Wnt signaling mediates acquisition of blood-brain barrier properties in naïve endothelium derived from human pluripotent stem cells.

Gastfriend, Benjamin D; Nishihara, Hideaki; Canfield, Scott G; Foreman, Koji L; Engelhardt, Britta; Palecek, Sean P; Shusta, Eric V (2021). Wnt signaling mediates acquisition of blood-brain barrier properties in naïve endothelium derived from human pluripotent stem cells. eLife, 10 eLife Sciences Publications 10.7554/eLife.70992

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Endothelial cells (ECs) in the central nervous system (CNS) acquire their specialized blood-brain barrier (BBB) properties in response to extrinsic signals, with Wnt/β-catenin signaling coordinating multiple aspects of this process. Our knowledge of CNS EC development has been advanced largely by animal models, and human pluripotent stem cells (hPSCs) offer the opportunity to examine BBB development in an in vitro human system. Here, we show that activation of Wnt signaling in hPSC-derived naïve endothelial progenitors, but not in matured ECs, leads to robust acquisition of canonical BBB phenotypes including expression of GLUT-1, increased claudin-5, decreased PLVAP, and decreased permeability. RNA-seq revealed a transcriptome profile resembling ECs with CNS-like characteristics, including Wnt-upregulated expression of LEF1, APCDD1, and ZIC3. Together, our work defines effects of Wnt activation in naïve ECs and establishes an improved hPSC-based model for interrogation of CNS barriergenesis.

Item Type:

Journal Article (Original Article)

Division/Institute:

04 Faculty of Medicine > Pre-clinic Human Medicine > Theodor Kocher Institute

UniBE Contributor:

Nishihara, Hideaki, Engelhardt, Britta

Subjects:

600 Technology > 610 Medicine & health

ISSN:

2050-084X

Publisher:

eLife Sciences Publications

Language:

English

Submitter:

Andrea Stettler

Date Deposited:

21 Dec 2021 09:38

Last Modified:

05 Dec 2022 15:58

Publisher DOI:

10.7554/eLife.70992

PubMed ID:

34755601

Uncontrolled Keywords:

Wnt signaling barriergenesis blood–brain barrier developmental biology endothelial cells human human pluripotent stem cells neuroscience

BORIS DOI:

10.48350/162848

URI:

https://boris.unibe.ch/id/eprint/162848

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