吞噬作用
酵母多糖
流式细胞术
巨噬细胞
PI3K/AKT/mTOR通路
蛋白激酶B
化学
炎症
细胞内
下调和上调
细胞生物学
药理学
生物
免疫学
信号转导
体外
生物化学
基因
作者
Éssia de Almeida Lima,Luiz Henrique Agra Cavalcante‐Silva,Deyse Cristina Madruga Carvalho,Mariana Mendonça Soares,Anna Beatriz Araujo Medeiros,Chaquip D. Netto,Paulo R. R. Costa,Sandra Rodrigues‐Mascarenhas
标识
DOI:10.1080/08820139.2025.2449949
摘要
Phagocytosis is an important function of macrophages. However, when it's dysregulated, it could compromise homeostasis. Thus, this study aimed to assess the inhibitory activity of pterocarpanquinone LQB 118 on murine macrophage phagocytosis. We used peritoneal macrophages isolated from mice to evaluate the impact of LQB 118 (5 μM) on the modulation of phagocytic activity and possible action mechanism related: IL-12 (by ELISA), NO (by Griess reaction),ROS production (by flow cytometry), and intracellular signaling proteins (iNOS, P-Akt, P-mTOR, NF-κB, and P-NF-κB) (by flow cytometry).The macrophages were stimulated with zymosan to assess both phagocytic activity and flow cytometry assays. Treatment with LQB 118 resulted in a reduction in the phagocytosis of zymosan particles by macrophages. This effect could potentially be attributed to LQB's inhibition of IL-12 production and mTOR/NF-κB signaling. Furthermore, LQB 118 decreased the levels of ROS and NO without interfering with iNOS and Akt activation. These findings show the anti-phagocytic activity of LQB 118 on macrophage, highlighting the potential of this compound as a candidate for modulating macrophage-driven inflammation.
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