Carnitine palmitoyltransferase 1 facilitates fatty acid oxidation in a non-cell-autonomous manner

Cell Rep. 2024 Dec 24;43(12):115006. doi: 10.1016/j.celrep.2024.115006. Epub 2024 Dec 12.

Abstract

Mitochondrial fatty acid oxidation is facilitated by the combined activities of carnitine palmitoyltransferase 1 (Cpt1) and Cpt2, which generate and utilize acylcarnitines, respectively. We compare the response of mice with liver-specific deficiencies in the liver-enriched Cpt1a or the ubiquitously expressed Cpt2 and discover that they display unique metabolic, physiological, and molecular phenotypes. The loss of Cpt1a or Cpt2 results in the induction of the muscle-enriched isoenzyme Cpt1b in hepatocytes in a Pparα-dependent manner. However, hepatic Cpt1b does not contribute substantively to hepatic fatty acid oxidation when Cpt1a is absent. Liver-specific double knockout of Cpt1a and Cpt1b or Cpt2 eliminates the mitochondrial oxidation of non-esterified fatty acids. However, Cpt1a/Cpt1b double knockout mice retain fatty acid oxidation by utilizing extracellular long-chain acylcarnitines that are dependent on Cpt2. These data demonstrate the non-cell-autonomous intercellular metabolism of fatty acids in hepatocytes.

Keywords: CP: Metabolism; Cpt1; Cpt2; acylcarnitine; biochemistry; fasting; liver; metabolism.

MeSH terms

  • Animals
  • Carnitine / analogs & derivatives
  • Carnitine / metabolism
  • Carnitine O-Palmitoyltransferase* / genetics
  • Carnitine O-Palmitoyltransferase* / metabolism
  • Fatty Acids* / metabolism
  • Hepatocytes* / metabolism
  • Liver / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout*
  • Mitochondria / metabolism
  • Oxidation-Reduction*
  • PPAR alpha / metabolism

Substances

  • Carnitine O-Palmitoyltransferase
  • Fatty Acids
  • CPT1B protein, mouse
  • PPAR alpha
  • acylcarnitine
  • Carnitine