Measurement of long-chain fatty acid uptake into adipocytes

Methods Enzymol. 2014:538:107-34. doi: 10.1016/B978-0-12-800280-3.00007-4.

Abstract

The ability of white and brown adipose tissue to efficiently take up long-chain fatty acids is key to their physiological functions in energy storage and thermogenesis, respectively. Several approaches have been taken to determine uptake rates by cultured cells and primary adipocytes including radio- and fluorescently labeled fatty acids. In addition, the recent description of activatable bioluminescent fatty acids has opened the possibility for expanding these in vitro approaches to real-time monitoring of fatty acid uptake kinetics by adipose depots in vivo. Here, we will describe some of the most useful experimental paradigms to quantitatively determine long-chain fatty acid uptake by adipocytes in vitro and provide the reader with detailed instruction on how bioluminescent probes for in vivo imaging can be synthesized and used in living mice.

Keywords: Adipocytes; Brown adipose tissue; Fatty acid transport proteins; Fatty acid uptake; In vivo imaging; Long-chain fatty acids; White adipose tissue.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes / metabolism*
  • Adipose Tissue / cytology
  • Adipose Tissue / metabolism*
  • Animals
  • Biological Transport
  • Boron Compounds / analysis
  • Boron Compounds / metabolism
  • Cells, Cultured
  • Fatty Acids / analysis*
  • Fatty Acids / metabolism*
  • Fluorescent Dyes / analysis
  • Fluorescent Dyes / metabolism
  • Humans
  • Luminescent Agents / analysis
  • Luminescent Agents / metabolism
  • Luminescent Measurements / methods*
  • Mice
  • Molecular Probes / analysis
  • Molecular Probes / metabolism
  • Optical Imaging / methods*
  • Whole Body Imaging / methods

Substances

  • 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene
  • Boron Compounds
  • Fatty Acids
  • Fluorescent Dyes
  • Luminescent Agents
  • Molecular Probes