Smedts F, Ramaekers F, Robben H, Pruszczynski M, van Muijen G, Lane B, Leigh I, Vooijs P
Department of Pathology, University Hospital Nijmegen, The Netherlands.
Am J Pathol. 1990 Mar;136(3):657-68.
The expression of keratins in normal cervical epithelia, metaplastic epithelium, and cervical intraepithelial neoplasia (CIN) grades I, II, and III is investigated with a panel of keratin polypeptide-specific monoclonal antibodies. This approach allowed the detection of individual keratins 4, 7, 8, 10, 13, 14, 18, and 19 at the single-cell level. By using an antibody recognizing keratins 5 and 8 (RCK 102) and two antibodies specific for keratin 8 (CAM 5.2 and M 20), it was also possible to derive information on the distribution of keratin 5. Our results show that during immature squamous metaplasia there is an acquisition of keratins typical of squamous epithelium, ie, keratins 4, 5, 13, and 14. This process continues during further differentiation to mature squamous metaplasia. In premalignant lesions the expression pattern of the progenitor reserve cells and immature squamous metaplastic epithelium is partly conserved. However, in most cases an induction in the expression of the keratins 4, 13, and 14 was observed. Furthermore, CIN III shows a more extensive expression of keratins typical of simple epithelia, ie, keratins 8 and 18, as compared to CIN I and CIN II.
使用一组角蛋白多肽特异性单克隆抗体,研究了正常宫颈上皮、化生上皮以及宫颈上皮内瘤变(CIN)I级、II级和III级中角蛋白的表达情况。这种方法能够在单细胞水平检测到单个角蛋白4、7、8、10、13、14、18和19。通过使用识别角蛋白5和8的抗体(RCK 102)以及两种角蛋白8特异性抗体(CAM 5.2和M 20),还能够获取有关角蛋白5分布的信息。我们的结果表明,在未成熟鳞状化生过程中,出现了鳞状上皮典型的角蛋白,即角蛋白4、5、13和14。在进一步分化为成熟鳞状化生的过程中,这一过程持续进行。在癌前病变中,祖细胞储备细胞和未成熟鳞状化生上皮的表达模式部分得以保留。然而,在大多数情况下,观察到角蛋白4、13和14的表达有所诱导。此外,与CIN I和CIN II相比,CIN III显示出更广泛的单层上皮典型角蛋白,即角蛋白8和18的表达。