Litvinov S V, Balzar M, Winter M J, Bakker H A, Briaire-de Bruijn I H, Prins F, Fleuren G J, Warnaar S O
Department of Pathology, Leiden University, Leiden 2300 RC, The Netherlands.
J Cell Biol. 1997 Dec 1;139(5):1337-48. doi: 10.1083/jcb.139.5.1337.
The contribution of noncadherin-type, Ca2+-independent cell-cell adhesion molecules to the organization of epithelial tissues is, as yet, unclear. A homophilic, epithelial Ca2+-independent adhesion molecule (Ep-CAM) is expressed in most epithelia, benign or malignant proliferative lesions, or during embryogenesis. Here we demonstrate that ectopic Ep-CAM, when expressed in cells interconnected by classic cadherins (E- or N-cadherin), induces segregation of the transfectants from the parental cell type in coaggregation assays and in cultured mixed aggregates, respectively. In the latter assay, Ep-CAM-positive transfectants behave like cells with a decreased strength of cell-cell adhesion as compared to the parental cells. Using transfectants with an inducible Ep-CAM-cDNA construct, we demonstrate that increasing expression of Ep-CAM in cadherin-positive cells leads to the gradual abrogation of adherens junctions. Overexpression of Ep-CAM has no influence on the total amount of cellular cadherin, but affects the interaction of cadherins with the cytoskeleton since a substantial decrease in the detergent-insoluble fraction of cadherin molecules was observed. Similarly, the detergent-insoluble fractions of alpha- and beta-catenins decreased in cells overexpressing Ep-CAM. While the total beta-catenin content remains unchanged, a reduction in total cellular alpha-catenin is observed as Ep-CAM expression increases. As the cadherin-mediated cell-cell adhesions diminish, Ep-CAM-mediated intercellular connections become predominant. An adhesion-defective mutant of Ep-CAM lacking the cytoplasmic domain has no effect on the cadherin-mediated cell-cell adhesions. The ability of Ep-CAM to modulate the cadherin-mediated cell-cell interactions, as demonstrated in the present study, suggests a role for this molecule in development of the proliferative, and probably malignant, phenotype of epithelial cells, since an increase of Ep-CAM expression was observed in vivo in association with hyperplastic and malignant proliferation of epithelial cells.
非钙黏蛋白型、不依赖Ca2+的细胞间黏附分子对上皮组织构建的作用目前尚不清楚。一种同源性、上皮性不依赖Ca2+的黏附分子(Ep-CAM)在大多数上皮组织、良性或恶性增殖性病变组织中或胚胎发育过程中表达。在此我们证明,异位表达的Ep-CAM,当在通过经典钙黏蛋白(E-钙黏蛋白或N-钙黏蛋白)相互连接的细胞中表达时,在共聚集试验和培养的混合聚集体中分别诱导转染细胞与亲代细胞类型分离。在后者的试验中,与亲代细胞相比,Ep-CAM阳性转染细胞表现得像细胞间黏附强度降低的细胞。使用带有可诱导Ep-CAM-cDNA构建体的转染细胞,我们证明在钙黏蛋白阳性细胞中Ep-CAM表达增加会导致黏着连接逐渐消失。Ep-CAM的过表达对细胞钙黏蛋白的总量没有影响,但会影响钙黏蛋白与细胞骨架的相互作用,因为观察到钙黏蛋白分子的去污剂不溶性部分大幅减少。同样,在过表达Ep-CAM的细胞中,α-连环蛋白和β-连环蛋白的去污剂不溶性部分也减少。虽然β-连环蛋白的总量保持不变,但随着Ep-CAM表达增加,观察到细胞内α-连环蛋白总量减少。随着钙黏蛋白介导的细胞间黏附减弱,Ep-CAM介导的细胞间连接变得占主导地位。缺乏细胞质结构域的Ep-CAM黏附缺陷突变体对钙黏蛋白介导的细胞间黏附没有影响。如本研究所示,Ep-CAM调节钙黏蛋白介导的细胞间相互作用的能力表明该分子在上皮细胞增殖性(可能还有恶性)表型的发展中起作用,因为在体内观察到Ep-CAM表达增加与上皮细胞的增生和恶性增殖相关。