Grifolic acid induces mitochondrial membrane potential loss and cell death of RAW264.7 macrophages
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Detection of Inflammasome Activation and Pyroptotic Cell Death in Murine Bone Marrow-derived Macrophages
Published on: May 21, 2018
Yufeng Zhao1, Hai Zhang2, Aili Yan1
1Institute of Basic Medical Sciences, Xi'an Medical University, Xi'an, Shaanxi 710021, P.R. China.
Abstract:
Grifolic acid is a phenolic compound that was first extracted from the mushroom Albatrellus confluens; it acts as an agonist of the free fatty acid receptor (FFAR4). FFAR4 is expressed in macrophages and mediates the anti‑inflammatory effects of n‑3 unsaturated free fatty acids. In the present study, the effects of grifolic acid on macrophages were observed in mouse RAW264.7 cells. It was demonstrated that grifolic acid (2.5‑20 µmol/l) treatment reduced RAW264.7 cell viability in a dose‑ and time‑dependent manner. The number of apoptotic cells significantly increased following grifolic acid treatment compared with the untreated control cells. Grifolic acid treatment resulted in a significant decrease in cellular adenosine 5'‑triphosphate (ATP) content in RAW264.7 cells. Mitochondrial membrane potential (MMP), as measured by JC‑1 staining, was significantly diminished by grifolic acid treatment in a dose‑ and time‑dependent manner. Treatment with cyclosporine A, a protector of MMP, attenuated grifolic acid‑induced reduction of MMP and viability in RAW264.7 cells. FFAR4 knockdown did not significantly influence grifolic acid‑induced reduction of cell viability, ATP levels or MMP. In conclusion, grifolic acid may induce macrophage cell death by reducing MMP and by inhibiting ATP production probably in an FFAR4‑independent manner.
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.

