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首页> 外文期刊>Melanoma research >Cytoplasmic Ca~(2+) concentration changes evoked by muscarinic cholinergic stimulation in primary and metastatic melanoma cell lines
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Cytoplasmic Ca~(2+) concentration changes evoked by muscarinic cholinergic stimulation in primary and metastatic melanoma cell lines

机译:毒蕈碱胆碱能刺激引起的原发性和转移性黑素瘤细胞株的细胞质Ca〜(2+)浓度变化

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摘要

Experiments were performed to explore differences between cultured primary and metastatic melanoma cell lines in their muscarinic acetylcholine receptor-mediated intracellular Ca~(2+) signalization. The expression of type 1 and type 3 muscarinic receptors was detected and compared at the protein level using both immunocytochemistry and semiquantitative western blotting. The functionality of muscarinic receptors was tested by applying carbamylcholine (CCh; 1 mmol/l) and by recording the associated increases in cytoplasmic Ca~(2+) using Ca~(2+) imaging with the application of the Ca~(2+) indicator dye, fluo-4. These data indicate that the expression levels of the receptor proteins were not significantly different in the metastatic (HT199, HT168-M1) and the primary (WM35) cell lines. Although Ca~(2+) transients were evoked in all the three cell lines by CCh, the proportion of the CCh-positive cells was smaller amongst the WM35 cells. The Ca~(2+) transients could be effectively blocked by atropine (0.1 mmol/l). The time courses of the Ca~(2+) transients were highly variable, and in some instances they showed a late (plateau-like) component whose presence crucially depended on the influx of extracellular Ca~(2+) . When the extracellular Ca~(2+) concentration was reduced, the duration of the CCh-evoked transients was considerably decreased; a phenomenon that was more pronounced in the metastatic cell lines. Although there are no fundamental differences in the muscarinic receptor-mediated Ca~(2+) signalization of the primary and metastatic cell lines, the quantitative differences showed in this study may partially explain the increased malignancy and migratory potential of the metastatic cells.
机译:进行实验以探索经培养的原发性和转移性黑素瘤细胞系在毒蕈碱乙酰胆碱受体介导的细胞内Ca〜(2+)信号转导中的差异。使用免疫细胞化学和半定量蛋白质印迹法检测并比较了1型和3型毒蕈碱受体的表达。通过应用氨甲酰胆碱(CCh; 1 mmol / l)并通过使用Ca〜(2+)成像使用Ca〜(2+)成像来记录胞质Ca〜(2+)的相关增加,来测试毒蕈碱受体的功能。 )指示染料,fluo-4。这些数据表明,在转移性(HT199,HT168-M1)和原代(WM35)细胞系中,受体蛋白的表达水平没有显着差异。尽管通过CCh在所有三个细胞系中引起Ca〜(2+)瞬变,但是在WM35细胞中CCh阳性细胞的比例较小。 Ca〜(2+)瞬变可被阿托品(0.1 mmol / l)有效阻断。 Ca〜(2+)瞬变的时间过程是高度可变的,在某些情况下,它们显示出晚期(高原样)成分,其存在关键取决于细胞外Ca〜(2+)的流入。当细胞外Ca〜(2+)浓度降低时,CCh诱发的瞬变的持续时间显着减少。这种现象在转移细胞系中更为明显。尽管在毒蕈碱受体介导的原代和转移细胞系的Ca〜(2+)信号转导方面没有根本差异,但本研究显示的定量差异可能部分解释了转移细胞的恶性和迁移潜力增加。

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