Year: 2019
Type: article
Abstract: Angiogenesis is driven by the coordinated collective branching of specialized leading "tip" and trailing "stalk" endothelial cells (ECs). While Notch-regulated negative feedback suppresses excessive tip selection, roles for positive feedback in EC identity decisions remain unexplored. Here, by integrating computational modeling with in vivo experimentation, we reveal that positive feedback critically modulates the magnitude, timing, and robustness of angiogenic responses. In silico modeling predicts that positive-feedback-mediated amplification of VEGF signaling generates an ultrasensitive bistable switch that underpins quick and robust tip-stalk decisions. In agreement, we define a positive-feedback loop exhibiting these properties in vivo , whereby Vegf-induced expression of the atypical tetraspanin, tm4sf18 , amplifies Vegf signaling to dictate the speed and robustness of EC selection for angiogenesis. Consequently, tm4sf18 mutant zebrafish select fewer motile ECs and exhibit stunted hypocellular vessels with unstable tip identity that is severely perturbed by even subtle Vegfr attenuation. Hence, positive feedback spatiotemporally shapes the angiogenic switch to ultimately modulate vascular network topology.
Source: Cell Reports
Authors: Donna J. Page, Raphael Thuret, Lakshmi Venkatraman, Tokiharu Takahashi, Katie Bentley, Shane P. Herbert
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $5,448
Awards: Transcriptional Control of Endothelial Tip Cell Behaviour and New Blood Vessel Sprouting., G1075485332, G1235485622, Transcriptional Control of Endothelial Tip Cell Behaviour and New Blood Vessel Sprouting., G4187036355, Spatiotemporal control of endothelial tip/stalk cell identity in angiogenesis, G5570099221, 14 NSFBIO: Asymmetric division and the temporal dynamics of cell motility, Bilateral BBSRC-NSF/BIO: Asymmetric division and the temporal dynamics of cell motility
OpenAlex ID: W2945353962
