首页> 美国卫生研究院文献>The Journal of Neuroscience >Non-neuronal cell-conditioned medium regulates muscarinic receptor expression in cultured sympathetic neurons
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Non-neuronal cell-conditioned medium regulates muscarinic receptor expression in cultured sympathetic neurons

机译:非神经元细胞条件培养基调节培养的交感神经元中毒蕈碱受体的表达

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摘要

Regulation of muscarinic receptor expression was examined in cultured sympathetic neurons of the neonatal rat superior cervical ganglion. Receptor concentration was determined by measuring binding of the muscarinic antagonist 1-quinuclidinyl[phenyl-4-3H] benzilate (3H-QNB). 3H-QNB bound to one apparent class of noninteracting sites on sympathetic neuron membranes with a Kd of 28.9 pM and a Bmax of 2.91 pmol/mg protein. Binding increased as a linear function of tissue protein and was saturable. The number of receptors per milligram protein increased approximately 6-fold during 16 d of culture, and receptor numbers were down-regulated by treatment with the agonist carbachol. These observations suggested that measurement of 3H-QNB binding would provide a reliable estimate of muscarinic receptor number on cultured sympathetic neurons. To determine whether nonneuronal cells produce soluble factors that influence muscarinic receptor expression, the effects of treatment with rat fibroblast-conditioned medium (RFCM) were examined. Exposure of sympathetic neurons to 50% RFCM resulted in a 57% decrease in muscarinic receptor numbers without a change in the apparent Kd. The decrease in 3H-QNB binding in response to RFCM was dose-related, with a minimum dose of 15% RFCM required to observe a significant effect. In contrast to the carbachol-induced down- regulation, the reduction in binding after RFCM treatment was not prevented by atropine, indicating that the effect was not mediated by acetylcholine stimulation of muscarinic receptors. Binding of 125I- alpha-bungarotoxin, which labels a nonfunctional membrane site distinct from nicotinic receptors, was not altered by treatment with RFCM, indicating the selectivity of the change in membrane muscarinic receptors.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:在新生大鼠上颈神经节的交感神经元中检测毒蕈碱受体表达的调节。受体浓度通过测量毒蕈碱拮抗剂1-奎宁环基[苯基-4-3H]苯甲酸酯(3H-QNB)的结合来确定。 3H-QNB以28.9 pM的Kd和2.91 pmol / mg蛋白质的Bmax结合到交感神经元膜上的一类明显的非相互作用位点。结合作为组织蛋白的线性功能而增加,并且是饱和的。在培养的16天中,每毫克蛋白质的受体数量增加了约6倍,并且通过激动剂卡巴胆碱的处理下调了受体数量。这些观察结果表明,对3H-QNB结合的测量将提供培养的交感神经元上毒蕈碱受体数目的可靠估计。为了确定非神经元细胞是否产生影响毒蕈碱受体表达的可溶性因子,检查了大鼠成纤维细胞条件培养基(RFCM)的治疗效果。交感神经元暴露于50%RFCM可使毒蕈碱受体数量减少57%,而表观Kd不变。对RFCM的响应3H-QNB结合的减少与剂量有关,观察到显着效果所需的最低剂量为15%RFCM。与卡巴胆碱引起的下调相反,RFCM治疗后结合的减少并未被阿托品所阻止,这表明该作用不是由毒蕈碱受体的乙酰胆碱刺激介导的。用RFCM处理并没有改变125I-α-真菌毒素的结合,该结合标记了一个不同于烟碱样受体的非功能性膜部位,表明膜毒蕈碱受体变化的选择性。(摘要摘录于250字)

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