pH-sensitive glass microelectrodes and intracellular pH measurements.

1. Some properties of the open-tipped, uninsulated, pH-sensitive glass microelectrode were examined in several electrical experiments. 2. Based on these observations, technical and theoretical problems were considered for application to the pH measurement in small cells. 3. The intracellular pH, (pH)i, of the epithelial cell in rat duodenum measured was approximately 7.0. A reduction in (pH)i was apparent (about 0.3) with the addition of 20 mM-glucose to the bathing fluid. 4. It was concluded that with certain limitations such uninsulated, open-tipped microelectrodes may be successfully utilized for intracellular pH measurements.     

Application of antimony microelectrodes to intracellular pH monitoring

Some novel studies of the properties of the antimony microelectrode used for intracellular pH measurements are described. First, it is shown that currents in the picoampere range, such as those encountered as leakage in some electrometers, induce important changes in pH sensitivity. The response time of the electrode has also been measured and indicates that the electrode exhibits a rapid time course which would be very useful for dynamic cytoplasmic pH investigations. An example of internal pH recording during cellular acidification in Xenopus laevis oocyte is also presented.     

Biological and artificial ion exchangers: Electrical measurements with glass microelectrodes

Summary Biological (stratum corneum) and artificial (cation-exchange resin beads, Bio-Rad AG 50W-X2) ion exchangers were impaled by glass microelectrodes filled with KCl solution. The electrical potential difference recorded in these structures in reference to the external bathing medium was shown to be dependent on the KCl concentration of both the external and the microelectrode filling solutions. The potentials were interpreted on the grounds of the fixed charge theory of membrane potentials as a consequence of two phase boundary potentials (Donnan potentials), one at the matrix-external solution interface and the other at the matrix-microelectrode solution interface. The contribution of a diffusion component for the recorded potential was considered.     

Single-unit pH-sensitive double-barreled microelectrodes for extracellular use

The purpose of this study is to systematically describe the construction of pH-sensitive double-barreled microelectrodes for extracellular use. The most important advantages of these microelectrodes are as follows: the reference and the pH barrels are next to each other, and therefore the measured pH is not affected by asymmetric or slowly spreading direct current potential. The diameter of the tip of the microelectrodes is between 7 and 35 micron. These pH-sensitive microelectrodes are generally stable and Nernstian. They can be used repeatedly both in vivo and in vitro to measure tissue extracellular fluid pH. Some applications are described.     

The apoplastic pH of the Zea mays root cortex as measured with pH-sensitive microelectrodes: aspects of regulation

In the root cortex of Zea mays the apoplastic pH andaspects of its regulation were investigated using pH-sensitivemicroelectrodes. To measure the pH directly in different cell layers of theapoplast sharp double-barrelled electrodes were applied, whereas bluntpH-electrodes were used simultaneously to measure the pH at the rootsurface. Recordings carried out 8-10 mm behind the root tip show that theapoplastic pH is maintained between 5.1 and 5.6, depending on the givenexperimental conditions, i.e. varying external [K⁺],[Ca²⁺], pH, weak buffering, as well as perfusion ofthe test medium. When the medium pH (bulk) differs considerably from theapoplastic pH, a small pH gradient is built up between the root surface(unstirred layer) and the outer cortex layers. In a standing medium thesegradients equilibrate. The apoplastic pH responds to increases in external[K⁺] and [CA²⁺] with anacidification, which is attributed to ion-exchange properties of the cellwall constituents. Stimulation of proton pump activity with fusicoccinacidifies the apoplast from pH 5.6 to pH 4.8, while deactivation of thepump with cyanide/salicylhydroxamic acid increases the pH of the apoplastfrom 5.6 to 6.2, and further to pH 6.6 with CCCP. TheCa²⁺ channel antagonists nifedipine andLa³⁺ also increase the apoplastic pH. It issuggested that not only the proton pump, but also the cation channels maycontribute to the regulation of the apoplastic pH.Keywords:Apoplast, ion-selective microelectrodes, pH, unstirred layer,Zea mays, root.     

Simultaneous measurements of intracellular pH in the leech giant glial cell using 2'',7''-bis-(2-carboxyethyl)-5,6-carboxyfluorescein and ion-sensitive microelectrodes.

We have employed two independent techniques to measure the intracellular pH (pHi) in giant glial cells of the leech Hirudo medicinalis, using the fluorescent dye 2',7'-bis-(2-carboxyethyl)-5,6-carboxyfluorescein (BCECF) and double-barreled neutral-carrier, pH-sensitive microelectrodes, which also record the membrane potential. We have compared two procedures for calibrating the ratio of the BCECF signal, excited at 440 nm and 495 nm: 1) the cell membrane was H(+)-permeabilized with nigericin in high-K+ saline at different external pH (pHo) values, and 2) the pHi of intact cells was perturbed in CO2/HCO3(-) -buffered saline of different pH, and the BCECF ratio was calibrated according to a simultaneous microelectrode pH reading. As indicated by the microelectrode measurements, the pHi did not fully equilibrate to the pHo values in nigericin-containing, high-K+ saline, but deviated by -0.12 +/- 0.02 (mean +/- SEM, n = 37) pH units. In intact cells, the microelectrode readings yielded up to 0.15 pH unit lower values than the calibrated BCECF signal. In addition, larger dye injections into the cells (> 100 microM) caused an irreversible membrane potential loss indicative of some damage to the cells. The amplitude and kinetics of slow pHi changes were equally followed by both sensors, and the dye ratio recorded slightly higher amplitudes during faster pHi shifts as induced by the addition and removal of NH4+.     

Comparative measurements of membrane potentials with microelectrodes and voltage-sensitive dyes

The usefulness of a new voltage-sensitive fluorescent dye, the membrane permeant negatively charged oxonol dye diBA-C4-(3)-, was evaluated by measuring the membrane potentials of BICR/M1R-k and L cells with glass microelectrodes and simultaneously recording the fluorescence of the stained cells. The membrane potential of BICR/M1R-k cells was varied between -25 mV and -90 mV by changing the bicarbonate concentration in the medium or by voltage clamping. To avoid any interference by the inserted electrodes with the fluorescence measurement of the cytoplasm, the cells were fused by polyethyleneglycol to form giant cells (homokaryons). These homokaryons also allowed penetration by two glass microelectrodes without causing a serious leakage of the plasma membrane. The slow responding dye diBA-C4-(3)- had a fluorescence response of about 1% per mV. Mathematical analysis of the fluorescence changes after voltage clamping revealed a first-order reaction with a rate constant between 0.1 min-1 and 0.8 min-1, depending on the cell size which was determined by the number of nuclei per homokaryon. A model for the mechanism of the fluorescence changes is proposed.     

Regulation of intracellular pH

The approach that most animal cells employ to regulate intracellular pH (pH(i)) is not too different conceptually from the way a sophisticated system might regulate the temperature of a house. Just as the heat capacity (C) of a house minimizes sudden temperature (T) shifts caused by acute cold and heat loads, the buffering power (beta) of a cell minimizes sudden pH(i) shifts caused by acute acid and alkali loads. However, increasing C (or beta) only minimizes T (or pH(i)) changes; it does not eliminate the changes, return T (or pH(i)) to normal, or shift steady-state T (or pH(i)). Whereas a house may have a furnace to raise T, a cell generally has more than one acid-extruding transporter (which exports acid and/or imports alkali) to raise pH(i). Whereas an air conditioner lowers T, a cell generally has more than one acid-loading transporter to lower pH(i). Just as a house might respond to graded decreases (or increases) in T by producing graded increases in heat (or cold) output, cells respond to graded decreases (or increases) in pH(i) with graded increases (or decreases) in acid-extrusion (or acid-loading) rate. Steady-state T (or pH(i)) can change only in response to a change in chronic cold (or acid) loading or chronic heat (or alkali) loading as produced, for example, by a change in environmental T (or pH) or a change in the kinetics of the furnace (or acid extrudes) or air conditioner (or acid loaders). Finally, just as a temperature-control system might benefit from environmental sensors that provide clues about cold and heat loading, at least some cells seem to have extracellular CO(2) or extracellular HCO(3)(-) sensors that modulate acid-base transport.     

Novel super pH-sensitive nanoparticles responsive to tumor extracellular pH

The objective of this study was to evaluate Camptothecin (CAMP)-loaded poly(N-isopropylacrylamide) (NIPAAm)/chitosan nanoparticles as a pH-sensitive carrier for specifically targeting tumors. The synthesis and properties of the system was studied by adjusting the mass ratio of NIPAAm and chitosan. The drug release characteristics of nanoparticles in vitro were investigated. The results showed that when the charge ratio between NIPAAm and chitosan of 4:1 (w/w) was achieved, the drug-loaded nanoparticles were most sensitive to tumor pH. Encapsulation efficiencies and loading were 73.7% and 8.4%, respectively. The cumulative release rate of CAMP was optimal at pH 6.8 and decreased rapidly either below pH 6.5 or above pH 6.9 in 37 °C. Based on MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium) test and fluorescence microscopy results, CAMP-loaded nanoparticles showed cytotoxicity at pH 6.8 but minimal cytotoxicity at pH 7.4. The pH-sensitive poly NIPAAm/chitosan nanoparticles provided some distinct advantages in delivering anti-cancer drugs to targeted tissues.     

Measurement of intracellular nitrate concentrations in Chara using nitrate-selective microelectrodes

Nitrate-selective microelectrodes have been made using a quaternary ammonium sensor, methyl-tridodecylammonium nitrate, in a Polyvinylchloride matrix. These electrodes showed a log-linear response from 0.1 to 100 mol · m^?3 nitrate with a typical slope of 55.6 mV per decade change in nitrate concentration. The only physiologically significant interfering anion was chloride but the lower limit of nitrate detection was 0.5 mol · m^?3 in the presence of 100 mol · m^?3 chloride which means this interference will not be important in most physiological situations. These microelectrodes were used to measure nitrate concentrations in internodal cells of Chara corallina cultured under low nitrate and nitrate-replete conditions for 6 to 30 weeks. Cells maintained in low nitrate only showed measurements which were less than the detection limit of the electrodes, while cells grown under nitrate-replete conditions showed two populations of measurements having means of 1.6 and 6.2 mol · m^?3. Chemical analysis of the high-nitrate cells indicated that they contained a mean nitrate concentration of 5.9 mol · m^?3. As vacuolar nitrate concentration would dominate this whole-cell measurement, it is concluded that the higher concentration measured with the electrodes represents vacuolar nitrate concentration and the lower value represents the cytoplasmic concentration. This intracellular distribution of nitrate could only be achieved passively if the electrical potential difference across the tonoplast is between +25 and + 35 mV.     

Application of fluorescence lifetime imaging of enhanced green fluorescent protein to intracellular pH measurements.

We have shown that the intracellular pH of a single HeLa cell expressing the enhanced green fluorescent protein (EGFP) can be imaged using the fluorescence lifetime of EGFP, which can be interpreted in terms of the pH-dependent ionic equilibrium of the p-hydroxybenzylidene-imidazolidinone structure of the chromophore of EGFP.