4.6 Article

Brown adipose tissue takes up plasma triglycerides mostly after lipolysis

期刊

JOURNAL OF LIPID RESEARCH
卷 56, 期 1, 页码 51-59

出版社

ELSEVIER
DOI: 10.1194/jlr.M052746

关键词

cholesterol; chylomicrons; lipoproteins/metabolism; lipids; lipoprotein lipase; fatty acid metabolism

资金

  1. Netherlands CardioVascular Research Initiative: 'the Dutch Heart Foundation' [CVON2011-19]
  2. Netherlands CardioVascular Research Initiative 'Dutch Federation of University Medical Centers' [CVON2011-19]
  3. Netherlands CardioVascular Research Initiative 'Netherlands Organisation for Health Research and Development' [CVON2011-19]
  4. Netherlands CardioVascular Research Initiative 'Royal Netherlands Academy of Sciences' [CVON2011-19]
  5. Netherlands Lung Foundation [3.2.10.048]
  6. Board of Directors of Leiden University Medical Center

向作者/读者索取更多资源

Brown adipose tissue (BAT) produces heat by burning TGs that are stored within intracellular lipid droplets and need to be replenished by the uptake of TG-derived FA from plasma. It is currently unclear whether BAT takes up FA via uptake of TG-rich lipoproteins (TRLs), after lipolysis-mediated liberation of FA, or via a combination of both. Therefore, we generated glycerol tri[H-3] oleate and [C-14] cholesteryl oleate double-labeled TRL-mimicking particles with an average diameter of 45, 80, and 150 nm (representing small VLDL to chylomicrons) and injected these intravenously into male C57Bl/6J mice. At room temperature (21 degrees C), the uptake of H-3-activity by BAT, expressed per gram of tissue, was much higher than the uptake of 14 C-activity, irrespective of particle size, indicating lipolysis-mediated uptake of TG-derived FA rather than whole particle uptake. Cold exposure (7 degrees C) increased the uptake of FA derived from the differently sized particles by BAT, while retaining the selectivity for uptake of FA over cholesteryl ester (CE). At thermoneutrality (28 degrees C), total FA uptake by BAT was attenuated, but the specificity of uptake of FA over CE was again largely retained. Altogether, we conclude that, in our model, BAT takes up plasma TG preferentially by means of lipolysis-mediated uptake of FA.

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