Vogt W, Schmidt G, Hinsch B
Immunology. 1979 Jan;36(1):139-43.
The effects of propamidine and their dose dependency, on utilization of the third and fifth complement components in immune haemolysis have been compared. While C3 utilization is not disturbed that of C5 is markedly inhibited by propamidine in concentrations as low as 0.5 mM. Both, binding of C5 to surface-fixed C3b and cleavage of C5 by convertases C42 and C3bBb, are also inhibited in the presence of propamidine. Since neither C3 cleavage by these enzymes nor even C5 cleavage by the cobra venom factor-supported convertase CFVBb is significantly reduced a general convertase-inhibiting effect of propamidine is ruled out. Rather the effect on utilization of C5 is the result of interference with binding of C5 is the result of interference with binding of C5 to C3b and hence impairment of its accessibility to the convertases. These findings thus further support the role of surface fixed C3b in C5 activation proposed earlier.
已比较了丙脒对免疫溶血中第三和第五补体成分利用的影响及其剂量依赖性。虽然丙脒浓度低至0.5 mM时对C3的利用没有干扰,但对C5的利用有明显抑制作用。在丙脒存在的情况下,C5与表面固定的C3b的结合以及C42和C3bBb转化酶对C5的裂解均受到抑制。由于这些酶对C3的裂解,甚至眼镜蛇毒因子支持的转化酶CFVBb对C5的裂解均未显著降低,因此排除了丙脒具有一般转化酶抑制作用的可能性。相反,对C5利用的影响是由于干扰了C5与C3b的结合,从而损害了其对转化酶的可及性。因此,这些发现进一步支持了先前提出的表面固定C3b在C5激活中的作用。