Thoman M L, Meuth J L, Morgan E L, Weigle W O, Hugli T E
J Immunol. 1984 Nov;133(5):2629-33.
The C3d-K fragment generated from human iC3b by plasma kallikrein is a potent suppressant of cellular proliferation. Originally characterized as inhibiting human and murine T lymphocyte function, C3d-K is shown in these studies to suppress mitogen-induced B cell growth, the spontaneous proliferation of several tumor cell lines, as well as all forms of T cell proliferation, including that induced by interleukin 2 (IL 2). In addition, synthesis of IL 2 in mixed lymphocyte cultures is blocked by C3d-K, but not IL 2 synthesis induced by Con A. The C3d-K fragment has no effect on resting cells; however, sensitivity to the inhibitory effect of C3d-K is acquired during the activation process. Because the proliferation of mitogen-activated spleen cells is not inhibited by exposure to C3d-K for the initial 24 hr of culture, only late steps in the cell activation process are C3d-K sensitive. When C3d-K is present throughout the course of the 72-hr culture, suppression was observed. Data obtained with the tumor cell lines suggest that once suppression is achieved, it is long-lasting even in the absence of C3d-K.
血浆激肽释放酶从人iC3b产生的C3d-K片段是一种有效的细胞增殖抑制剂。C3d-K最初被鉴定为抑制人和鼠T淋巴细胞功能,在这些研究中显示它能抑制丝裂原诱导的B细胞生长、几种肿瘤细胞系的自发增殖以及所有形式的T细胞增殖,包括白细胞介素2(IL-2)诱导的增殖。此外,混合淋巴细胞培养中IL-2的合成被C3d-K阻断,但伴刀豆球蛋白A诱导的IL-2合成不受影响。C3d-K片段对静息细胞无作用;然而,在激活过程中细胞会获得对C3d-K抑制作用的敏感性。由于在培养的最初24小时暴露于C3d-K不会抑制丝裂原激活的脾细胞增殖,所以细胞激活过程中只有后期步骤对C3d-K敏感。当在72小时培养过程中全程存在C3d-K时,可观察到抑制作用。从肿瘤细胞系获得的数据表明,一旦实现抑制,即使不存在C3d-K,抑制作用也是持久的。