Fearon D T, Daha M R, Weiler J M, Austen K F
Transplant Rev. 1976;32:12-25. doi: 10.1111/j.1600-065x.1976.tb00226.x.
As C3 cleavage represents the most critical step in the elaboration of the biologic effects of the complement system, the modulation of this reaction by formation and function of the C3b-dependent C3 convertase may well determine whether the initial activation of the complement sequence eventuates in beneficial or detrimental effects to the host. Stabilization of the amplification C3b-dependent convertase, C3bBb, is achieved with P and C3NeF, respectively, after their binding which exhibits different molecular and temperature requirements. Control of this amplifying step occurs at three levels: intrinsic decay of the inherently labile C3bBb convertase; extrinsic decay by displacement of Bb from the convertase with beta1H; and inactivation by C3bINA of C3b after its generation from native C3 or removal of protective Bb by intrinsic or extrinsic decay. In the presence of the stabilizing factors the control proteins must function in sequence with beta1H-mediated decay preceding C3b inactivation.
由于C3裂解是补体系统生物学效应发挥过程中最关键的一步,C3b依赖性C3转化酶的形成和功能对该反应的调节很可能决定补体序列的初始激活最终对宿主产生有益还是有害的影响。分别通过P和C3NeF与扩增性C3b依赖性转化酶C3bBb结合来实现其稳定,这种结合表现出不同的分子和温度要求。对这一扩增步骤的控制发生在三个层面:固有不稳定的C3bBb转化酶的内在衰变;β1H将Bb从转化酶上置换导致的外在衰变;C3bINA在天然C3产生C3b后对其进行灭活,或通过内在或外在衰变去除保护性Bb。在存在稳定因子的情况下,控制蛋白必须按顺序发挥作用,β1H介导的衰变先于C3b灭活。