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Expression profiling of genes regulated by sphingosine kinase1 signaling in a murine model of hyperoxia induced neonatal bronchopulmonary dysplasia

机译:鞘氨醇激酶1信号调节的基因在高氧诱导的新生支气管肺发育不良的小鼠模型中的表达谱

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摘要

BackgroundSphingosine- 1-Phosphate (S1P) is a bioactive lipid and an intracellular as well as an extracellular signaling molecule. S1P ligand specifically binds to five related cell surface G-protein-coupled receptors (S1P1-5). S1P levels are tightly regulated by its synthesis catalyzed by sphingosine kinases (SphKs) 1 & 2 and catabolism by S1P phosphatases, lipid phosphate phosphatases and S1P lyase. We previously reported that knock down of SphK1 (Sphk1 −/−) in a neonatal mouse BPD model conferred significant protection against hyperoxia induced lung injury. To better understand the underlying molecular mechanisms, genome-wide gene expression profiling was performed on mouse lung tissue using Affymetrix MoGene 2.0 array.
机译:背景鞘氨醇-1-磷酸酯(S1P)是一种生物活性脂质,是一种细胞内以及细胞外信号分子。 S1P配体与五个相关的细胞表面G蛋白偶联受体(S1P1-5)特异性结合。 S1P水平受鞘氨醇激酶(SphKs)1和2催化的合成以及S1P磷酸酶,脂质磷酸磷酸酶和S1P裂解酶的分解代谢的严格调控。我们以前曾报道过,在新生小鼠BPD模型中,SphK1(Sphk1 -/-)的敲除可提供对高氧诱导的肺损伤的显着保护作用。为了更好地理解潜在的分子机制,使用Affymetrix MoGene 2.0阵列在小鼠肺组织上进行了全基因组基因表达谱分析。

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