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@MISC{Mller:282929,
author = {Müller, Stephan A and Lichtenthaler, Stefan},
title = {{D}ataset: {A} proteomics resource for human i{PSC}-derived
endothelial cells (i{EC}), smooth muscle cells (i{SMC}),
pericytes (i{PC}) and astrocytes (i{AS}) in comparison to
human primary cells - technical and biological replicates
({P}roject {PXD}066414)},
publisher = {PRoteomics IDEntifications Database},
reportid = {DZNE-2025-01390},
year = {2025},
abstract = {Integrity of the blood-brain barrier (BBB) is critical for
brain homeostasis, and its malfunction contributes to
neurovascular and neurodegenerative disorders. So far,
mechanistic studies on BBB function have been mostly
conducted in rodent and non-physiological in vitro models,
which recapitulate some disease features, but have limited
translatability to humans and pose challenges for drug
discovery. Here we report on a fully human iPSC-derived,
microfluidic 3D BBB model consisting of endothelial cells
(EC), mural cells, and astrocytes. Our model expresses
typical cell fate markers, forms a barrier in vessel-like
tubes, and enables perfusion, including with human blood. We
optimized iPSC differentiations and validated cellular fates
by comparison to published datasets and extensive
benchmarking vs. primary cells with proteomic profiles
provided in an online database
(https://dbNeuroVasP.isd-muc.de).},
cin = {AG Lichtenthaler},
cid = {I:(DE-2719)1110006},
pnm = {352 - Disease Mechanisms (POF4-352)},
pid = {G:(DE-HGF)POF4-352},
typ = {PUB:(DE-HGF)32},
url = {https://pub.dzne.de/record/282929},
}