Liao Hsiang-Ruei, Chien Ching-Ru, Chen Jih-Jung, Lee Tzung-Yan, Lin Shinn-Zhi, Tseng Ching-Ping
Graduate Institute of Natural Products, College of Medicine, Chang-Gung University, Tao-Yuan, Taiwan.
Graduate Institute of Natural Products, College of Medicine, Chang-Gung University, Tao-Yuan, Taiwan.
Chem Biol Interact. 2015 Jul 5;236:90-101. doi: 10.1016/j.cbi.2015.05.004. Epub 2015 May 14.
The undesirable respiratory burst in neutrophils can lead to inflammation and tissue damage. This study investigates the effect and the underlying mechanism of 2-(4-hydroxy-3-prop-2-enyl-phenyl)-4-prop-2-enyl-phenol (honokiol), a lignan extracted from the stem bark of Magnolia officinalis Rehd. et Wils (Magnoliaceae), on N-formyl-L-methionyl-L-leucyl-L-phenylalanine (fMLP)-induced respiratory burst in human neutrophils. Signaling pathways regulated by honokiol which modulate fMLP-induced respiratory burst and cathepsin G release were evaluated by phosphorylation of Src family kinase induced by fMLP, Src family kinases activities and by immunoblotting analysis of the downstream targets of Src kinase. Briefly, honokiol inhibited fMLP-induced superoxide anion production (IC50 = 9.80 ± 0.21 μM, n = 4), cathepsin G release (IC50 = 14.23 ± 1.43 μM, n = 4) and migration (IC50 = 5.69 ± 1.51 μM, n = 4) in a concentration dependent manner. Further, honokiol specifically suppresses fMLP-induced Lyn (a member of the Src kinase family) phosphorylation, by inhibiting Lyn kinase activity. Consequently, honokiol attenuated the downstream targets of Lyn kinase, such as Tec translocation from the cytosol to the inner leaflet of the plasma membrane, phosphorylation of AKT, P38, PLCγ2, protein kinase C and membrane localization of p47(phox). On the other hand, fMLP-induced phosphorylation of Hck, Fgr kinase activity (other members of Src kinase), downstream phosphorylation of Vav1 and extracellular signal-regulated kinase remained unaffected. In addition, honokiol neither inhibited NADPH oxidase activity nor increased cyclic AMP levels. Honokiol is not a competitive or allosteric antagonist of fMLP. In conclusion, honokiol specifically modulates fMLP-mediated neutrophil activation by inhibiting Lyn activation which subsequently interferes with the activation of PLCγ2, AKT, p38, protein kinase C, and p47(phox).
中性粒细胞中不良的呼吸爆发可导致炎症和组织损伤。本研究调查了从厚朴(木兰科)茎皮中提取的木脂素2-(4-羟基-3-丙烯基苯基)-4-丙烯基苯酚(厚朴酚)对N-甲酰-L-蛋氨酰-L-亮氨酰-L-苯丙氨酸(fMLP)诱导的人中性粒细胞呼吸爆发的影响及其潜在机制。通过fMLP诱导的Src家族激酶磷酸化、Src家族激酶活性以及对Src激酶下游靶点的免疫印迹分析,评估了厚朴酚调节fMLP诱导的呼吸爆发和组织蛋白酶G释放的信号通路。简而言之,厚朴酚以浓度依赖的方式抑制fMLP诱导的超氧阴离子产生(IC50 = 9.80 ± 0.21 μM,n = 4)、组织蛋白酶G释放(IC50 = 14.23 ± 1.43 μM,n = 4)和迁移(IC50 = 5.69 ± 1.51 μM,n = 4)。此外,厚朴酚通过抑制Lyn激酶活性,特异性抑制fMLP诱导的Lyn(Src激酶家族成员)磷酸化。因此,厚朴酚减弱了Lyn激酶的下游靶点,如Tec从细胞质向质膜内小叶的转位、AKT、P38、PLCγ2、蛋白激酶C的磷酸化以及p47(phox)的膜定位。另一方面,fMLP诱导的Hck磷酸化、Fgr激酶活性(Src激酶的其他成员)、Vav1的下游磷酸化和细胞外信号调节激酶不受影响。此外,厚朴酚既不抑制NADPH氧化酶活性,也不增加环磷酸腺苷水平。厚朴酚不是fMLP的竞争性或变构拮抗剂。总之,厚朴酚通过抑制Lyn激活,特异性调节fMLP介导的中性粒细胞活化,随后干扰PLCγ2、AKT、p38、蛋白激酶C和p47(phox)的激活。