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一种可转移因子对培养的神经杂交细胞中镍偶联受体的异源上调,其表达以环磷酸腺苷依赖性、细胞特异性方式受到抑制。

Heterologous up-regulation of Ni-coupled receptors in cultured neural hybrid cells by a transferable factor, whose expression is inhibited in a cyclic AMP-dependent, cell-specific manner.

作者信息

Noronha-Blob L, Lowe V C, Kinnier W J, U'Prichard D C

机构信息

Nova Pharmaceutical Corporation, Baltimore, Maryland 21224.

出版信息

Mol Pharmacol. 1987 Nov;32(5):669-77.

PMID:2824982
Abstract

Opiate, muscarinic, and alpha 2-adrenergic receptors on NCB-20 and NG108-15 neuroblastoma hybrid cells were up-regulated by treatment of the cells with media (CM) conditioned by previous incubation with either cell type. NG cells treated with CM from both NCB and NG cells (NCB-CM or NG-CM) showed a 2-fold increase in opiate receptor density relative to untreated cells, with no change in ligand affinities. Opiate receptor density on NG cells was also enhanced approximately 2-fold by CM derived from dibutyryl cyclic AMP (dBc)-treated NG cells (NG-dBc-CM) but not by CM from dBc-treated NCB cells, (NCB-dBc-CM). The data suggest that a transferable factor that up-regulates NG opiate receptors is produced by untreated NCB and NG cells, and is either suppressed or inactivated in dBc-treated NCB cells but not in dBc-treated NG cells. Muscarinic and alpha 2-adrenergic receptor site densities on NG cells were also up-regulated approximately 2-fold by NCB-CM but not by NCB-dBc-CM. Thus, the factor induced a heterologous up-regulation of three classes of Ni-coupled receptor sites on NG cells. The up-regulating factor, which accumulates in the media with time in culture, also acts directly upon cells that are synthesizing/secreting the factor (auto-up-regulation). Thus, opiate receptor density increased in untreated NCB and NG cells, as well as in dBc-treated NG cells, as a function of cell growth, but did not increase on dBc-treated NCB cells. Coupling of NG opiate receptors to adenylate cyclase (AC) was not altered by CM. Prostaglandin E1-stimulated AC was maximally inhibited by (approximately 40%) by 1 microM DADLE with the same efficiency and potency in untreated as in CM-treated NG cell membranes. Furthermore, NCB-dBc-CM which does not induce NG opiate receptor up-regulation and NCB-CM, which does induce it, had no effect on inhibition of AC by DADLE. The up-regulating factor is a relatively small molecule (molecular weight = 3000-6000), whose synthesis and/or secretion is suppressed by dBc in NCB but not in the related NG hybrid. This unique cell specificity may be exploited to study the mechanism of opiate, muscarinic, and alpha 2-adrenergic receptor expression and turnover in cultured neural hybrid cells.

摘要

用经先前与任何一种细胞类型共同孵育处理过的培养基(CM)处理NCB - 20和NG108 - 15神经母细胞瘤杂交细胞,可使阿片受体、毒蕈碱受体和α2 - 肾上腺素能受体上调。用来自NCB细胞和NG细胞的CM(NCB - CM或NG - CM)处理的NG细胞,相对于未处理的细胞,阿片受体密度增加了2倍,配体亲和力无变化。来自二丁酰环磷腺苷(dBc)处理的NG细胞的CM(NG - dBc - CM)也使NG细胞上的阿片受体密度提高了约2倍,但来自dBc处理的NCB细胞的CM(NCB - dBc - CM)则没有这种作用。数据表明,未处理的NCB细胞和NG细胞产生一种可转移的上调NG阿片受体的因子,该因子在dBc处理的NCB细胞中被抑制或失活,但在dBc处理的NG细胞中未被抑制或失活。NG细胞上的毒蕈碱受体和α2 - 肾上腺素能受体位点密度也被NCB - CM上调了约2倍,但未被NCB - dBc - CM上调。因此,该因子诱导了NG细胞上三类与Ni偶联的受体位点的异源上调。随着培养时间的推移在培养基中积累的上调因子,也直接作用于正在合成/分泌该因子的细胞(自上调)。因此,未处理的NCB细胞和NG细胞以及dBc处理的NG细胞中的阿片受体密度随细胞生长而增加,但在dBc处理的NCB细胞中未增加。CM未改变NG阿片受体与腺苷酸环化酶(AC)的偶联。在未处理的和经CM处理的NG细胞膜中,1 microM DADLE对前列腺素E1刺激的AC的最大抑制作用(约40%)效率和效力相同。此外,不诱导NG阿片受体上调的NCB - dBc - CM和诱导上调的NCB - CM对DADLE抑制AC均无影响。上调因子是一种相对较小的分子(分子量 = 3000 - 6000),其合成和/或分泌在NCB细胞中被dBc抑制,但在相关的NG杂交细胞中未被抑制。这种独特的细胞特异性可用于研究培养的神经杂交细胞中阿片受体、毒蕈碱受体和α2 - 肾上腺素能受体的表达及周转机制。

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