6R-Tetrahydrobiopterin induces dopamine synthesis in a human neuroblastoma cell line, LA-N-1 - A cellular model of Dopa-responsive dystonia

被引:2
|
作者
Zuddas, A
Mancosu, C
Lilliu, V
Sorrentino, G
di Porzio, U
Cianchetti, C
机构
[1] Univ Cagliari, Dept Neurosci, I-09124 Cagliari, Italy
[2] Univ Naples Parthenope, Fac Motor Sci, Naples, Italy
[3] CNR, Int Inst Genet & Biophys, I-80125 Naples, Italy
关键词
D O I
10.1016/S0006-8993(02)02694-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Dopa-responsive dystonia (DRD) is an extrapyramidal disorder caused by deficit of 5,6,7,8-tetrahydrobiopterin (BH4), cofactor for tyrosine hydroxylase (TH). In these patients the nigrostriatal dopaminergic neurons normally express TH and the cellular machinery for the dopamine uptake. LA-N-1 is a human neuroblastoma cell line expressing tyrosine hydroxylase. Here we show that LA-N-1 cells are able to take up exogenous dopamine (DA) by an high-affinity mechanism; significant amounts of serotonin and its metabolite 5HIAA, but neither DA nor its metabolites, DOPAC and HVA, could be measured in the cell culture homogenate. 5,6,7,8-Tetrahydrobiopterin, cofactor for both tyrosine and tryptophan hydroxylases, is able to activate dopamine synthesis and also decreases the content of 5HIAA by 50%, indicating that LA-N-1 might be a useful model for studying dopamine-serotonin interaction in cultured cells and the neuronal mechanism of DRD. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:257 / 262
页数:6
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