Cited by 242Adipokines, Inflammation, and Metabolic DiseasesAdipose Tissue and MetabolismCardiovascular Disease and Adiposity

Interplay between the immune system and adipose tissue in obesity

Open access
Exley, Mark A, Hand, Laura, O'Shea, Donal, Lynch, Lydia·2014·Journal of Endocrinology

Abstract

Obesity is a major risk factor for metabolic disease, with white adipose tissue (WAT) inflammation emerging as a key underlying pathology. Alongside its major role in energy storage, WAT is an important endocrine organ, producing many bioactive molecules, termed adipokines, which not only serve as regulators of systemic metabolism, but also possess immunoregulatory properties. Furthermore, WAT contains a unique immune cell repertoire, including an accumulation of leukocytes that are rare in other locations. These include alternatively activated macrophages, invariant natural killer T cells, and regulatory T cells. Disruption of resident adipose leukocyte homeostasis contributes to obesity-associated inflammation and consequent metabolic disorder. Despite many recent advances in this new field of immuno-metabolism, fundamental questions of why and how inflammation arises as obesity develops are not yet fully understood. Exploring the distinct immune system of adipose tissue is fundamental to our understanding of the endocrine as well as immune systems. In this review, we discuss the roles of adipose tissue leukocytes in the transition to obesity and progression of inflammation and highlight potential anti-inflammatory therapies for combating obesity-related pathology.

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  • Obesity promotes inflammatory pathways in visceral fat through adipocyte hypertrophy and hyperplasia and the accumulation of immune cells including macrophages, mast cells, and T lymphocytes producing pro-inflammatory cytokines.

    “Obesity promotes inflammatory pathways in visceral fat through adipocyte hypertrophy and hyperplasia and the accumulation of immune cells including macrophages, mast cells, and T lymphocytes producing pro-inflammatory cytokines (148–150).”

    From Health Consequences of Sarcopenic Obesity: A Narrative Review (2020) · cites this paper as [149]

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  1. Platell C, Cooper D, Papadimitriou JM & Hall JC 2000 The omentum. World Journal of Gastroenterology 6 169-176.

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Authors
Exley, M. A., Hand, L., O'Shea, D., & Lynch, L.
Affiliations
University College Dublin (IE)
Venue
Journal of Endocrinology
Published
2014-09-16
Volume
223
Issue
2
Pages
R41-R48
ISSN
  • 0022-0795 (ISSN-L)
  • 1479-6805
OpenAlex
W2145456795
Cited by
242
References
66
Citations by year
2026: 8 · 2025: 8 · 2024: 12 · 2023: 26 · 2022: 25 · 2021: 20 · 2020: 24 · 2019: 18 · 2018: 20 · 2017: 22 · 2016: 24 · 2015: 35
FWCI
3.60
Type
journal article
Language
en
Open access
Locations
  • Journal of Endocrinology (publishedVersion)
  • PubMed (publishedVersion)
  • Research Explorer (The University of Manchester) (publishedVersion)
Funders
National Cancer Institute (P01CA017094, CA017094)
Topics
  • Health Sciences › Medicine › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
  • Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Disease and Adiposity
Keywords
obesity, white adipose tissue, adipose tissue inflammation, adipokines, M2 macrophages, invariant natural killer T cells, regulatory T cells, metabolic disorders, anti-inflammatory therapy
MeSH terms
Adipose Tissue, Animals, Eosinophils, Humans, Immune System, Inflammation, Lymphocytes, Macrophages, Obesity

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