Dynamics of fat cell turnover in humans (original) (raw)
- Letter
- Published: 04 May 2008
- Erik Arner1,
- Pål O. Westermark2,
- Samuel Bernard3,
- Bruce A. Buchholz4,
- Olaf Bergmann1,
- Lennart Blomqvist5,
- Johan Hoffstedt5,
- Erik Näslund6,
- Tom Britton7,
- Hernan Concha5,
- Moustapha Hassan5,
- Mikael Rydén5,
- Jonas Frisén1 &
- …
- Peter Arner5
Nature volume 453, pages 783–787 (2008)Cite this article
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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 diabetes1,2. Owing to the increase in obesity, life expectancy may start to decrease in developed countries for the first time in recent history3. 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 important4,5. 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 DNA6. 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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Acknowledgements
We thank M. Stahlberg and T. Bergman for help with high-performance liquid chromatography (HPLC), D. Kurdyla, P. Zermeno and A. Williams for producing graphite, and S. Zdunek for comments on the statistics and modelling. This study was supported by grants from Knut och Alice Wallenbergs Stiftelse, the Human Frontiers Science Program, the Swedish Research Council, the Swedish Cancer Society, the Swedish Heart and Lung foundation, the Novo Nordic Foundation, the Swedish Diabetes Foundation, the Foundation for Strategic Research, the Karolinska Institute, the Tobias Foundation, AFA Life Insurance Health Foundation and NIH/NCRR (RR13461). This work was performed in part under the auspices of the US Department of Energy by University of California, Lawrence Livermore National Laboratory under contract W-7405-Eng-48.
Author Contributions K.L.S., P.A. and J.F. designed the study and wrote the manuscript. E.A., P.O.W., S.B., O.B. and T.B. were responsible for the modelling and statistics. K.L.S. and B.A.B. performed sample preparation and 14C accelerator mass spectrometry measurements. L.B., J.H. and E.N. collected clinical material. H.C., M.H. and M.R. performed studies on fat cell purity.
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Authors and Affiliations
- Department of Cell and Molecular Biology, Karolinska Institute, SE-171 77 Stockholm, Sweden
Kirsty L. Spalding, Erik Arner, Olaf Bergmann & Jonas Frisén - Institute for Theoretical Biology (ITB), Humboldt University Berlin and Charité, Invalidenstrasse 43, 10115 Berlin, Germany ,
Pål O. Westermark - Institute of Applied and Computational Mathematics, Foundation of Research and Technology, 71110 Heraklion Crete, Greece
Samuel Bernard - Center for Accelerator Mass Spectrometry, Lawrence Livermore National Laboratory, 7000 East Avenue, L-397, Livermore, California 94551, USA ,
Bruce A. Buchholz - Department of Medicine, Karolinska University Hospital, SE-141 86 Stockholm, Sweden
Lennart Blomqvist, Johan Hoffstedt, Hernan Concha, Moustapha Hassan, Mikael Rydén & Peter Arner - Division of Surgery, Department of Clinical Science, Danderyds Hospital, Karolinska Institutet, SE-182 88 Stockholm, Sweden
Erik Näslund - Department of Mathematics, Stockholm University, 106 91 Stockholm, Sweden
Tom Britton
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Correspondence toKirsty L. Spalding, Jonas Frisén or Peter Arner.
Supplementary information
Supplementary information
The file contains Supplementary Notes including model and curve fit for fat cell data measuring average fat cell volume against body fat mass; Supplementary Table showing all data from the thirty-five people whose adipose DNA was carbon dated; modelling of 14C data; methodologies and additional references. (PDF 1007 kb)
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Spalding, K., Arner, E., Westermark, P. et al. Dynamics of fat cell turnover in humans.Nature 453, 783–787 (2008). https://doi.org/10.1038/nature06902
- Received: 30 November 2007
- Accepted: 07 March 2008
- Published: 04 May 2008
- Issue Date: 05 June 2008
- DOI: https://doi.org/10.1038/nature06902
Editorial Summary
Obesity: Fat cell numbers are for life
The storage of lipids in pre-existing fat cells is thought to be a major factor in obesity, but beyond that it is not known for certain when in life adipocytes are generated and whether alterations in this process may contribute to obesity. Now a survey of total adipocyte numbers in hundreds of individuals, combined with analysis of the integration of carbon-14 derived from nuclear bomb tests into genomic DNA, has provided a clear picture of metabolism of adipose tissues. The number of fat cells in the body is a major determinant for fat mass in adults, but that number is set during childhood and adolescence and hardly varies during adulthood. Surprisingly, there is a remarkably high turnover of adipocytes within a constant total population. Neither adipocyte death nor generation rate alters during early onset obesity. This newly discovered phenomenon of adipocyte turnover could provide a new target for therapeutic intervention in obesity.