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磷脂及磷脂前体的轴突-髓鞘转运。通过轴突运输标记髓鞘磷酸肌醇。

Axon-myelin transfer of phospholipids and phospholipid precursors. Labeling of myelin phosphoinositides through axonal transport.

作者信息

Ledeen R W, Golly F, Haley J E

机构信息

Albert Einstein College of Medicine, Department of Neurology, Bronx, NY 10461.

出版信息

Mol Neurobiol. 1992 Summer-Fall;6(2-3):179-90. doi: 10.1007/BF02780551.

Abstract

Previous studies have provided evidence for axon-to-myelin transfer of intact lipids and lipid precursors for reutilization by myelin enzymes. Several of the lipid constituents of myelin showed significant contralateral/ipsilateral ratios of incorporated radioactivity, indicative of axonal origin, whereas proteins and certain other lipids did not participate in this transfer-reutilization process. The present study will examine the labeling of myelin phosphoinositides by this pathway. Both 32PO4 and [3H]inositol were injected monocularly into 7-9-wk-old rabbits and myelin was isolated 7 or 21 days later from pooled optic tracts and superior colliculi. In total lipids 32P counts of the isolated myelin samples showed significant contralateral/ipsilateral ratios as well as increasing magnitude of contralateral-ipsilateral differences during the time interval. Thin-layer chromatographic isolation of the myelin phosphoinositides revealed significant 32P-labeling of these species, with PIP and PIP2 showing time-related increases. This resembled the labeling pattern of the major phospholipids from rabbit optic system myelin in a previous study and suggested incorporation of axon-derived phosphate by myelin-associated enzymes. The 32P label in PI, on the other hand, remained constant between 7 and 21 days, suggesting transfer of intact lipid. This was supported by the labeling pattern with [3H]inositol, which also showed no increase over time for PI. These results suggest axon-myelin transfer of intact PI followed by myelin-localized incorporation of axon-derived phosphate groups into PIP and PIP2. The general topic of axon-myelin transfer of phospholipids and phospholipid precursors is reviewed.

摘要

先前的研究已经为完整脂质和脂质前体从轴突到髓磷脂的转移提供了证据,以便髓磷脂酶重新利用。髓磷脂的几种脂质成分显示出掺入放射性的显著对侧/同侧比率,表明其来源于轴突,而蛋白质和某些其他脂质不参与这种转移-再利用过程。本研究将通过该途径检测髓磷脂磷酸肌醇的标记情况。将32PO4和[3H]肌醇单眼注射到7-9周龄的兔子体内,7天或21天后从汇集的视束和上丘中分离出髓磷脂。在分离的髓磷脂样品的总脂质中,32P计数显示出显著的对侧/同侧比率,并且在该时间间隔内对侧-同侧差异的幅度不断增加。通过薄层层析分离髓磷脂磷酸肌醇,发现这些物质有显著的32P标记,磷脂酰肌醇-4-磷酸(PIP)和磷脂酰肌醇-4,5-二磷酸(PIP2)显示出与时间相关的增加。这与先前一项研究中兔视神经系统髓磷脂主要磷脂的标记模式相似,表明髓磷脂相关酶掺入了轴突来源的磷酸盐。另一方面,磷脂酰肌醇(PI)中的32P标记在7至21天之间保持恒定,表明完整脂质的转移。这得到了[3H]肌醇标记模式的支持,该模式也显示PI没有随时间增加。这些结果表明完整的PI从轴突转移到髓磷脂,随后髓磷脂将轴突来源的磷酸基团局部掺入PIP和PIP2。本文综述了磷脂和磷脂前体从轴突到髓磷脂转移的一般主题。

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