Nelson D H, Murray D K
Proc Natl Acad Sci U S A. 1982 Nov;79(21):6690-2. doi: 10.1073/pnas.79.21.6690.
An acute increase in the sphingomyelin content of a plasma membrane-enriched fraction of 3T3-L1 cells was produced by incubation of the cells with 0.1 microM dexamethasone for 4 hr. Dexamethasone also stimulated the activity of the pathway of sphingomyelin synthesis by utilizing the phosphorylcholine of phosphatidylcholine as a donor to ceramide to synthesize the phospholipid (phosphatidylcholine:ceramide cholinephosphotransferase). Dexamethasone-stimulated increase in the utilization of 14C-labeled choline of phosphatidylcholine for the synthesis of sphingomyelin was inhibited by the addition of cycloheximide to the incubation. Therefore, it appears that corticosteroid stimulation of new protein synthesis was required to produce the effect. An increase in the enzymatic pathway by 83% and of the sphingomyelin content of the plasma membrane-enriched fraction by 50% after incubation with dexamethasone for 4 hr demonstrates the rapidity with which the hormone can produce considerable remodeling of the membrane. The increase in the synthetic pathway in the plasma membrane-enriched fraction was sufficient to account for the measured increase in sphingomyelin. It appears likely that the large increase in membrane sphingomyelin could contribute significantly to the many demonstrated effects of corticosteroids upon membrane processes, including transport, receptors, and enzymatic activity.
将3T3-L1细胞用0.1微摩尔地塞米松孵育4小时,可使富含质膜的部分中鞘磷脂含量急剧增加。地塞米松还通过利用磷脂酰胆碱的磷酸胆碱作为神经酰胺的供体来合成磷脂(磷脂酰胆碱:神经酰胺胆碱磷酸转移酶),从而刺激鞘磷脂合成途径的活性。向孵育体系中添加环己酰亚胺可抑制地塞米松刺激的磷脂酰胆碱中14C标记胆碱用于鞘磷脂合成的利用率增加。因此,似乎需要皮质类固醇刺激新的蛋白质合成才能产生这种效应。用地塞米松孵育4小时后,酶促途径增加83%,富含质膜部分的鞘磷脂含量增加50%,这表明该激素能迅速对膜进行相当程度的重塑。富含质膜部分合成途径的增加足以解释所测得的鞘磷脂增加。膜鞘磷脂的大幅增加很可能对皮质类固醇在膜过程中的许多已证实的作用有显著贡献,包括转运、受体和酶活性。