O'Bryant Zaven, Leng Tiandong, Liu Mingli, Inoue Koichi, Vann Kiara T, Xiong Zhi-Gang
Neuroscience Institute, Morehouse School of Medicine, 720 Westview Drive SW, Atlanta, GA, 30310-1945, USA.
Mol Brain. 2016 Jun 24;9(1):68. doi: 10.1186/s13041-016-0249-8.
Cultured neuronal cell lines can express properties of mature neurons if properly differentiated. Although the precise mechanisms underlying neuronal differentiation are not fully understood, the expression and activation of ion channels, particularly those of Ca(2+)-permeable channels, have been suggested to play a role. In this study, we explored the presence and characterized the properties of acid-sensing ion channels (ASICs) in NS20Y cells, a neuronal cell line previously used for the study of neuronal differentiation. In addition, the potential role of ASICs in cell differentiation was explored. Reverse Transcription Polymerase Chain Reaction and Western blot revealed the presence of ASIC1 subunits in these cells. Fast drops of extracellular pH activated transient inward currents which were blocked, in a dose dependent manner, by amiloride, a non-selective ASIC blocker, and by Psalmotoxin-1 (PcTX1), a specific inhibitor for homomeric ASIC1a and heteromeric ASIC1a/2b channels. Incubation of cells with PcTX1 significantly reduced the differentiation of NS20Y cells induced by cpt-cAMP, as evidenced by decreased neurite length, dendritic complexity, decreased expression of functional voltage gated Na(+) channels. Consistent with ASIC1a inhibition, ASIC1a knockdown with small interference RNA significantly attenuates cpt-cAMP-induced increase of neurite outgrowth. In summary, we described the presence of functional ASICs in NS20Y cells and demonstrate that ASIC1a plays a role in the differentiation of these cells.
如果经过适当分化,培养的神经元细胞系可以表达成熟神经元的特性。尽管神经元分化背后的确切机制尚未完全了解,但已有人提出离子通道,特别是钙通透性通道的表达和激活可能发挥作用。在本研究中,我们探究了NS20Y细胞(一种先前用于神经元分化研究的神经元细胞系)中酸敏感离子通道(ASICs)的存在并对其特性进行了表征。此外,还探究了ASICs在细胞分化中的潜在作用。逆转录聚合酶链反应和蛋白质免疫印迹显示这些细胞中存在ASIC1亚基。细胞外pH值的快速下降激活了瞬时内向电流,该电流被非选择性ASIC阻滞剂阿米洛利以及同源ASIC1a和异源ASIC1a/2b通道的特异性抑制剂Psalmotoxin-1(PcTX1)以剂量依赖性方式阻断。用PcTX1孵育细胞显著降低了cpt-cAMP诱导的NS20Y细胞分化,这可通过神经突长度缩短、树突复杂性降低以及功能性电压门控钠通道表达减少来证明。与ASIC1a抑制一致,用小干扰RNA敲低ASIC1a可显著减弱cpt-cAMP诱导的神经突生长增加。总之,我们描述了NS20Y细胞中功能性ASICs的存在,并证明ASIC1a在这些细胞的分化中发挥作用。