Abstract

BackgroundPolychlorinated biphenyls (PCBs) are persistent environmental pollutants that preferentially accumulate in lipid-rich tissues of contaminated organisms. Although the adipose tissue constitutes a major intern reservoir of PCBs and recent epidemiological studies associate PCBs to the development of obesity and its related disorders, little is known about the mechanisms involved in their uptake by the adipose tissue and their intracellular localization in fat cells.Methodology/Principal FindingsWe have examined the intracellular distribution of PCBs in mouse cultured adipocytes and tested the potential involvement of caveolin-1, an abundant adipocyte membrane protein, in the uptake of these compounds by fat cells. We show that 2,4,4′-trichlorobiphenyl (PCB-28), 2,3′,4,4′,5-pentachlorobiphenyl (PCB-118) and 2,2′,4,4′,5,5′-hexachlorobiphenyl (PCB-153) congeners rapidly and extensively accumulate in 3T3-L1 or mouse embryonic fibroblast (MEF) derived cultured adipocytes. The dynamics of accumulation differed between the 3 congeners tested. By subcellular fractionation of primary adipocytes, we demonstrate that these pollutants were almost exclusively recovered within the lipid droplet fraction and practically not associated to cell membranes. The absence of caveolin-1 expression in primary adipocytes from cav-1 deficient mice did not modify lipid droplet selective targeting of PCBs. In cav-1 KO MEF differentiated adipocytes, PCB accumulation was decreased, which correlated with reduced cell triglyceride content. Conversely, adenoviral mediated cav-1 overexpressing in 3T3-L1 cells, which had no impact on total cell lipid content, did not change PCB accumulation.Conclusion/SignificanceOur data indicate that caveolin-1 per se is not required for selective PCB accumulation, but rather point out a primary dependence on adipocyte triglyceride content. If the crucial role of lipid droplets in energy homeostasis is considered, the almost exclusive accumulation of PCBs in these organelles warrants future attention as the impairment of their function could be linked to the worldwide obesity epidemic.

Highlights

  • Polychlorinated biphenyls (PCBs) are persistent environmental pollutants that are found at elevated concentrations in the adipose tissue of contaminated organisms [1]

  • Within the following 8 h, up to 80% of each PCB congener present in the second dose had accumulated in the adipocytes (Fig. 1B), indicating an important capacity for PCBs accumulation in cultured fat cells

  • We used several culture models of adipocytes to investigate the mechanisms of PCB accumulation within the adipose tissue

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Summary

Introduction

Polychlorinated biphenyls (PCBs) are persistent environmental pollutants that are found at elevated concentrations in the adipose tissue of contaminated organisms [1]. A recent study demonstrated increased persistent organic pollutant (POP) total body burden in obese subjects and increased POP serum concentrations after bariatric surgery leading to drastic weight loss [7]. How these compounds interfere with metabolic regulation remains poorly understood [4,7,8]. Polychlorinated biphenyls (PCBs) are persistent environmental pollutants that preferentially accumulate in lipid-rich tissues of contaminated organisms. The adipose tissue constitutes a major intern reservoir of PCBs and recent epidemiological studies associate PCBs to the development of obesity and its related disorders, little is known about the mechanisms involved in their uptake by the adipose tissue and their intracellular localization in fat cells

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