Department of Vascular Cell Biology, Max Planck Institute for Molecular Biomedicine, Münster, Germany.
Cell Mol Life Sci. 2011 Nov;68(22):3757-70. doi: 10.1007/s00018-011-0676-8. Epub 2011 Apr 17.
The non-receptor tyrosine kinase Syk is a well-characterized hematopoietic signal transducer, which is also expressed in non-hematopoietic cells. In epithelial cells, the function of Syk is not wholly known. It interacts with the receptor tyrosine kinase DDR1 and is frequently lost from metastatic mammary tumors. Here, using genetic tracing, we demonstrate Syk expression in murine mammary epithelium, myoepithelium and skin epithelium, but not in intestinal or lung epithelia. Investigating possible functions of Syk, we found a substantial suppression of cell mobility that depended on Syk kinase activity in trans-well migration and wounding assays. Co-expression of DDR1 resulted in constitutive interaction and strong activation of Syk kinase. Most importantly, Syk-mediated migration inhibition was blocked in the presence of DDR1, while conversely DDR1 knockdown restored migration inhibition. Our study identifies Syk as a potent inhibitor of epithelial migration and describes a first functional consequence of the interaction with the collagen receptor DDR1.
非受体酪氨酸激酶 Syk 是一种特征明确的造血信号转导物,也在非造血细胞中表达。在上皮细胞中,Syk 的功能尚不完全清楚。它与受体酪氨酸激酶 DDR1 相互作用,并且经常从转移性乳腺肿瘤中丢失。在这里,我们使用遗传追踪技术证明了 Syk 在小鼠乳腺上皮细胞、肌上皮细胞和皮肤上皮细胞中的表达,但不在肠道或肺上皮细胞中表达。研究 Syk 可能的功能,我们发现细胞迁移受到显著抑制,这依赖于 Trans-well 迁移和划痕实验中转录后迁移中 Syk 激酶的活性。DDR1 的共表达导致 Syk 激酶的组成性相互作用和强烈激活。最重要的是,在存在 DDR1 的情况下,Syk 介导的迁移抑制被阻断,而相反,DDR1 的敲低恢复了迁移抑制。我们的研究将 Syk 鉴定为上皮细胞迁移的有效抑制剂,并描述了与胶原受体 DDR1 相互作用的第一个功能后果。