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日本血吸虫卵刺激诱导中性粒细胞释放嗜酸性粒细胞趋化因子。

Eosinophil chemotactic factor release from neutrophils induced by stimulation with Schistosoma japonicum eggs.

作者信息

Owhashi M, Kirai N, Horii Y

机构信息

Faculty of Integrated Arts and Sciences, University of Tokushima, Japan.

出版信息

Parasitol Res. 1997;83(1):42-6. doi: 10.1007/s004360050205.

DOI:10.1007/s004360050205
PMID:9000232
Abstract

The neutrophil is one of the sources of eosinophil chemotactic factor (ECF) in the presence of some stimulants. In the present study we showed that guinea-pig neutrophils could release ECF upon stimulation with Schistosoma japonicum eggs. ECF release from neutrophils began as early as 5 min after the stimulation and reached a peak at 20 min. When homogenate of the eggs was separated into a water-soluble fraction as soluble egg antigen (SEA) and a water-insoluble fraction (eggshell), both preparations possessed a potent neutrophil-stimulating activity to release ECF. The ECF release was dependent on the concentration of eggshells or SEA or on the number of neutrophils. The neutrophil-stimulating activity of eggshells was stable to heat, HCl, or pronase treatment but sensitive to NaOH treatment. When the eggs or eggshells were washed with acetone or Tween-20, they lost the neutrophil-stimulating activity to release ECF, indicating that the neutrophil-stimulating factor (NSF) possesses a lipid nature. The molecular weight of NSF extracted from the eggshells was estimated to be about 1000 Da by gel chromatography on Sephadex G25. The possible role of eggshells in the formation of eosinophil-rich granulomatous lesions in schistosomiasis japonica is discussed.

摘要

在某些刺激物存在的情况下,中性粒细胞是嗜酸性粒细胞趋化因子(ECF)的来源之一。在本研究中,我们发现豚鼠中性粒细胞在受到日本血吸虫卵刺激后可释放ECF。中性粒细胞释放ECF最早在刺激后5分钟开始,并在20分钟时达到峰值。当将虫卵匀浆分离成水溶性部分即可溶性虫卵抗原(SEA)和水不溶性部分(卵壳)时,这两种制剂都具有强大的刺激中性粒细胞释放ECF的活性。ECF的释放取决于卵壳或SEA的浓度或中性粒细胞的数量。卵壳刺激中性粒细胞的活性对热、盐酸或链霉蛋白酶处理稳定,但对氢氧化钠处理敏感。当用丙酮或吐温-20洗涤虫卵或卵壳时,它们失去了刺激中性粒细胞释放ECF的活性,这表明中性粒细胞刺激因子(NSF)具有脂质性质。通过在Sephadex G25上进行凝胶色谱法估计,从卵壳中提取的NSF的分子量约为1000 Da。本文讨论了卵壳在日本血吸虫病富含嗜酸性粒细胞的肉芽肿性病变形成中的可能作用。

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Eosinophil chemotactic factor release from neutrophils induced by stimulation with Schistosoma japonicum eggs.日本血吸虫卵刺激诱导中性粒细胞释放嗜酸性粒细胞趋化因子。
Parasitol Res. 1997;83(1):42-6. doi: 10.1007/s004360050205.
2
Isolation of Schistosoma japonicum egg-derived neutrophil stimulating factor: its role on eosinophil chemotactic factor release from neutrophils.日本血吸虫卵源性中性粒细胞刺激因子的分离:其对中性粒细胞释放嗜酸性粒细胞趋化因子的作用。
Int Arch Allergy Appl Immunol. 1985;78(4):415-20. doi: 10.1159/000233924.
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Schistosoma japonicum: identification and characterization of neutrophil chemotactic factors from egg antigen.日本血吸虫:来自虫卵抗原的中性粒细胞趋化因子的鉴定与特性分析
Exp Parasitol. 1985 Oct;60(2):229-38. doi: 10.1016/0014-4894(85)90026-8.
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J Immunol. 1982 Nov;129(5):2226-31.
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Eosinophil chemotactic factor in schistosome eggs: a comparative study of eosinophil chemotactic factors in the eggs of Schistosoma japonicum and S. mansoni in vitro.血吸虫卵中的嗜酸性粒细胞趋化因子:日本血吸虫和曼氏血吸虫卵中嗜酸性粒细胞趋化因子的体外比较研究
Am J Trop Med Hyg. 1983 Mar;32(2):359-66. doi: 10.4269/ajtmh.1983.32.359.
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Schistosoma mekongi: a prominent neutrophil chemotactic activity of egg antigen with reference to that of Schistosoma japonicum.湄公血吸虫:与日本血吸虫相比,虫卵抗原具有显著的中性粒细胞趋化活性。
Exp Parasitol. 2005 Aug;110(4):335-41. doi: 10.1016/j.exppara.2005.03.001.
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Kinetic study of eosinophil chemotactic factor production with reference to eosinophilia and granuloma formation in mice infected with Schistosoma japonicum.日本血吸虫感染小鼠中嗜酸性粒细胞趋化因子产生的动力学研究及其与嗜酸性粒细胞增多和肉芽肿形成的关系
Int J Parasitol. 1996 Jul;26(7):705-11. doi: 10.1016/0020-7519(96)00054-9.
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Eosinophil and neutrophil chemotactic activities of adult worm extracts of Schistosoma japonicum in vivo and in vitro.日本血吸虫成虫提取物在体内和体外的嗜酸性粒细胞及中性粒细胞趋化活性
J Parasitol. 1984 Dec;70(6):955-61.
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Eosinophil chemotactic lymphokine produced by spleen cells of Schistosoma japonicum-infected mice.日本血吸虫感染小鼠脾细胞产生的嗜酸性粒细胞趋化性淋巴因子。
Int Arch Allergy Appl Immunol. 1987;82(1):20-5. doi: 10.1159/000234284.
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Low molecular weight eosinophil chemotactic factor (ECF) in the serum of murine schistosomiasis japonica.日本血吸虫病小鼠血清中的低分子量嗜酸性粒细胞趋化因子(ECF)
Int Arch Allergy Appl Immunol. 1986;79(2):178-81. doi: 10.1159/000233967.

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