Wang J P, Tsao L T, Raung S L, Lin P L, Lin C N
Department of Medical Research, Taichung Veterans General Hospital, Taiwan.
Free Radic Biol Med. 1999 Mar;26(5-6):580-8. doi: 10.1016/s0891-5849(98)00230-5.
In this study, the underlying mechanisms of stimulation by cyclocommunin, a natural pyranoflavonoid, of respiratory burst in rat neutrophils was investigated. Cyclocommunin evoked a concentration-dependent stimulation of superoxide anion (O2*-) generation with a slow onset and long lasting profile. The maximum response (16.4+/-2.3 nmol O2*-/10 min per 10(6) cells) was observed at 3-10 microM cyclocommunin. Cyclocommunin did not activate NADPH oxidase in a cell-free system. Cells pretreated with pertussis toxin or n-butanol did not affect the cyclocommunin-induced O2*- generation. However, a protein kinase inhibitor staurosporine and EGTA greatly reduced the O2*-generation caused by cyclocommunin. Treatment of neutrophils with phorbol 12-myristate 13-acetate (PMA), but not with formylmethionyl-leucyl-phenylalanine (fMLP), for 20 min significantly reduced the O2*- generation following the subsequent stimulation of cells with cyclocommunin. Cyclocommunin did not affect the cellular mass of phosphatidic acid (PA). Neither the tyrosine kinase inhibitor, genistein, nor the p38 mitogen-activated protein kinase (MAPK) inhibitor, SB203580, affected cyclocommunin-induced O2*- generation. The enzyme activities of neutrophil cytosolic and membrane-associated protein kinase C (PKC) were both increased significantly with 100 microM cyclocommunin. The membrane-associated PKC-theta and PKC-beta were increased following the stimulation of neutrophils with 30 and 100 microM cyclocommunin, respectively. Cyclocommunin reduced the [3H]phorbol 12,13-dibutyrate ([3H]PDB) binding to cytosolic PKC in a concentration-dependent manner. Cyclocommunin (> or =3 microM) significantly evoked a slow and long lasting [Ca2+]i elevation in neutrophils, and a phospholipase C (PLC) inhibitor U73122 greatly inhibited these Ca2+ responses. Moreover, the increase in cellular inositol bis- and trisphosphate (IP2 and IP3) levels were observed in neutrophils stimulated with 30 microM cyclocommunin for 3 min. Collectively, these results indicate that the stimulation of respiratory burst by cyclocommunin is probably mediated by the synergism of PKC activation and [Ca2+]i elevation in rat neutrophils.
在本研究中,对天然吡喃黄酮类化合物环香豆素刺激大鼠中性粒细胞呼吸爆发的潜在机制进行了研究。环香豆素以浓度依赖性方式刺激超氧阴离子(O2*-)生成,起效缓慢且持续时间长。在3 - 10 microM环香豆素浓度下观察到最大反应(16.4±2.3 nmol O2*-/10 min/10(6)个细胞)。环香豆素在无细胞体系中不激活NADPH氧化酶。用百日咳毒素或正丁醇预处理的细胞不影响环香豆素诱导的O2*-生成。然而,蛋白激酶抑制剂星形孢菌素和乙二醇双四乙酸(EGTA)显著降低了环香豆素引起的O2*-生成。用佛波醇12 - 肉豆蔻酸酯13 - 乙酸酯(PMA)而非甲酰甲硫氨酰 - 亮氨酰 - 苯丙氨酸(fMLP)处理中性粒细胞20分钟,可显著降低随后用环香豆素刺激细胞后的O2*-生成。环香豆素不影响磷脂酸(PA)的细胞含量。酪氨酸激酶抑制剂染料木黄酮和p38丝裂原活化蛋白激酶(MAPK)抑制剂SB203580均不影响环香豆素诱导的O2*-生成。用100 microM环香豆素处理后,中性粒细胞胞质和膜相关蛋白激酶C(PKC)的酶活性均显著增加。用30和100 microM环香豆素刺激中性粒细胞后,膜相关的PKC - θ和PKC - β分别增加。环香豆素以浓度依赖性方式降低[3H]佛波醇12,13 - 二丁酸酯([3H]PDB)与胞质PKC的结合。环香豆素(≥3 microM)显著引起中性粒细胞中[Ca2+]i缓慢且持久的升高,磷脂酶C(PLC)抑制剂U73122极大地抑制了这些Ca2+反应。此外,在用30 microM环香豆素刺激中性粒细胞3分钟后,观察到细胞内肌醇二磷酸和三磷酸(IP2和IP3)水平升高。总体而言,这些结果表明环香豆素对呼吸爆发的刺激可能是由大鼠中性粒细胞中PKC激活和[Ca2+]i升高的协同作用介导的。