Abstract

Endothelial cells that form the inner layer of blood and lymphatic vessels are important regulators of vascular functions and centrally involved in the pathogenesis of vascular diseases. In addition to the vascular endothelial growth factor (VEGF) receptor pathway, the angiopoietin (Ang)–Tie system is a second endothelial cell specific ligand–receptor signalling system necessary for embryonic cardiovascular and lymphatic development. The Ang–Tie system also regulates postnatal angiogenesis, vessel remodelling, vascular permeability and inflammation to maintain vascular homoeostasis in adult physiology. This system is implicated in numerous diseases where the vasculature has an important contribution, such as cancer, sepsis, diabetes, atherosclerosis and ocular diseases. Furthermore, mutations in the TIE2 signalling pathway cause defects in vascular morphogenesis, resulting in venous malformations and primary congenital glaucoma. Here, we review recent advances in the understanding of the Ang–Tie signalling system, including cross-talk with the vascular endothelial protein tyrosine phosphatase (VE-PTP) and the integrin cell adhesion receptors, focusing on the Ang–Tie system in vascular development and pathogenesis of vascular diseases.

Highlights

  • Endothelial cells (EC) that form the inner layer of blood and lymphatic vessels are key mediators of vascular functions, including the growth of new blood (angiogenesis) and lymphatic vessels (lymphangiogenesis), tissue fluid homeostasis, vascular permeability and inflammation

  • Endothelial cells (EC) that form the inner layer of blood and lymphatic vessels are key mediators of vascular functions, including the growth of new blood and lymphatic vessels, tissue fluid homeostasis, vascular permeability and inflammation

  • The TIE2 and PIK3CA mutations resulted in the formation of venous malformations (VM) lesions when mutant genes were expressed by transplanted ECs in mice [30,150], and in a genetic mouse model [31,32], respectively. These results indicate that the TIE2 receptor and the PIK3CA signal transducer participate in the same VM signalling pathway, opening new possibilities for evidence-based molecular therapies against VMs [29,31,32,150]

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Summary

Introduction

Endothelial cells (EC) that form the inner layer of blood and lymphatic vessels are key mediators of vascular functions, including the growth of new blood (angiogenesis) and lymphatic vessels (lymphangiogenesis), tissue fluid homeostasis, vascular permeability and inflammation. Tie1 in blood and lymphatic vascular development The constitutive deletion of Tie1 resulted in haemorrhages and death of mouse embryos by E13.5. Lymphatic development occurred normally in Ang2-deficient embryos, but subsequent remodelling of the vessels resulted in narrowing of the lymphatic capillaries associated with abnormal vascular smooth muscle cell (SMC) coverage and defective lymphatic valve formation of collecting lymphatic vessels [45,47,48].

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