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Department of Animal Science and Technology/Institute of Biotechnology, National Taiwan University, Taipei 106, Taiwan
Abstract
The nuclear transcription factor, peroxisome proliferator activated receptor
(PPAR
), triggers adipocyte differentiation by regulating lipogenic genes. A ligand for PPAR
is necessary to activate PPAR
function. Fatty acids are potential ligands for PPAR
activation. The current experiment was designed to determine the potential for individual fatty acids to activate porcine PPAR
ectopically expressed in myoblasts. The expression of adipocyte fatty acid binding protein (aP2) and adiponectin in myoblasts stably expressing porcine PPAR
was increased when docosahexaenoic acid (DHA) was added to the adipogenic medium. The response was positively related to the DHA concentration and suggests that DHA may bind to and activate porcine PPAR
leading to increased expression of aP2 and adiponectin. The conditioned media collected from myoblasts expressing PPAR
between d 3 and 6 or between d 6 and 9, but not DHA itself activated the aP2 gene promoter-driven luciferase activity. These results suggest that a metabolite of DHA is the ligand binding to and activating porcine PPAR
. The metabolite and pathway for its production are currently unknown.
Key Words: adipocyte differentiation adipocyte fatty acid binding protein adiponectin docosahexaenoic acid peroxisome proliferator-activated receptor
pig
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