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经二甲基亚砜或六亚甲基双乙酰胺诱导分化的Friend红白血病细胞以及用诱导剂处理的非诱导性克隆中醚键连接甘油磷脂的特征

Characteristics of ether-linked glycerophospholipids in Friend erythroleukaemia cells differentiated by dimethyl sulphoxide or hexamethylenebisacetamide and in non-inducible clones treated with the inducers.

作者信息

Fallani A, Arcangeli A, Ruggieri S

机构信息

Instituto di Patologia Generale dell'Università di Firenze, Italy.

出版信息

Biochem J. 1988 Oct 15;255(2):731-5.

Abstract

The present study deals with changes in ether-linked glycerophospholids which accompany differentiation of Friend erythroleukaemia (FEL) cells by dimethyl sulphoxide (DMSO) and hexamethylenebisacetamide (HMBA). We also tested clones of FEL cells non-inducible by DMSO or HMBA for ether-linked lipid changes not related to the differentiation process. FEL cells contained appreciable proportions of alkenylacyl and alkylacyl subfractions in phosphatidylethanolamine (PE) and phosphatidylcholine (PC). Compared with FEL cells, clones non-inducible by DMSO or HMBA had a greater amount of alkenylacyl PE associated with a lack of alkenylacyl PC. The differentiation of FEL cells by DMSO or HMBA was accompanied by a reduction of alkylacyl PE and PC. DMSO- and HMBA-differentiated FEL cells showed changes in alkenyl- and alkyl-chain profiles, some of which were also observed in non-inducible FEL cells treated with DMSO or HMBA.

摘要

本研究探讨了在二甲基亚砜(DMSO)和六亚甲基双乙酰胺(HMBA)诱导下,Friend红白血病(FEL)细胞分化过程中醚键连接的甘油磷脂的变化。我们还检测了对DMSO或HMBA无诱导反应的FEL细胞克隆中与分化过程无关的醚键连接脂质的变化。FEL细胞在磷脂酰乙醇胺(PE)和磷脂酰胆碱(PC)中含有相当比例的烯基酰基和烷基酰基亚组分。与FEL细胞相比,对DMSO或HMBA无诱导反应的克隆中烯基酰基PE含量更高,且缺乏烯基酰基PC。DMSO或HMBA诱导FEL细胞分化伴随着烷基酰基PE和PC的减少。经DMSO和HMBA诱导分化的FEL细胞在烯基链和烷基链谱上出现了变化,其中一些变化在用DMSO或HMBA处理的无诱导反应的FEL细胞中也有观察到。

相似文献

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Lipid changes associated with erythroid differentiation of Friend erythroleukemia cells.
Toxicol Pathol. 1987;15(2):170-7. doi: 10.1177/019262338701500207.

本文引用的文献

4
Changes in phospholipid and ganglioside during differentiation of mouse myeloid leukemia cells.
Biochem Biophys Res Commun. 1980 Nov 28;97(2):452-62. doi: 10.1016/0006-291x(80)90285-5.

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