Institute of Biomaterials & Bioengineering, Tokyo Medical and Dental University, Bldg 21-4-403B, 2-3-10 Kanda-Surugadai, Chiyoda, Tokyo 101-0062, Japan.
Department of Physiology, UT Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390, USA.
Biosensors (Basel). 2016 Mar 30;6(2):11. doi: 10.3390/bios6020011.
We present a novel method for the rapid measurement of pH fluxes at close proximity to the surface of the plasma membrane in mammalian cells using an ion-sensitive field-effect transistor (ISFET). In conjuction with an efficient continuous superfusion system, the ISFET sensor was capable of recording rapid changes in pH at the cells' surface induced by intervals of ammonia loading and unloading, even when using highly buffered solutions. Furthermore, the system was able to isolate physiologically relevant signals by not only detecting the transients caused by ammonia loading and unloading, but display steady-state signals as would be expected by a proton transport-mediated influence on the extracellular proton-gradient. Proof of concept was demonstrated through the use of 5-(N-ethyl-N-isopropyl)amiloride (EIPA), a small molecule inhibitor of sodium/hydrogen exchangers (NHE). As the primary transporter responsible for proton balance during cellular regulation of pH, non-electrogenic NHE transport is notoriously difficult to detect with traditional methods. Using the NHE positive cell lines, Chinese hamster ovary (CHO) cells and NHE3-reconstituted mouse skin fibroblasts (MSF), the sensor exhibited a significant response to EIPA inhibition, whereas NHE-deficient MSF cells were unaffected by application of the inhibitor.
我们提出了一种新的方法,使用离子敏感场效应晶体管(ISFET)在哺乳动物细胞的质膜附近快速测量 pH 通量。结合高效的连续灌注系统,ISFET 传感器能够记录由氨加载和卸载间隔引起的细胞表面 pH 的快速变化,即使使用高度缓冲的溶液也是如此。此外,该系统不仅能够检测到由氨加载和卸载引起的瞬变,还能够显示稳态信号,这是质子转运对细胞外质子梯度的影响所预期的,从而能够分离出与生理相关的信号。这通过使用 5-(N-乙基-N-异丙基)阿米洛利(EIPA)来证明,EIPA 是一种钠/氢交换器(NHE)的小分子抑制剂。作为细胞调节 pH 过程中质子平衡的主要转运蛋白,非电中性的 NHE 转运蛋白很难用传统方法检测到。使用 NHE 阳性细胞系中国仓鼠卵巢(CHO)细胞和 NHE3 重组的小鼠皮肤成纤维细胞(MSF),该传感器对 EIPA 抑制表现出显著的响应,而 NHE 缺陷型 MSF 细胞不受抑制剂的影响。