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The signal transduction mechanism involved in kazinol B-stimulated superoxide anion generation in rat neutrophils

机译:Kazinol B刺激大鼠中性粒细胞产生超氧阴离子的信号转导机制

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摘要

In this study, the underlying mechanism of stimulation of respiratory burst by kazinol B, a natural isoprenylated flavan, in rat neutrophils in vitro was investigated.Kazinol B concentration-dependently stimulated the superoxide anion (O2[dot over 2]−) generation, with a lag but transient activation profile, in neutrophils but not in a cell-free system. The maximum response (13.2±1.4 nmol O2[dot over 2]− 10 min−1 per 106 cells) was observed at 10 μM kazinol B.Pretreatment of neutrophils with phorbol 12-myristate 13-acetate (PMA) or formylmethionyl-leucyl-phenylalanine (fMLP) significantly enhanced the O2[dot over 2]− generation following the subsequent stimulation of cells with kazinol B.Cells pretreated with EGTA or a protein kinase inhibitor staurosporine effectively attenuated the kazinol B-induced O2[dot over 2]− generation. However, a p38 mitogen-activated protein kinase (MAPK) inhibitor SB203580 and a phosphoinositide 3-kinase (PI3K) inhibitor wortmannin had no effect on the kazinol B-induced response.Kazinol B significantly stimulated [Ca2+]i elevation in neutrophils, with a lag and slow rate of rise activation profile, and this response was attenuated by a phospholipase C (PLC) inhibitor U73122. Kazinol B also stimulated the inositol bis- and trisphosphate (IP2 and IP3) formation with a 1 min lag time.The membrane-associated PKC-α and PKC-θ but not PKC-ι were increased following the stimulation of neutrophils with kazinol B. It was more rapid and sensitive in the activation of PKC-θ than PKC-α by kazinol B. Kazinol B partially inhibited the [3H]phorbol 12,13-dibutyrate ([3H]PDB) binding to the neutrophil cytosolic PKC.Neither the cellular mass of phosphatidic acid (PA) and phosphatidylethanol (PEt), in the presence of ethanol, nor the protein tyrosine phosphorylation were stimulated by kazinol B. In addition, the kazinol B-induced O2[dot over 2]− generation remained relatively unchanged in cells pretreated with ethanol or a tyrosine kinase inhibitor genistein.Collectively, these results indicate that the stimulation of the respiratory burst by kazinol B is probably mediated by the synergism of PKC activation and [Ca2+]i elevation in rat neutrophils.
机译:在这项研究中,研究了天然的异戊二烯化黄酮Kazinol B体外刺激大鼠中性粒细胞刺激呼吸爆发的潜在机制。KazinolB浓度依赖性地刺激了超氧阴离子(O2 [dot over 2]-)的生成,在嗜中性粒细胞中有一个滞后但短暂的激活曲线,但在无细胞系统中则不是。在10μM的Kazinol B溶液中观察到最大响应(每106个细胞13.2±1.4 nmol O2 [点]-10 min-1)。用佛波醇12-肉豆蔻酸酯13-乙酸酯(PMA)或甲酰基甲硫基-亮基-在随后用卡宾醇B刺激细胞后,苯丙氨酸(fMLP)显着增强了O2 [2点]-的生成。用EGTA或蛋白激酶抑制剂staurosporine预处理的细胞有效减弱了卡嗪醇B诱导的O2 [2点以上]- 。然而,p38丝裂原活化蛋白激酶(MAPK)抑制剂SB203580和磷酸肌醇3激酶(PI3K)抑制剂渥曼青霉素对Kazinol B诱导的反应无影响。KazinolB显着刺激中性粒细胞的[Ca2 +] i升高。滞后和缓慢的上升激活曲线速率,并且该反应被磷脂酶C(PLC)抑制剂U73122减弱。卡嗪醇B还以1/5分钟的滞后时间刺激肌醇双磷酸酯和三磷酸肌醇(IP2和IP3)的形成。在用卡嗪醇B刺激嗜中性粒细胞后,膜相关的PKC-α和PKC-θ增加,但PKC-1不增加。卡扎尼醇B对PKC-α的活化比PKC-α更快,更灵敏。卡扎尼醇B部分抑制[3H] phorbol 12,13-dibutyrate([3H] PDB)与中性粒细胞胞浆PKC的结合。 Kazinol B刺激细胞中磷脂酸(PA)和磷脂酰乙醇(PEt)的细胞质量,蛋白酪氨酸磷酸化也不受卡扎尼醇B的刺激。此外,卡扎尼醇B诱导的O2 [2点以上]生成保持相对不变总之,这些结果表明,卡扎诺尔B对呼吸爆发的刺激可能是由大鼠中性粒细胞的PKC活化和[Ca2 +] i升高的协同作用介导的。

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