Biology and function of adipose tissue macrophages, dendritic cells and B cells. (April 2018)

• Record Type: Journal Article
• Authors: Ivanov, Stoyan; Merlin, Johanna; Lee, Man Kit Sam; Murphy, Andrew J.; Guinamard, Rodolphe R.
• Is Part Of: Atherosclerosis. Volume 271(2018)
• Page Start: 102
• Page End: 110
• Publication Date: 2018-04
• Subjects: Macrophage -- Dendritic cell -- B cell -- Adipose tissue -- Obesity; Arteriosclerosis -- Periodicals; Electronic journals; 616.136
• DOI: 10.1016/j.atherosclerosis.2018.01.018
• Languages: English
• ISSNs: 0021-9150

Abstract

Abstract: The increasing incidence of obesity and its socio-economical impact is a global health issue due to its associated co-morbidities, namely diabetes and cardiovascular disease [1–5 ]. Obesity is characterized by an increase in adipose tissue, which promotes the recruitment of immune cells resulting in low-grade inflammation and dysfunctional metabolism. Macrophages are the most abundant immune cells in the adipose tissue of mice and humans. The adipose tissue also contains other myeloid cells (dendritic cells (DC) and neutrophils) and to a lesser extent lymphocyte populations, including T cells, B cells, Natural Killer (NK) and Natural Killer T (NKT) cells. While the majority of studies have linked adipose tissue macrophages (ATM) to the development of low-grade inflammation and co-morbidities associated with obesity, emerging evidence suggests for a role of other immune cells within the adipose tissue that may act in part by supporting macrophage homeostasis. In this review, we summarize the current knowledge of the functions ATMs, DCs and B cells possess during steady-state and obesity. Highlights: Adipose tissue contains a large and diverse pattern of immune cells. Adipose tissue macrophages play a critical role in the maintenance of adipose tissue homeostasis and obesity development. Dendritic cells and B cells emerge as new players in adipose tissue control.