Department of Pediatrics, University of Alabama School of Medicine, 1719 6th Ave. S., CIRC 252A, Birmingham, AL 35294, USA.
J Membr Biol. 2010 Oct;237(2-3):59-69. doi: 10.1007/s00232-010-9306-x. Epub 2010 Oct 8.
Medulloblastoma is a pediatric high-grade cerebellar malignancy derived from neuronal precursors. Although electrophysiologic characteristics of cerebellar granule neurons at all stages of cell development have been well described, such characterization has not been reported for medulloblastoma. In this study we attempt to characterize important electrophysiologic features of medulloblastoma that may distinguish it from the surrounding cerebellum. Using patient-derived cell lines and tumor tissues, we show that medulloblastoma cells have no inward Na+ current or transient K+ current involved in action potential generation and propagation, typically seen in granule neurons. Expression and function of calcium-activated, large-conductance K+ channels are diminished in medulloblastoma, judged by electrophysiology and Western analysis. The resting membrane potential of medulloblastoma cells in culture is quite depolarized compared to granule neurons. Interestingly, medulloblastoma cells express small, fast-inactivating calcium currents consistent with T-type calcium channels, but these channels are activated only from hyperpolarized potentials, which are unlikely to occur. Additionally, a background acid-sensitive K+ current is present with features characteristic of TASK1 or TASK3 channels, such as inhibition by ruthenium red. Western analysis confirms expression of TASK1 and TASK3. In describing the electrophysiologic characteristics of medulloblastoma, one can see features that resemble other high-grade malignancies as opposed to normal cerebellar granule neurons. This supports the notion that the malignant phenotype of medulloblastoma is characterized by unique changes in ion channel expression.
髓母细胞瘤是一种起源于神经元前体细胞的小儿高级别小脑恶性肿瘤。虽然小脑颗粒神经元在细胞发育的各个阶段的电生理特征已经得到了很好的描述,但髓母细胞瘤的特征尚未报道。在这项研究中,我们试图描述髓母细胞瘤的重要电生理特征,这些特征可能使其与周围小脑区分开来。使用患者来源的细胞系和肿瘤组织,我们表明髓母细胞瘤细胞没有内向钠电流或与动作电位产生和传播有关的瞬时钾电流,这在颗粒神经元中通常可见。钙激活的大电导钾通道的表达和功能在髓母细胞瘤中减少,通过电生理学和 Western 分析判断。与颗粒神经元相比,培养中的髓母细胞瘤细胞的静息膜电位相当去极化。有趣的是,髓母细胞瘤细胞表达小的、快速失活的钙电流,与 T 型钙通道一致,但这些通道仅在超极化电位下被激活,这是不太可能发生的。此外,存在背景酸敏感的钾电流,其特征与 TASK1 或 TASK3 通道相似,如钌红抑制。Western 分析证实了 TASK1 和 TASK3 的表达。在描述髓母细胞瘤的电生理特征时,可以看到与其他高级别恶性肿瘤相似的特征,而不是正常小脑颗粒神经元。这支持髓母细胞瘤的恶性表型的特征是离子通道表达的独特变化的观点。