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Center for Cell Analysis and Modeling, University of Connecticut Health Center, Farmington, Connecticut
Correspondence: Address reprint requests to Leslie M. Loew, Center for Cell Analysis and Modeling, University of Connecticut Health Center, Farmington, CT 06030-1507. E-mail: les{at}volt.uchc.edu.
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ABSTRACT |
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 TOP ABSTRACT INTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONSUPPLEMENTARY MATERIALACKNOWLEDGEMENTSREFERENCES |
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INTRODUCTION |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONSUPPLEMENTARY MATERIALACKNOWLEDGEMENTSREFERENCES |
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). This phenomenon has gained broad interest in the last decade, since phase separation is thought to organize molecules in cell plasma membranes and plays an important role in cell function (2). The liquid-ordered phase domains in plasma membranes are defined as rafts. With cold, nonionic detergent extraction methods, rafts have been isolated from plasma membranes as a detergent-resistant fraction that is enriched in glycosphingolipids, cholesterol, and specific membrane proteins (3).
Biophysical studies on lipid phases are most readily performed on model membranes instead of cells. This is because chemical components and physical conditions are under total experimental control in model membranes. The domains of model membranes can be at the micrometer scale, allowing them to be resolved by light microscopy. Phase separation has been studied under the microscope using fluorescent probes. Most probes partition preferentially into one phase: for instance, lissamine rhodamine 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine and perylene segregate preferentially into the liquid-disordered and liquid-ordered phases, respectively (4). Laurdan uses a different mechanism to differentiate the two phases. It exhibits an emission spectrum shift of up to 50 nm and a photoselection effect in the domains of different phases (5,6). Thus, laurdan labels both phases but displays distinct optical properties in each. Laurdan is excited with near-ultraviolet light, making it advantageous to use two-photon fluorescence (TPF) microscopy. This has the added advantage in cellular applications (7) of minimizing bleaching and the damaging effects of ultraviolet excitation, as only the dye molecules in the optical section are excited.
However, imaging of rafts in live cells has not been widely reported and can be quite challenging. Most of the probes used in model membranes are mixed with lipids before vesicle development, so the loading method cannot be readily applied to live cells. Cell biologists often turn to fluorescently labeled toxins and antibodies, which bind to lipids or proteins in rafts; these include cholera toxin subunit B for GM1 and antibodies against caveolins (8,9). Fluorescent-protein-tagged constructs of proteins known to associate with rafts have also permitted the visualization of domains in live cells (10). These probes indicate the location of a certain chemical component, but not the physical phase of the domains, which defines rafts; of course, specific labels and antibodies can also be problematic for live-cell imaging experiments. Furthermore, analysis of the diffusion rate of molecules in plasma membranes suggests that the size of rafts may be at the nanometer scale, which is not resolvable by light microscopy (11). For example, electron microscopy reveals caveolae, raft-like structures, with a size of 25–150 nm in diameter (12). An additional consideration is that, according to biochemical analysis, rafts are thought to be heterogeneous in both lipid and protein components (13), so labeling a particular chemical component may not visualize the general distribution of rafts. Indeed, biophysical studies on model membrane domains and cell biological studies on cell membrane heterogeneity suffer from a dearth of common tools. Therefore, information derived from model membrane studies is not readily connected to cell membrane physiology.
Di-4-ANEPPDHQ is a potentiometric styryl dye that has recently been introduced for studies of neuronal activity (14). It is reasonably water-soluble yet has a high avidity for membrane. Thus, a simple solution of the dye in extracellular medium readily stains live cells. It inserts into one leaflet of the bilayer membrane, with its chromophore aligned by the surrounding lipid molecules. Di-4-ANEPPDHQ is conveniently excited by blue light, including the common 488-nm laser line available in all confocal microscopes. As with other styryl dyes (15), it has a high-fluorescence quantum efficiency and large Stokes shift when bound to membranes, but very little fluorescence in water. This minimizes background fluorescence contributions. Its spectra are solvatochromic and electrochromic, with the latter effect providing the basis for its sensitivity to membrane potential.
In this article, we explore environmental influences on the optical properties of di-4-ANEPPDHQ that promise to make it an excellent probe of membrane domains. We find that the local cholesterol concentration and lipid phase affect the dye's emission spectrum. Given these optical properties, di-4-ANEPPDHQ successfully differentiates liquid-ordered and -disordered phases in giant unilamellar vesicles (GUVs) with both single photon fluorescence (SPF) and TPF. The dye also has a much higher second harmonic generation (SHG) signal in the liquid-disordered phase. A preliminary account of this work has appeared as a Biophysical Letter (16). Here we provide data that helps explain the physical origin of these optical phenomena and further apply the method to a variety of model membrane systems.
We also successfully demonstrate the applicability of di-4-ANEPPDHQ in a live cell system, polarized neutrophils, which have lipid rafts concentrated at the front lamellipodia (7). The dye shows a smaller red/green fluorescence ratio in the front lamellipodia compared to those of the rest of the cell. The ratio difference between the front and rear disappears after cholesterol depletion, which breaks up rafts. We anticipate that the dye will reveal membrane heterogeneity in other cells and become a unifying tool for both model-membrane and live-cell investigations of lipid domains.
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MATERIALS AND METHODS |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONSUPPLEMENTARY MATERIALACKNOWLEDGEMENTSREFERENCES |
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).
Vesicle development
Large unilamellar vesicles (LUVs)
A solution of 5 mg lipids in 0.2 ml chloroform was prepared with the desired molar ratio of lipids. The solutions were dried under argon, and held in a vacuum chamber for 1 h to completely evaporate the solvent. Distilled deionized water (2 ml) was added to hydrate the lipids for 1 h. The lipid suspension is pushed through a polycarbonate membrane with 3-µm pores in a miniextruder system (Avanti Polar Lipids) 21 times. If there is DPPC in the lipid mix, the hydration and extrusion are done at 60°C to keep the lipid in liquid phase during the procedure.
GUVs
Twenty microliters of 1 mg/ml lipid solution in chloroform was spread evenly on two indium-tin-oxide-coated glass slides (Delta Technologies, Stillwater, MN). The chloroform was evaporated under argon and held in a vacuum chamber for 1 h. The two slides were separated by 0.39-mm-thick Teflon spacers with the lipid layers facing each other, forming a capacitor sandwich. The space between the slides was filled with Millipore water and connected to a function generator (10 MHz, Wavetek, San Diego, CA), producing a 10-Hz sinusoidal wave of 3 V for 1 h. The GUVs were developed at 60°C if there was DPPC or brain sphingomyelin in the lipid mixture (17,18).
Cell preparation
Neutrophil isolation
Polymorphonuclear leukocytes from mouse bone marrow were isolated from femurs as described (19), with some modifications. Marrow cells were flushed from the bones using Hank's balanced salt solution (HBSS) without Ca2+/Mg2+ (GIBCO, Grand Island, NY) + 0.1% BSA + 5 mM Hepes (GIBCO). Red blood cells were lysed with 0.15 mM NH4Cl, 1 mM KHCO3, 0.1 mM Na2 EDTA for 4 min at room temperature. The remaining leukocytes were washed twice in HBSS (Ca2+/Mg2+-free) + 0.1% BSA + 5 mM Hepes and resuspended in 3 ml of a 45% Percoll solution in HBSS (Ca2+/Mg2+-free). The leukocytes were loaded on a Percoll density gradient, which had a Percoll concentration of 81%, 62%, 55%, and 50% from the bottom to the top. Cells were centrifuged at 1600 g for 30 min at room temperature. The neutrophil band between the 81% and 62% layers was harvested, and washed twice in fresh HBSS (Ca2+/Mg2+-free) + 0.1% BSA + 5 mM Hepes.
Polarization
The cells were plated in coverglass-bottom dishes and incubated for 5 min. The chemoattractant ligand fMLP (10 µM) was added and after 10 min incubation the polarized neutrophils were ready for imaging.
Cholesterol depletion
Plated cells were incubated in buffer solution with 10 mM methylated ß-cyclodextrin (Cycoldextrin Technologies Development, High Springs, FL) for 15 min at 37°C. After the cylcodextrin solution was washed away, cells were polarized with ligand.
Staining
LUVs were stained with 2 and 1 µM di-4-ANEPPDHQ added into cuvettes in spectrum-shift and affinity studies, respectively. GUVs were stained by 10 µM di-4-ANEPPDHQ. Neutrophils were treated with 3 µM di-4-ANEPPDHQ in buffer solution and immediately transferred to the microscope for imaging.
Spectrum measurement
LUVs
In a cuvette, 1 ml of the LUV suspension from the extruder is diluted by water to 3 ml and stained with 2 µM di-4-ANEPPDHQ. The spectra were measured by a Fluorolog spectrofluorometer (SPEX, Hoboken, NJ). The sample temperature was controlled by an MGU Lauda circulation bath (Brinkmann, Westbury, NY). For emission spectra measurement, 475 nm excitation was used, and for excitation spectra measurement, 630 nm emission was used. All spectra were corrected for the wavelength dependence of the monochromators, and, for emission spectra, for the detector sensitivity at different wavelengths.
Affinity analysis
LUV suspensions of 0, 0.02, 0.04, 0.06, 0.08, 0.1, 0.2, 0.4, 0.6, 0.8, 1, 2, 3, 4, and 5 mg/ml were each equilibrated with 1 µM di-4-ANEPPDHQ, and emission spectra were recorded. The signal intensity at the peak wavelength was used in a one-site saturable binding analysis.
Imaging
For confocal SPF imaging of GUVs, we used a Zeiss Meta multiwavelength confocal microscope system mounted on an Axiovert 200M microscope (Carl Zeiss, Thornwood, NY). The di-4-ANEPPDHQ fluorescence is excited by the 488-nm line of an argon ion laser, collected by a plan-Apochromat 63x/1.4 oil DIC objective, and filtered through emission channels of either BP 650–710 nm or BP 500–550 nm. The lambda function of the Meta system was used to collect emission spectra from 521 to 703 nm.
The neutrophils images are taken with an LSM 510 confocal microscope mounted on a Zeiss Alexiovert. The samples are excited by a 488-nm argon ion laser line. The fluorescence emission is collected by a plan-Apochromat 63x/1.4 oil DIC objective and filtered through either LP 650-nm or BP 505–550 nm emission channels. Ratio images are calculated by dividing the emission intensity from the LP650 channel by the emission intensity from the BP 505–550 channel on a pixel by pixel basis. In a separate set of experiments, we used the Meta system to acquire spectra from the front and rear of polarized neutrophils as described above for the GUVs.
The excitation for both TPF and SHG, femtosecond laser pulses at 910 nm, is from a Mira 900 Ti:sapphire ultrafast laser (Coherent, Santa Clara, CA) pumped by a 10 W Verdi doubled solid-state laser (Coherent). The laser is circularly polarized by a half-waveplate (CVI Laser) and a quarter-waveplate (CVI Laser). A Fluoview scanning confocal imaging system (Olympus America, Melville, NY) directs the scanning beam into the sample through an IR-Achroplan 40x/0.8NA water-immersion objective on an Axioskop microscope (Zeiss). TPF is collected backward through the objective and a bandpass filter (either 540/50 or 675/50 nm), and detected by a photomultiplier tube (Hamamatsu, Tokyo, Japan). The SHG is collected forward through a 0.9 NA condenser and a 455-nm filter onto a photon-counting head (Hamamatsu). Both TPF and SHG signals are input to the Fluoview amplifier board (Olympus America) (20).
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RESULTS |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONSUPPLEMENTARY MATERIALACKNOWLEDGEMENTSREFERENCES |
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). Compared with widely used ANEPPS dyes that are zwitterionic, di-4-ANEPPDHQ has two positive charges on its headgroup (Fig. 1), which give it two unique properties. First, it is water soluble without the need of detergents or cyclodextrin as vehicles. Second, its double positive charge retards the rate of flipping from the outer leaflet of the bilayer to the inner leaflet. This will also decrease the rate of internalization of the dye, which can produce significant background fluorescence in cell studies. These two properties make di-4-ANEPPDHQ a better membrane probe than the ANEPPS dyes while retaining the general styryl attributes of low aqueous fluorescence, high membrane fluorescence, and large Stokes shift.
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We developed LUVs with different lipid components and used temperature to control their phase transitions. We stained these vesicles with di-4-ANEPPDHQ and measured the dye's excitation and emission spectra with a spectrofluorometer. The basic components of the vesicles are DOPC, DPPC, and cholesterol. DOPC and DPPC have the same headgroup and differ in the length and saturation of fatty acid chains. DOPC is an unsaturated lipid with a transition temperature of –21°C, whereas DPPC is a saturated lipid with a transition temperature of 41°C (22).
To test the chemical components' influence, we first measured the dye's spectra in LUVs of pure DOPC and pure DPPC at 60°C (Fig. 2). At this temperature, the vesicles of each lipid are in the liquid-disordered phase. Di-4-ANEPPDHQ's excitation and emission spectra in DPPC LUVs are slightly blue-shifted relative to its spectra in DOPC LUVs. Therefore, we conclude that di-4-ANEPPDHQ is not particularly sensitive to the environmental difference caused by the unsaturation of the fatty acid chains of the phosphatidylcholines. In other words, the dye will not readily distinguish the liquid-ordered and liquid-disordered phase domains based on a concentration difference in these saturated and unsaturated lipids alone.
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), so the only difference between these vesicles is the cholesterol concentration. In Fig. 3, the excitation spectrum blue-shifts a little with increasing cholesterol concentration, whereas the emission spectrum shows significant changes. Increasing the cholesterol concentration from 0 to 40 mol % shifts the peak of the emission spectrum from 628 nm to 588 nm. Another obvious change is that the emission spectrum is getting narrower: the half-peak width changes from 169 nm to 122 nm. We also examined the effect of varying cholesterol concentrations in DOPC LUVs at room temperature. The spectra showed similar changes with increasing cholesterol concentration (data not shown). Therefore, we conclude that di-4-ANEPPDHQ's fluorescence emission is sensitive to the cholesterol concentration.
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). We changed the temperature to control the phase transition, and measured di-4-ANEPPDHQ's spectra. Fig. 4 a shows the excitation and emission spectra at different temperatures. From the emission spectra, we can see that the fluorescence intensity decreases with the temperature increase. To observe the spectrum shift more clearly, we normalized all the spectra by the area under the curves (Fig. 4 b). The excitation spectrum does not change, whereas the emission spectrum blue-shifts with the temperature decrease. The emission peak wavelengths at 60°C and 20°C are around 602 nm and 570 nm, respectively. The emission spectrum also gets narrower with the temperature decrease. The half-peak width changes from 152 nm at 60°C to 114 nm at 20°C.
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). The phase diagram derived from these studies shows that small-scale (r < 1 µm) liquid-ordered phase domains will appear within the liquid-disordered phase domains when the temperature is decreased to close to the transition temperature. With further temperature decrease, the membrane will eventually become homogeneous in the liquid-ordered phase. Therefore, we suspect that the rapid emission shift in Fig. 4 b mainly reflects the phase transition and is not some other effect of the temperature change. To test the effect of temperature in the absence of a phase transition, we measured the temperature dependence with LUVs composed of pure DOPC as a control. DOPC has a transition temperature of –21°C, so in this control experiment, changing temperature from 20°C to 60°C does not cause a phase transition. In Fig. 5 a, we observed a fluorescence intensity decrease with temperature increase, as in Fig. 4 a. In Fig. 5 b, the spectra are normalized, showing no shift in the excitation spectrum, and a very small and continuous emission-spectrum blue shift from 638 nm to 630 nm as temperature decreases from 60°C to 20°C. The rate of emission change is analyzed by plotting the emission ratios at 690:580 nm against the temperatures (Fig. 5 c), revealing a linear relationship within this temperature range. Additionally, the emission spectrum (Fig. 5 b) does not show any signifcant narrowing as a function of temperature. Comparing Figs. 4 and 5, we can draw the following conclusions: 1), di-4-ANEPPDHQ's fluorescence intensity decreases as the temperature increases; and 2), the dye's emission spectrum blue-shifts and narrows during the membrane phase transition from the liquid-disordered to the liquid-ordered phase.
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To test this idea, we used di-4-ANEPPDHQ to stain GUVs with DOPC, DPPC, and cholesterol in a mixture of 2:2:1 molar ratio. At room temperature, membranes with this composition form separate liquid-ordered and -disordered phases (18). DOPC is more concentrated in the disordered phase, whereas DPPC and cholesterol are more concentrated in the ordered phase. In Fig. 6, a–c, di-4-ANEPPDHQ shows opposite contrast patterns for the green (500–550 nm) and red (650–710 nm) emission band channels, reflecting domain phase separation within the GUV. Based on our analysis of the LUV data of Figs. 2–5
, we assign the greener domains in the GUV images to the liquid-ordered, cholesterol-enriched phase and the redder domains to the liquid-disordered, cholesterol-depleted phase. To confirm this, we have shown that perylene, a probe known to partition preferentially into the liquid-ordered phase (4), colocalizes with the greener di-4-ANEPPDHQ emission. Using the spectral recording capabilities of the multielement detector in the Zeiss Meta confocal microscope, we were able to obtain emission spectra from these two regions. Fig. 6 d shows the normalized emission spectra of di-4-ANEPPDHQ in the liquid-ordered (greener) and liquid-disordered (redder) domains of GUVs with this composition. The emission peak in the green domain is 
575 nm, whereas in the red domain it is 607 nm. From Fig. 6 d, we can also see that the green emission spectrum is narrower than the red one, as predicted. This is not as large as the 60-nm spectral difference displayed between the LUVs composed of pure DOPC versus DPPC/cholesterol; the smaller spectral difference between the domains in the GUVs presumably reflects the incomplete segregation of lipids into the two domains (see Discussion). From these averaged normalized emission spectra, we can assess the relative contrast between the two domains within the wavelength ranges corresponding to the emission filters used for Fig. 6, a–c; the intensity ratio for liquid-ordered/liquid-disordered is 3.7 within the 500–550 nm green band, whereas it is 0.23 for the 650–710 nm channel. This explains why the choice of filters in Fig. 6, a–c, permits ready visualization of the separated phases.
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). Egg phosphatidylcholine is a mixture of L-
-phosphatidylcholines with various fatty acid chains, and its main component is 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine, an unsymmetric phospholipid with a low transition temperature of –2°C (22). Brain sphingomyelin is a mixture of different ceramide-1-phosphocholines, and its main component is stearoyl sphingomyelin, with a high transition temperature of 41.5°C (24). 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine and stearoyl sphingomyelin are common cell plasma membrane components, so this test can provide a first indication of whether di-4-ANEPPDHQ might be suited for cell biological applications. The two lipids differ not only in their fatty acid chains, which determine the transition temperature, but also in their backbone structures. Therefore they indicate whether the dye's sensitivity will be affected by factors other than the fatty acid chains. Di-4-ANEPPDHQ again displayed emission spectral differences between the two coexisting phases that permitted visualization of domains in images of these GUVs. (Fig. 7). The images in Fig. 7 were acquired using the same emission wavelengths as the images in Fig. 6. The spectrum peak in the ordered phase is around 596 nm, whereas in the disordered phase it is 639 nm (Fig. 7 d). Thus, both spectra are red-shifted compared to the simpler mixture of synthetic lipids analyzed in Fig. 6; this may reflect an overall greater disorder in both domains of the natural lipid GUVs. The spectrum in the disordered domains is also broader than in the ordered domains. Analysis of the relative contrast in the two domains shows that the intensity ratio for liquid-ordered/liquid-disordered is 2.3 within the 500–550 nm green band, whereas it is 0.53 for the 650–710 nm channel. These contrast ratios are substantial, but not as great as those found for the synthetic lipids; this accounts for the poorer contrast in Fig. 7, a–c, compared to Fig. 6, a–c. This experiment shows that the dye also distinguishes domains with natural lipids with various backbone structures and complex mixtures of fatty acids.
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–27). The styryl chromophore of di-4-ANEPPDHQ displays strong resonance-enhanced hyperpolarizability, and in membranes the dye is aligned by the surrounding lipids, with the molecules arranged in the same orientation in a single leaflet. Therefore, membrane-bound di-4-ANEPPDHQ generates second harmonics. The signal intensity of SHG is quadratic with respect to the dye's concentration, so one hypothesis for the higher SHG signal in the liquid-disordered phase is that the dye preferentially partitions into the liquid-disordered phase over the liquid-ordered phase. A significant, but lower, concentration of dye in the liquid-ordered phase could produce sufficient fluorescence emission to account for the comparable intensities from both phases, if the fluorescence quantum efficiency of the dye were higher in liquid-ordered than in liquid-disordered phases.
To estimate di-4-ANEPPDHQ's relative affinity to membranes in liquid-ordered and liquid-disordered phases, we titrated 1 µM of dye with LUVs at concentrations from 0 to 5 mg/ml and measured the fluorescence enhancement associated with dye binding. The fluorescence at wavelengths corresponding to maximal excitation and emission of the bound form is plotted against the lipid concentration of the LUV suspensions (Fig. 9). We then fit the data to a one-site saturable binding model via nonlinear least-squares analysis (15):
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is the fluorescence when all of the dye is bound; F0 is the almost negligible fluorescence from aqueous dye in the absence of lipid; Kd is the parameter for the relative affinity of the dye to the LUV, measured in mg/ml. We made LUVs of pure DOPC and 2:1 DPPC/cholesterol, and measured their emission spectra at room temperature, at which LUVs of the two mixtures would be in disordered and ordered phases, respectively. Excited with 475 nm, the peak emission in DOPC LUVs is 620 nm, whereas in DPPC/cholesterol LUVs it is 568 nm. The ordered-phase data fits the one-site saturable binding model (Fig. 10 a), in which F0 = 407, F = 2.6 x 104, and Kd = 0.691 mg/ml. The disordered-phase data does not fit a one-site saturable binding model; it can be fit with a sum of high- and low-affinity binding isotherms:
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1 = 6488, Kd1 = 0.063 mg/ml, F2 = 3.1 x 106, and Kd2 = 3.4 x 104 mg/ml. The first binding form has high affinity, whereas the second binding form has very low affinity. Because the Kd2 value of 3.4 x 104 is much higher than the lipid concentrations used here, the second binding form shows an essentially linear fluorescent increase with increasing lipid concentration in this range. From Fig. 10 b, when the lipid concentration is low, binding form 1 is the main contributor to the fluorescence. In the GUV experiments, the lipid concentration in the preparation is 0.1 mg/ml, which is in the low concentration range of the titration curve, so the high-affinity binding site is the major binding form at this lipid concentration and contributes 98% of the fluorescence in the disordered phase domain. Therefore, the dye's relative affinities to the disordered phase and ordered phase are estimated by comparing Kd1 = 0.063 mg/ml and Kd = 0.691 mg/ml, respectively. Thus, the dye's concentration should be 10 times higher in the disordered phase than in the ordered phase, explaining the higher SHG signal in the disordered phase.
After this series of studies on di-4-ANEPPDHQ in model membranes, we tested the efficacy of the dye to image lipid domains in cells. Because individual rafts are smaller than the spatial resolution of the light microscope (11), we chose polarized neutrophils, which are thought to have a high density of rafts in their front lamellipodia, with the expectation that the dye could show shorter emission wavelength in the region of high raft localization.
Neutrophils can be activated by a chemoattractant fMLP (formyl-methionyl-leucyl-phenylalanine). This is an important step for the recruitment of leukocytes during the inflammatory response. After activation, neutrophils are polarized with a blunted leading edge and a narrower posterior. F-actin in the lamellipodia in the front drives the cell to migrate toward the direction of higher chemoattractant gradient. This morphology change and motility is mediated by the polarized distribution of proteins and lipids, such as F-actin and PIP3 (28). Membrane reorganization during polarization recruits rafts to the front lamellipodia. Immunofluorescent staining of raft markers, sphingolipid GM3 and calcium channel TRPC-1, indicates that after polarization rafts are concentrated toward the leading edge of neutrophils. Cholesterol depletion disrupts rafts and abolishes the reorganization of the two markers during the polarization (29,30). Raft distribution in the neutrophils is also supported by emission spectrophotometry studies of cells stained by laurdan. Laurdan's spectrum blue-shifts in the liquid-ordered phase. Its emission spectrum from the front lamellipodia blue-shifts compared with the cell body and nonpolarized cell. The difference disappeared after cholesterol depletion (30). Therefore, we regard polarized neutrophils as a well studied cell system to test di-4-ANEPPDHQ.
To visualize lipid-domain heterogeneity with our probe, we divided images with emission at >650 nm by images acquired simultaneously through a 505–550 nm emission bandpass filter. Since the liquid-disordered phase has a dye emission spectrum that is shifted to the red compared to the dye in the liquid-ordered phase, a ratio of red/green emission intensities provides an indication of the relative population of domains at each point in the membrane. Similarly, the dye responds to high cholesterol by shifting its emission spectrum to the green, so the emission ratio for red/green wavelength bands will be sensitive to cholesterol concentration. We calculated this ratio for each pixel and can display and analyze the pattern of ratio values in the resulting image. Since rafts are presumed to be composed of high cholesterol in a liquid-ordered phase, pixels with low red/green ratios will correspond to patches of membranes with a higher density of rafts than pixels with high red/green ratios. The nonpolarized neutrophils are approximately spherical (Fig. 10, a and b). Di-4-ANEPPDHQ does not show significant ratio heterogeneity along the membranes in these cells. In polarized neutrophils (Fig. 10, c and d), di-4-ANEPPDHQ has a smaller ratio value in the lamellipodia at the leading edge. After cholesterol depletion, the neutrophils still can be polarized by fMLP, but the ratio difference of di-4-ANEPPDHQ between the front and back (Fig. 10, e and f) is largely abolished.
Fig. 11 is a statistical summary of several such experiments on polarized neutrophils with and without cholesterol depletion. The depleted groups show generally higher red/green ratios in the plasma membranes (Fig. 11 a). We divided the red/green ratio of the front lamellipodia by that of the back lamellopodia to reveal the difference between the two areas; if this value of ratios is 1, no asymmetry is indicated. The value is 0.87 in the polarized neutrophils and 0.96 in the cholesterol-depleted neutrophils (Fig. 11 b). The number is closer to 1 after cholesterol depletion, which is consistent with the disruption of raft domains by removal of cholesterol. The data displayed in Fig. 11 c show that the front and rear of the cells have significantly differing emission spectra—approaching the separation obtained from the resolved domains of the natural lipid GUVs (Fig. 7). Significantly, the difference in the front versus the rear spectra is abolished upon cholesterol depletion (Fig. 11 d). This suggests that the spectral difference in the normal polarized cells is a result of a biased distribution of cholesterol toward the leading edge of the cell, as would be associated with a high density of rafts.
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DISCUSSION |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONSUPPLEMENTARY MATERIALACKNOWLEDGEMENTSREFERENCES |
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Di-4-ANEPPDHQ shows green and red emission in the ordered and disordered phases, respectively. To further understand the mechanism, we undertook a series of studies with LUVs of different lipid composition and different phases. We found that the dye's emission spectrum is primarily influenced by two factors, cholesterol concentration and the lipid phases. The emission spectrum blue-shifted with cholesterol concentration increase, and it also blue-shifted in the liquid-ordered phase relative to the liquid-disordered phase.
Cholesterol affects lipid membranes in two ways. First, it is known that cholesterol changes the lipid membrane's dipole potential (31,32). Second, it changes the packing of lipid molecules in the membrane (33). Both of these effects could influence di-4-ANEPPDHQ's fluorescence.
Dipole potentials are intramembrane potentials originating from oriented dipoles at the membrane/water interface. The polar molecules contributing to dipole potentials include water, the polar headgroups of lipid molecules, and the ester linkages of acyl chains to the glycerol backbone of phospholipids. Dipole potentials in the membrane bilayer are positive in the center, with a magnitude of several hundred millivolts. Cholesterol increases the dipole potentials, and styryl dyes have been shown to sense the dipole potential changes in lipid membranes (32). In theory, dipole potentials can affect the energy difference between the excited and ground states of dye molecules. Both the excitation and emission spectra would be influenced, and they would be shifted in the same direction and to a similar extent. This has been demonstrated by studying the spectra of another styryl dye, d-4-ANEPPS (32). A cholesterol analog, 6-ketocholestanol, which increases dipole potential (34), blue-shifts di-4-ANEPPS' excitation and emission spectra to a similar extent, amounting to just a few nanometers (32). Interestingly, in our experiments, increasing cholesterol concentration in the LUVs blue-shifts both the excitation and emission spectra of di-4-ANEPPDHQ, but to a much greater extent in the emission spectrum. Therefore, we conclude that cholesterol's influence on the dipole potential contributes to the dye's emission-spectrum shift, but it cannot account for the large magnitude of the shift.
As cholesterol also changes the order of lipids in membranes, a second hypothesis for the origin of the emission shift is that it reflects a change in the local molecular ordering of the dye molecule's environment. Membranes with pure lipid will be in a liquid-disordered phase above their transition temperature and in a solid phase below the transition temperature. Cholesterol in the lipid membrane disrupts molecular packing when the membrane is below the lipid's transition temperature, whereas it orders the acyl chains of lipids when the temperature is higher than the transition temperature. Thus, an intermediate phase, the liquid-ordered phase, has been established for cholesterol-containing membranes (35,36). Therefore, cholesterol could increase the order or rigidity of the molecular environment surrounding di-4-ANEPPDHQ, thereby decreasing the dye's Stokes shift. The Stokes shift reflects the energy lost when the excited dye molecules relax to a lower energy geometry and a lower energy distribution of solvent molecules before emitting fluorescence. Styryl dyes are known to have large Stokes shifts, reflecting the formation of twisted excited states and a large reorganization of solvent around the redistributed charge within the excited state (37,38). When the environment becomes more ordered, conformation change and rearrangement of the solvent may be limited. Therefore, there will be less energy lost and more energy released as fluorescence from dyes in the rigid environment. The data of Fig. 3 could then be explained as an increased order or rigidity in the neighborhood of dye molecules as the cholesterol concentration is increased.
The same hypothesis concerning the Stokes shift could also explain the phase transition's effect on di-4-ANEPPDHQ. The lipid rigidity increases when the membrane phase changes from liquid-disordered to -ordered. In Fig. 4, there is no obvious excitation shift but a large emission blue shift during the phase transition.
Comparing emission spectra from LUVs of DOPC and 7:3 DPPC/cholesterol, there is a 60 nm peak difference. In GUVs of 2:2:1 DPPC/DOPC/cholesterol, the spectra from the ordered and disordered phases have a shift of 30 nm, which is smaller than the maximum possible difference of 60 nm obtained from the LUV experiments. In the GUVs, the chemical components are not totally segregated into the two phases, so not all the DOPC is in the disordered phase and not all the DPPC and cholesterol are in the ordered phase. Cholesterol in particular does not show dramatically preferential partitioning between the two phases. In GUVs made from 7:7:5 DOPC/DPPC/cholesterol, after phase separation at 25°C, NMR shows that in the ordered phase 32 mol % of the lipid molecules are cholesterol, whereas in the disordered phase 22 mol % of the lipids are cholesterol (39). Although the formula of GUVs used in our experiment (2:2:1 DOPC/DPPC/cholesterol) is slightly different from that used in the NMR study, we would still expect only moderately preferential partitioning of cholesterol into the liquid-ordered phase. Thus, the emission spectrum shift of 30 nm mainly reflects the phase difference rather than a large difference in cholesterol concentration. This also helps explains why the natural lipids (Fig. 7) show a somewhat poorer contrast between the two phase-separated domains in the red and green emission channels. The partitioning of the different lipids between the two phases will be even less clean for this heterogeneous mixture of natural lipids. Furthermore, the more complex lipid mixture will tend to somewhat diminish the order even within the liquid-ordered phase, thus accounting for the red shift of both spectra in Fig. 7 compared to those of Fig. 6. Thus, the LUV spectra represent extremes that can be used to gauge the domain characteristics in the GUVs and in cells.
Di-4-ANEPPDHQ differentiates the two domains not only by its fluorescence but also by its SHG signals. Its higher SHG intensity in the liquid-disordered phase reflects the higher concentration of the dye. The affinity of the dye to LUV composed of DOPC, representing a liquid-disordered membrane, is 11 times higher than the affinity for 2:1 DPPC/cholesterol, representing the liquid-ordered phase, at room temperature. If we assume that all the DOPC is in the GUVs' liquid-disordered phase and all the DPPC and cholesterol are in the liquid-ordered phase, we would conclude that the concentration of di-4-ANEPPDHQ in the liquid-disordered phase is 11 times that in the liquid-ordered phase. Thus, based on the quadratic dependence of SHG intensity on concentration (26), we might expect to see the SHG signal intensity in the disordered phase to be 121 times that in the liquid-ordered phase. The relative SHG signal measured in the disordered phase to that in the ordered phase is actually 7:1, which is much smaller than the expected 121:1. It corresponds to only a 2.6-fold higher concentration in the disordered phase. We explain the smaller ratio in two ways. First, the implicit assumption concerning the concentration of lipids in the two phases of the GUVs is not reasonable. As explained above, the lipids do not partition into the two phases with a complete segregation. Therefore, the affinities estimated in LUVs of DOPC and 2:1 DPPC/cholesterol can work only as an upper limit for the GUV experiment. Second, the concentration of the dye is not the only factor influencing the SHG signal intensity. The alignment of the dyes is another important factor. SHG depends on coherent scattering of polar molecules, which need to be aligned in the same orientation, so the signal will be strongest if the dye chromophores are parallel to each other. In the ordered phase the acyl chains are straighter, and the lipids are more tightly packed. This will improve alignment of the dye molecules and increase the SHG signal in the ordered phase, partially counteracting the effect of a higher concentration of the dye in the disordered phase.
In summary, di-4-ANEPPDHQ shows significant fluorescent emission spectrum shifts in liquid-ordered and -disordered phase domains coexisting in GUVs. This appears to primarily reflect the membrane rigidity in the different phases. The dye also shows SHG intensity contrast between the two domains, reflecting both the dye's concentration and alignment in the two phases.
Di-4-ANEPPDHQ has been used to measure the transmembrane potential changes in live cells, and we provide evidence that it can also be used as a probe for rafts in neutrophil plasma membranes. Compared to other probes currently used to study membrane domains in live cells, di-4-ANEPPDHQ has some benefits. First, it loads into cells from a water solution. Most membrane probes are not water soluble, so they need organic solvents, such as DMSO and ethanol, or vehicles, such as Pluronic F127 or 
-cyclodextrin, to be mixed with buffer solutions for cells. These may disturb cell membranes and cause artifacts. Second, the dye loads into cells rapidly. Laurdan requires 30–60 min to stain cells (7), during which period it may be internalized by endocytosis. Signals from intracellular organelles complicate the image analysis. Di-4-ANEPPDHQ stains the plasma membrane rapidly, so the stained cells can be imaged immediately. Before any obvious endocytosis is observed, there is a time window during which clean fluorescent images of plasma membrane can be acquired. The length of the time window depends on the type of cell and the temperature. Furthermore, if rafts are detected by SHG from the dye, the internal staining will not show up in the SHG images. Third, di-4-ANEPPDHQ can be imaged by multiple optical methods, including confocal microscopy with commonly available visible wavelengths. Fourth, di-4-ANEPPDHQ's fluorescence senses the environmental differences between phases, as required for detecting rafts with different chemical components. Probes such as cholera toxin subunit B, which bind to certain chemical components in rafts, may not detect all rafts in cells because of the heterogeneity of rafts. It should be cautioned that, as with other environmentally sensitive probes, the spectrum of di-4-ANEPPDHQ could be influenced by interactions with membrane proteins that cannot be predicted from its spectral characterization in lipid vesicles. However, the fact that the emission spectra originating from the front and rear of the cell are distinct in normal cells (Fig. 11 c), but become indistinguishable in cholesterol-depleted cells (Fig. 11 d), argues that, at least in the case of neutrophils, the dye is sensitive to a differential distribution of cholesterol-enriched raft domains. We anticipate that di-4-ANEPPDHQ will become a valuable probe for visualizing lipid domains in live cells.
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONSUPPLEMENTARY MATERIALACKNOWLEDGEMENTSREFERENCES |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONSUPPLEMENTARY MATERIALACKNOWLEDGEMENTSREFERENCES |
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This study was funded by the National Institute of Biomedical Imaging and Bioengineering via a National Institutes of Health grant (No. EB001963).
Submitted on August 18, 2005; accepted for publication December 15, 2005.
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