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不同的犬尿氨酸途径酶限制了各种人类细胞类型中喹啉酸的形成。

Different kynurenine pathway enzymes limit quinolinic acid formation by various human cell types.

作者信息

Heyes M P, Chen C Y, Major E O, Saito K

机构信息

Laboratory of Neurotoxicology, NIMH, Bethesda, MD 20892-1262, USA.

出版信息

Biochem J. 1997 Sep 1;326 ( Pt 2)(Pt 2):351-6. doi: 10.1042/bj3260351.

Abstract

Substantial increases in the tryptophan-kynurenine pathway metabolites, l-kynurenine and the neurotoxin quinolinic acid, occur in human brain, blood and systemic tissues during immune activation. Studies in vitro have shown that not all human cells are capable of synthesizing quinolinate. To investigate further the mechanisms that limit l-kynurenine and quinolinate production, the activities of kynurenine pathway enzymes and the ability of different human cells to convert pathway intermediates into quinolinate were compared. Stimulation with interferon gamma substantially increased indoleamine 2,3-dioxygenase activity and L-kynurenine production in primary peripheral blood macrophages and fetal brains (astrocytes and neurons), as well as cell lines derived from macrophage/monocytes (THP-1), U373MG astrocytoma, SKHEP1 liver and lung (MRC-9). High activities of kynurenine 3-hydroxylase, kynureninase or 3-hydroxyanthranilate 3,4-dioxygenase were found in interferon-gamma-stimulated macrophages, THP-1 cells and SKHEP1 cells, and these cells made large amounts of quinolinate when supplied with L-tryptophan, L-kynurenine, 3-hydroxykynurenine or 3-hydroxyanthranilate. Quinolinate production by human fetal brain cultures and U373MG cells was restricted by the low activities of kynurenine 3-hydroxylase, kynureninase and 3-hydroxyanthranilate 3,4-dioxygenase, and only small amounts of quinolinate were synthesized when cultures were supplied with L-tryptophan or 3-hydroxyanthranilate. In MRC-9 cells, quinolinate was produced only from 3-hydroxykynurenine and 3-hydroxyanthranilate, consistent with their low kynurenine 3-hydroxylase activity. The results are consistent with the notion that indoleamine 2,3-dioxygenase is an important regulatory enzyme in the production of L-kynurenine and quinolinate. Kynurenine 3-hydroxylase and, in some cells, kynureninase and 3-hydroxyanthranilate 3,4-dioxygenase are important determinants of whether a cell can make quinolinate.

摘要

在免疫激活过程中,人脑中的色氨酸 - 犬尿氨酸途径代谢产物、L - 犬尿氨酸和神经毒素喹啉酸在血液及全身组织中显著增加。体外研究表明,并非所有人类细胞都能合成喹啉酸。为进一步探究限制L - 犬尿氨酸和喹啉酸生成的机制,对犬尿氨酸途径中各种酶的活性以及不同人类细胞将途径中间产物转化为喹啉酸的能力进行了比较。用γ - 干扰素刺激可显著提高原代外周血巨噬细胞和胎儿脑(星形胶质细胞和神经元)以及源自巨噬细胞/单核细胞的细胞系(THP - 1)、U373MG星形细胞瘤、SKHEP1肝癌细胞和肺细胞(MRC - 9)中的吲哚胺2,3 - 双加氧酶活性及L - 犬尿氨酸生成量。在γ - 干扰素刺激的巨噬细胞、THP - 1细胞和SKHEP1细胞中发现了较高活性的犬尿氨酸3 - 羟化酶、犬尿氨酸酶或3 - 羟基邻氨基苯甲酸3,4 - 双加氧酶,当向这些细胞提供L - 色氨酸、L - 犬尿氨酸、3 - 羟基犬尿氨酸或3 - 羟基邻氨基苯甲酸时,它们会大量生成喹啉酸。人胎儿脑培养物和U373MG细胞中喹啉酸的生成受到犬尿氨酸3 - 羟化酶、犬尿氨酸酶和3 - 羟基邻氨基苯甲酸3,4 - 双加氧酶低活性的限制,当向培养物中提供L - 色氨酸或3 - 羟基邻氨基苯甲酸时,仅合成少量喹啉酸。在MRC - 9细胞中,喹啉酸仅由3 - 羟基犬尿氨酸和3 - 羟基邻氨基苯甲酸生成,这与其犬尿氨酸3 - 羟化酶活性较低一致。这些结果与吲哚胺2,3 - 双加氧酶是L - 犬尿氨酸和喹啉酸生成过程中的一种重要调节酶这一观点相符。犬尿氨酸3 - 羟化酶以及在某些细胞中的犬尿氨酸酶和3 - 羟基邻氨基苯甲酸3,4 - 双加氧酶是细胞能否生成喹啉酸的重要决定因素。

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