Koopman W J, Sandberg A L, Wahl S M, Mergenhagen S E
J Immunol. 1976 Jul;117(1):331-6.
C3a, C3b, C3c, and C3d were generated from purified guinea pig C3 by trypsin treatment. These fragments were characterized immunochemically and functionally by rosette inhibition. C3b is capable of binding to both C3b and C3d receptors on lymphocytes whereas C3d binds only to C3D receptors. C3b stimulates guinea pig spleen cells to elaborate a macrophage chemotactic factor which is similar in m.w. to that generated in response to PHA or LPS and is antigenically unrelated to C3 or C5. In contrast, neither C3a, C3c, or C3d stimulate guinea pig lymphocytes. Neither C3 nor any of its major fragments induce cellular proliferation. These data are compatible with the hypothesis that C3b triggers spleen cells to release a macrophage chemotactic factor by cross-linking C3b and C3d receptors.
通过胰蛋白酶处理从纯化的豚鼠补体3(C3)中生成了C3a、C3b、C3c和C3d。这些片段通过玫瑰花结抑制进行了免疫化学和功能表征。C3b能够与淋巴细胞上的C3b和C3d受体结合,而C3d仅与C3D受体结合。C3b刺激豚鼠脾细胞产生一种巨噬细胞趋化因子,其分子量与对植物血凝素(PHA)或脂多糖(LPS)反应产生的趋化因子相似,并且在抗原性上与C3或C5无关。相比之下,C3a、C3c或C3d均不刺激豚鼠淋巴细胞。C3及其任何主要片段均不诱导细胞增殖。这些数据与以下假设相符:C3b通过交联C3b和C3d受体触发脾细胞释放巨噬细胞趋化因子。