Halperin J A, Taratuska A, Nicholson-Weller A
Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
J Clin Invest. 1993 May;91(5):1974-8. doi: 10.1172/JCI116418.
The membrane attack complex of complement (MAC) can induce reversible changes in cell membrane permeability resulting in significant but transient intracellular ionic changes in the absence of cell lysis. Because ion fluxes and cytosolic ionic changes are integral steps in the signaling cascade initiated when growth factors bind to their receptors, we hypothesized that the MAC-induced reversible changes in membrane permeability could stimulate cell proliferation. Using purified terminal complement components we have documented a mitogenic effect of the MAC for quiescent murine 3T3 cells. The MAC enhances the mitogenic effects of serum and PDGF, and also stimulates cell proliferation in the absence of other exogenous growth factors. MAC-induced mitogenesis represents a novel effect of the terminal complement complex that could contribute to focal tissue repair or pathological cell proliferation locally at sites of complement activation.
补体膜攻击复合物(MAC)可诱导细胞膜通透性发生可逆性变化,在不发生细胞裂解的情况下导致显著但短暂的细胞内离子变化。由于离子通量和胞质离子变化是生长因子与其受体结合时启动的信号级联反应中的重要步骤,我们推测MAC诱导的细胞膜通透性可逆性变化可能刺激细胞增殖。使用纯化的补体末端成分,我们已证明MAC对静止的小鼠3T3细胞具有促有丝分裂作用。MAC增强了血清和血小板衍生生长因子(PDGF)的促有丝分裂作用,并且在没有其他外源性生长因子的情况下也能刺激细胞增殖。MAC诱导的有丝分裂代表补体末端复合物的一种新作用,可能有助于在补体激活部位局部进行局灶性组织修复或病理性细胞增殖。