Rogers S W, Mandelzys A, Deneris E S, Cooper E, Heinemann S
Department of Pharmacology, University of Colorado Health Sciences Center, Denver 80262.
J Neurosci. 1992 Dec;12(12):4611-23. doi: 10.1523/JNEUROSCI.12-12-04611.1992.
The expression of neuronal nicotinic ACh receptors (nAChRs) and the subunits that compose these receptors by PC12 cells exposed to NGF has been studied. The analysis of total RNA reveals that the neuronal nAChR subunits alpha 3, alpha S, beta 2, beta 3, and beta 4, but not alpha 2 and alpha 4, are expressed in our PC12 cells. Within 48 hr of adding NGF to cultures, the RNA corresponding to alpha 3, alpha 5, beta 3, and beta 4 is decreased, but the beta 2 RNA increases for up to 6 d after NGF treatment. To determine the influence of NGF treatment on subunit protein expression, subunit-specific antisera were prepared. Immunocytochemistry detected antigen for alpha 3, alpha 5, beta 2, beta 3, and beta 4 (but not alpha 2 and alpha 4) in both NGF-treated and nontreated PC12 cells. The expression of nAChR subunit proteins, as measured by direct binding of antibodies to PC12 cells, does not change subsequent to 6 d of treatment with NGF. Whole-cell recording of PC12 cells shows that both the individual cell current density and response to the agonist cytisine were not altered after 5-7 d in NGF. However, the number of cells exhibiting detectable ACh-induced currents doubled. These results indicate that NGF increases the number of PC12 cells expressing ACh-sensitive nAChR currents but the activation is not the result of altering the amounts of individual nAChR subunit proteins. These data, taken together with the decrease in most nAChR subunit RNAs (except beta 2), suggest that NGF regulation of nAChRs may be through a posttranscriptional mechanism.
研究了暴露于神经生长因子(NGF)的PC12细胞中神经元烟碱型乙酰胆碱受体(nAChRs)及其组成亚基的表达情况。总RNA分析显示,神经元nAChR亚基α3、α5、β2、β3和β4在我们的PC12细胞中有表达,但α2和α4没有表达。在向培养物中添加NGF后的48小时内,与α3、α5、β3和β4对应的RNA减少,但β2 RNA在NGF处理后长达6天增加。为了确定NGF处理对亚基蛋白表达的影响,制备了亚基特异性抗血清。免疫细胞化学在NGF处理和未处理的PC12细胞中均检测到α3、α5、β2、β3和β4(但不是α2和α4)的抗原。通过抗体与PC12细胞的直接结合测量,nAChR亚基蛋白的表达在NGF处理6天后没有变化。PC12细胞的全细胞记录显示,在NGF中培养5 - 7天后,单个细胞的电流密度和对激动剂氧化苦参碱的反应均未改变。然而,表现出可检测到的乙酰胆碱诱导电流的细胞数量增加了一倍。这些结果表明,NGF增加了表达对乙酰胆碱敏感的nAChR电流的PC12细胞数量,但这种激活不是单个nAChR亚基蛋白量改变的结果。这些数据与大多数nAChR亚基RNA(β2除外)的减少一起表明,NGF对nAChRs的调节可能是通过转录后机制。