Department of Chemistry and Biochemistry, Faculty of Chemistry and Chemical Technology, University of Ljubljana, Večna pot 113, Ljubljana, SI 1000, Slovenia.
Department of Bioengineering and Therapeutic Sciences, Department of Pharmaceutical Chemistry, California Institute for Quantitative Biosciences, University of California, San Francisco, 1700 4th Street, Suite 503B, San Francisco, CA, 94158, USA.
Sci Rep. 2018 Sep 5;8(1):13269. doi: 10.1038/s41598-018-31482-7.
Cell-surface tumor marker EpCAM plays a key role in proliferation, differentiation and adhesion processes in stem and epithelial cells. It is established as a cell-cell adhesion molecule, forming intercellular interactions through homophilic association. However, the mechanism by which such interactions arise has not yet been fully elucidated. Here, we first show that EpCAM monomers do not associate into oligomers that would resemble an inter-cellular homo-oligomer, capable of mediating cell-cell adhesion, by using SAXS, XL-MS and bead aggregation assays. Second, we also show that EpCAM forms stable dimers on the surface of a cell with pre-formed cell-cell contacts using FLIM-FRET; however, no inter-cellular homo-oligomers were detectable. Thus, our study provides clear evidence that EpCAM indeed does not function as a homophilic cell adhesion molecule and therefore calls for a significant revision of its role in both normal and cancerous tissues. In the light of this, we strongly support the previously suggested name Epithelial Cell Activating Molecule instead of the Epithelial Cell Adhesion Molecule.
细胞表面肿瘤标志物 EpCAM 在干细胞和上皮细胞的增殖、分化和黏附过程中发挥关键作用。它被确立为一种细胞间黏附分子,通过同源结合形成细胞间相互作用。然而,这种相互作用产生的机制尚未完全阐明。在这里,我们首先通过 SAXS、XL-MS 和珠聚集实验表明,EpCAM 单体不会形成类似细胞间同源寡聚物的寡聚体,而这种寡聚体能够介导细胞-细胞黏附。其次,我们还表明,EpCAM 在预先形成细胞-细胞接触的细胞表面形成稳定的二聚体,使用 FLIM-FRET;然而,没有检测到细胞间同源寡聚物。因此,我们的研究提供了明确的证据表明,EpCAM 实际上不作为同亲性细胞黏附分子发挥作用,因此需要对其在正常组织和癌组织中的作用进行重大修正。有鉴于此,我们强烈支持之前提出的上皮细胞激活分子的名称,而不是上皮细胞黏附分子。