Abstract
Intimate communication between neural and vascular cells is critical for normal brain development and function. Germinal matrix (GM), a key primordium for the brain reward circuitry, is unique among brain regions for its distinct pace of angiogenesis and selective vulnerability to hemorrhage during development. A major neonatal condition, GM hemorrhage can lead to cerebral palsy, hydrocephalus, and mental retardation. Here we identify a brain-region-specific neural progenitor-based signaling pathway dedicated to regulating GM vessel development. This pathway consists of cell-surface sphingosine-1-phosphate receptors, an intracellular cascade including Gα co-factor Ric8a and p38 MAPK, and target gene integrin β8, which in turn regulates vascular TGF-β signaling. These findings provide insights into region-specific specialization of neurovascular communication, with special implications for deciphering potent early-life endocrine, as well as potential gut microbiota impacts on brain reward circuitry. They also identify tissue-specific molecular targets for GM hemorrhage intervention.
Original language | English (US) |
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Pages (from-to) | 366-381.e4 |
Journal | Developmental cell |
Volume | 41 |
Issue number | 4 |
DOIs | |
State | Published - May 22 2017 |
Externally published | Yes |
Keywords
- angiogenesis
- basal ganglia
- G-protein-coupled receptor
- germinal matrix
- integrin
- neural stem cell
- neurovascular signaling
- radial glia
- sphigosine-1-phosphate
- TGF
ASJC Scopus subject areas
- Molecular Biology
- Biochemistry, Genetics and Molecular Biology(all)
- Developmental Biology
- Cell Biology