Please use this identifier to cite or link to this item: https://doi.org/10.1038/srep04031
Title: Dll4-containing exosomes induce capillary sprout retraction in a 3D microenvironment
Authors: Sharghi-Namini, S.
Tan, E.
Ong, L.-L.S.
Ge, R. 
Asada, H.H.
Issue Date: 7-Feb-2014
Citation: Sharghi-Namini, S., Tan, E., Ong, L.-L.S., Ge, R., Asada, H.H. (2014-02-07). Dll4-containing exosomes induce capillary sprout retraction in a 3D microenvironment. Scientific Reports 4 : -. ScholarBank@NUS Repository. https://doi.org/10.1038/srep04031
Abstract: Delta-like 4 (Dll4), a membrane-bound Notch ligand, plays a fundamental role in vascular development and angiogenesis. Dll4 is highly expressed in capillary endothelial tip cells and is involved in suppressing neighboring stalk cells to become tip cells during angiogenesis. Dll4-Notch signaling is mediated either by direct cell-cell contact or by Dll4-containing exosomes from a distance. However, whether Dll4-containing exosomes influence tip cells of existing capillaries is unknown. Using a 3D microfluidic device and time-lapse confocal microscopy, we show here for the first time that Dll4-containing exosomes causes tip cells to lose their filopodia and trigger capillary sprout retraction in collagen matrix. We demonstrate that Dll4 exosomes can freely travel through 3D collagen matrix and transfer Dll4 protein to distant tip cells. Upon reaching endothelial sprout, it causes filopodia and tip cell retraction. Continuous application of Dll4 exosomes from a distance lead to significant reduction of sprout formation. This effect correlates with Notch signaling activation upon Dll4-containing exosome interaction with recipient endothelial cells. Furthermore, we show that Dll4-containing exosomes increase endothelial cell motility while suppressing their proliferation. These data revealed novel functions of Dll4 in angiogenesis through exosomes.
Source Title: Scientific Reports
URI: http://scholarbank.nus.edu.sg/handle/10635/100491
ISSN: 20452322
DOI: 10.1038/srep04031
Appears in Collections:Staff Publications

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