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首页> 外文期刊>European Biophysics Journal >Influence of the whole-cell patch-clamp configuration on electrophysiological properties of the voltage-dependent sodium current expressed in MDA-MB-231 breast cancer cells
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Influence of the whole-cell patch-clamp configuration on electrophysiological properties of the voltage-dependent sodium current expressed in MDA-MB-231 breast cancer cells

机译:全细胞膜片钳配置对MDA-MB-231乳腺癌细胞中表达的电压依赖性钠电流的电生理特性的影响

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摘要

Voltage-gated ionic channels are known to be involved in oncogenesis. However, only a few studies describe the functional characteristics of these channels or the mechanisms by which they are involved in the proliferation and invasive processes. Breast cancer cells proliferate and migrate under the constant activation of growth factors, hormones, extracellular matrix interactions, etc. It would thus not be surprising if the activity of the ionic channels was modulated by intracellular regulation pathways such as kinases or phosphatases, which in turn can affect oncogenic properties. In the present study, we investigated some of the electrophysiological properties of the fast inward sodium current found in the breast cancer cell line MDA-MB-231 with two configurations of the patch-clamp technique. With perforated patch, a configuration which allows to keep the cytoplam intact, the mean current amplitude was lower, the relative conductance–voltage relationship was shifted to more positive potentials and the recovery from inactivation was accelerated when compared to ruptured patch, where the cytoplasm is dialysed by the intrapipette solution. There was no difference in availability–voltage (pseudo-steady-state inactivation) relationship and in time to peak of the current. These results suggest that regulation mechanisms, possibly involving kinases or phosphatases, are switched off when the cytoplasm is diluted. We propose that such a regulation can modulate the functioning of the channels even in the absence of membrane voltage changes, which in turn can affect oncogenic properties. This finding is of importance when evaluating the physiopathological role of ionic channel in cancer development.
机译:已知电压门控离子通道参与致癌作用。但是,只有少数研究描述了这些通道的功能特性或它们参与增殖和侵袭过程的机制。乳腺癌细胞在生长因子,激素,细胞外基质相互作用等的持续激活下增殖和迁移。因此,如果离子通道的活性受到细胞内调节途径(如激酶或磷酸酶)的调节,这就不足为奇了。会影响致癌特性。在本研究中,我们研究了使用膜片钳技术的两种配置在乳腺癌细胞系MDA-MB-231中发现的快速内向钠电流的一些电生理特性。与穿孔的贴片相比,穿孔的贴片可以保持细胞质完整,平均电流幅度更低,相对电导-电压关系转移到更多的正电位,与破裂的贴片相比,加速了从失活的恢复用移液器溶液透析。可用性-电压(伪稳态失活)关系以及达到电流峰值的时间没有差异。这些结果表明,稀释细胞质时可能会关闭可能涉及激酶或磷酸酶的调节机制。我们提出,即使在没有膜电压变化的情况下,这样的调节也可以调节通道的功能,这反过来又会影响致癌特性。当评估离子通道在癌症发展中的生理病理作用时,这一发现很重要。

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