Abstract

Angiopoietin-like 4 (ANGPTL4) is a target of hypoxia that accumulates in the endothelial extracellular matrix. While ANGPTL4 is known to regulate angiogenesis and vascular permeability, its context-dependent role related to vascular endothelial growth factor (VEGF) has been suggested in capillary morphogenesis. We here thus develop in vitro 3D models coupled to imaging and morphometric analysis of capillaries to decipher ANGPTL4 functions either alone or in the presence of VEGF. ANGPTL4 induces the formation of barely branched and thin endothelial capillaries that display linear adherens junctions. However, ANGPTL4 counteracts VEGF-induced formation of abundant ramified capillaries presenting cell–cell junctions characterized by VE-cadherin containing reticular plaques and serrated structures. We further deciphered the early angiogenesis steps regulated by ANGPTL4. During the initial activation of endothelial cells, ANGPTL4 alone induces cell shape changes but limits the VEGF-induced cell elongation and unjamming. In the growing sprout, ANGPTL4 maintains cohesive VE-cadherin pattern and sustains moderate 3D cell migration but restricts VEGF-induced endothelium remodeling and cell migration. This effect is mediated by differential short- and long-term regulation of P-Y1175-VEGFR2 and ERK1-2 signaling by ANGPTL4. Our in vitro 3D models thus provide the first evidence that ANGPTL4 induces a specific capillary morphogenesis but also overcomes VEGF effect.

Highlights

  • Angiogenesis orchestrates the establishment of a functional vascular plexus from pre-existing vessels and responds to oxygen and nutrients requirement during physiological or pathophysiological tissue remodeling

  • Hypoxia is a major stimulus of angiogenesis, triggering the expression of growth factors like vascular endothelial growth factor (VEGF) as well as components or proteins associated to the extracellular matrix (ECM) [2,3]

  • Regulation of capillary formation and morphogenesis by Angiopoietin-like 4 (ANGPTL4) was explored in presence or absence of VEGF using in vitro 3D angiogenesis models characterized by lumen formation and deposition of a polarized basement membrane [4,22]

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Summary

Introduction

Angiogenesis orchestrates the establishment of a functional vascular plexus from pre-existing vessels and responds to oxygen and nutrients requirement during physiological or pathophysiological tissue remodeling. Sprouting angiogenesis consists of many stages regulated by a spatial and dynamic balance involving a multitude of actors. Hypoxia is a major stimulus of angiogenesis, triggering the expression of growth factors like vascular endothelial growth factor (VEGF) as well as components or proteins associated to the extracellular matrix (ECM) [2,3]. ECM-associated proteins are known to regulate angiogenesis both directly and through fine-tuning of VEGF signaling. In keeping with the latter, we previously reported that transglutaminase 2 is accumulated in the hypoxic endothelial

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