Stepwise phosphorylation of leukotriene B-4 receptor 1 defines cellular responses to leukotriene B-4

作者：Nakanishi Yoshimitsu; Tan Modong; Ichiki Takako; Inoue Asuka; Yoshihara Jun ichi; Maekawa Naoto; Takenoshita Itsuki; Yanagida Keisuke; Yamahira Shinya; Yamaguchi Satoshi; Aoki Junken; Nagamune Teruyuki; Yokomizo Takehiko; Shimizu Takao; Nakamura Motonao^*

来源：Science Signaling, 2018, 11(544): eaao5390.

DOI：10.1126/scisignal.aao5390

Leukotriene B-4 (LTB4) receptor type 1 (BLT1) is abundant in phagocytic and immune cells and plays crucial roles in various inflammatory diseases. BLT1 is phosphorylated at several serine and threonine residues upon stimulation with the inflammatory lipid LTB4. Using Phos-tag gel electrophoresis to separate differentially phosphorylated forms of BLT1, we identified two distinct types of phosphorylation, basal and ligand-induced, in the carboxyl terminus of human BLT1. In the absence of LTB4, the basal phosphorylation sites were modified to various degrees, giving rise to many different phosphorylated forms of BLT1. Different concentrations of LTB4 induced distinct phosphorylation events, and these ligand-induced modifications facilitated additional phosphorylation events at the basal phosphorylation sites. Because neutrophils migrate toward inflammatory sites along a gradient of LTB4, the degree of BLT1 phosphorylation likely increases in parallel with the increase in LTB4 concentration as the cells migrate. At high concentrations of LTB4, deficiencies in these two types of phosphorylation events impaired chemotaxis and b-hexosaminidase release, a proxy for degranulation, in Chinese hamster ovary (CHO-K1) and rat basophilic leukemia (RBL-2H3) cells, respectively. These results suggest that an LTB4 gradient around inflammatory sites enhances BLT1 phosphorylation in a stepwise manner to facilitate the precise migration of phagocytic and immune cells and the initiation of local responses, including degranulation.

• 出版日期2018-8-21