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首页> 外文期刊>Neurochemical research >Involvement of lysophosphatidic acid, sphingosine 1-phosphate and ceramide 1-phosphate in the metabolization of phosphatidic acid by lipid phosphate phosphatases in bovine rod outer segments.
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Involvement of lysophosphatidic acid, sphingosine 1-phosphate and ceramide 1-phosphate in the metabolization of phosphatidic acid by lipid phosphate phosphatases in bovine rod outer segments.

机译:溶血磷脂酸,1-磷酸鞘氨醇和1-磷酸神经酰胺参与牛杆外段脂磷脂磷酸酶代谢磷脂酸的过程。

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摘要

The aim of the present research was to evaluate the generation of [2-3H]diacylglycerol ([2-3H]DAG) from [2-3H]-Phosphatidic acid ([2-3H]PA) by lipid phosphate phosphatases (LPPs) at different concentrations of lysophosphatidic acid (LPA), sphingosine 1-phosphate (S1P), and ceramide 1-phosphate (C1P) in purified ROS obtained from dark-adapted retinas (DROS) or light-adapted retinas (BLROS) as well as in ROS membrane preparations depleted of soluble and peripheral proteins. Western blot analysis revealed the presence of LPP3 exclusively in all membrane preparations. Immunoblots of entire ROS and depleted ROS did not show dark-light differences in LPP3 levels. LPPs activities were diminished by 53% in BLROS with respect to DROS. The major competitive effect on PA hydrolysis was exerted by LPA and S1P in DROS and by C1P in BLROS. LPPs activities in depleted ROS were similar to the activity observed in entire DROS and BLROS, respectively. LPA, S1P and C1P competed at different extent in depleted DROS and BLROS. Sphingosine and ceramide inhibited LPPs activities in entire and depleted DROS. Ceramide also inhibited LPPs activities in entire and in depleted BLROS. Our findings are indicative of a different degree of competition between PA and LPA, S1P and C1P by LPPs depending on the illumination state of the retina.
机译:本研究的目的是评估脂质磷酸磷酸酶(LPP)从[2-3H]-磷脂酸([2-3H] PA)生成[2-3H]二酰甘油([2-3H] DAG)从暗适应视网膜(DROS)或浅适应视网膜(BLROS)以及在ROS膜制剂中的可溶性蛋白和外周蛋白耗竭。蛋白质印迹分析表明,LPP3仅在所有膜制品中存在。整个ROS和耗尽的ROS的免疫印迹未显示LPP3水平的暗光差异。与DROS相比,BLROS中LPP的活性降低了53%。 DPA中的LPA和S1P以及BLROS中的C1P发挥了对PA水解的主要竞争作用。耗尽的ROS中的LPPs活性分别类似于整个DROS和BLROS中观察到的活性。 LPA,S1P和C1P在耗尽的DROS和BLROS中竞争程度不同。鞘氨醇和神经酰胺在整个和耗尽的DROS中抑制LPPs活性。神经酰胺还抑制整个和耗尽BLROS中LPP的活性。我们的发现表明,LPP根据肺的照射状态,在PA与LPA,S1P和C1P之间存在不同程度的竞争。

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