Karl M, Saviolakis G A, Gravanis A, Chrousos G P, Margioris A N
Developmental Endocrinology Branch, NICHD, National Institutes of Health, Bethesda, MD 20892, USA.
Regul Pept. 1996 Feb 22;61(2):99-104. doi: 10.1016/0167-0115(95)00144-1.
Most adrenal chromaffin cells synthesize opioids derived from proenkephalin but not from prodynorphin. However, human pheochromocytomas and the PC12 rat pheochromocytoma cell line synthesize dynorphins. The aim of this study was to confirm the presence of the authentic prodynorphin transcript and its dynorphin product in PC12 cells. We have found that the sequence of a 458 bp cDNA fragment derived from RT-PCR amplification of total PC12 RNA was in complete accordance with the published sequence of the equivalent region of the prodynorphin gene. It encodes the potent endogenous kappa opioid agonists alpha-neo-endorphin, dynorphin A and dynorphin B. Furthermore, immunoaffinity-purified PC12 cell extracts were subjected to RP-HPLC. Most of its IR-dynorphin eluted on a peak exhibiting the retention time of similarly treated rat anterior pituitary. The expression of the prodynorphin gene in pheochromocytomas can be explained as either the result of (a) the process of dedifferentiation of chromaffin cells to pheochromocytoma which may thus cause the expression of a previously unexpressed prodynorphin or that (b) those pheochromocytomas expressing the prodynorphin gene derive from the few, centrally located chromaffin cells, which express this gene even under normal conditions.
大多数肾上腺嗜铬细胞合成源自脑啡肽原而非强啡肽原的阿片样物质。然而,人嗜铬细胞瘤和PC12大鼠嗜铬细胞瘤细胞系合成强啡肽。本研究的目的是证实PC12细胞中存在真实的强啡肽原转录本及其强啡肽产物。我们发现,通过对PC12总RNA进行RT-PCR扩增得到的一个458 bp cDNA片段的序列与已发表的强啡肽原基因等效区域的序列完全一致。它编码强效内源性κ阿片样激动剂α-新内啡肽、强啡肽A和强啡肽B。此外,对免疫亲和纯化的PC12细胞提取物进行反相高效液相色谱分析。其大部分免疫反应性强啡肽在一个峰上洗脱,该峰的保留时间与同样处理的大鼠垂体前叶相似。嗜铬细胞瘤中强啡肽原基因的表达可以解释为以下两种情况之一:(a)嗜铬细胞向嗜铬细胞瘤去分化的过程,这可能导致先前未表达的强啡肽原的表达;或者(b)那些表达强啡肽原基因的嗜铬细胞瘤源自少数位于中央的嗜铬细胞,这些细胞即使在正常条件下也表达该基因。