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白细胞衍生的中性粒细胞趋化因子-2的特性及其在大鼠变应性炎症中中性粒细胞浸润中的可能作用。

Characterization of leukocyte-derived neutrophil chemotactic factor-2 and its possible roles in neutrophil infiltration in allergic inflammation in rats.

作者信息

Tanabe J, Watanabe M, Fujimoto N, Mue S, Ohuchi K

机构信息

Department of Pathophysiological Biochemistry, Faculty of Pharmaceutical Sciences, Tohoku University, Miyagi, Japan.

出版信息

Int Arch Allergy Immunol. 1995 Oct;108(2):148-57. doi: 10.1159/000237132.

Abstract

This study sought to clarify the responsible chemotactic factor for neutrophils in allergic inflammation in rats. When the leukocytes collected from the pouch fluid 4 h after injection of the antigen solution into the air pouch were incubated, the neutrophil chemotactic activity in the conditioned medium increased time-dependently with higher levels for the leukocytes from the immunized rats than the nonimmunized ones. The chemotactic activity did not result from cytokine-induced neutrophil chemoattractant (CINC) because CINC concentrations in the conditioned medium were low. Neutrophil chemotactic factors in the conditioned medium were separated by isoelectric focusing into two factors, leukocyte-derived neutrophil chemotactic factor (LDNCF)-1 and LDNCF-2. The activity of LDNCF-2 was more than 75% of the total chemotactic activity in the conditioned medium. LDNCF-2 was purified by gel chromatography and reverse-phase HPLC. The N-terminal amino acid sequence (1-20) of the purified LDNCF-2 was identical to the 32-51 amino acid sequence of the pro-form of rat macrophage inflammatory protein (MIP)-2. Higher levels of MIP-2 mRNA in the leukocytes from the immunized rats than that from the non-immunized rats were proved by the reverse transcription-polymerase chain reaction. In vivo, concentrations of CINC in the pouch fluid were low, and did not represent the chemotactic activity in the pouch fluid. These results suggest that LDNCF-2 (MIP-2) is an important chemotactic factor for neutrophils in the allergic inflammation in rats.

摘要

本研究旨在阐明大鼠过敏性炎症中嗜中性粒细胞的趋化因子。将抗原溶液注入气袋4小时后,从气袋液中收集的白细胞进行孵育,条件培养基中的嗜中性粒细胞趋化活性随时间增加,免疫大鼠的白细胞趋化活性水平高于未免疫大鼠。趋化活性并非由细胞因子诱导的嗜中性粒细胞趋化因子(CINC)引起,因为条件培养基中CINC的浓度较低。通过等电聚焦将条件培养基中的嗜中性粒细胞趋化因子分离为两个因子,即白细胞衍生的嗜中性粒细胞趋化因子(LDNCF)-1和LDNCF-2。LDNCF-2的活性占条件培养基中总趋化活性的75%以上。通过凝胶色谱和反相高效液相色谱法纯化LDNCF-2。纯化后的LDNCF-2的N端氨基酸序列(1-20)与大鼠巨噬细胞炎性蛋白(MIP)-2前体形式的32-51氨基酸序列相同。逆转录聚合酶链反应证明,免疫大鼠白细胞中的MIP-2 mRNA水平高于未免疫大鼠。在体内,气袋液中CINC的浓度较低,并不代表气袋液中的趋化活性。这些结果表明,LDNCF-2(MIP-2)是大鼠过敏性炎症中嗜中性粒细胞的重要趋化因子。

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