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Conversion of n-3 polyunsaturated fatty acids(PUFAs) and incorporation of docosahexaenoic acid(DHA) in cultured neural cells

机译:n-3多不饱和脂肪酸(PUFAs)的转化和二十二碳六烯酸(DHA)在培养的神经细胞中的掺入

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Docosahexaenoic acid(DHA,22:6n-3)in membrane phospholipids originates from dietary intake of preformed DHA and from conversion of its essential precursor alpha-linolenic acid(ALA,7 8:3n-3).Cultured cells,especially nervous cells,are increasingly used to explore the uptake,metabolism and gene transcription effects of n-3 fatty acids,raising the question of the specific metabolic fate of different fatty acids and of the physiological relevance of their concentrations in the culture medium.This paper reports experimental data that 1)compare the dose-dependent incorporation of preformed DHA into the ethanolamine phosphoglycerolipids(EPC)of neural and cerebral endothelial cells in culture with that of the developing rat brain,2)evaluate the pathway of DHA synthesis from ALA,eicosapentaenoic acid(EPA,20:5n-3)or n-3 docosapentaenoic acid(DPA,22:5n-3)in a model of neuronal cells,theSHSYSY human neuroblastoma cells,and 3)characterize in these cells the mRNA expression profile of genes involved in the fatty acid metabolism.The incorporation of preformed DHA in EPC followed,both in vivo and in vitro,a dose-response curve from which two parameters were drawn:the DHAmax,i.e.the plateau-value of the linearized dose-response curve(expressed in weight % of total fatty acids),and the DHA5 0,the concentration of DHA in the diet or in the culture medium corresponding to an incorporation of DHA in EPC equal to one-half the DHAmax.The ratio of DHAmax to DHA50 reflects the propensity(so-called the 'avidity' for DHA)of cells or tissues to incorporate the exogenous DHA.The DHAmax and the DHAmax/DHASO ratio values of SH-SY5Y cells and of rat brain endothelial cells in culture were compared to those of the frontal cortex and hippocampus of rats chronically deficient in n-3 fatty acids and supplemented with preformed DHA.The same DHAmax/DHASO ratio values were found in SH-SYS Y(5.2)cells and in rat brain areas(5.1-5.7)when the DHA doses were expressed in mu mol DHA/liter of culture medium and in mu mol DHA/10 g diet,respectively.The SH-SY5Y cells were able to produce neoformed EPA,DPA and DHA from supplemental ALA.The incorporation of neoformed EPA and DPA in EPC followed a dose-response saturating curve,while that of DHA was bell-shaped.The different pattern of neoformed DPA and neoformed DHA suggests that the conversion pathway was limited at the terminal step of DHA synthesis.The mRNA profile showed that two enzymes of the peroxisomal fi-oxidation system,the L-and D-bifunctional proteins,were expressed at lower levels than those of the endoplasmic reticulum pathway(DELTA 6-desaturase).These data show that incorporation of preformed DHA in cultured neuroblastoma cells match physiological values,indicating that DHA uptake,acyl-CoA activation,and phospholipid acyltransferases are active.However,the synthesis and incorporation of newly formed DHA in SH-SY5Y cells responds to a critical concentration-window of precursors which could originate from the low basal expression level of peroxisomal enzymes.
机译:膜磷脂中的二十二碳六烯酸(DHA,22:6n-3)来源于膳食中预先形成的DHA的摄入及其必需的前体α-亚麻酸(ALA,7 8:3n-3)的转化。培养的细胞,尤其是神经细胞,越来越多地被用于探索n-3脂肪酸的吸收,代谢和基因转录效应,提出了不同脂肪酸的具体代谢命运以及其在培养基中浓度的生理相关性的问题。 (1)将预先形成的DHA与发育中的大鼠大脑的神经和大脑内皮细胞的乙醇胺磷酸甘油脂(EPC)的剂量依赖性掺入进行比较; 2)评价ALA,二十碳五烯酸(EPA)合成DHA的途径,20:5n-3)或n-3二十二碳五烯酸(DPA,22:5n-3)在神经元细胞模型,SHSYSY人成神经细胞瘤细胞模型中的行为,以及3)在这些细胞中表征所涉及基因的mRNA表达谱在体内和体外均遵循预先形成的DHA在EPC中的掺入量-剂量曲线,从中得出两个参数:DHAmax,即线性化剂量-反应曲线的平稳值( DHA5为0,DHA在饮食或培养基中的浓度相当于DHA在EPC中的含量等于DHAmax的一半.DHAmax与DHA50的比值反映了将细胞或组织掺入外源DHA的倾向(所谓的DHA亲和力)与培养的SH-SY5Y细胞和大鼠脑内皮细胞的DHAmax和DHAmax / DHASO比值进行比较长期缺乏n-3脂肪酸并补充预先形成的DHA的大鼠的额叶皮层和海马区。当SH-SYS Y(5.2)细胞和大鼠脑区域(5.1-5.7)时,发现相同的DHAmax / DHASO比值DHA剂量以μmol DHA /升培养基和SH-SY5Y细胞分别能够以μmol DHA / 10 g的饮食量从补充的ALA中产生新形成的EPA,DPA和DHA.EPC中新形成的EPA和DPA的掺入遵循剂量-反应饱和曲线,而DHA是钟形的。新形成的DPA和新形成的DHA的不同模式表明,转化途径在DHA合成的最终步骤受到限制。mRNA图谱显示过氧化物酶体氧化系统的两​​种酶L和D -双功能蛋白的表达水平低于内质网途径(DELTA 6-去饱和酶)的表达。这些数据表明,在培养的成神经母细胞瘤细胞中掺入预先形成的DHA符合生理值,表明DHA摄取,酰基辅酶A活化和磷脂酰基转移酶是有活性的。但是,SH-SY5Y细胞中新形成的DHA的合成和掺入反应了可能源自低基础表达的前体的临界浓度窗口。一过氧化物酶体酶。

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