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神经母细胞瘤(N1E - 115、N2A)和嗜铬细胞瘤(PC - 12)克隆的四氢生物蝶呤和总生物蝶呤含量以及PC - 12细胞中儿茶酚胺合成对四氢生物蝶呤浓度的依赖性。

Tetrahydrobiopterin and total biopterin content of neuroblastoma (N1E-115, N2A) and pheochromocytoma (PC-12) clones and the dependence of catecholamine synthesis on tetrahydrobiopterin concentration in PC-12 cells.

作者信息

Bräutigam M, Dreesen R, Herken H

出版信息

J Neurochem. 1984 Feb;42(2):390-6. doi: 10.1111/j.1471-4159.1984.tb02690.x.

DOI:10.1111/j.1471-4159.1984.tb02690.x
PMID:6693875
Abstract

Tetrahydrobiopterin content was determined in several clonal cell lines by reversed-phase HPLC and subsequent electrochemical detection. The same chromatography system was used to determine the total biopterin (tetrahydrobiopterin and 7,8-dihydrobiopterin) by fluorescence detection. The catecholamine-producing clones neuroblastoma N1E-115 and pheochromocytoma PC-12 contained 96 and 60 ng tetrahydrobiopterin/mg protein, respectively. The corresponding amount for the neuroblastoma clone N2A was 36 ng/mg protein. The tetrahydrobiopterin content in C-6 glioma cells was below the limit of detection. The total biopterin is about 20% above the tetrahydrobiopterin content. Tetrahydrobiopterin and biopterin from the cells were identified by coelution with standard solutions and by potential-current relationship or emission and excitation spectra, respectively. Addition of 2,4-diamino-6-hydroxypyrimidine, an inhibitor of biopterin synthesis from GTP, to the culture medium of PC-12 cells resulted in a dose-dependent decrease of tetrahydrobiopterin and total biopterin content within 4 h, suggesting that the cells are capable of synthesising the biopterin which was found. A decrease in intracellular tetrahydrobiopterin levels by different concentrations of 2,4-diamino-6-hydroxypyrimidine reduces the cellular production of dihydroxyphenylalanine after inhibition of aromatic L-amino acid decarboxylase, indicating that the concentration of tetrahydrobiopterin might be a limiting factor for catecholamine synthesis in catecholamine-producing cells.

摘要

采用反相高效液相色谱法及后续电化学检测法测定了几种克隆细胞系中的四氢生物蝶呤含量。使用相同的色谱系统通过荧光检测法测定总生物蝶呤(四氢生物蝶呤和7,8 - 二氢生物蝶呤)。产生儿茶酚胺的克隆神经母细胞瘤N1E - 115和嗜铬细胞瘤PC - 12中四氢生物蝶呤含量分别为96和60 ng/ mg蛋白质。神经母细胞瘤克隆N2A的相应含量为36 ng/ mg蛋白质。C - 6胶质瘤细胞中的四氢生物蝶呤含量低于检测限。总生物蝶呤比四氢生物蝶呤含量高约20%。通过与标准溶液共洗脱以及分别通过电位 - 电流关系或发射和激发光谱鉴定了细胞中的四氢生物蝶呤和生物蝶呤。向PC - 12细胞培养基中添加2,4 - 二氨基 - 6 - 羟基嘧啶(一种从GTP合成生物蝶呤的抑制剂)导致4小时内四氢生物蝶呤和总生物蝶呤含量呈剂量依赖性下降,这表明细胞能够合成所发现的生物蝶呤。不同浓度的2,4 - 二氨基 - 6 - 羟基嘧啶降低细胞内四氢生物蝶呤水平后,在抑制芳香族L - 氨基酸脱羧酶后会减少二羟基苯丙氨酸的细胞生成,这表明四氢生物蝶呤的浓度可能是产生儿茶酚胺细胞中儿茶酚胺合成的限制因素。

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