Department of Cell Biology, Institute of Ophthalmology, University College London, London EC1V 9EL, England, UK.
J Cell Biol. 2014 Mar 3;204(5):821-38. doi: 10.1083/jcb.201304115. Epub 2014 Feb 24.
MarvelD3 is a transmembrane component of tight junctions, but there is little evidence for a direct involvement in the junctional permeability barrier. Tight junctions also regulate signaling mechanisms that guide cell proliferation; however, the transmembrane components that link the junction to such signaling pathways are not well understood. In this paper, we show that MarvelD3 is a dynamic junctional regulator of the MEKK1-c-Jun NH2-terminal kinase (JNK) pathway. Loss of MarvelD3 expression in differentiating Caco-2 cells resulted in increased cell migration and proliferation, whereas reexpression in a metastatic tumor cell line inhibited migration, proliferation, and in vivo tumor formation. Expression levels of MarvelD3 inversely correlated with JNK activity, as MarvelD3 recruited MEKK1 to junctions, leading to down-regulation of JNK phosphorylation and inhibition of JNK-regulated transcriptional mechanisms. Interplay between MarvelD3 internalization and JNK activation tuned activation of MEKK1 during osmotic stress, leading to junction dissociation and cell death in MarvelD3-depleted cells. MarvelD3 thus couples tight junctions to the MEKK1-JNK pathway to regulate cell behavior and survival.
MarvelD3 是紧密连接的跨膜成分,但几乎没有证据表明其直接参与连接通透性屏障。紧密连接还调节指导细胞增殖的信号机制;然而,将连接与这种信号通路的跨膜成分尚不清楚。在本文中,我们表明 MarvelD3 是 MEKK1-c-Jun NH2-末端激酶 (JNK) 通路的动态连接调节剂。在分化的 Caco-2 细胞中表达 MarvelD3 会导致细胞迁移和增殖增加,而在转移性肿瘤细胞系中重新表达则会抑制迁移、增殖和体内肿瘤形成。MarvelD3 的表达水平与 JNK 活性呈负相关,因为 MarvelD3 将 MEKK1 募集到连接中,导致 JNK 磷酸化下调和 JNK 调节的转录机制抑制。MarvelD3 的内化和 JNK 激活之间的相互作用在渗透胁迫期间调节 MEKK1 的激活,导致 MarvelD3 耗尽的细胞中连接解离和细胞死亡。因此,MarvelD3 将紧密连接与 MEKK1-JNK 通路连接起来,以调节细胞行为和存活。