Wentworth P A, Ziegler H K
J Immunol. 1987 May 15;138(10):3167-73.
Experiments were performed to analyze the mechanism by which lipopolysaccharide (LPS) modulates the expression of Ia by murine peritoneal macrophages in vivo. We investigated the effect of LPS on Ia expression in T cell deficient mice by using the congenitally athymic nude mouse model. Injection (i.p) of LPS into athymic (nu/nu) mice resulted in a dramatic increase in the expression and biosynthesis of Ia by peritoneal macrophages 7 days after injection. The magnitude and kinetics of this induction were equivalent to increases observed after LPS injection of euthymic (nu/+) mice. Viable Listeria monocytogenes also increased Ia expression in athymic mice, but in contrast to the induction observed in euthymic mice at 3 and 7 days after injection, increased Ia expression was not seen until 7 days. Ia induction by either LPS or L. monocytogenes in athymic mice was not due to the presence or development of mature T cell function as defined by assays for T cell mitogenesis and interleukin 2 production. We conclude that increased macrophage Ia expression by LPS and L. monocytogenes in vivo can occur in the absence of mature functioning T cells.
进行实验以分析脂多糖(LPS)在体内调节小鼠腹腔巨噬细胞Ia表达的机制。我们通过使用先天性无胸腺裸鼠模型,研究了LPS对T细胞缺陷小鼠Ia表达的影响。向无胸腺(nu/nu)小鼠腹腔注射LPS后7天,腹腔巨噬细胞Ia的表达和生物合成显著增加。这种诱导的幅度和动力学与向正常胸腺(nu/+)小鼠注射LPS后观察到的增加相当。活的单核细胞增生李斯特菌也增加了无胸腺小鼠的Ia表达,但与正常胸腺小鼠注射后3天和7天观察到的诱导情况不同,直到7天才观察到Ia表达增加。在无胸腺小鼠中,LPS或单核细胞增生李斯特菌诱导Ia并非由于成熟T细胞功能的存在或发展,成熟T细胞功能通过T细胞有丝分裂和白细胞介素2产生的检测来定义。我们得出结论,在没有成熟功能T细胞的情况下,LPS和单核细胞增生李斯特菌在体内可增加巨噬细胞Ia表达。