| Literature DB >> 28514658 |
Si Chen1, Nathalie Tisch2, Marcel Kegel3, Rosario Yerbes2, Robert Hermann1, Hannes Hudalla1, Cecilia Zuliani1, Gülce Sila Gülcüler1, Klara Zwadlo1, Jakob von Engelhardt3, Carmen Ruiz de Almodóvar2, Ana Martin-Villalba4.
Abstract
The development of neurons and vessels shares striking anatomical and molecular features, and it is presumably orchestrated by an overlapping repertoire of extracellular signals. CNS macrophages have been implicated in various developmental functions, including the morphogenesis of neurons and vessels. However, whether CNS macrophages can coordinately influence neurovascular development and the identity of the signals involved therein is unclear. Here, we demonstrate that activity of the cell surface receptor CD95 regulates neuronal and vascular morphogenesis in the post-natal brain and retina. Furthermore, we identify CNS macrophages as the main source of CD95L, and macrophage-specific deletion thereof reduces both neurovascular complexity and synaptic activity in the brain. CD95L-induced neuronal and vascular growth is mediated through src-family kinase (SFK) and PI3K signaling. Together, our study highlights a coordinated neurovascular development instructed by CNS macrophage-derived CD95L, and it underlines the importance of macrophages for the establishment of the neurovascular network during CNS development.Entities:
Keywords: CD95; CD95L; CNS macrophages; angiogenesis; cortex; microglia; neurovascular development; retina; vessel
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Year: 2017 PMID: 28514658 DOI: 10.1016/j.celrep.2017.04.056
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423