Nelson W J, Shore E M, Wang A Z, Hammerton R W
Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111.
J Cell Biol. 1990 Feb;110(2):349-57. doi: 10.1083/jcb.110.2.349.
Cell-cell contact is an important determinant in the formation of functionally distinct plasma membrane domains during the development of epithelial cell polarity. In cultures of Madin-Darby canine kidney (MDCK) epithelial cells, cell-cell contact induces the assembly and accumulation of the Na+,K+-ATPase and elements of the membrane-cytoskeleton (ankyrin and fodrin) at the regions of cell-cell contact. Epithelial cell-cell contact appears to be regulated by the cell adhesion molecule uvomorulin (E-cadherin) which also becomes localized at the lateral plasma membrane of polarized cells. We have sought to determine whether the colocalization of these proteins reflects direct molecular interactions which may play roles in coordinating cell-cell contact and the assembly of the basal-lateral domain of the plasma membrane. Recently, we identified a complex of proteins containing the Na+,K+-ATPase, ankyrin, and fodrin in extracts of whole MDCK cells (Nelson, W.J., and R. W. Hammerton. 1989. J. Cell Biol. 108:893-902). We have now examined cell extracts for protein complexes containing the cell adhesion molecule uvomorulin. Proteins were solubilized from whole MDCK cells and fractionated in sucrose gradients. The sedimentation profile of solubilized uvomorulin is well separated from the majority of cell surface proteins, suggesting that uvomorulin occurs in a protein complex. A distinct portion of uvomorulin (30%) cosediments with ankyrin and fodrin (approximately 10.5S). Further fractionation of cosedimenting proteins in nondenaturing polyacrylamide gels reveals a discrete band of proteins that binds antibodies specific for uvomorulin, Na+,K+-ATPase, ankyrin, and fodrin. Significantly, ankyrin and fodrin, but not Na+K+-ATPase, coimmunoprecipitate in a complex with uvomorulin using uvomorulin antibodies. This result indicates that separate complexes exist containing ankyrin and fodrin with either uvomorulin or Na+,K+-ATPase. These results are discussed in the context of the possible roles of uvomorulin-induced cell-cell contact in the assembly of the membrane-cytoskeleton and associated membrane proteins (e.g., Na+,K+-ATPase) at the contact zone and in the development of cell polarity.
细胞间接触是上皮细胞极性发育过程中功能不同的质膜结构域形成的重要决定因素。在Madin-Darby犬肾(MDCK)上皮细胞培养物中,细胞间接触诱导Na⁺,K⁺-ATP酶以及膜细胞骨架成分(锚蛋白和血影蛋白)在细胞间接触区域组装和积累。上皮细胞间接触似乎受细胞黏附分子桥粒芯蛋白(E-钙黏蛋白)调控,该蛋白也定位于极化细胞的侧质膜。我们试图确定这些蛋白质的共定位是否反映了直接的分子相互作用,这种相互作用可能在协调细胞间接触以及质膜基底外侧结构域的组装中发挥作用。最近,我们在整个MDCK细胞提取物中鉴定出了一种包含Na⁺,K⁺-ATP酶、锚蛋白和血影蛋白的蛋白质复合物(纳尔逊,W.J.,和R.W.哈默顿。1989。《细胞生物学杂志》108:893 - 902)。我们现在已经检测了细胞提取物中是否存在包含细胞黏附分子桥粒芯蛋白的蛋白质复合物。蛋白质从整个MDCK细胞中溶解出来,并在蔗糖梯度中进行分级分离。溶解的桥粒芯蛋白的沉降分布与大多数细胞表面蛋白明显分开,这表明桥粒芯蛋白存在于一种蛋白质复合物中。桥粒芯蛋白的一个独特部分(30%)与锚蛋白和血影蛋白(约10.5S)共同沉降。在非变性聚丙烯酰胺凝胶中对共同沉降的蛋白质进一步分级分离,揭示出一条离散的蛋白带,它能结合针对桥粒芯蛋白、Na⁺,K⁺-ATP酶、锚蛋白和血影蛋白的特异性抗体。值得注意的是,使用桥粒芯蛋白抗体时,锚蛋白和血影蛋白而非Na⁺K⁺-ATP酶能与桥粒芯蛋白在一个复合物中共免疫沉淀。这一结果表明存在分别包含与桥粒芯蛋白或Na⁺,K⁺-ATP酶结合的锚蛋白和血影蛋白的复合物。我们将在桥粒芯蛋白诱导的细胞间接触在接触区膜细胞骨架及相关膜蛋白(如Na⁺,K⁺-ATP酶)组装以及细胞极性发育中可能发挥的作用的背景下讨论这些结果。