Synthesis of sphingomyelin by oligodendrocytes—how and where?

Jan P. Vos , M.Luisa Giudici , Petra van der Bijl , Matthijs Lopes-Cardozo
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引用次数: 4

Abstract

Sphingomyelin (SM) biosynthesis in cultured oligodendrocytes (OC) was evaluated: (i) with [14C] tracers (choline, ethanolamine, serine) to pinpoint the major metabolic routes; (ii) with fluorescent and truncated, radiolabeled ceramide analogs to determine the relative activities of SM-synthase in intra- and extra-Golgi compartments of OC. In contrast to a general contention in the literature that SM synthase is absent from the brain, our data show that (choline → CDP-choline → phosphatidylcholine (PC) → SM) is the major anabolic route with only a minor contribution to PC via methylation of phosphatidylethanolamine (PE). SM synthase activity was found to be equally divided between intra- and extra-Golgi compartments of OC. Moreover, significant SM-synthase activity was recovered in purified myelin preparations. Our results shed new light on the possible involvement of sphingolipid-derived mediators in myelination.

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少突胶质细胞合成鞘磷脂的途径和位置?
对培养的少突胶质细胞(OC)中鞘磷脂(SM)的生物合成进行评估:(i)用[14C]示踪剂(胆碱、乙醇胺、丝氨酸)确定主要代谢途径;(ii)用荧光和截断的、放射性标记的神经酰胺类似物来测定OC内部和外部高尔基区室中sm合酶的相对活性。与文献中普遍认为SM合成酶在大脑中不存在的观点相反,我们的数据显示(胆碱→cdp -胆碱→磷脂酰胆碱(PC)→SM)是主要的合成代谢途径,只有少量的PC通过磷脂酰乙醇胺(PE)甲基化而产生。SM合成酶活性在OC的高尔基区室和高尔基区室之间分布均匀。此外,在纯化的髓磷脂制剂中恢复了显著的sm合成酶活性。我们的结果为鞘脂衍生介质可能参与髓鞘形成提供了新的线索。
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