Kwon Hyouk-Bum, Mackie Duncan I, Bonnavion Remy, Mercier Alan Le, Helker Christian S M, Son Taekwon, Guenter Stefan, Serafin D Stephen, Kim Kyu-Won, Offermanns Stefan, Caron Kathleen M, Stainier Didier Y R
Department of Developmental Genetics, Max Planck Institute for Heart and Lung Research, Bad Nauheim, 61231, Germany.
Department of Cell Biology & Physiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, United States.
ACS Pharmacol Transl Sci. 2020 Jun 24;3(4):676-689. doi: 10.1021/acsptsci.0c00020. eCollection 2020 Aug 14.
The G protein-coupled receptor 182 (GPR182) is an orphan GPCR, the expression of which is enriched in embryonic endothelial cells (ECs). However, the physiological role and molecular mechanism of action of GPR182 are unknown. Here, we show that GPR182 negatively regulates definitive hematopoiesis in zebrafish and mice. In zebrafish, expression is enriched in the hemogenic endothelium (HE), and display an increased expression of HE and hematopoietic stem cell (HSC) marker genes. Notably, we find an increased number of myeloid cells in compared to wild-type. Further, by time-lapse imaging of zebrafish embryos during the endothelial-to-hematopoietic transition, we find that HE/HSC cell numbers are increased in compared to wild-type. mice also exhibit an increased number of myeloid cells compared to wild-type, indicating a conserved role for GPR182 in myelopoiesis. Using cell-based small molecule screening and transcriptomic analyses, we further find that GPR182 regulates the leukotriene B4 (LTB4) biosynthesis pathway. Taken together, these data indicate that GPR182 is a negative regulator of definitive hematopoiesis in zebrafish and mice, and provide further evidence for LTB4 signaling in HSC biology.
G蛋白偶联受体182(GPR182)是一种孤儿GPCR,其表达在胚胎内皮细胞(ECs)中富集。然而,GPR182的生理作用和分子作用机制尚不清楚。在这里,我们表明GPR182对斑马鱼和小鼠的确定性造血起负调节作用。在斑马鱼中,其表达在造血内皮(HE)中富集,并且显示出HE和造血干细胞(HSC)标记基因的表达增加。值得注意的是,我们发现与野生型相比,[此处原文缺失相关内容]中的髓样细胞数量增加。此外,通过对斑马鱼胚胎在内皮向造血转变过程中的延时成像,我们发现与野生型相比,[此处原文缺失相关内容]中的HE/HSC细胞数量增加。[此处原文缺失相关内容]小鼠与野生型相比也表现出髓样细胞数量增加,表明GPR182在髓系造血中具有保守作用。通过基于细胞的小分子筛选和转录组分析,我们进一步发现GPR182调节白三烯B4(LTB4)生物合成途径。综上所述,这些数据表明GPR182是斑马鱼和小鼠确定性造血的负调节因子,并为LTB4信号在HSC生物学中的作用提供了进一步证据。