Signaling Mechanisms of EphrinB1 in Cell Adhesion, Migration and Invasion

我们目前的研究兴趣是研究Eph受体酪氨酸激酶及其ePhin配体信号影响细胞-细胞黏附和形态发生运动的机制。通过对这些信号转导途径的阐明，可以提高我们对肿瘤发生的认识。细胞-细胞黏附系统在正常发育和形态发生中起着重要作用。这种黏附系统的失活被认为在癌症的侵袭和转移中起着关键作用。非洲爪蛙胚胎非常适合研究这些过程，因为这种青蛙有一个很好的特征和不变的细胞命运图，而且在实验期间可以很容易地追踪到细胞谱系。突变的受体、配体和其他蛋白质可以在胚胎中异位表达。因此，它们对信号转导、运动和分化的影响可以在发育中的脊椎动物中从形态和组织学以及生化方面进行评估。我们的实验室目前正在利用非洲爪哇的卵母细胞和胚胎系统以及人类培养的细胞系来研究非洲爪哇Eph受体酪氨酸激酶和eparinB跨膜配体在细胞信号和功能中的作用。目前，我们的重点放在这些Eph家族成员发出影响形态发生运动的信号的机制上。Eph家族成员参与了许多发育过程的调控，并被发现在转移性癌症中表达下调，例如前列腺癌、卵巢癌、乳腺癌、结肠癌、神经母细胞瘤、肺癌和黑色素瘤。我们的实验室继续进行这些研究，检测控制细胞黏附和细胞运动的ewitinB1的近端和远端信号。我们最近发现有证据表明，ewitinB1信号通过其细胞内结构域与Disheveled(Dsh)相互作用，并选择平面细胞极性(PCP)途径来控制视网膜前体细胞进入眼场。利用生化分析和功能得失实验，我们的数据表明，在眼场形成过程中，dsh与ewitinB1联系在一起，并通过PCP通路的下游成员介导ewitinB1信号传递。因此，我们使用眼场作为一个模型系统来理解ewitinB1是如何控制细胞运动的。最近，我们研究了ewitinB1影响细胞-细胞连接的机制。大量证据表明，在细胞的正常迁移以及细胞和组织边界的形成过程中，需要有肾上腺素配体。这些过程依赖于细胞黏附系统，细胞黏附系统在发育过程中的正常形态发生过程以及侵袭和转移过程中起着至关重要的作用。虽然ewitinB配体是双向信号分子，但ewitinB1信号通过其胞内结构域调节上皮细胞细胞间黏附的确切机制尚不清楚。在这里，我们提供了证据表明，ePhrinB1与PAR极性复合体蛋白PAR-6(一种建立紧密连接所需的支架蛋白)相结合，并可以与小的GTPase CDc42竞争与PAR-6的结合。这种竞争导致PAR复合体失活，导致紧密连接的丧失。此外，ewitinB1和PAR-6之间的相互作用被ewitinB1胞内域的酪氨酸磷酸化所破坏。因此，我们已经确定了一种机制，通过ewitinB1信号调节上皮细胞中的细胞-细胞连接，这可能会影响我们如何设计关于转移疾病中这些分子的治疗干预措施。

Our current research interests are aimed toward examining the mechanism by which Eph receptor tyrosine kinases and their ephrin ligands signal events affecting cell-cell adhesion and morphogenetic movements. From the elucidation of these signal transduction pathways we may improve our understanding of oncogenesis. The cell-cell adhesion system plays a major role in normal development and morphogenesis. Inactivation of this adhesion system is thought to play a critical role in cancer invasion and metastasis. The Xenopus embryo is well suited for investigations of these processes because the frog has a well characterized and invariant cell fate map and cell lineage can be easily traced during experiments. Mutant receptors, ligands, and other proteins can be ectopically expressed in embryos. Thus, their effects on signal transduction, motility, and differentiation can be assessed morphologically and histologically as well as biochemically in a developing vertebrate. Our laboratory is currently investigating the role of the Xenopus Eph receptor tyrosine kinases and ephrinB transmembrane ligands in cell signaling and function using the Xenopus oocyte and embryo systems, as well as human cultured cell lines. At present, our emphasis is placed upon the mechanism by which these Eph family members send signals affecting morphogenetic movements. Members of the Eph family have been implicated in regulating numerous developmental processes and have been found to be de-regulated in metastatic cancers, for example, prostate, ovarian, breast, colon, neuroblastoma, lung, and melanoma. Our laboratory has continued these studies examining proximal and distal signaling from ephrinB1 that controls cell adhesion and cell movement. We recently found evidence that ephrinB1 signals via its intracellular domain to control retinal progenitor movement into the eye field by interacting with Dishevelled (dsh), and co-opting the planar cell polarity (PCP) pathway. Using biochemical analysis and gain or loss of function experiments, our data suggest that dsh associates with ephrinB1 and mediates ephrinB1 signaling via downstream members of the PCP pathway during eye field formation. thus, we have used the eye field as a model system for understanding how ephrinB1 controls cell movement. Most recently we have examined the mechanisms by which ephrinB1 affects cell-cell junctions. A body of evidence is emerging that shows a requirement for ephrin ligands in the proper migration of cells, and the formation of cell and tissue boundaries. These processes are dependent on the cellcell adhesion system, which plays a crucial role in normal morphogenetic processes during development, as well as in invasion and metastasis19. Although ephrinB ligands are bi-directional signalling molecules, the precise mechanism by which ephrinB1 signals through its intracellular domain to regulate cell-cell adhesion in epithelial cells remains unclear. Here, we present evidence that ephrinB1 associates with the Par polarity complex protein Par-6 (a scaffold protein required for establishing tight junctions) and can compete with the small GTPase Cdc42 for association with Par-6. This competition causes inactivation of the Par complex, resulting in the loss of tight junctions. Moreover, the interaction between ephrinB1 and Par-6 is disrupted by tyrosine phosphorylation of the intracellular domain of ephrinB1. Thus, we have identified a mechanism by which ephrinB1 signalling regulates cell-cell junctions in epithelial cells, and this may influence how we devise therapeutic interventions regarding these molecules in metastatic disease.