Abstract

The microvasculature is a heterogeneous, dynamic and versatile component of the systemic circulation, with a unique ability to locally self‐regulate and to respond to organ demand and environmental stimuli. Endothelial cells from different organs display considerable variation, but it is currently unclear to what extent functional properties of organ‐specific endothelial cells are intrinsic, acquired and/or reprogrammable. Vascular function is a fundamental pillar of homeostasis, and dysfunction results in systemic consequences for the organism. Additionally, vascular failure can occur downstream of organ disease or environmental stress, often driving an exacerbation of symptoms and pathologies originally independent of the local circulation. The understanding of the molecular mechanisms underlying endothelial physiology and metabolism holds the promise to inform and improve diagnosis, prognosis and treatment options for a myriad of conditions as unrelated as cancer, neurodegeneration or pulmonary hypertension, and likely everything in between, if we consider that also treatments for such conditions are primarily distributed via the bloodstream. However, studying endothelial function has its challenges: the origin, isolation, culture conditions and preconditioning stimuli make this an extremely variable cell type to study and difficult to source. Animal models exist but are neither trivial to generate, nor necessarily adequately translatable to human disease. In this article, we aim to illustrate the breadth of microvascular functions in different environments, highlighting current and pioneering studies that have advanced our insight into the importance of the integrity of this tissue, as well as the limitations posed by its heterogeneity and plasticity.

Highlights

  • The microvascular system is arguably the largest organ in the human body, covering a surface area of 1–7 m2, and only rivalled in mass by the liver and skin [1]

  • Microvascular function is currently too loose a term to reflect the functional heterogeneity observed along the vascular tree, in terms of vessel type and location within specialized tissues

  • Activated endothelial cells (EC) are prothrombotic [63], due to the surface expression of intercellular adhesion molecules that promote platelet interaction and binding of circulating myeloid cells [3,64]. Essential as this function is for control of blood flow and tissue remodelling, it needs to be reversible

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Summary

Background

The microvascular system is arguably the largest organ in the human body, covering a surface area of 1–7 m2, and only rivalled in mass by the liver and skin [1]. This knowledge is limited in the representation of the impact of EC dysfunction as both cause and effect of other conditions, including lifestyle and ageing, which can neither be generalized and applied to all EC populations, nor seamlessly translated between model organisms This viewpoint article will not review detailed molecular aspects of current knowledge of EC biology; instead, it will emphasize general aspects of local control of vascular function and the challenges of adequately modelling these studies, while providing an overview of existing new and exciting developments in the field, to highlight the potential applications and implications of harnessing microvascular properties to improve human health

Regulation and regulators of EC function in different tissues
Metabolic shifts as mediators of EC form and function
Findings
Author contributions
Full Text
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