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升高的环磷酸腺苷(cAMP)水平可诱导MDCK细胞多层化,而不破坏细胞表面极性。

Elevated cAMP levels induce multilayering of MDCK cells without disrupting cell surface polarity.

作者信息

Ullrich O, Haase W, Koch-Brandt C

机构信息

Institut für Biochemie, J. Gutenberg-Universität, Mainz, Germany.

出版信息

J Cell Sci. 1993 Mar;104 ( Pt 3):719-26. doi: 10.1242/jcs.104.3.719.

Abstract

The effect of hormones on the morphology and cell surface polarity of the epithelial cell line MDCK was examined. When MDCK cells were seeded in high densities in media containing FCS a regular monolayer was formed. However, in serum-free medium supplemented with insulin, transferrin, prostaglandin E1, hydrocortisone and triiodothyronine, the development of a multilayer with intercellular lumina was observed. In hormone-depletion studies we identified PGE1 as the inducer of these multilayers. Since dibutyryl cyclic AMP and the phosphodiesterase inhibitor isobutyl methylxanthine could substitute for PGE1, we conclude that an elevated intracellular cAMP level resulted in formation of the multilayer. Further analysis by electron microscopy and immunocytochemistry revealed a polarized organization of the multilayered cells. Junctional complexes, enclosing microvilli-rich membrane domains, were found at the apices of adjacent cells facing the medium and those surrounding the intercellular lumina. Surprisingly, cells participating in the formation of both the free surface and the surface of the intercellular lumen, exhibited two distinct membranes with microvilli, each separated by junctional complexes. Immunolocalization of membrane marker proteins demonstrated that an apical 114 kDa membrane protein was localized to the free cell surfaces, the same membrane domains where extensive microvilli were also observed. The distribution of a basolateral 58 kDa membrane protein was restricted to sites of cell contact. These results provided evidence that nontransformed epithelial MDCK cells form multilayers in response to elevated cAMP levels; however, they retain the potential of developing cell surface polarity.

摘要

研究了激素对上皮细胞系MDCK的形态和细胞表面极性的影响。当MDCK细胞以高密度接种于含胎牛血清(FCS)的培养基中时,会形成规则的单层。然而,在补充了胰岛素、转铁蛋白、前列腺素E1、氢化可的松和三碘甲状腺原氨酸的无血清培养基中,观察到形成了具有细胞间腔隙的多层结构。在激素去除研究中,我们确定前列腺素E1是这些多层结构的诱导剂。由于二丁酰环磷酸腺苷(dibutyryl cyclic AMP)和磷酸二酯酶抑制剂异丁基甲基黄嘌呤(isobutyl methylxanthine)可以替代前列腺素E1,我们得出结论,细胞内cAMP水平升高导致了多层结构的形成。通过电子显微镜和免疫细胞化学的进一步分析揭示了多层细胞的极性组织。在面向培养基的相邻细胞顶端以及围绕细胞间腔隙的细胞顶端发现了封闭富含微绒毛膜结构域的连接复合体。令人惊讶的是,参与形成自由表面和细胞间腔表面的细胞表现出两种不同的带有微绒毛的膜,每种膜都由连接复合体分隔开。膜标记蛋白的免疫定位表明,一种顶端114 kDa的膜蛋白定位于游离细胞表面,即也观察到大量微绒毛的相同膜结构域。一种基底外侧58 kDa膜蛋白的分布局限于细胞接触部位。这些结果证明,未转化的上皮MDCK细胞在细胞内cAMP水平升高时会形成多层结构;然而,它们保留了发展细胞表面极性的潜力。

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