Perivascular adipose tissue – an immune cell metropolis
Autor: | Sophie N Saxton, Anthony M. Heagerty, Sarah B Withers |
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Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
Pathology
medicine.medical_specialty Lydia Becker Institute Physiology Cell Adrenergic Adipose tissue 030204 cardiovascular system & hematology Diet High-Fat Nitric Oxide Nitric oxide Contractility Mice 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Immune system Physiology (medical) ResearchInstitutes_Networks_Beacons/lydia_becker_institute_of_immunology_and_inflammation medicine Animals Obesity Nutrition and Dietetics Adiponectin business.industry General Medicine Eosinophils medicine.anatomical_structure Adipose Tissue chemistry Hypertension business 030217 neurology & neurosurgery Ex vivo Signal Transduction |
Zdroj: | Saxton, S, Heagerty, A & Withers, S 2020, ' Perivascular adipose tissue – an immune cell metropolis ', Experimental Physiology . https://doi.org/10.1113/EP087872 PDFPDF |
ISSN: | 0958-0670 |
DOI: | 10.1113/EP087872 |
Popis: | 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 which 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 directly contribute to healthy perivascular adipose tissue function. These immune cells contribute to adrenergic signalling, nitric oxide and adiponectin dependent mechanisms in perivascular adipose tissue. Perivascular adipose tissue is a heterogenous tissue which surrounds most blood vessels in the body. This review focuses on the contribution of eosinophils located within the adipose tissue to vascular contractility. High fat diet reduces the number of these immune cells with perivascular adipose tissue, and this loss is linked with 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, nitric oxide and adiponectin dependent mechanisms in perivascular adipose tissue. Exploring whether manipulation of these pathways in obesity can alleviate cardiovascular complications is now important to determine whether eosinophils are a valid target for obesity-related disease. This article is protected by copyright. All rights reserved. [Abstract copyright: This article is protected by copyright. All rights reserved.] |
Databáze: | OpenAIRE |
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