Why the study?
While obesity-induced metabolic dysfunction depends on adipose depot type, pericardial adipose tissue is a lesser known visceral depot whose transcriptional and morphological signature remained uncharacterized.
Does a high-fat diet alter the transcriptional and morphological signature of pericardial adipose tissue in a mouse model compared to a chow diet?
Does a high-fat diet alter the transcriptional and morphological signature of pericardial adipose tissue in a mouse model compared to a chow diet?
Pericardial adipose tissue possesses a unique transcriptional and histological signature with features of both beige and pro-inflammatory depots, which may contribute to obesity-associated metabolic dysfunction.
Pericardial adipose tissue may link high-fat diet to cardiometabolic dysfunction; hypothesis-generating for human translation and therapeutic targeting.
Obesity is a major risk factor for a plethora of metabolic disturbances including diabetes and cardiovascular disease. Accumulating evidence is showing that there is an adipose tissue depot-dependent relationship with obesity-induced metabolic dysfunction. While some adipose depots, such as subcutaneous fat, are generally metabolically innocuous, others such as visceral fat, are directly deleterious. A lesser known visceral adipose depot is the pericardial adipose tissue depot. We therefore set out to examine its transcriptional and morphological signature under chow and high-fat fed conditions, in comparison with other adipose depots, using a mouse model. Our results revealed that under chow conditions pericardial adipose tissue has uncoupling-protein 1 gene expression levels which are significantly higher than classical subcutaneous and visceral adipose depots. We also observed that under high-fat diet conditions, the pericardial adipose depot exhibits greatly upregulated transcript levels of inflammatory cytokines. Our results collectively indicate, for the first time, that the pericardial adipose tissue possesses a unique transcriptional and histological signature which has features of both a beige (brown fat-like) but also pro-inflammatory depot, such as visceral fat. This unique profile may be involved in metabolic dysfunction associated with obesity.
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Al‐Dibouni et al. (2020) studied this question.
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