Plxnd1-mediated mechanosensing of blood flow controls the caliber of the Dorsal Aorta via the transcription factor Klf2

作者：Jia He, Adriana Blazeski, Uthayanan Nilanthi, Javier Menéndez, S. Pirani, Daniel S. Levic, Michel Bagnat, Manvendra K. Singh, José G. Raya, Guillermo García‐Cardeña, Jesús Torres‐Vázquez · 发表于：bioRxiv (Cold Spring Harbor Laboratory) · 年份：2024 · DOI：10.1101/2024.01.24.576555 · 被引用次数：4 · 研究领域：Congenital heart defects research、Angiogenesis and VEGF in Cancer、Zebrafish Biomedical Research Applications

SUMMARY The cardiovascular system generates and responds to mechanical forces. The heartbeat pumps blood through a network of vascular tubes, which adjust their caliber in response to the hemodynamic environment. However, how endothelial cells in the developing vascular system integrate inputs from circulatory forces into signaling pathways to define vessel caliber is poorly understood. Using vertebrate embryos and in vitro -assembled microvascular networks of human endothelial cells as models, flow and genetic manipulations, and custom software, we reveal that Plexin-D1, an endothelial Semaphorin receptor critical for angiogenic guidance, employs its mechanosensing activity to serve as a crucial positive regulator of the Dorsal Aorta’s (DA) caliber. We also uncover that the flow-responsive transcription factor KLF2 acts as a paramount mechanosensitive effector of Plexin-D1 that enlarges endothelial cells to widen the vessel. These findings illuminate the molecular and cellular mechanisms orchestrating the interplay between cardiovascular development and hemodynamic forces. Highlights Plexin-D1 mechanosensing of blood flow tunes the caliber of the Dorsal Aorta (DA) The DA widens without raising endothelial cell numbers, which can change separate from the caliber The Kruppel-like transcription factor 2 (KLF2) is a key Plexin-D1 mechano-effector during development KLF2 increases endothelial cell size to expand the DA caliber