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首页> 外文期刊>Scientific reports. >Non-Faradaic Electrochemical Detection of Exocytosis from Mast and Chromaffin Cells Using Floating-Gate MOS Transistors
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Non-Faradaic Electrochemical Detection of Exocytosis from Mast and Chromaffin Cells Using Floating-Gate MOS Transistors

机译:非法拉第电化学检测使用浮栅MOS晶体管对肥大细胞和嗜铬细胞的胞吐作用

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摘要

We present non-faradaic electrochemical recordings of exocytosis from populations of mast and chromaffin cells using chemoreceptive neuron MOS (CνMOS) transistors. In comparison to previous cell-FET-biosensors, the CνMOS features control (CG), sensing (SG) and floating gates (FG), allows the quiescent point to be independently controlled, is CMOS compatible and physically isolates the transistor channel from the electrolyte for stable long-term recordings. We measured exocytosis from RBL-2H3 mast cells sensitized by IgE (bound to high-affinity surface receptors FcεRI) and stimulated using the antigen DNP-BSA. Quasi-static I-V measurements reflected a slow shift in surface potential ( ) which was dependent on extracellular calcium ([Ca]o) and buffer strength, which suggests sensitivity to protons released during exocytosis. Fluorescent imaging of dextran-labeled vesicle release showed evidence of a similar time course, while un-sensitized cells showed no response to stimulation. Transient recordings revealed fluctuations with a rapid rise and slow decay. Chromaffin cells stimulated with high KCl showed both slow shifts and extracellular action potentials exhibiting biphasic and inverted capacitive waveforms, indicative of varying ion-channel distributions across the cell-transistor junction. Our approach presents a facile method to simultaneously monitor exocytosis and ion channel activity with high temporal sensitivity without the need for redox chemistry.
机译:我们目前使用化学感受性神经元MOS(CνMOS)晶体管从肥大和嗜铬细胞的群体中的胞吐作用的非法拉第电化学记录。与以前的单元FET生物传感器相比,CνMOS具有控制(CG),传感(SG)和浮栅(FG)的功能,允许独立控制静态点,具有CMOS兼容并将晶体管通道与电解质物理隔离稳定的长期录音。我们测量了由IgE致敏的RBL-2H3肥大细胞的胞吐作用(结合到高亲和力表面受体FcεRI),并使用抗原DNP-BSA进行刺激。准静态I-V测量反映了表面电位()的缓慢变化,这取决于细胞外钙([Ca] o )和缓冲液的强度,这表明对胞吐过程中释放的质子敏感。右旋糖酐标记的囊泡释放的荧光成像显示了类似的时程证据,而未敏化的细胞未显示对刺激的反应。瞬态记录显示出波动具有快速上升和缓慢衰减。用高KCl刺激的嗜铬细胞既显示缓慢移动,又显示出双相和倒电容波形的细胞外动作电位,表明跨细胞-晶体管连接的离子通道分布变化。我们的方法提出了一种简便的方法,可以同时监测胞吐作用和离子通道活性,同时具有较高的时间敏感性,而无需氧化还原化学反应。

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