Nephrology Division, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States of America.
Image and Data Analysis Core, Department of Cell Biology, Harvard Medical School, Boston, MA, United States of America.
PLoS One. 2019 Feb 8;14(2):e0211943. doi: 10.1371/journal.pone.0211943. eCollection 2019.
The initial steps in the synthesis of leukotrienes are the translocation of 5-lipoxygenase (5-LO) to the nuclear envelope and its subsequent association with its scaffold protein 5-lipoxygenase-activating protein (FLAP). A major gap in our understanding of this process is the knowledge of how the organization of 5-LO and FLAP on the nuclear envelope regulates leukotriene synthesis. We combined single molecule localization microscopy with Clus-DoC cluster analysis, and also a novel unbiased cluster analysis to analyze changes in the relationships between 5-LO and FLAP in response to activation of RBL-2H3 cells to generate leukotriene C4. We identified the time-dependent reorganization of both 5-LO and FLAP into higher-order assemblies or clusters in response to cell activation via the IgE receptor. Clus-DoC analysis identified a subset of these clusters with a high degree of interaction between 5-LO and FLAP that specifically correlates with the time course of LTC4 synthesis, strongly suggesting their role in the initiation of leukotriene biosynthesis.
白三烯合成的初始步骤是 5-脂氧合酶(5-LO)向核膜易位及其随后与支架蛋白 5-脂氧合酶激活蛋白(FLAP)的结合。我们对这一过程的理解存在一个主要的空白,即不知道核膜上 5-LO 和 FLAP 的组织如何调节白三烯的合成。我们结合单分子定位显微镜和 Clus-DoC 聚类分析,以及一种新的无偏聚类分析,分析了 RBL-2H3 细胞激活后 5-LO 和 FLAP 之间关系的变化,以生成白三烯 C4。我们发现,通过 IgE 受体,5-LO 和 FLAP 会在细胞激活时发生时间依赖性的重组,形成更高阶的组装或簇。Clus-DoC 分析确定了这些簇中的一部分,它们之间的 5-LO 和 FLAP 相互作用程度很高,与 LTC4 合成的时间进程特异性相关,强烈表明它们在白三烯生物合成的启动中起作用。