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Perilipin ablation results in a lean mouse with aberrant adipocyte lipolysis, enhanced leptin production, and resistance to diet-induced obesity
被引:616
作者:
Tansey, JT
Sztalryd, C
Gruia-Gray, J
Roush, DL
Zee, JV
Gavrilova, O
Reitman, ML
Deng, CX
Li, C
Kimmel, AR
Londos, C
机构:
[1] NIDDKD, Cellular & Dev Biol Lab, NIH, Bethesda, MD 20892 USA
[2] NIDDKD, Diabet Branch, NIH, Bethesda, MD 20892 USA
[3] NIDDKD, Genet Dev & Dis Branch, NIH, Bethesda, MD 20892 USA
来源:
关键词:
D O I:
10.1073/pnas.101042998
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Perilipin coats the lipid droplets of adipocytes and is thought to have a role in regulating triacylglycerol hydrolysis. To study the role of perilipin in vivo, we have created a perilipin knockout mouse. Perilipin null (peri(-/-)) and wild-type (peri(+/+)) mice consume equal amounts of food, but the adipose tissue mass in the null animals is reduced to approximate to 30% of that in wild-type animals. Isolated adipocytes of perilipin null mice exhibit elevated basal lipolysis because of the loss of the protective function of perilipin. They also exhibit dramatically attenuated stimulated lipolytic activity, indicating that perilipin is required for maximal lipolytic activity. Plasma leptin concentrations in null animals were greater than expected for the reduced adipose mass. The peri(-/-) animals have a greater lean body mass and increased metabolic rate but they also show an increased tendency to develop glucose intolerance and peripheral insulin resistance. When fed a high-fat diet, the perilipin null animals are resistant to diet-induced obesity but not to glucose intolerance. The data reveal a major role for perilipin in adipose lipid metabolism and suggest perilipin as a potential target for attacking problems associated with obesity.
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页码:6494 / 6499
页数:6
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