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Dynamics of fat cell turnover in humans
Authors:Spalding Kirsty L  Arner Erik  Westermark Pål O  Bernard Samuel  Buchholz Bruce A  Bergmann Olaf  Blomqvist Lennart  Hoffstedt Johan  Näslund Erik  Britton Tom  Concha Hernan  Hassan Moustapha  Rydén Mikael  Frisén Jonas  Arner Peter
Affiliation:Department of Cell and Molecular Biology, Karolinska Institute, SE-171 77 Stockholm, Sweden. kirsty.spalding@ki.se
Abstract:Obesity is increasing in an epidemic manner in most countries and constitutes a public health problem by enhancing the risk for cardiovascular disease and metabolic disorders such as type 2 diabetes. Owing to the increase in obesity, life expectancy may start to decrease in developed countries for the first time in recent history. The factors determining fat mass in adult humans are not fully understood, but increased lipid storage in already developed fat cells (adipocytes) is thought to be most important. Here we show that adipocyte number is a major determinant for the fat mass in adults. However, the number of fat cells stays constant in adulthood in lean and obese individuals, even after marked weight loss, indicating that the number of adipocytes is set during childhood and adolescence. To establish the dynamics within the stable population of adipocytes in adults, we have measured adipocyte turnover by analysing the integration of 14C derived from nuclear bomb tests in genomic DNA. Approximately 10% of fat cells are renewed annually at all adult ages and levels of body mass index. Neither adipocyte death nor generation rate is altered in early onset obesity, suggesting a tight regulation of fat cell number in this condition during adulthood. The high turnover of adipocytes establishes a new therapeutic target for pharmacological intervention in obesity.
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