Issa-Chergui B, Goldner-Sauvé A, Colle E, Prud'homme G J, Lapchak P H, van der Meide P H, Seemayer T A
McGill University-Montreal Children's Hospital Research Institute, Canada.
Diabetologia. 1988 Sep;31(9):675-80. doi: 10.1007/BF00278751.
A study of Class I and II major histocompatibility complex gene product expression by a rat insulinoma cell line (RINm5F) was performed using monoclonal antibodies and immunoperoxidase techniques. RINm5F cells were incubated with different concentrations of gamma interferon. RINm5F cells exhibit low levels of Class I molecules and are normally devoid of Class II gene products. Upon exposure to gamma interferon, RINm5F cells showed a dramatic increase in Class I expression. This expression was homogenous and could be detected on all cells after 18 h of incubation with as little as 1 unit/ml of interferon. In contrast, de novo Class II expression was not homogeneous and required 36 h of incubation with 10 units/ml of interferon. The number of RINm5F cells expressing Class II antigens was dose- and time-dependent. Interferon treatment did not affect the morphology of RINm5F cells as determined by ultrastructural analysis. Withdrawal of interferon from the culture medium for as long as 78 h diminished but did not abolish the expression of Class I and Class II molecules already induced. The ability of interferon to enhance expression of Class I gene products and induce de novo expression of Class II molecules on B-cell-derived RINm5F cells supports the hypothesis that aberrant expression of major histocompatibility complex gene products on pancreatic B cells may be an important factor in triggering the immune response in Type 1 (insulin dependent) diabetes mellitus.
利用单克隆抗体和免疫过氧化物酶技术,对大鼠胰岛素瘤细胞系(RINm5F)的I类和II类主要组织相容性复合体基因产物表达进行了研究。将RINm5F细胞与不同浓度的γ干扰素一起孵育。RINm5F细胞I类分子水平较低,通常不表达II类基因产物。暴露于γ干扰素后,RINm5F细胞的I类表达显著增加。这种表达是均匀的,在用低至1单位/毫升的干扰素孵育18小时后,所有细胞上均可检测到。相比之下,II类的从头表达并不均匀,需要用10单位/毫升的干扰素孵育36小时。表达II类抗原的RINm5F细胞数量呈剂量和时间依赖性。超微结构分析表明,干扰素处理不影响RINm5F细胞的形态。从培养基中撤去干扰素长达78小时,可减少但不能消除已诱导的I类和II类分子的表达。干扰素增强I类基因产物表达并诱导B细胞来源的RINm5F细胞上II类分子从头表达的能力支持了这样一种假说,即胰腺B细胞上主要组织相容性复合体基因产物的异常表达可能是引发1型(胰岛素依赖型)糖尿病免疫反应的一个重要因素。