Mertens C, Kuhn C, Moll R, Schwetlick I, Franke W W
Division of Cell Biology, German Cancer Research Center, Heidelberg, Germany.
Differentiation. 1999 Jun;64(5):277-90. doi: 10.1046/j.1432-0436.1999.6450277.x.
Plakophilin 2 (PKP2) is a widespread protein which shows a remarkable dual location: On the one hand, it appears as a constitutive karyoplasmic protein and on the other it is a desmosomal plaque component of most, probably all, desmosome-possessing tissues and cell culture lines. Here we report on its desmosomal occurrence as revealed by immunocytochemical results obtained with three PKP2-specific murine monoclonal antibodies (mAbs) PP2-62, PP2-86 and PP2-150. These mAbs detect PKP2 in characteristic desmosomes of most normal cells, including simple and stratified epithelia as well as non-epithelial tissues such as myocardium and lymph node follicles. In addition, however, several normal tissues consistently display a differentiation-related PKP2 distribution, for example an absence of immunostaining in the "keratinizing" local specializations of the thymic epithelial reticulum, i.e. Hassall's corpuscles, and the restriction of PKP2 to the stratum basale of most stratified squamous epithelia, in contrast to its absence in upper strata, which contain PKP1- or PKP3-rich desmosomes instead. Taking advantage of the reactivity of mAb PP2-150 with formalin-fixed, paraffin-embedded material, a series of human carcinomas (n = 37) has also been analyzed. The results suggest that mAbs to PKP2 may serve as markers for the identification and characterization of carcinomas derived from--or corresponding to--simple or complex epithelia. Thus consistent PKP2 immunostaining has been observed in all 18 cases of adenocarcinomas tested, but more variable and heterogeneous staining has been noted in squamous cell carcinomas, depending on the specific tumor type. The potential value of such mAbs for cell typing in normal and embryonic tissues and for detecting cell subpopulations with different degrees of differentiation is discussed with respect to their possible application in tumor diagnosis.
桥粒芯蛋白2(PKP2)是一种广泛存在的蛋白质,具有显著的双重定位:一方面,它表现为一种组成型核质蛋白;另一方面,它是大多数(可能是所有)具有桥粒的组织和细胞系中的桥粒斑成分。在此,我们报告通过使用三种PKP2特异性鼠单克隆抗体(mAb)PP2 - 62、PP2 - 86和PP2 - 150获得的免疫细胞化学结果所揭示的其在桥粒中的存在情况。这些单克隆抗体在大多数正常细胞的特征性桥粒中检测到PKP2,包括单层和复层上皮以及非上皮组织,如心肌和淋巴结滤泡。然而,此外,一些正常组织始终呈现与分化相关的PKP2分布,例如胸腺上皮网状结构的“角质化”局部特化结构(即哈氏小体)中无免疫染色,并且与上层缺乏PKP2形成对比的是,大多数复层鳞状上皮的基底层中存在PKP2,而上层含有富含PKP1或PKP3的桥粒。利用单克隆抗体PP2 - 150与福尔马林固定、石蜡包埋材料的反应性,还分析了一系列人类癌组织(n = 37)。结果表明,针对PKP2的单克隆抗体可作为鉴定和表征源自简单或复层上皮或与之对应的癌组织的标志物。因此,在所检测的18例腺癌病例中均观察到一致的PKP2免疫染色,但在鳞状细胞癌中观察到的染色更具变异性和异质性,这取决于具体的肿瘤类型。关于这些单克隆抗体在肿瘤诊断中的可能应用,讨论了它们在正常和胚胎组织细胞分型以及检测不同分化程度细胞亚群方面的潜在价值。