Simultaneous pH Measurement in Endocytic and Cytosolic Compartments in Living Cells using Confocal Microscopy

Summary

Several methods are available for measuring intracellular pH but very few of these allow simultaneous measurement of cytoplasmic and organellar pH. Here, we describe in detail a rapid and accurate methodology to simultaneously measure cytoplasmic and vesicular pH by ratiometric imaging of living cells.

Abstract

Intracellular pH is tightly regulated and differences in pH between the cytoplasm and organelles have been reported¹. Regulation of cellular pH is crucial for homeostatic control of physiological processes that include: protein, DNA and RNA synthesis, vesicular trafficking, cell growth and cell division. Alterations in cellular pH homeostasis can lead to detrimental functional changes and promote progression of various diseases². Various methods are available for measuring intracellular pH but very few of these allow simultaneous measurement of pH in the cytoplasm and in organelles. Here, we describe in detail a rapid and accurate method for the simultaneous measurement of cytoplasmic and organellar pH by using confocal microscopy on living cells³. This goal is achieved with the use of two pH-sensing ratiometric dyes that possess selective cellular compartment partitioning. For instance, SNARF-1 is compartmentalized inside the cytoplasm whereas HPTS is compartmentalized inside endosomal/lysosomal organelles. Although HPTS is commonly used as a cytoplasmic pH indicator, this dye can specifically label vesicles along the endosomal-lysosomal pathway after being taken up by pinocytosis^3,4. Using these pH-sensing probes, it is possible to simultaneously measure pH within the endocytic and cytoplasmic compartments. The optimal excitation wavelength of HPTS varies depending on the pH while for SNARF-1, it is the optimal emission wavelength that varies. Following loading with SNARF-1 and HPTS, cells are cultured in different pH-calibrated solutions to construct a pH standard curve for each probe. Cell imaging by confocal microscopy allows elimination of artifacts and background noise. Because of the spectral properties of HPTS, this probe is better suited for measurement of the mildly acidic endosomal compartment or to demonstrate alkalinization of the endosomal/lysosomal organelles. This method simplifies data analysis, improves accuracy of pH measurements and can be used to address fundamental questions related to pH modulation during cell responses to external challenges.

Protocol

1. Preparation of Solutions for Cellular pH Calibration

1. Add the following compounds to five separate 50 ml conical tubes to prepare 5 solutions to be used for calibration:
   • NaCl (1 ml of 1 M NaCl) (1 M NaCl = 0.58 g in 10 ml H₂0)
   • KCl (6.75 ml of 1 M KCl) (1 M KCl = 0.75 g in 10 ml H₂0)
   • Glucose (1 ml of 1 M D-Glucose) ( 1M D-Glucose = 1.80 g in 10 ml H₂0)
   • MgS0₄ (0.05 ml of 1 M MgSO₄) (1 M MgSO₄= 1.20 g in 10 ml H₂0)
   • 20 mM HEPES (1 ml of 1M HEPES) (1 M HEPES = 2.38 g in 10 ml H₂0)
   • CaCl₂ (0.05 ml of 1M CaCl₂) (1 M CaCl₂= 1.47 g in 10 ml H₂0)
     Prepare all solutions in double distilled H₂O (ddH₂O).
2. Complete each solution with 35 ml of ddH₂O and mix with a magnetic stirrer until solution is achieved.
3. Adjust the pH of each solution with 1 N KOH or 1 N HCl to obtain pH values of 5.5, 6.0, 6.5, 7.0 and 7.5. Then, adjust the volume with deionized water to a final volume of 50 ml.
4. Measure 5 mg of nigericin and add it to 670 μl of absolute EtOH to prepare a 10 mM nigericin stock solution.
   Caution: nigericin is highly toxic and must be handled with great care (gloves, safety glasses and mask). Mix the solution by inversion until the nigericin is completely dissolved.
5. Add 0.05 ml of 10 mM nigericin (final concentration 10 μM) to each calibration solution. Nigericin is an ionophore that increases cell membrane permeability and causes equilibration of intracellular and extracellular pH in the presence of a depolarizing concentration of extracellular K⁺.
6. Calibration solutions can be stored up to 1 month at 4 °C

2. Cell Preparation

1. Under a biological safety hood, seed cells in 35 mm x 10 mm culture dishes in 2 ml of growth medium supplemented with 10% fetal bovine serum and antibiotics. Use the amount of cells needed to ensure approximately 50% confluence after 24 hr.
   NOTE: In our experiments, we use the HT-1080 cell line and plate 1 x 10⁵ cells per culture dish.
2. Determine the number of culture dishes needed for the experiment and plate 5 additional culture dishes to be used for calibration.
3. Place culture dishes in a 37 °C/5% CO₂ incubator for at least 24 hr.

3. Preparation of pH-sensing Probes

1. Prepare a 1M stock solution of the fluorescent pH probe 8-hydroxypyrene-1,3,6 trisulfonic acid, trisodium salt (HPTS/pyranine) in ddH₂0. This solution must be stored at RT and protected from light.
2. Prepare a stock solution of 1 mM 5-(and-6)-carboxyl seminaphthorhodafluor acetoxymethyl ester acetate (C-SNARF-1 AM; called thereafter SNARF-1) by dissolving 1 mg of SNARF-1 in 1.76 ml of DMSO. Thoroughly mix by repeated pipetting. SNARF-1 solution must be stored at -20 °C and protected from light.

4. Cell Labeling

1. Sixteen hours before live-cell imaging, add 2 μl of 1M HPTS stock solution (final concentration 1 mM) to each culture dish containing 2 ml of complete medium.
2. Return the culture dishes to the incubator. The HPTS probe is cell-impermeant, therefore to label organelles the probe must be taken up by pinocytosis. This condition requires that cell incubations with HPTS are performed in serum-supplemented culture medium.
3. Following incubation with HPTS, wash the cells twice with sterile PBS and add 2 ml of serum-free medium for at least 2 hr. Incubation with SNARF-1 needs to be performed in serum-free medium because serum may prevent the uptake of the probe.
4. Add 10 μl of a 1 mM SNARF-1 stock solution to obtain a final concentration of 5 μM and allow cells to incubate for 20 min at 37° C, under dim light. C-SNARF-1 concentration and time of incubation may vary according to cell type.
5. At the end of incubation, wash cells twice in sterile PBS and add 2 ml of serum-free medium.

5. Addition of pH Modulators

1. To assess whether the method can detect pH changes in cells, different reagents that modulate intracellular pH can be used:
   • Bafilomycin A1, a specific inhibitor of V-ATPase⁵
   • Na⁺/H⁺ exchanger isoform 1 (NHE-1)⁶
   • NH₄Cl, a weak base that increases intracellular pH⁷
   1. Prepare stock solutions of the reagents mentioned above:
      • Bafilomycin A1: add 10 μg of bafilomycin A1 to 160 μl of DMSO to obtain a stock solution of 100 μM
      • EIPA: add 25 mg of EIPA to 1.67 ml of methanol to obtain a final concentration of 50 mM
      • NH₄Cl: dissolve 0.53 g of ammonium chloride in 10 ml of ddH₂O to obtain a final concentration of 1 mM.
      
      Note: All stock solutions must be kept at 4 °C except for bafilomycin A1 which must be stored at -20 °C and protected from light.
   2. In separate culture dishes, add one of the reagents as described below:
      • 2 μl of 100 μM bafilomycin A1 (final concentration 100 nM)
      • 1 μl of 50 mM EIPA (final concentration 25 μM)
      • 40 μl of 1M NH₄Cl (final concentration 20 mM)
   3. Incubate the cells for 30 min at 37 °C.
2. Proceed to image acquisition.

6. Specifications of the Live-cell Imaging Microscope and Acquisition Settings

1. Perform live-cell imaging using a 40X objective mounted on a spectral inverted scanning confocal microscope equipped with a motorized XY stage, a chamber that accommodates glass bottom culture dishes in an environmentally controlled (temperature, humidity, CO₂) stage incubator.
2. The confocal instrument (Olympus FV1000) used here is equipped with:
   • A diode laser 405 nm
   • A 40 mW argon laser (458 nm, 488 nm, 515 nm)
   • A helium neon laser (543 nm)
   • Fluorite 10X objective, NA0.4
   • A LUCPLFLN 40X objective, NA0.60
   • A PLAPONSC PLAN APO 60X oil objective, NA1.4
   • A dichroic mirror DM 405/458/488/543
   • A SDM 560 and a SDM 640 dichroic filters
   • A BA655-755 barrier filter
   • A beam splitter BS20/80
   • Data analysis software for image acquisition and analysis,
3. Once the stage incubator has warmed up to 37 °C and the microscope is set up, place a culture dish previously incubated with HPTS and SNARF-1 into the confocal stage imaging chamber.
4. After locating an area of interest, adjust the software acquisition settings Figure 1.
   • Set up two virtual channel sets.
   • Initiate the first phase that corresponds to HPTS excitation at 405 nm and emission collection at 505 - 525 nm and SNARF-1 excitation at 543 nm and emission collection at 570 - 600 nm.
   • Initiate the second phase that corresponds to HPTS excitation at 458 nm and emission collection at 505 - 525 nm and SNARF-1 excitation at 543 nm and emission collection at 640 - 650 nm.
   • The confocal aperture is set to 175 μm by default and optimal aperture needs to be manually set at 300 μm.
   • Take Image by stacking serial horizontal optical sections (800 x 800 pixels) of 0.4 μm thickness.

NOTE: A 40X objective is useful to observe several cells simultaneously and works well for organelle viewing. However, spatial resolution and signal intensity are better achieved using a 60X oil objective. In addition, there is no excitation or emission cross-talk between the two dyes.

7. Calibration of pH-sensing Probes

1. Before calibration, remove medium from the culture dish previously incubated with HPTS and SNARF-1, wash twice with sterile PBS and then add 2 ml of one of the five calibration solutions.
2. Place the culture dish into the confocal stage chamber.
3. Proceed to time-lapse image acquisition according to the following settings:
   1. Set the number of images and interval duration times for the experiment.
      NOTE: We typically use a 1 min interval between images for up to 30 min.
   2. Program the shutter to close between the acquisition of each image.
4. Record the fluorescence intensity per min in a spreadsheet software and determine the time when fluorescence intensity is steady. Intracellular pH is usually stable after 15 - 20 min.
5. Repeat steps 7.1 to 7.4 using a new culture dish for each remaining calibration solution.

8. Data Acquisition

1. Once calibration has been done, acquire sample data from 4-5 randomly chosen fields containing 15-20 cells per field. Two images are obtained for each field: one for HPTS labeling (vesicles) and the second for SNARF-1 labeling (cytosol).
2. Background fluorescence (extracellular area) is digitally subtracted from fluorescent images of both probes. Labeled vesicles and cytosol from their respective stored images are selected using a binary mask. For each pH-sensing probe, fluorescence intensities are measured on a numerical scale (0-4,095 gray level scale). A mean intensity for all pixels in the organelle or cytoplasm is calculated and values are used to calculate fluorescence ratios.

9. Data Analysis

1. Various software packages are commercially available for data analysis. i.e. Fluoview Software.
2. In a spreadsheet, record values and calculate fluorescence ratios as follows: In the case of HPTS, R = (F_{458 nm}/F_{405 nm}) and, in the case of SNARF-1, R = (F_{644 nm}/F_{584 nm}).
3. Plot the data using scientific graphing software such as GraphPad Prism. The plot should portray fluorescence ratios (Y-axis) as a function of pH (X-axis). Curve fitting is achieved using non-linear regression.
4. Collect fluorescence intensities of the samples as described in step 8.2 and calculate fluorescence ratios. Use calibration curves to transform ratios into pH values.

Results

For the simultaneous measurement of pH in both intracellular and endosomal/lysosomal cell compartments, the ratiometric fluorescent pH-sensing probes SNARF-1 and HPTS were used. SNARF-1 is restricted to the cytosolic compartment whereas HPTS allows ratiometric pH measurement of the endosomal/lysosomal compartment. Cell loading with HPTS for 16 hr allows its selective localization in endosomes/lysosomes⁴. A typical example of fluorescence recorded from HT-1080 cells loaded with the pH-sensing probes is shown in...

Discussion

Quantitative pH measurement in live-cell imaging of different cellular compartments is needed to accurately measure pH variations in cell responses to external challenges. However, one of the major hurdles that remains is to easily and specifically target cellular compartments. In this respect, a few studies have highlighted the use of HPTS as an intracellular pH indicator introduced into cells by electroporation or microinjection^8-10. These techniques suffer from serious drawbacks, namely electroporation caus...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
Solutions for calibration
Sodium chloride	Fischer	L-11621
Potassium chloride	Fischer	M-12445
D-Glucose (dextrose)	Fischer	D16-1
Magnesium sulfate	Fischer	M65-500
HEPES	Sigma-Aldrich	H3375
Calcium chloride dihydrate	Fischer	M-1612
Deionized water	N/A	N/A
Nigericin	Calbiochem	481990	Toxic by inhalation or in contact with skin
Keep protected from the light at 4 °C
Culture dishes ∅ 35mm	BD Biosciences	354456
pH-sensing probes
8-Hydroxypyrene-1,3,6-trisulfonic acid (HPTS)	Life technologies	H-348	Keep away from the light at room temperature
5-(and-6)-Carboxy SNARF®-1, Acetoxymethyl Ester, Acetate	Life technologies	C-1271	Keep away from the light and humidity at -20 °C
Dimethyl Sufoxide (DMSO)	Fischer	BP231-1	Harmful
Phosphate buffered saline (PBS) 100X
Potassium chloride	Fischer	M-12445	20 g
Sodium phosphate monobasic	Fischer	S369-1	115 g
Potassium phosphate monobasic	J.T Baker	3246-01	20 g
Deionized water	N/A	N/A	Bring to 1 L
Autoclave and adjust pH to 7.4
Phosphate buffered saline (PBS) 1X
PBS 100X	N/A	N/A	50 ml
Sodium chloride	Fischer	L-11621	40.5 g
Deoinized water	N/A	N/A	Bring to 5 L
pH modulators
Bafilomycin A1	Sigma-Aldrich	B-1793
5-(N-Ethyl-N-isopropyl)amiloride (EIPA)	Sigma-Aldrich	A3085
Ammonium chloride	Fischer	A649-500