Takashima N, Kawachi H, Oite T, Nishi S, Arakawa M, Shimizu F
Department of Immunology, Niigata University School of Medicine, Japan.
Clin Exp Immunol. 1993 Jan;91(1):135-40. doi: 10.1111/j.1365-2249.1993.tb03368.x.
The effect of chlorpromazine, one of several calmodulin antagonists that inhibit cytoskeletal movement, on the local kinetics of injected proteinuria-inducing MoAb 5-1-6 was examined to test the hypothesis that proteinuria is inhibited if the antigen recognized by MoAb 5-1-6 or injected MoAb remains on the surface of epithelial foot processes. MoAb 5-1-6 was injected into both chlorpromazine-treated (5 mg/100 g body weight) and untreated rats. As a positive control for the chlorpromazine treatment, anti-Fx1A serum was also injected into other chlorpromazine-treated and untreated rats. Chlorpromazine inhibited neither the change in localization of injected MoAb 5-1-6 nor proteinuria, although it showed an inhibitory effect on redistribution of immune complex and the fixation of complement in passive Heymann glomerulonephritis induced by injection of anti-Fx1A serum. We conclude that the kinetics of bound MoAb 5-1-6 are regulated by a system different from that operating in passive Heymann glomerulonephritis.
氯丙嗪是几种抑制细胞骨架运动的钙调蛋白拮抗剂之一,研究了其对注射的蛋白尿诱导性单克隆抗体5-1-6局部动力学的影响,以检验如下假设:如果单克隆抗体5-1-6识别的抗原或注射的单克隆抗体保留在上皮足突表面,则蛋白尿会受到抑制。将单克隆抗体5-1-6注射到氯丙嗪处理组(5mg/100g体重)和未处理的大鼠体内。作为氯丙嗪处理的阳性对照,抗Fx1A血清也被注射到其他氯丙嗪处理组和未处理的大鼠体内。氯丙嗪既没有抑制注射的单克隆抗体5-1-6定位的变化,也没有抑制蛋白尿,尽管它对注射抗Fx1A血清诱导的被动海曼肾小球肾炎中免疫复合物的重新分布和补体的固定有抑制作用。我们得出结论,结合的单克隆抗体5-1-6的动力学受不同于被动海曼肾小球肾炎中作用机制的系统调节。