Chu Tianjiao, Wang Yuman, Wang Shihao, Li Jinze, Li Zheng, Wei Zihao, Li Jing, Bian Yifei
Innovation Research Institute of Traditional Chinese Medicine, Shandong University of Traditional Chinese Medicine, Ji'nan 250355, PR China; School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, PR China.
Innovation Research Institute of Traditional Chinese Medicine, Shandong University of Traditional Chinese Medicine, Ji'nan 250355, PR China.
J Adv Res. 2024 Nov 17. doi: 10.1016/j.jare.2024.11.016.
Antioxidants represented by kaempferol have been shown to be effective against atherosclerosis (AS). However, the underlying mechanisms still remain unclear.
The aim of this research was to reveal the mechanism of kaempferol regarding the treatment of AS and accumulation of foam cell.
We explored the contribution of kaempferol to the levels of inflammatory factors, scavenger receptor CD36, mitochondrial membrane potential, ROS, MAPK/NF-κB, Nrf2/HO-1, Ca and Piezo1 levels in RAW264.7 macrophages exposed to ox-LDL. In addition, to explore whether kaempferol inhibits ox-LDL-induced foamy macrophage through Piezo1, we extracted macrophages from Piezo1 macrophage-specific knockout (Piezo1) mice. For further validation, ApoE and Piezo1 macrophage-specific knockout mice (Piezo1/ ApoE) were generated.
The results showed that kaempferol notably suppressed inflammatory response, CD36 expression, mitochondrial membrane potential elevation, ROS production, MAPK/NF-κB expression, Ca influx, and increased Nrf2/HO-1 levels in RAW264.7. In addition, depletion of macrophage Piezo1 also effectively reduced lipid droplet deposition, inflammatory factor expression, oxidative damage, MAPK/NF-κB, Ca influx, and increased Nrf2/HO-1 expression in mouse BMDMs, and the results were still consistent after kaempferol treatment. In vivo studies have shown that kaempferol significantly reduces atherosclerotic plaque formation. However, the beneficial effect of kaempferol was attenuated in Piezo1 depletion mice.
These results collectively provide compelling evidence that kaempferol regulates CD36-mediated mitochondrial ROS production by inhibiting the Piezo1 channels and Ca influx, and then regulates the downstream pathways of NF-κB/MAPK and HO-1/Nrf2, inhibiting to the formation of foam cells. In conclusion, this study revealed a potential mechanism by which the natural antioxidant kaempferol prevents foamy macrophage.
以山奈酚为代表的抗氧化剂已被证明对动脉粥样硬化(AS)有效。然而,其潜在机制仍不清楚。
本研究旨在揭示山奈酚治疗AS及泡沫细胞积累的机制。
我们探究了山奈酚对暴露于氧化型低密度脂蛋白(ox-LDL)的RAW264.7巨噬细胞中炎症因子水平、清道夫受体CD36、线粒体膜电位、活性氧(ROS)、丝裂原活化蛋白激酶/核因子κB(MAPK/NF-κB)、核因子E2相关因子2/血红素加氧酶-1(Nrf2/HO-1)、钙和Piezo1水平的影响。此外,为探究山奈酚是否通过Piezo1抑制ox-LDL诱导的泡沫巨噬细胞形成,我们从Piezo1巨噬细胞特异性敲除(Piezo1 -/-)小鼠中提取巨噬细胞。为进一步验证,构建了载脂蛋白E(ApoE)和Piezo1巨噬细胞特异性敲除小鼠(Piezo1 -/-/ApoE -/-)。
结果显示,山奈酚显著抑制RAW264.7细胞中的炎症反应、CD36表达、线粒体膜电位升高、ROS产生、MAPK/NF-κB表达、钙内流,并增加Nrf2/HO-1水平。此外,巨噬细胞Piezo1缺失也有效减少了小鼠骨髓来源巨噬细胞(BMDMs)中的脂滴沉积、炎症因子表达、氧化损伤、MAPK/NF-κB、钙内流,并增加了Nrf2/HO-1表达,山奈酚处理后结果仍然一致。体内研究表明,山奈酚显著减少动脉粥样硬化斑块形成。然而,在Piezo1缺失小鼠中,山奈酚的有益作用减弱。
这些结果共同提供了令人信服的证据,表明山奈酚通过抑制Piezo1通道和钙内流来调节CD36介导的线粒体ROS产生,进而调节NF-κB/MAPK和HO-1/Nrf2的下游通路,抑制泡沫细胞的形成。总之,本研究揭示了天然抗氧化剂山奈酚预防泡沫巨噬细胞形成的潜在机制。