Dataset DZNE-2025-01390

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Dataset: A proteomics resource for human iPSC-derived endothelial cells (iEC), smooth muscle cells (iSMC), pericytes (iPC) and astrocytes (iAS) in comparison to human primary cells - technical and biological replicates (Project PXD066414)

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2025
PRoteomics IDEntifications Database

PRoteomics IDEntifications Database ()

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).


Contributing Institute(s):
  1. Neuroproteomics (AG Lichtenthaler)
Research Program(s):
  1. 352 - Disease Mechanisms (POF4-352) (POF4-352)

Appears in the scientific report 2025
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The record appears in these collections:
Document types > Other Resources > Datasets
Institute Collections > M DZNE > M DZNE-AG Lichtenthaler
Public records
Publications Database

 Record created 2025-12-17, last modified 2025-12-18


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