Koizumi T, Nakao Y, Matsui T, Katakami Y, Nakagawa T, Fujita T
Immunology. 1986 Sep;59(1):43-9.
MRL/MP-lpr/lpr (MRL/l) mice spontaneously develop an age-related autoimmune disease concomitant with interleukin-2 (IL-2) defects. Induction of IL-2 receptor (IL-2R), IL-2 production and subsequent de novo DNA synthesis in MRL/l mice by the tumour-promoting phorbol ester 12-o-tetradecanoyl phorbol 13-acetate (TPA) and calcium ionophore (A23187) were examined. These two compounds given together induced significant IL-2R expression, IL-2 production, and de novo DNA synthesis of spleen cells from this murine strain, as did concanavalin A (Con A) plus TPA. TPA and A23187 may bypass the early steps of activation by mitogens in murine lymphocytes. However, even though these IL-2 defects could be overcome to some extent, the response of MRL/l mice to these stimuli was considerably lower than the enhanced IL-2R expression and IL-2 production of MRL/MP-+/+(MRL/n) control mice. These results suggested that the failure to respond to mitogens in these mice may be due, at least in part, to failure of receptor signal transduction, and to defects of molecular and biochemical reactions following signal transduction.
MRL/MP-lpr/lpr(MRL/l)小鼠会自发发展出一种与年龄相关的自身免疫性疾病,并伴有白细胞介素-2(IL-2)缺陷。研究了促肿瘤佛波酯12-o-十四酰佛波醇13-乙酸酯(TPA)和钙离子载体(A23187)对MRL/l小鼠白细胞介素-2受体(IL-2R)的诱导、IL-2的产生以及随后的从头DNA合成。这两种化合物共同作用可诱导该小鼠品系脾细胞显著表达IL-2R、产生IL-2以及从头合成DNA,伴刀豆球蛋白A(Con A)加TPA的作用效果相同。TPA和A23187可能绕过了鼠淋巴细胞中丝裂原激活的早期步骤。然而,尽管这些IL-2缺陷在一定程度上可以被克服,但MRL/l小鼠对这些刺激的反应明显低于MRL/MP-+/+(MRL/n)对照小鼠增强的IL-2R表达和IL-2产生。这些结果表明,这些小鼠对丝裂原无反应可能至少部分是由于受体信号转导失败以及信号转导后分子和生化反应的缺陷。