König W, Frickhofen N, Tesch H
Immunology. 1979 Apr;36(4):733-42.
An eosinophil chemotactic factor(s) (ECF) can be generated from human polymorphonuclear neutrophils by the calcium ionophore, phagocytosis, arachidonic acid and hypotonic lysis. In kinetic studies it is observed that peak ECF activity is released prior to the maximum of lysosomal enzyme release with the calcium ionophore, phagocytosis and arachidonic acid, while under conditions of hypotonic exposure ECF activity appears after the maximum of enzyme release. The ECF obtained by hypotonic exposure shows a fluctuating pattern with sharp peaks and steep fall-offs in activity. The ECF-release for each stimulus is temperature dependent; extracellular calcium is required when the ionophore or phagocytosis are used as stimuli, while with arachidonic acid and hypotonic exposure no extracellular calcium is necessary for ECF-release. On Sephadex G-25 each preparation of ECF eluted in the low molecular weight range at approximately 500 daltons. Eosinophils can be deactivated and cross-deactivated with the various ECF-preparations indicating either a molecular identity or a common mode of action on eosinophils.
嗜酸性粒细胞趋化因子(ECF)可通过钙离子载体、吞噬作用、花生四烯酸和低渗裂解从人多形核中性粒细胞中产生。在动力学研究中观察到,在用钙离子载体、吞噬作用和花生四烯酸刺激时,ECF活性峰值在溶酶体酶释放最大值之前释放,而在低渗暴露条件下,ECF活性在酶释放最大值之后出现。通过低渗暴露获得的ECF呈现出波动模式,活性有 sharp peaks 和 steep fall-offs。每种刺激的ECF释放都依赖于温度;当使用离子载体或吞噬作用作为刺激时,需要细胞外钙,而对于花生四烯酸和低渗暴露,ECF释放不需要细胞外钙。在Sephadex G - 25上,每种ECF制剂在低分子量范围内以约500道尔顿的分子量被洗脱。嗜酸性粒细胞可以被各种ECF制剂失活和交叉失活,这表明它们在嗜酸性粒细胞上具有分子同一性或共同作用模式。