Neuropilin-1–Expressing Microglia Are Associated With Nascent Retinal Vasculature Yet Dispensable for Developmental Angiogenesis
Author(s) -
Agnieszka Dejda,
Gaëlle Mawambo,
JeanFrançois Daudelin,
Khalil Miloudi,
Naoufal Akla,
Chintan Patel,
Elisabeth M. M. A. Andriessen,
Nathalie Labrecque,
Florian Sennlaub,
Przemysław Sapieha
Publication year - 2016
Publication title -
investigative ophthalmology and visual science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.935
H-Index - 218
eISSN - 1552-5783
pISSN - 0146-0404
DOI - 10.1167/iovs.15-18598
Subject(s) - microglia , retinal , angiogenesis , neuropilin 1 , biology , retina , microbiology and biotechnology , semaphorin , neuroscience , immunology , vascular endothelial growth factor , cancer research , inflammation , receptor , genetics , biochemistry , vegf receptors
Neuropilin-1 (NRP-1) is a transmembrane receptor that is critical for vascular development within the central nervous system (CNS). It binds and influences signaling of several key angiogenic factors, such as VEGF-165, semaphorin 3A, platelet derived growth factor, and more. Neuropilin-1 is expressed by neurons and endothelial cells as well as a subpopulation of proangiogenic macrophages/microglia that are thought to interact with endothelial tip cells to promote vascular anastomosis during brain vascularization. We previously demonstrated a significant role for NRP-1 in macrophage chemotaxis and showed that NRP-1-expressing microglia are major contributors to pathologic retinal angiogenesis. Given this influence on CNS angiogenesis, we now investigated the involvement of microglia-resident NRP-1 in developmental retinal vascularization.
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