Noda M, Kato I, Hirayama T, Matsuda F
Infect Immun. 1982 Jan;35(1):38-45. doi: 10.1128/iai.35.1.38-45.1982.
The cytotoxic action of the S component of leukocidin from Staphylococcus aureus on rabbit polymorphonuclear leukocytes was supported by the following observations, (i) Leukocytes displayed a large chemotactic response to the S component (10(-10) M) as well as to the chemotactic factor N-formylmethionylleucylphenylalanine (10(-11) M). (ii) The S component stimulated high levels of phospholipase A2 activity in the cell membranes, with concomitant synthesis and release of prostaglandins. (iii) Uptake of 45Ca into leukocytes exposed to the S component was about double the rate of uptake into untreated cells. The increased 45Ca uptake into the cells was not inhibited by trifluoperazine and ruthenium red. (iv) Indomethacin and alloxazine, which had no effects on the binding of the S component to the cells, attenuated markedly the stimulation of phospholipase A2 activity, the syntheses of prostaglandins, and the increased uptake of 45Ca caused by the S component. The F component of leukocidin, bound to rabbit leukocytes with the aid of the S component, rapidly induced complete release of 86Rb from preloaded leukocytes. This release resulted from stimulation of ouabain-insensitive (Na+ + K+)-adenosine triphosphatase activity and inhibition of cyclic AMP-dependent protein kinase.
金黄色葡萄球菌杀白细胞素S成分对兔多形核白细胞的细胞毒性作用得到以下观察结果的支持:(i)白细胞对S成分(10⁻¹⁰ M)以及趋化因子N-甲酰甲硫氨酰亮氨酰苯丙氨酸(10⁻¹¹ M)表现出强烈的趋化反应。(ii)S成分刺激细胞膜中高水平的磷脂酶A2活性,同时合成并释放前列腺素。(iii)暴露于S成分的白细胞对⁴⁵Ca的摄取率约为未处理细胞摄取率的两倍。细胞对⁴⁵Ca摄取的增加不受三氟拉嗪和钌红的抑制。(iv)吲哚美辛和咯嗪对S成分与细胞的结合没有影响,但能显著减弱S成分引起的磷脂酶A2活性刺激、前列腺素合成以及⁴⁵Ca摄取增加。杀白细胞素F成分借助S成分与兔白细胞结合后,能迅速诱导预先加载的白细胞完全释放⁸⁶Rb。这种释放是由于对哇巴因不敏感的(Na⁺ + K⁺)-腺苷三磷酸酶活性受到刺激以及环磷酸腺苷依赖性蛋白激酶受到抑制所致。