几丁质类肝素对小鼠腹膜巨噬细胞活化及单因子产生的影响。

Molecular biotherapy Pub Date : 1990-06-01
K Nishimura, S Nishimura, N Nishi, S Tokura, I Azuma
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引用次数: 0

摘要

研究了几丁质磺化衍生物(几丁质肝素)对小鼠腹腔巨噬细胞的激活和单因子的产生。与70%去乙酰化几丁质(DAC-70)相比,所有几丁质肝素对腹腔巨噬细胞的细胞溶解活性的增强效果都较差。腹腔注射甲壳素类肝素对巨噬细胞数量几乎没有增加或减少的作用,对循环集落刺激因子的活性没有影响。在体外实验中,只有n-磺化DAC-70能刺激巯基乙酸诱导的腹腔巨噬细胞产生白细胞介素-1。但其作用弱于DAC-70。几丁质肝素类对正常小鼠脾细胞无或弱有丝分裂活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of chitin heparinoids on the activation of peritoneal macrophages and on the production of monokines in mice.

Sulfonated derivatives of chitin which showed anticoagulant activity (chitin heparinoids) were studied with regard to the activation of mouse peritoneal macrophages and the production of monokines. In comparison with 70% deacetylated chitin (DAC-70), which was the most adjuvant-active derivative of chitin, all chitin heparinoids were less effective for the augmentation of cytolytic activity of peritoneal macrophages. The number of macrophages was hardly increased or decreased by intraperitoneal injection of chitin heparinoids, and the activity of circulating colony-stimulating factor was not changed by their treatment. Only N-sulfonated DAC-70 stimulated the production of interleukin-1 by thioglycolate-induced peritoneal macrophages in vitro. However, its effect was weaker than that of DAC-70. Chitin heparinoids showed no or weak mitogenic activity on normal mouse spleen cells.

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