4.3 Article

The pathobiology of perivascular adipose tissue (PVAT), the fourth layer of the blood vessel wall

Journal

CARDIOVASCULAR PATHOLOGY
Volume 61, Issue -, Pages -

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.carpath.2022.107459

Keywords

Artery; Tunica adiposa; White adipose tissue; Brown adipose tissue; Beige adipose tissue; Atherosclerosis

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Perivascular adipose tissue (PVAT) is a metabolically active adipose tissue depot surrounding human blood vessels. It plays a role in vascular homeostasis and can contribute to the development of vascular dysfunction. PVAT is composed of white, brown, and beige adipose tissue, and its dysfunction can influence the initiation and growth of atherosclerotic plaque. PVAT interacts with the arterial wall through various mechanisms, including modulation of smooth muscle cell contractility and secretion of anti-inflammatory molecules.
The perivascular adipose tissue (PVAT) is an adipose tissue depot which surrounds most human blood vessels. It is metabolically active and has both a protective and a pathogenic role in vascular biology and pathobiology. It regulates vascular homeostasis and promotes vascular dysfunction. The purpose of this review is to consider the origin, structure, function, and dysfunction of this unique adipose depot con-sisting of white (WAT), brown (BAT) and beige adipose tissue, to support the concept that PVAT may be considered the fourth layer of the normal arterial wall (tunica adiposa), in which dysfunction cre-ates a microenvironment that regulates, in part, the initiation and growth of the fibro-inflammatory lipid atherosclerotic plaque. Experimental in-vivo and in-vitro studies and human investigations show that the adipocytes, extracellular matrix, nerve fibers and vasa vasorum found in PVAT form a functional adipose tissue unit adjacent to, but not anatomically separated from, the adventitia. PVAT maintains and regu-lates the structure and function of the normal arterial wall through autocrine and paracrine mechanisms, that include modulation of medial smooth muscle cell contractility and secretion of anti-inflammatory molecules. PVAT shows regional phenotypic heterogeneity which may be important in its effect on the wall of specific sections of the aorta and its muscular branches during perturbations and various injuries including obesity and diabetes. In atherosclerosis, a pan-vascular microenvironment is created that func-tionally links the intima-medial atherosclerotic plaque to the adventitia and PVAT beneath the plaque, highlighting the local impact of PVAT on atherogenesis. PVAT adipocytes have inflammatory effects which in response to injury show activation and phenotypic changes, some of which are considered to have direct and indirect effects on the intima and media during the initiation, growth, and development of complicated atherosclerotic plaques. Thus, it is important to maintain the integrity of the full vascular microenvironment so that design of experimental and human studies include investigation of PVAT. The era of discarding PVAT tissue in both experimental and human research and clinical vascular studies should end. (c) 2022 Elsevier Inc. All rights reserved.

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