Lancillotti F, Darwiche N, Celli G, De Luca L M
Laboratory of Cellular Carcinogenesis and Tumor Promotion, National Cancer Institute, Bethesda, MD 20892.
Cancer Res. 1992 Nov 15;52(22):6144-52.
We induced vitamin A depletion to define early and late changes during the histogenesis of squamous metaplasia of hamster tracheal epithelium. An early change is the "minimal morphological change" (MMC), in which the mucociliary epithelium is separated from the basement membrane by a continuous layer of basal cells. Immunohistochemistry showed an exclusive localization of the keratins K5 and K14 in basal cells of normal and MMC epithelia. At the MMC stage no staining was observed above the basal layer with antibodies to K5, but upon progression of the lesion to a squamous focus all cells from basal to terminally differentiated were positive for K5 and K14. In contrast, when we used antibodies to the keratins K6 or K13 all cells were negative in the normal epithelium and in the MMC epithelium. Successive layers of suprabasal squamous cells found in squamous metaplasia failed to express normal epidermal differentiation marker keratins K1 and K10 but expressed the proliferation marker keratin K6 and the internal stratified epithelium keratin K13, not normally found in the epidermis or in the trachea. Hamster tracheal epithelial cells could be maintained in culture in serum-free medium for at least 4 weeks in the presence of retinoic acid (RA). In non-RA-containing medium, cells from vitamin A-deficient hamsters showed markedly reduced growth and an increase in the expression of keratins K5, K6, K13, and K14. Since our previous work had implicated retinoids in the control of cell adhesiveness, we were interested to find out whether changes in cell adhesion occur in vitamin A-deficient hamster tracheal epithelial cells, compared to normal cells. Functional assays demonstrated that hamster tracheal epithelial cells, obtained from non-RA-treated tracheas or maintained in culture, displayed reduced attachment to laminin, compared to RA-treated cells. Immunofluorescence studies did not show a decrease either in the alpha 6 integrin subunit, which was localized in the basal aspect of basal cells, or in basement membrane laminin. However, the expression of laminin-binding protein 37 decreased as the epithelium changed from pseudostratified to stratified. Therefore, a coordinated pattern of changes in keratin gene expression, as well as in the expression of laminin-binding protein 37, the precursor to the cell surface laminin receptor 67LR, and in adhesive properties takes place in tracheal epithelium when its phenotype changes from mucociliary to the preneoplastic stage of squamous metaplasia.
我们诱导仓鼠气管上皮鳞状化生的组织发生过程中出现维生素A缺乏,以确定早期和晚期变化。早期变化是“最小形态学变化”(MMC),即黏液纤毛上皮通过连续的基底细胞层与基底膜分离。免疫组织化学显示角蛋白K5和K14仅定位于正常和MMC上皮的基底细胞中。在MMC阶段,用K5抗体在基底细胞层上方未观察到染色,但随着病变进展为鳞状病灶,从基底细胞到终末分化的所有细胞K5和K14均呈阳性。相比之下,当我们使用角蛋白K6或K13抗体时,正常上皮和MMC上皮中的所有细胞均为阴性。在鳞状化生中发现的相继的基底上层鳞状细胞层未能表达正常表皮分化标志物角蛋白K1和K10,但表达增殖标志物角蛋白K6和内部复层上皮角蛋白K13,这些在表皮或气管中通常不存在。在视黄酸(RA)存在的情况下,仓鼠气管上皮细胞可以在无血清培养基中培养至少4周。在不含RA的培养基中,来自维生素A缺乏仓鼠的细胞生长明显减少,角蛋白K5、K6、K13和K14的表达增加。由于我们之前的工作表明类视黄醇参与细胞黏附的控制,我们有兴趣了解与正常细胞相比,维生素A缺乏的仓鼠气管上皮细胞中是否发生细胞黏附变化。功能分析表明,与经RA处理的细胞相比,从未经RA处理的气管获得或在培养中维持的仓鼠气管上皮细胞对层粘连蛋白的附着减少。免疫荧光研究未显示定位于基底细胞基底侧的α6整合素亚基或基底膜层粘连蛋白减少。然而,随着上皮从假复层变为复层,层粘连蛋白结合蛋白37的表达降低。因此,当气管上皮的表型从黏液纤毛变为鳞状化生的肿瘤前阶段时,角蛋白基因表达以及层粘连蛋白结合蛋白37(细胞表面层粘连蛋白受体67LR的前体)的表达和黏附特性会发生协调的变化模式。