TY - JOUR
T1 - UCP1 induction during recruitment of brown adipocytes in white adipose tissue is dependent on cyclooxygenase activity
AU - Madsen, Lise
AU - Pedersen, Lone M
AU - Lillefosse, Haldis Haukaas
AU - Fjaere, Even
AU - Bronstad, Ingeborg
AU - Hao, Qin
AU - Petersen, Rasmus Koefoed
AU - Hallenborg, Philip
AU - Ma, Tao
AU - De Matteis, Rita
AU - Araujo, Pedro
AU - Mercader, Josep
AU - Bonet, M Luisa
AU - Hansen, Jacob B
AU - Cannon, Barbara
AU - Nedergaard, Jan
AU - Wang, Jun
AU - Cinti, Saverio
AU - Voshol, Peter
AU - Døskeland, Stein Ove
AU - Kristiansen, Karsten
PY - 2010/1/30
Y1 - 2010/1/30
N2 - Background: The uncoupling protein 1 (UCP1) is a hallmark of brown adipocytes and pivotal for cold- and diet-induced thermogenesis. Methodology/Principal Findings: Here we report that cyclooxygenase (COX) activity and prostaglandin E2 (PGE2) are crucially involved in induction of UCP1 expression in inguinal white adipocytes, but not in classic interscapular brown adipocytes. Cold-induced expression of UCP1 in inguinal white adipocytes was repressed in COX2 knockout (KO) mice and by administration of the COX inhibitor indomethacin in wild-type mice. Indomethacin repressed b-adrenergic induction of UCP1 expression in primary inguinal adipocytes. The use of PGE2 receptor antagonists implicated EP4 as a main PGE2 receptor, and injection of the stable PGE2 analog (EP3/4 agonist) 16,16 dm PGE2 induced UCP1 expression in inguinal white adipose tissue. Inhibition of COX activity attenuated diet-induced UCP1 expression and increased energy efficiency and adipose tissue mass in obesity-resistant mice kept at thermoneutrality. Conclusions/Significance: Our findings provide evidence that induction of UCP1 expression in white adipose tissue, but not in classic interscapular brown adipose tissue is dependent on cyclooxygenase activity. Our results indicate that cyclooxygenase-dependent induction of UCP1 expression in white adipose tissues is important for diet-induced thermogenesis providing support for a surprising role of COX activity in the control of energy balance and obesity development.
AB - Background: The uncoupling protein 1 (UCP1) is a hallmark of brown adipocytes and pivotal for cold- and diet-induced thermogenesis. Methodology/Principal Findings: Here we report that cyclooxygenase (COX) activity and prostaglandin E2 (PGE2) are crucially involved in induction of UCP1 expression in inguinal white adipocytes, but not in classic interscapular brown adipocytes. Cold-induced expression of UCP1 in inguinal white adipocytes was repressed in COX2 knockout (KO) mice and by administration of the COX inhibitor indomethacin in wild-type mice. Indomethacin repressed b-adrenergic induction of UCP1 expression in primary inguinal adipocytes. The use of PGE2 receptor antagonists implicated EP4 as a main PGE2 receptor, and injection of the stable PGE2 analog (EP3/4 agonist) 16,16 dm PGE2 induced UCP1 expression in inguinal white adipose tissue. Inhibition of COX activity attenuated diet-induced UCP1 expression and increased energy efficiency and adipose tissue mass in obesity-resistant mice kept at thermoneutrality. Conclusions/Significance: Our findings provide evidence that induction of UCP1 expression in white adipose tissue, but not in classic interscapular brown adipose tissue is dependent on cyclooxygenase activity. Our results indicate that cyclooxygenase-dependent induction of UCP1 expression in white adipose tissues is important for diet-induced thermogenesis providing support for a surprising role of COX activity in the control of energy balance and obesity development.
U2 - 10.1371/journal.pone.0011391
DO - 10.1371/journal.pone.0011391
M3 - Journal article
C2 - 20613988
SN - 1932-6203
VL - 5
SP - 1
EP - 13
JO - PLoS Computational Biology
JF - PLoS Computational Biology
IS - 6
ER -