| Literature DB >> 28535372 |
Shang Ma1, Devi Santhosh2, Peeyush Kumar T3, Zhen Huang4.
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.Entities:
Keywords: G-protein-coupled receptor; TGF-β; angiogenesis; basal ganglia; germinal matrix; integrin; neural stem cell; neurovascular signaling; radial glia; sphigosine-1-phosphate
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Year: 2017 PMID: 28535372 PMCID: PMC5492999 DOI: 10.1016/j.devcel.2017.04.014
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270