Adrenergic differentiation potential in PC12 cells: Influence of sodium butyrate and dexamethasone

被引:24
作者
Ebert, SN [1 ]
Lindley, SE [1 ]
Bengoechea, TG [1 ]
Bain, D [1 ]
Wong, DL [1 ]
机构
[1] STANFORD UNIV,SCH MED,DEPT PSYCHIAT & BEHAV SCI,NANCY PRITZKER LAB DEV & MOL NEUROBIOL,STANFORD,CA 94305
来源
MOLECULAR BRAIN RESEARCH | 1997年 / 47卷 / 1-2期
关键词
phenylethanolamine N-methyltransferase (PNMT); adrenergic expression; transcriptional control; sodium butyrate; dexamethasone; synergistic activation;
D O I
10.1016/S0169-328X(97)00032-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The ability of sodium butyrate and dexamethasone to promote adrenergic differentiation in PC12 cells was examined using the gene encoding the epinephrine biosynthetic enzyme, phenylethanolamine N-methyltransferase (PNMT1), as a marker. Sodium butyrate and dexamethasone independently stimulated expression of PNMT mRNA in PC12 cells, and the combined action of these drugs led to synergistic activation of the PNMT gene. Despite the induction of the PNMT gene, epinephrine is not produced in these cells, in part due to the absence of a corresponding induction in PNMT enzymatic activity. Another contributing factor appears to be a reduction in the precursor catecholamines, norepinephrine and dopamine, in the presence of sodium butyrate. Thus, while sodium butyrate and dexamethasone can induce PNMT gene expression, treatment of PC12 cells with these drugs appears insufficient for full acquisition of the adrenergic phenotype. (C) 1997 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:24 / 30
页数:7
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