = {PUB:(DE-HGF)16},
pubmed = {38976151},
UT = {WOS:001264639700002},
doi = {10.1007/s12021-024-09673-7},
url = {https://juser.fz-juelich.de/record/1028714},
}