Ohuchi Hideyo, Hamada Aska, Matsuda Hironao, Takagi Akira, Tanaka Masayuki, Aoki Junken, Arai Hiroyuki, Noji Sumihare
Department of Life Systems, Institute of Technology and Science, University of Tokushima, Tokushima, Japan.
Dev Dyn. 2008 Nov;237(11):3280-94. doi: 10.1002/dvdy.21736.
Lysophospholipids (LPs) such as lysophosphatidic acid (LPA) and sphingosine-1-phosphate (S1P) are known to mediate various biological responses, including cell proliferation, migration, and differentiation. To better understand the role of these lipids in mammalian early development, we applied whole-mount in situ hybridization techniques to E8.5 to E12.5 mouse embryos. We determined the expression patterns of the following LP receptor genes, which belong to the G protein-coupled receptor (GPCR) family: EDG1 to EDG8 (S1P1 to S1P5 and LPA1 to LPA3), LPA4 (GPR23/P2Y9), and LPA5 (GPR92). We found that the S1P/LPA receptor genes exhibit overlapping expression patterns in a variety of organ primordia, including the developing brain and cardiovascular system, presomitic mesoderm and somites, branchial arches, and limb buds. These results suggest that multiple receptor systems for LPA/S1P lysophospholipids may be functioning during organogenesis.
溶血磷脂(LPs),如溶血磷脂酸(LPA)和1-磷酸鞘氨醇(S1P),已知可介导多种生物学反应,包括细胞增殖、迁移和分化。为了更好地理解这些脂质在哺乳动物早期发育中的作用,我们将全胚胎原位杂交技术应用于E8.5至E12.5的小鼠胚胎。我们确定了以下属于G蛋白偶联受体(GPCR)家族的LP受体基因的表达模式:EDG1至EDG8(S1P1至S1P5和LPA1至LPA3)、LPA4(GPR23/P2Y9)和LPA5(GPR92)。我们发现,S1P/LPA受体基因在包括发育中的脑和心血管系统、前体节中胚层和体节、鳃弓和肢芽在内的各种器官原基中表现出重叠的表达模式。这些结果表明,LPA/S1P溶血磷脂的多个受体系统可能在器官发生过程中发挥作用。