In:
eLife, eLife Sciences Publications, Ltd, Vol. 4 ( 2015-10-17)
Abstract:
The body stores energy in the form of fat molecules. Most of these molecules are stored in white fat cells. Other fat cells, the so-called brown fat cells, consume fats and produce heat to maintain body temperature in cold conditions. The capacity of brown fat cells to consume fats has led researchers to investigate whether brown fat cells might be a key to combat obesity. When an organism is cold, fat is shuttled to the brown fat cells. An enzyme called lipoprotein lipase is involved in a process that allows these fat molecules to be taken up by brown fat cells. However, it was not clear exactly how this process works. A protein called Angiopoietin-like 4 (ANGPTL4) inhibits the activity of lipoprotein lipase in white fat cells and is also found at high levels in brown fat cells. Here, Dijk et al. used genetic and biochemical approaches to study the role of ANGPTL4 in the fat cells of mice. The experiments show that when mice are exposed to cold, the levels of ANGPTL4 decrease in the brown fat cells. This allows the activity of lipoprotein lipase to increase so that these cells are able to take up more fat molecules. However, the opposite happens in white fat cells during cold exposure. The levels of ANGPTL4 increase, which decreases the activity of lipoprotein lipase in white fat cells to allow fat molecules to be shuttled specifically to the brown fat cells. Further experiments suggest that the opposite regulation of ANGPTL4 in brown and white fat cells could be due to a protein called AMPK. This protein is found at higher levels in brown fat cells than in white fat cells and is produced by brown fat cells during cold exposure. Taken together, Dijk et al. show that organs and cells work together to ensure that fat molecules are appropriately distributed to cells in need of energy, such as to brown fat cells during cold. How these findings could be used to stimulate fat consumption by brown fat cells in humans remains open for further investigation.
Type of Medium:
Online Resource
ISSN:
2050-084X
DOI:
10.7554/eLife.08428.001
DOI:
10.7554/eLife.08428.002
DOI:
10.7554/eLife.08428.003
DOI:
10.7554/eLife.08428.004
DOI:
10.7554/eLife.08428.005
DOI:
10.7554/eLife.08428.006
DOI:
10.7554/eLife.08428.007
DOI:
10.7554/eLife.08428.008
DOI:
10.7554/eLife.08428.009
DOI:
10.7554/eLife.08428.010
DOI:
10.7554/eLife.08428.011
DOI:
10.7554/eLife.08428.012
DOI:
10.7554/eLife.08428.013
DOI:
10.7554/eLife.08428.014
DOI:
10.7554/eLife.08428.015
Language:
English
Publisher:
eLife Sciences Publications, Ltd
Publication Date:
2015
detail.hit.zdb_id:
2687154-3