Adult Epicardial Fat Exhibits Beige Features

Author:

Sacks Harold S.12,Fain John N.3,Bahouth Suleiman W.4,Ojha Shalini5,Frontini Andrea6,Budge Helen5,Cinti Saverio6,Symonds Michael E.5

Affiliation:

1. Endocrinology and Diabetes Division (H.S.S.), VA Greater Los Angeles Healthcare System, Los Angeles, California 90073

2. Department of Medicine (H.S.S.), David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California 90095

3. Departments of Microbiology, Immunology, and Biochemistry (J.N.F.), Tennessee 38163

4. Pharmacology (S.W.B.), College of Medicine, University of Tennessee Health Science Center, Memphis, Tennessee 38163

5. The Early Life Nutrition Research Unit (S.O., H.B., M.E.S.), Academic Division of Child Health, School of Clinical Sciences, University Hospital, Nottingham NG7 2UH, United Kingdom

6. Department of Experimental and Clinical Medicine (A.F., S.C.), Obesity Center, United Hospitals-University of Ancona (Politecnica delle Marche), Ancona 60020, Italy

Abstract

Context: Human epicardial fat has been designated previously as brown-like fat. The supraclavicular fat depot in man has been defined as beige coexistent with classical brown based on its gene expression profile. Objective: The aim of the study was to establish the gene expression profile and morphology of human epicardial and visceral paracardial fat compared with sc fat. Setting: The study was conducted at a tertiary care hospital cardiac center. Patients: Epicardial, visceral paracardial, and sc fat samples had been taken from middle-aged patients with severe coronary atherosclerosis or valvular heart disease. Interventions: Gene expression was determined by reverse transcription- quantitative PCR and relative abundance of the mitochondrial uncoupling protein-1 (UCP-1) by Western blotting. Epicardial tissue sections from patients were examined by light microscopy, UCP-1 immunohistochemistry, and cell morphometry. Main Outcome Measures: We hypothesized that epicardial fat has a mixed phenotype with a gene expression profile similar to that described for beige cell lineage. Results: Immunoreactive UCP-1 was clearly measurable in each epicardial sample analyzed but was undetectable in each of the 4 other visceral and sc depots. Epicardial fat exhibited high expression of genes for UCP-1, PRDM16, PGC-1α, PPARγ, and the beige adipocyte-specific marker CD137, which were also expressed in visceral paracardial fat but only weakly in sternal, upper abdominal, and lower extremity sc fat. Histology of epicardial fat showed small unilocular adipocytes without UCP-1 immunostaining. Conclusion: UCP-1 is relatively abundant in epicardial fat, and this depot possesses molecular features characteristic of those found in vitro in beige lineage adipocytes.

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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