Apolipoprotein D modulates arachidonic acid signaling in cultured cells: implications for psychiatric disorders

Elizabeth A Thomas, Roshni C George, J.Gregor Sutcliffe
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Abstract

Deficiencies in arachidonic acid (AA) parameters have been reported in schizophrenic patients. AA is a primary binding ligand for apolipoprotein D (apoD), which is increased in response to antipsychotic drug treatment and elevated in subjects with schizophrenia and bipolar disorder. In this study, we investigated whether apoD might modulate AA signaling/mobilization in cultured embryonic kidney (HEK) 293T cells. Immunofluorescent labeling revealed both cytosolic and membrane-bound expression of apoD protein in apoD-transfected cells. In cells expressing apoD, phorbal 12-myristate 13-acetate-induced AA release was inhibited compared to controls and membrane levels of AA were elevated, as indicated by the amount of AA maximally incorporated into membrane phospholipids. In addition, exogenous apoD added directly to the incubation media prevented cellular uptake of free [3H]AA. These results suggest that apoD acts to stabilize membrane-associated AA by preventing release and sequestering free AA in the cell. These actions of apoD may be beneficial to psychiatric patients.
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载脂蛋白D调节培养细胞中的花生四烯酸信号:对精神疾病的影响
花生四烯酸(AA)参数缺乏在精神分裂症患者中有报道。AA是载脂蛋白D (apoD)的主要结合配体,在抗精神病药物治疗中增加,在精神分裂症和双相情感障碍患者中升高。在本研究中,我们研究了apoD是否可能调节培养的胚胎肾(HEK) 293T细胞中的AA信号传导/动员。免疫荧光标记显示apoD转染细胞中apoD蛋白的胞质和膜结合表达。在表达apoD的细胞中,与对照组相比,12-肉豆蔻酸13-乙酸酯诱导的AA释放被抑制,AA的膜水平升高,这表明AA最大程度地融入膜磷脂中。此外,直接添加到培养培养基中的外源apoD阻止了细胞对游离[3H]AA的摄取。这些结果表明,apoD通过阻止释放和隔离细胞中的游离AA来稳定膜相关AA。apoD的这些作用可能对精神病患者有益。
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来源期刊
Prostaglandins, leukotrienes, and essential fatty acids
Prostaglandins, leukotrienes, and essential fatty acids Clinical Biochemistry, Endocrinology, Diabetes and Metabolism
CiteScore
5.30
自引率
0.00%
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0
审稿时长
64 days
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