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MicroRNA-9 Couples Brain Neurogenesis and Angiogenesis
Author(s) -
Romain Madelaine,
Steven A. Sloan,
Nina Huber,
James H. Notwell,
Louis C. Leung,
Gemini Skariah,
Caroline Halluin,
Sergiu P. Paşca,
Gill Bejerano,
Mark A. Krasnow,
Ben A. Barres,
Philippe Mourrain
Publication year - 2017
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2017.07.051
Subject(s) - neurogenesis , angiogenesis , microrna , biology , microbiology and biotechnology , neuroscience , transcription factor , vascular endothelial growth factor , cancer research , vegf receptors , genetics , gene
In the developing brain, neurons expressing VEGF-A and blood vessels grow in close apposition, but many of the molecular pathways regulating neuronal VEGF-A and neurovascular system development remain to be deciphered. Here, we show that miR-9 links neurogenesis and angiogenesis through the formation of neurons expressing VEGF-A. We found that miR-9 directly targets the transcription factors TLX and ONECUTs to regulate VEGF-A expression. miR-9 inhibition leads to increased TLX and ONECUT expression, resulting in VEGF-A overexpression. This untimely increase of neuronal VEGF-A signal leads to the thickening of blood vessels at the expense of the normal formation of the neurovascular network in the brain and retina. Thus, this conserved transcriptional cascade is critical for proper brain development in vertebrates. Because of this dual role on neural stem cell proliferation and angiogenesis, miR-9 and its downstream targets are promising factors for cellular regenerative therapy following stroke and for brain tumor treatment.

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