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ARTICLE |
regulates adipogenesis in myoblasts
1 Department of Animal Science and Technology/Institute of Biotechnology, National Taiwan University, Taipei 106, Taiwan
* To whom correspondence should be addressed. E-mail: sding{at}ntu.edu.tw.
| Abstract |
|---|
Peroxisome-proliferator-activated receptor
(PPAR
) plays a critical role in regulating adipogenesis. The expression of PPAR
precedes that of PPAR
during adipocyte differentiation in rodents. The current experiment was designed to study the function of porcine PPAR
and the interaction of PPAR
and PPAR
in adipocyte differentiation. Inhibition of myogenesis was observed in mouse myoblasts expressing porcine PPAR
, similar to myoblasts expressing PPAR
. Treatment of myoblasts expressing PPAR
with ligands for both PPAR
and
enhanced lipogenesis and adipogenesis to a greater extent than treatment with a PPAR
ligand alone, suggesting that both genes were involved in regulating lipogenesis and adipogenesis. The ability to transdifferentiate myoblasts into adipocytes was decreased in myoblasts co-expressing PPAR
with either wild-type or mutated PPAR
(serine 112 was mutated to alanine; the mutated PPAR
is more active than wild-type) compared with myoblasts expressing PPAR
alone. Adipocyte differentiation in myoblasts co-expressing PPAR
and mutated PPAR
was greater than in myoblasts co-expressing PPAR
and wild-type PPAR
, confirming that the serine 112 is important for the function of PPAR
. Taken together, our results demonstrate that overexpression of PPAR
inhibits myotube formation and also enhances adipocyte differentiation. However, the complexity and interaction of PPAR
and PPAR
in adipogenesis are not clearly understood.
Key Words:
Adipocyte differentiation, myogenin, peroxisome proliferator-activated receptor
, peroxisome proliferator-activated receptor
, pigs
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