Schulz O, Edwards A D, Schito M, Aliberti J, Manickasingham S, Sher A, Reis e Sousa C
Immunobiology Laboratory, Imperial Cancer Research Fund, London, United Kingdom.
Immunity. 2000 Oct;13(4):453-62. doi: 10.1016/s1074-7613(00)00045-5.
CD40 ligation triggers IL-12 production by dendritic cells (DC) in vitro. Here, we demonstrate that CD40 cross-linking alone is not sufficient to induce IL-12 production by DC in vivo. Indeed, resting DC make neither the IL-12 p35 nor IL-12 p40 subunits and express only low levels of CD40. Nevertheless, after DC activation by microbial stimuli that primarily upregulate IL-12 p40 and augment CD40 expression, CD40 ligation induces a significant increase in IL-12 p35 and IL-12 p70 heterodimer production. Similarly, IL-12 p70 is produced during T cell activation in the presence but not in the absence of microbial stimuli. Thus, production of bioactive IL-12 by DC can be amplified by T cell-derived signals but must be initiated by innate signals.
CD40连接在体外可触发树突状细胞(DC)产生白细胞介素-12(IL-12)。在此,我们证明仅CD40交联不足以在体内诱导DC产生IL-12。实际上,静息DC既不产生IL-12 p35亚基也不产生IL-12 p40亚基,且仅表达低水平的CD40。然而,在主要上调IL-12 p40并增强CD40表达的微生物刺激激活DC后,CD40连接可诱导IL-12 p35和IL-12 p70异二聚体产生显著增加。同样,在有微生物刺激而非无微生物刺激的情况下,T细胞激活过程中会产生IL-12 p70。因此,DC产生具有生物活性的IL-12可被T细胞衍生信号放大,但必须由先天信号启动。