Induction of tyrosine hydroxylase expression by the transcription factor Pitx3

被引:40
作者
Messmer, Kirsten
Remington, Mary P.
Skidmore, Frank
Fishman, Paul S.
机构
[1] Univ Maryland, Sch Med, Dept Neurol, Baltimore, MD 21201 USA
[2] Univ Maryland, Sch Med, Dept Pharmacol & Expt Therapeut, Baltimore, MD 21201 USA
[3] Baltimore VA Med Ctr, Neurol Serv, Baltimore, MD USA
[4] Baltimore VA Med Ctr, Res Serv, Baltimore, MD USA
关键词
Pitx3; Nurr1; Parkinson's disease; embryonic stem cells; transcription factor;
D O I
10.1016/j.ijdevneu.2006.11.003
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Transcription factors are fate determining regulatory factors in dopaminergic neuronal development and differentiation. Among them, Nurrl is the most extensively studied, but the importance of Pitx3 has recently been appreciated. Over-expression of both factors has been utilized to enhance the dopaminergic differentiation of stem cells for transplantation into models of Parkinson's disease. Previous studies however have seen conflicting results regarding the induction of tyrosine hydroxylase expression and dopaminergic differentiation induced by over-expression of Pitx3. Here we show that over-expression of Pitx3 and Nurrl induced endogenous tyrosine hydroxylase expression as well as a tyrosine hydroxylase promoter-reporter construct in a human non-neuronal and mouse embryonic stem cell lines. Combined simultaneous expression of Nurrl and Pitx3 however did not lead to enhancement of tyrosine hydroxylase expression over that of either factor alone in either of the cell lines or with either method. These results suggest that other regulatory elements may also be involved in regulation of tyrosine hydroxylase expression. There was also a lack of a correlation between the expression levels of tyrosine hydroxylase with that of the transcription factor constructs. To yield a robust dopaminergic differentiation a combinatorial or successive treatment with different transcription factors may be more effective. (c) 2006 ISDN. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:29 / 37
页数:9
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