Cell Biology & Biophysics Unit, European Molecular Biology Laboratory (EMBL), Meyerhofstrasse 1, 69117 Heidelberg, Germany.
Division of Cell Biology, The Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, the Netherlands.
Cell Chem Biol. 2016 May 19;23(5):629-634. doi: 10.1016/j.chembiol.2015.11.019. Epub 2016 May 5.
Lysophosphatidic acid (LPA) is a serum-borne lipid mediator that binds to a variety of different G protein-coupled receptors to trigger an exceptionally wide range of biological effects, including cell survival and differentiation, cancer cell migration, and embryonic development. Here we synthesized caged LPA (cgLPA), a "photolysable" coumarin-masked derivative of LPA. We demonstrate that illumination of cgLPA with 405 nm light liberates bioactive LPA on a subsecond scale to evoke Ca(2+) signaling, Rho activation, and cytoskeletal contraction. In addition, we developed an "optotaxis" assay to attract melanoma cells through a stable chemotactic gradient by repeated liberation of LPA through local photolysis of extracellular cgLPA. We expect that this method of light-controlled chemotaxis will be generally applicable to a large variety of small molecules that drive cellular migration or other responses.
溶血磷脂酸(LPA)是一种血清来源的脂质介质,它可以与多种不同的 G 蛋白偶联受体结合,从而引发异常广泛的生物学效应,包括细胞存活和分化、癌细胞迁移和胚胎发育。在这里,我们合成了笼状溶血磷脂酸(cgLPA),这是一种“光解”香豆素掩蔽的 LPA 衍生物。我们证明,用 405nm 光照射 cgLPA 可以在亚秒级的时间尺度内释放出具有生物活性的 LPA,从而引发 Ca(2+)信号转导、Rho 激活和细胞骨架收缩。此外,我们开发了一种“光趋化性”测定法,通过局部光解细胞外 cgLPA 反复释放 LPA,从而利用稳定的趋化性梯度吸引黑素瘤细胞。我们预计这种光控趋化性方法将普遍适用于驱动细胞迁移或其他反应的各种小分子。