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在儿童期细菌感染期间,外周多形核白细胞中细胞溶质磷脂酶A2和环氧化酶-2的上调会增加血栓素的合成。

Thromboxane synthesis is increased by upregulation of cytosolic phospholipase A2 and cyclooxygenase-2 in peripheral polymorphonuclear leukocytes during bacterial infection in childhood.

作者信息

Zaitsu Masafumi, Hamasaki Yuhei, Nishimura Shinji, Matsuo Muneaki, Fujita Ichiro, Ishii Eiichi

机构信息

Department of Pediatrics, Faculty of Medicine, Saga Medical School, 5-1-1 Nabeshima, Saga 849-8501, Japan.

出版信息

Am J Hematol. 2003 Feb;72(2):115-20. doi: 10.1002/ajh.10280.

Abstract

Prostaglandins (PGs) and thromboxane (TX) are important mediators of inflammation. Recent studies revealed that PG and TX synthesis is controlled by the regulation of PG- and TX-synthesizing enzymes. In this study, we examined the TX synthesis and the expression of TX-synthesizing enzymes in activated peripheral polymorphonuclear leukocytes (PMNs) obtained from children with bacterial infection. Blood samples were obtained from controls and patients with bacterial infection. A23187-stimulated production of TXB(2), a stable metabolite of TXA(2) in PMNs, was measured by a specific radioimmunoassay. The mRNA expression of cytosolic phospholipase A(2) (cPLA(2)), cyclooxygenase (COX)-1, COX-2, and TXA(2) synthase was determined by RT-PCR. The synthesis of TXB(2) in PMNs was significantly increased in the patients [925.0 (550.0-1100.0) pg/10(6) cells], compared with the controls [550.0 (450.0-775.0) pg/10(6) cells]. The mRNA expression for cPLA(2) and COX-2 in PMNs was also enhanced in the patients. The results indicate that TX production in PMNs is significantly increased through possible transcriptional mechanisms of cPLA(2) and COX-2 during bacterial infection in children. The upregulation of TXA(2) synthesis may contribute to the process of acute inflammatory reaction caused by bacterial infection.

摘要

前列腺素(PGs)和血栓素(TX)是炎症的重要介质。最近的研究表明,PG和TX的合成受PG和TX合成酶调控。在本研究中,我们检测了从细菌感染患儿获得的活化外周多形核白细胞(PMNs)中TX的合成及TX合成酶的表达。从对照组和细菌感染患者采集血样。通过特异性放射免疫分析法测定A23187刺激后PMNs中TXA2的稳定代谢产物TXB2的生成量。采用逆转录聚合酶链反应(RT-PCR)测定胞质型磷脂酶A2(cPLA2)、环氧化酶(COX)-1、COX-2及TXA2合成酶的mRNA表达。与对照组[550.0(450.0 - 775.0)pg/10^6细胞]相比,患者PMNs中TXB2的合成显著增加[925.0(550.0 - 1100.0)pg/10^6细胞]。患者PMNs中cPLA2和COX-2的mRNA表达也增强。结果表明,在儿童细菌感染期间,通过cPLA2和COX-2可能的转录机制,PMNs中TX的生成显著增加。TXA2合成的上调可能有助于细菌感染引起的急性炎症反应过程。

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