Tracing insights into de novo lipogenesis in liver and adipose tissues

Semin Cell Dev Biol. 2020 Dec:108:65-71. doi: 10.1016/j.semcdb.2020.02.012. Epub 2020 Mar 19.

Abstract

Lipids play important roles in biology that include structural compartmentation as membranes, energy storage, and regulatory functions as signaling molecules. These molecules can be obtained via the surrounding environment (e.g. diet) or synthesized de novo. Fatty acid synthesis is an energetically demanding process and must therefore be tightly regulated to balance fatty acid availability with the functional and energetic needs of cells and tissues. Here we review key aspects of de novo lipogenesis (DNL) in mammalian systems. We highlight key nodes in the pathway that are used for quantitation of lipogenic fluxes and regulation of fatty acid diversity across tissues. Next, we discuss key aspects of DNL function in the major lipogenic tissues of mammals: liver, white adipose tissue (WAT), and brown adipose tissue (BAT), highlighting recent molecular discoveries that suggest potential roles for tissue specific DNL. Finally, we propose critical questions that will be important to address using the advanced approaches for DNL quantitation described herein.

Keywords: Adipose tissue; De novo lipogenesis; FASN; Fatty acids; Isotope tracing; Liver.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adipose Tissue / metabolism*
  • Animals
  • Fatty Acids / metabolism
  • Homeostasis
  • Humans
  • Isotope Labeling
  • Lipogenesis*
  • Liver / metabolism*

Substances

  • Fatty Acids