Human pluripotent stem cell-derived brain pericyte-like cells induce blood-brain barrier properties

Stebbins, M. J.; Gastfriend, B. D.; Canfield, S. G.; Lee, M.-S.; Richards, D.; Faubion, M. G.; Li, W.-J.; Daneman, R.; Palecek, S. P.; Shusta, E. V.

doi:10.1101/387100

bioRxiv · 10.1101/387100

Human pluripotent stem cell-derived brain pericyte-like cells induce blood-brain barrier properties

Stebbins, M. J.·Gastfriend, B. D.·Canfield, S. G.·Lee, M.-S.·Richards, D.·Faubion, M. G.·Li, W.-J.·Daneman, R.·Palecek, S. P.·Shusta, E. V.

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Abstract

Brain pericytes play an important role in the formation and maintenance of the neurovascular unit (NVU), and their dysfunction has been implicated in central nervous system (CNS) disorders. While human pluripotent stem cells (hPSCs) have been used to model other components of the NVU including brain microvascular endothelial cells (BMECs), astrocytes, and neurons, cells having brain pericyte-like phenotypes have not been described. In this study, we generated neural crest stem cells (NCSCs), the embryonic precursor to forebrain pericytes, from human pluripotent stem cells (hPSCs) and subsequently differentiated NCSCs to brain pericyte-like cells. The brain pericyte-like cells expressed marker profiles that closely resembled primary human brain pericytes, and they self-assembled with endothelial cells to support vascular tube formation. Importantly, the brain pericyte-like cells induced blood-brain barrier (BBB) properties in BMECs, including barrier enhancement and reduction of transcytosis. Finally, brain pericyte-like cells were incorporated with iPSC-derived BMECs, astrocytes, and neurons to form an isogenic human NVU model that should prove useful for the study of the BBB in CNS health, disease, and therapy.

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Stebbins, M. J., Gastfriend, B. D., Canfield, S. G., Lee, M.-S., Richards, D., Faubion, M. G., Li, W.-J., Daneman, R., Palecek, S. P., Shusta, E. V.. 2018-08-07. Human pluripotent stem cell-derived brain pericyte-like cells induce blood-brain barrier properties. https://doi.org/10.1101/387100

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