Saitoh M, Oyamada M, Oyamada Y, Kaku T, Mori M
Department of Pathology, Sapporo Medical University School of Medicine, Chuo-ku, Japan.
Carcinogenesis. 1997 Jul;18(7):1319-28. doi: 10.1093/carcin/18.7.1319.
We examined changes in the expression and localization of connexin proteins and transcripts by means of immunofluorescence and in situ hybridization in normal conditions, wound healing and carcinogenesis using hamster tongue epithelium, in which differentiation, migration and growth of keratinocytes takes place physiologically and pathologically. In normal hamster tongue epithelium, immunofluorescent staining showed that Cx26 and Cx43 proteins were localized differently during differentiation of keratinocytes, but in in situ hybridization, the localization of Cx26 and Cx43 transcripts overlapped considerably, suggesting that the different localization of Cx26 and Cx43 proteins in squamous epithelium is largely regulated at post-transcriptional levels. During wound healing, the expression and localization of connexin proteins and transcripts were changed drastically. Shortly (6 h) after injury the expression of Cx26 and Cx43 proteins decreased at wound edges, but by 1-3 days after injury the expression of both proteins increased and both proteins co-localized to the same spots in the epithelium near wound edges. During carcinogenesis, the increased expression of Cx26 and Cx43 proteins and their transcripts and co-localization of both proteins occurred in papillomas, and the expression of Cx26 was reduced as cancer cells became morphologically less differentiated. We also found, that during wound healing in papillomas, squamous cell carcinomas and keratinocytes, Cx26 and Cx43 proteins were localized aberrantly in the cytoplasm, especially around nuclei, rather than on plasma membranes. These results indicate that quantitative and qualitative changes in connexin expression are associated with differentiation, migration and proliferation of keratinocytes in squamous epithelium.
我们通过免疫荧光和原位杂交技术,利用仓鼠舌上皮研究了正常条件、伤口愈合和癌变过程中连接蛋白的表达和定位变化。在仓鼠舌上皮中,角质形成细胞的分化、迁移和生长在生理和病理状态下均可发生。在正常仓鼠舌上皮中,免疫荧光染色显示,Cx26和Cx43蛋白在角质形成细胞分化过程中的定位不同,但在原位杂交中,Cx26和Cx43转录本的定位有相当大的重叠,这表明鳞状上皮中Cx26和Cx43蛋白的不同定位在很大程度上是在转录后水平调控的。在伤口愈合过程中,连接蛋白的表达和定位发生了剧烈变化。损伤后不久(6小时),伤口边缘Cx26和Cx43蛋白的表达下降,但在损伤后1 - 3天,这两种蛋白的表达均增加,且在伤口边缘附近上皮细胞的相同位置共定位。在癌变过程中,Cx26和Cx43蛋白及其转录本的表达增加,且两种蛋白在乳头状瘤中共定位,随着癌细胞形态学上分化程度降低,Cx26的表达减少。我们还发现,在乳头状瘤、鳞状细胞癌和角质形成细胞的伤口愈合过程中,Cx26和Cx43蛋白异常定位于细胞质中,尤其是细胞核周围,而非质膜上。这些结果表明,连接蛋白表达的定量和定性变化与鳞状上皮中角质形成细胞的分化、迁移和增殖有关。