Elferink J G, de Koster B M
Department of Medical Biochemistry, University of Leiden, The Netherlands.
Eur J Pharmacol. 1993 Jul 15;246(2):157-61. doi: 10.1016/0922-4106(93)90093-o.
Human neutrophils retain the ability to migrate when they are electroporated; this enables the study of potential mediators by direct application to the cell interior. Cyclic GMP strongly enhances random migration by electroporated human neutrophils. The effect is maximal at a concentration of 10 microM. The potentiating effect of cGMP is chemokinetic. Chemotaxis of electroporated neutrophils activated by formylmethionylleucylphenylalanine (fMLP) is stimulated by cGMP at concentrations up to 10 microM; higher concentrations inhibit chemotaxis. Cyclic AMP resembles cGMP in that both activation and inhibition may occur. However, activation occurs over a very small concentration range, and inhibition is a predominant feature. Cyclic nucleotide-activated migration is dependent on Ca2+, in contrast with activation of migration by fMLP.
人中性粒细胞在进行电穿孔后仍保留迁移能力;这使得通过直接应用于细胞内部来研究潜在介质成为可能。环鸟苷酸(cGMP)能强烈增强经电穿孔的人中性粒细胞的随机迁移。在浓度为10微摩尔时,这种作用达到最大。cGMP的增强作用是化学动力学的。环磷腺苷(cAMP)与cGMP类似,两者都可能发生激活和抑制作用。然而,激活发生在非常小的浓度范围内,且抑制是主要特征。与甲酰甲硫氨酰亮氨酰苯丙氨酸(fMLP)激活迁移不同,环核苷酸激活的迁移依赖于钙离子。