Spreca A, Rambotti M G, Donato R
Department of Experimental Medicine and Biochemical Sciences, University of Perugia, Italy.
Histochem J. 1991 Mar;23(3):143-8. doi: 10.1007/BF01047459.
The cytochemical localization of particulate guanylate cyclase and adenylate cyclase activities in rabbit platelets were studied after stimulation with various agents, at the electron microscope level. In the presence of platelet aggregating agents such as thrombin and ADP, the particulate reaction product of guanylate cyclase activity was detectable on plasma membrane and on membranes of the open canalicular system. In contrast, samples incubated with platelet-activating factor showed no activation of the cyclase activity. Atrial natriuretic factor stimulated the particulate guanylate cyclase. The ultracytochemical localization of this activated cyclase was the same as that of thrombin- or ADP-stimulated guanylate cyclase. Adenylate cyclase activity was studied in platelets incubated with prostaglandin E1 plus or minus insulin. The enzyme reaction product was found at the same sites where guanylate cyclase was detected. Therefore guanylate and adenylate cyclase activities do not seem to be preferentially localised in platelet membranes.
在电子显微镜水平下,研究了用各种试剂刺激后兔血小板中颗粒型鸟苷酸环化酶和腺苷酸环化酶活性的细胞化学定位。在存在血小板聚集剂如凝血酶和ADP的情况下,可在质膜和开放小管系统的膜上检测到鸟苷酸环化酶活性的颗粒反应产物。相比之下,用血小板活化因子孵育的样品未显示环化酶活性的激活。心房利钠因子刺激颗粒型鸟苷酸环化酶。这种活化环化酶的超细胞化学定位与凝血酶或ADP刺激的鸟苷酸环化酶相同。在添加或不添加胰岛素的情况下,用前列腺素E1孵育血小板,研究腺苷酸环化酶活性。酶反应产物在检测到鸟苷酸环化酶的相同部位被发现。因此,鸟苷酸环化酶和腺苷酸环化酶活性似乎并非优先定位于血小板膜中。