Grifolic acid induces mitochondrial membrane potential loss and cell death of RAW264.7 macrophages

Yufeng Zhao1, Hai Zhang2, Aili Yan1

  • 1Institute of Basic Medical Sciences, Xi'an Medical University, Xi'an, Shaanxi 710021, P.R. China.

Molecular Medicine Reports
|December 20, 2017
PubMed

Insights

Grifolic acid, a mushroom compound, induces macrophage cell death by reducing mitochondrial membrane potential and inhibiting ATP production. These effects appear to be independent of the free fatty acid receptor 4 (FFAR4).

Area of Science:

  • Immunology
  • Pharmacology
  • Cell Biology

Background:

  • Grifolic acid, a phenolic compound from *Albatrellus confluens*, is a free fatty acid receptor 4 (FFAR4) agonist.
  • FFAR4, expressed in macrophages, mediates anti-inflammatory effects of n-3 unsaturated fatty acids.

Purpose of the Study:

  • To investigate the effects of grifolic acid on macrophages.
  • To elucidate the role of FFAR4 in grifolic acid's action on macrophages.

Main Methods:

  • Treatment of mouse RAW264.7 macrophage cells with grifolic acid.
  • Assessment of cell viability, apoptosis, cellular adenosine 5'-triphosphate (ATP) content, and mitochondrial membrane potential (MMP) using JC-1 staining.
  • Evaluation of grifolic acid effects with and without cyclosporine A treatment and FFAR4 knockdown.

Main Results:

  • Grifolic acid reduced RAW264.7 cell viability, increased apoptosis, decreased ATP content, and diminished MMP in a dose- and time-dependent manner.
  • Cyclosporine A partially protected against grifolic acid-induced reduction in MMP and viability.
  • FFAR4 knockdown did not significantly alter grifolic acid's effects on cell viability, ATP levels, or MMP.

Conclusions:

  • Grifolic acid induces macrophage cell death.
  • The mechanism involves reduction of MMP and inhibition of ATP production.
  • These effects are likely mediated in an FFAR4-independent manner.