Inhibition of Crif1 protects fatty acid-induced POMC neuron-like cell-line damage by increasing CPT-1 function

Am J Physiol Endocrinol Metab. 2024 May 1;326(5):E681-E695. doi: 10.1152/ajpendo.00420.2023. Epub 2024 Apr 10.

Abstract

Hypothalamic proopiomelanocortin (POMC) neurons are sensors of signals that reflect the energy stored in the body. Inducing mild stress in proopiomelanocortin neurons protects them from the damage promoted by the consumption of a high-fat diet, mitigating the development of obesity; however, the cellular mechanisms behind these effects are unknown. Here, we induced mild stress in a proopiomelanocortin neuron cell line by inhibiting Crif1. In proopiomelanocortin neurons exposed to high levels of palmitate, the partial inhibition of Crif1 reverted the defects in mitochondrial respiration and ATP production; this was accompanied by improved mitochondrial fusion/fission cycling. Furthermore, the partial inhibition of Crif1 resulted in increased reactive oxygen species production, increased fatty acid oxidation, and reduced dependency on glucose for mitochondrial respiration. These changes were dependent on the activity of CPT-1. Thus, we identified a CPT-1-dependent metabolic shift toward greater utilization of fatty acids as substrates for respiration as the mechanism behind the protective effect of mild stress against palmitate-induced damage of proopiomelanocortin neurons.NEW & NOTEWORTHY Saturated fats can damage hypothalamic neurons resulting in positive energy balance, and this is mitigated by mild cellular stress; however, the mechanisms behind this protective effect are unknown. Using a proopiomelanocortin cell line, we show that under exposure to a high concentration of palmitate, the partial inhibition of the mitochondrial protein Crif1 results in protection due to a metabolic shift warranted by the increased expression and activity of the mitochondrial fatty acid transporter CPT-1.

Keywords: energy balance; energy substrate; hypothalamus; obesity; respiration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carnitine O-Palmitoyltransferase* / genetics
  • Carnitine O-Palmitoyltransferase* / metabolism
  • Cell Cycle Proteins* / antagonists & inhibitors
  • Cell Cycle Proteins* / metabolism
  • Cell Line
  • Fatty Acids* / metabolism
  • Hypothalamus / drug effects
  • Hypothalamus / metabolism
  • Mice
  • Mitochondria* / drug effects
  • Mitochondria* / metabolism
  • Neurons / drug effects
  • Neurons / metabolism
  • Pro-Opiomelanocortin / genetics
  • Pro-Opiomelanocortin / metabolism
  • Reactive Oxygen Species / metabolism

Substances

  • Carnitine O-Palmitoyltransferase
  • Fatty Acids
  • Pro-Opiomelanocortin
  • Reactive Oxygen Species
  • Crif1 protein, mouse
  • Cell Cycle Proteins
  • GADD45GIP1 protein, human
  • CPT1B protein, mouse