Male D, Pryce G
Department of Neuropathology, Institute of Psychiatry, London, U.K.
Immunology. 1988 Jan;63(1):37-42.
Rat brain endothelium was examined in vitro to determine the sequence of events in MHC gene activation following IFN-gamma stimulation. The cell-triggering time, kinetics of mRNA synthesis, rate of MHC induction and rate of decay were measured by quantifying cell-surface MHC expression in the presence or absence of alpha-amanitin. Enhanced class I expression is triggered immediately after IFN-gamma stimulation, and is maximally induced by 4 hr of stimulation. New class I mRNA synthesis starts immediately and proceeds over the next 24 hr. This is followed by increased expression of class I molecules, which reaches plateau levels by 24 hr. While IFN-gamma is present, enhanced class I expression is maintained at 140-200% of that seen on resting cells. On removal of IFN-gamma, class I expression decays towards the levels seen on resting cells, with a half-life of approximately 40 hr. Class II molecules can be induced on these cells as well, but it requires the continuous presence of higher levels of IFN-gamma for more than 48 hr to trigger the cells. Induced class II molecules start to appear 2 days after pulsing and continue to increase until Day 4. If the IFN-gamma is removed from the cultures, class II expression declines rapidly towards zero, with a half-life of approximately 30 hr.
对大鼠脑内皮细胞进行体外研究,以确定γ干扰素刺激后MHC基因激活过程中的事件顺序。通过在有或无α-鹅膏蕈碱存在的情况下定量细胞表面MHC表达,来测量细胞触发时间、mRNA合成动力学、MHC诱导率和衰减率。I类表达在γ干扰素刺激后立即增强,刺激4小时后达到最大诱导水平。新的I类mRNA合成立即开始,并在接下来的24小时内持续进行。随后I类分子表达增加,到24小时达到平台期。在γ干扰素存在的情况下,I类表达维持在静息细胞的140%-200%。去除γ干扰素后,I类表达向静息细胞水平衰减,半衰期约为40小时。这些细胞上也可诱导II类分子,但需要持续存在更高水平的γ干扰素超过48小时才能触发细胞。诱导的II类分子在脉冲后2天开始出现,并持续增加直至第4天。如果从培养物中去除γ干扰素,II类表达迅速下降至零,半衰期约为30小时。