Cahill A L, Eertmoed A L, Mangoura D, Perlman R L
Department of Pediatrics, University of Chicago, IL 60637, USA.
J Neurochem. 1996 Sep;67(3):1217-24. doi: 10.1046/j.1471-4159.1996.67031217.x.
Chromaffin cells were isolated from bovine adrenal glands and fractionated into two distinct subpopulations by density gradient centrifugation on Percoll. Cells in the more dense fraction stored epinephrine (E) as their predominant catecholamine (81% of total catecholamines), contained high levels of phenylethanolamine N-methyltransferase (PNMT) activity, and exhibited intense PNMT immunoreactivity. This population of chromaffin cells was termed the E-rich cell population. Cells in the less dense fraction, the norepinephrine (NE)-rich cell population, stored predominantly NE (75% of total catecholamines). Although the NE-rich cells had only 3% as much PNMT activity as did the E-rich cells, 20% of the NE-rich cells were PNMT immunoreactive. This suggested that the PNMT-positive cells in the NE-rich cell cultures contained less PNMT per cell than did E-rich cells and may not be typical adrenergic cells. The regulation of PNMT mRNA levels and PNMT activity in primary cultures of E-rich and NE-rich cells was compared. At the time the cells were isolated, PNMT mRNA levels in NE-rich cells were approximately 20% of those in E-rich cells; within 48 h in culture, PNMT mRNA in both populations declined to almost undetectable levels. Treatment with dexamethasone increased PNMT mRNA levels and PNMT activity in both populations. In E-rich cells, dexamethasone restored PNMT mRNA to the level seen in freshly isolated cells and increased PNMT activity twofold. In NE-rich cells, dexamethasone increased PNMT mRNA to levels twice those found in freshly isolated cells and increased PNMT activity sixfold. Cycloheximide blocked the effects of dexamethasone on PNMT mRNA expression in NE-rich cells but had little effect in E-rich cells. Angiotensin II, forskolin, and phorbol 12,13-dibutyrate elicited large increases in PNMT mRNA levels in E-rich cells but had no effect in NE-rich cells. Our data suggest that PNMT expression is regulated differently in the two chromaffin cell subpopulations.
从牛肾上腺中分离出嗜铬细胞,并通过在Percoll上进行密度梯度离心将其分为两个不同的亚群。密度较大部分的细胞以肾上腺素(E)作为其主要儿茶酚胺储存(占总儿茶酚胺的81%),含有高水平的苯乙醇胺N-甲基转移酶(PNMT)活性,并表现出强烈的PNMT免疫反应性。这群嗜铬细胞被称为富含E的细胞群。密度较小部分的细胞,即富含去甲肾上腺素(NE)的细胞群,主要储存NE(占总儿茶酚胺的75%)。尽管富含NE的细胞的PNMT活性仅为富含E的细胞的3%,但20%的富含NE的细胞具有PNMT免疫反应性。这表明富含NE的细胞培养物中PNMT阳性细胞每细胞所含的PNMT比富含E的细胞少,可能不是典型的肾上腺素能细胞。比较了富含E和富含NE的细胞原代培养物中PNMT mRNA水平和PNMT活性的调节。在细胞分离时,富含NE的细胞中的PNMT mRNA水平约为富含E的细胞中的20%;在培养48小时内,两个群体中的PNMT mRNA均下降到几乎无法检测的水平。地塞米松处理增加了两个群体中的PNMT mRNA水平和PNMT活性。在富含E的细胞中,地塞米松将PNMT mRNA恢复到新鲜分离细胞中的水平,并使PNMT活性增加两倍。在富含NE的细胞中,地塞米松将PNMT mRNA增加到新鲜分离细胞中发现水平的两倍,并使PNMT活性增加六倍。放线菌酮阻断了地塞米松对富含NE的细胞中PNMT mRNA表达的影响,但对富含E的细胞影响很小。血管紧张素II、福斯可林和佛波醇12,13-二丁酸酯引起富含E的细胞中PNMT mRNA水平大幅增加,但对富含NE的细胞没有影响。我们的数据表明,PNMT表达在两个嗜铬细胞亚群中的调节方式不同。