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Perivascular adipose tissue: An immune cell metropolis.

Authors :
Saxton, S. N.
Heagerty, A. M.
Withers, S. B.
Source :
Experimental Physiology; Sep2020, Vol. 105 Issue 9, p1440-1443, 4p
Publication Year :
2020

Abstract

New Findings: What is the topic of this review?The review discusses how eosinophils can contribute to the function of perivascular adipose tissue and explores the mechanisms involved.What advances does it highlight?Understanding the communication between the cell populations that constitute perivascular adipose tissue function is important for exploring therapeutic options in the treatment of obesity‐related cardiovascular complications. This article highlights that eosinophils are able to contribute directly to healthy perivascular adipose tissue function. These immune cells contribute to adrenergic signalling and nitric oxide‐ and adiponectin‐dependent mechanisms in perivascular adipose tissue. Perivascular adipose tissue is a heterogeneous tissue that surrounds most blood vessels in the body. This review focuses on the contribution of eosinophils located within the adipose tissue to vascular contractility. A high‐fat diet reduces the number of these immune cells within perivascular adipose tissue, and this loss is linked to an increase in vascular contractility and hypertension. We explored the mechanisms by which eosinophils contribute to this function using genetically modified mice, ex vivo assessment of contractility and pharmacological tools. We found that eosinophils contribute to adrenergic signalling and nitric oxide‐ and adiponectin‐dependent mechanisms in perivascular adipose tissue. It is now important to explore whether manipulation of these pathways in obesity can alleviate cardiovascular complications, in order to determine whether eosinophils are a valid target for obesity‐related disease. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09580670
Volume :
105
Issue :
9
Database :
Complementary Index
Journal :
Experimental Physiology
Publication Type :
Academic Journal
Accession number :
145429925
Full Text :
https://doi.org/10.1113/EP087872