Author:
Nakamura Yoshihiko,Nakano Takafumi,Park Ji Hyun,Tanaka Masayoshi,Li Wenlu,Esposito Elga,Ahn Bum Ju,Durán-Laforet Violeta,Desai Rakhi,Sencan Ikbal,Sakadžić Sava,Lo Eng H.,Snyder Evan Y.,Tabaka Marcin,Hayakawa Kazuhide
Abstract
SummaryThe neural crest (NC) is a transient structure in vertebrate embryogenesis comprising highly migratory multipotent stem cells that give rise to a diverse array of cell types in organs throughout the body, including initiating neurovascular patterning. It is assumed that neural crest stem cells (NCSCs) disappear after development. Unexpectedly, using single-nucleus RNA-sequencing, we discovered residual quiescent NCSCs in the adult mouse meninges which are activated by injury and contribute to the brain’s homeostatic response. RNA velocity, pathway, and transcription factor analyses in a murine stroke model (combined with in vivo imaging) show that these adult NCSCs migrate towards the perivascular spaces of the infarct and undergo a perivascular stromal cell transition that is regulated by Ptp1b, Ghr, and Stat3. Loss- and gain-of-function experiments show that these “vestigial” NCSCs are required for restoring vascular endothelial barrier function via β-catenin and Stat3 signaling. These findings suggest that, in the adult, an unexpected reservoir of cells -- once pivotal to embryogenesis and vascular morphogenesis -- are re-invoked for neurovascular repair.
Publisher
Cold Spring Harbor Laboratory