Mattila P
Department of Bacteriology and Immunology, University of Helsinki, Finland.
FEBS Lett. 1991 Sep 2;289(1):86-90. doi: 10.1016/0014-5793(91)80914-o.
Activation of protein kinase C (PKC) has been linked to the regulation of class II expression on endothelial cells by interferon-gamma (IFN-gamma). PKC subtypes in endothelial cells were analyzed using three different approaches, the immunoperoxidase staining of native and IFN-gamma stimulated cells cultured on chamber slides as well as immuno- and Northern blotting. All approaches revealed that of the conventional subtypes, alpha is the predominant form of PKC in endothelial cells. Even though IFN-gamma is able to induce PKC translocation to particulate fractions, no translocation was detected in histological stainings. Western blot studies as well as mRNA studies revealed that IFN-gamma is unable to increase the total amount of PKC in endothelial cells.
蛋白激酶C(PKC)的激活已被证明与干扰素-γ(IFN-γ)对内皮细胞II类表达的调节有关。采用三种不同方法分析内皮细胞中的PKC亚型,即对培养在腔室载玻片上的天然细胞和IFN-γ刺激细胞进行免疫过氧化物酶染色,以及免疫印迹和Northern印迹。所有方法均显示,在内皮细胞中,传统亚型中α是PKC的主要形式。尽管IFN-γ能够诱导PKC转位至颗粒部分,但在组织学染色中未检测到转位。蛋白质印迹研究以及mRNA研究表明,IFN-γ无法增加内皮细胞中PKC的总量。