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Vol. 18, Issue 6, 2226-2243, June 2007

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Receptor Complexes Cotransported via Polarized Endocytic Pathways Form Clusters with Distinct Organizations

H. Wallrabe^*,, G. Bonamy^,,, A. Periasamy^*, and M. Barroso^||

*Department of Biology, W. M. Keck Center for Cellular Imaging, University of Virginia, Charlottesville, VA 22904; Hudson Alpha Institute for Biotechnology, Huntsville, AL 35801; and ^||Center for Cardiovascular Sciences, Albany Medical College, Albany, NY 12208

Submitted August 11, 2006; Revised February 8, 2007; Accepted March 26, 2007
Monitoring Editor: Francis Barr

	ABSTRACT

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
Previously, FRET confocal microscopy has shown that polymeric IgA-receptor (pIgA-R) is distributed in a clustered manner in apical endosomes. To test whether different membrane-bound components form clusters during membrane trafficking, live-cell quantitative FRET was used to characterize the organization of pIgA-R and transferrin receptor (TFR) in endocytic membranes of polarized MDCK cells upon internalization of donor- and acceptor-labeled ligands. We show that pIgA-R and TFR complexes form increasingly organized clusters during cotransport from basolateral to perinuclear endosomes. The organization of these receptor clusters in basolateral versus perinuclear/apical endosomes is significantly different; the former showing a mixed random/clustered distribution while the latter highly organized clusters. Our results indicate that although both perinuclear and apical endosomes comprise pIgA-R and TFR clusters, their E% levels are significantly different suggesting that these receptors are packed into clusters in a distinct manner. The quantitative FRET-based assay presented here suggests that different receptor complexes form clusters, with diverse levels of organization, while being cotransported via the polarized endocytic pathways.

	INTRODUCTION

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
Understanding how proteins are correctly localized and why that process goes awry in diseases is a fundamental question in biomedical research. Many diseases, such as cystic fibrosis and hypercholesterolemia, are due to defects in protein sorting and transport. The mechanism of protein transport has been analyzed but the molecular and biophysical basis for clustering at all levels of membrane trafficking pathways remains to be defined. Here, quantitative Förster resonance energy transfer (FRET) confocal imaging has been used to address the dynamics of protein clustering during receptor-mediated endocytic membrane trafficking in live polarized epithelial cells.

Polarized endocytic pathways include several compartments with different biochemical and molecular properties; for example, basolateral and apical early endosomes (BEE and AEE, respectively), common endosomes (CE), and apical recycling endosomes (ARE; see Figure 1; Rojas and Apodaca, 2002; Mostov et al., 2003). For this study, filter-grown polarized epithelial Madin-Darby canine kidney (MDCK) cells, stably transfected with polymeric IgA-receptor (pIgA-R) and transferrin receptor (TFR; MDCK-PTR cells), are used because they express TFR and pIgA-R at moderate levels and have been extensively used to characterize the polarized trafficking of these receptors using their respective fluorophore-labeled ligands, i.e., holo-transferrin (Tfn) and dimeric IgA or pIgA-R ligand (Apodaca et al., 1994; Barroso and Sztul, 1994; Gibson et al., 1998; Brown et al., 2000; Wang et al., 2000; Rojas and Apodaca, 2002; Mostov et al., 2003; see Figure 1A). Both TFR and pIgA-R are involved in physiologically significant cellular processes, such as iron uptake for TFR (Lawrence et al., 1999; Cheng et al., 2004) and secretory immunity for pIgA-R (Rojas and Apodaca, 2002). TFR undergoes basolateral recycling via BEE, CE, and AEE (see Figure 1A, arrows 1, 2b, 2a, 3a, 3b, and 5b; Odorizzi et al., 1996; Gibson et al., 1998; Sheff et al., 1999; Leung et al., 2000). Entrance of basolaterally internalized TFR into the AEE suggests that these endosomes play a role in the basolateral recycling of TFR (Leung et al., 2000). Although, the majority of pIgA-R transcytoses to the apical PM via the CE and the ARE (see Figure 1A, arrows 3c and 6), a smaller, but significant minority, recycles back to the basolateral surface together with TFR (see Figure 1A, arrow 2a or 3a; Apodaca et al., 1994; Barroso and Sztul, 1994; Gibson et al., 1998; Brown et al., 2000; Leung et al., 2000; Wang et al., 2000). In contrast to TFR, which is predominantly located at the basolateral PM, pIgA-R is also found at the apical PM (Figure 1A, arrow 4). On apical internalization, pIgA-R is delivered to the AEE and CE (Figure 1A, arrows 4, 5a, and 5b) and recycled back to the apical PM via the ARE (Figure 1A, arrow 6; Barroso and Sztul, 1994; Leung et al., 2000). Basolateral-to-apical transcytosis and apical PM localization, and internalization of TFR are only achieved upon treatment with brefeldin A (BFA; see Figure 2A), a fungal metabolite that disrupts the polar sorting of endocytic receptors (Wan et al., 1992; Futter et al., 1998; Wang et al., 2001).

An essential prerequisite for efficient membrane protein trafficking is the segregation of protein molecules within continuous membrane sheets to form microdomains with specific protein compositions. The sorting of membrane components from fluid-phase molecules has been suggested to depend on the endosomal geometry and iterative fractionation (Geuze et al., 1987; Dunn et al., 1989; Mayor et al., 1993). On the other hand, membrane-bound receptors may undergo a signal-mediated enrichment upon exiting the PM or endosomes to be delivered to their specific destinations (Maxfield and McGraw, 2004). Thus, an important step in endocytic receptor trafficking could be the concentration of receptor-ligand complexes in transport intermediates.

The organization of receptors in endocytic membranes has been analyzed using electron microscopy (Geuze et al., 1984; Stoorvogel et al., 1989). Demonstration that gold-labeled Tfn or gold-labeled pIgA-R ligand concentrate in discrete packaging sites, such as in clathrin-coated buds, in polarized MDCK cells has been hard to achieve because of technical difficulties in loading the endosomal system close to saturation (Geuze et al., 1984; Futter et al., 1998; Gibson et al., 1998). In polarized MDCK cells, some studies have suggested that receptors are organized in a nonuniform manner in endocytic membranes (Futter et al., 1998), whereas other studies have indicated that receptors are distributed in a random manner throughout endocytic tubules and vesicles (Gibson et al., 1998).

In this study, we used quantitative FRET confocal microscopy in live cells to investigate the nature of receptor organization in membranes of polarized endosomes Membrane-bound receptors can either be assembled in clusters, distributed randomly or possibly exhibit a continuum between these two states. The relationship between FRET and the geometric distribution of labeled membrane components is highly nonlinear. Thus, mathematical modeling has played a key role in identifying relevant parameters and developing criteria to reveal the presence of clustered receptors (Kenworthy and Edidin, 1998; Varma and Mayor, 1998; Kenworthy et al., 2000; Tcherkasskaya et al., 2002). The quantitative FRET assay presented here uses the efficiency of the energy transfer (E%) and its relationship to donor and acceptor (A) fluorescence intensities to establish whether the close proximity between membrane proteins is due to random associations ("molecular crowding") or specific nonrandom clustering (Zimet et al., 1995; Kenworthy and Edidin, 1998; Kenworthy et al., 2000; Pentcheva and Edidin, 2001; Zacharias et al., 2002; Wallrabe et al., 2003a,b, 2006; Bhatia et al., 2005; Wallrabe and Barroso, 2005). Our results show that clusters, comprising these two receptor-ligand complexes during cotransport, are formed with increasingly tighter organizations along the polarized endocytic pathway of live MDCK-PTR cells.

	MATERIALS AND METHODS

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
Culture of MDCK-PTR Cells on Filter Inserts
MDCK-PTR cells stably transfected with rabbit pIgA-R and human TFR (Brown et al., 2000; Wang et al., 2000) were grown to confluence in 100-mm cell culture dishes, trypsinized, centrifuged, and resuspended in DMEM/10% fetal bovine serum/Pen-Strep (Barroso and Sztul, 1994). Approximately 300,000 cells were placed on top of an inverted Transwell Clear insert (Corning Costar, Cambridge, MA), which allowed for their direct visualization through a coverslip using an inverted microscope (Brown et al., 2000; Wallrabe et al., 2003a). After 3–4 d in culture, the fully polarized monolayer was immediately used according to different internalization protocols (Barroso and Sztul, 1994; Wallrabe et al., 2003a). Cellular polarity was established by the reduced apical uptake and basolateral staining of apically internalized fluorophore-labeled Tfn (<10%) and ricin (<5%), using confocal microscopy (Barroso and Sztul, 1994).

Fluorophore-labeled Ligands
Alexa488 (donor) was conjugated to pIgA-R pseudoligands ([Fab]₂ fragments raised against rabbit pIgA-R extracellular domain) according to the manufacturer's (Invitrogen, Carlsbad, CA) protocol (Barroso and Sztul, 1994; Wallrabe et al., 2003a). Conjugation of Cy3 (acceptor) was performed, according to the manufacturer's (GE Healthcare, Waukesha, WI) instructions, to iron-free human Tfn (apo-Tfn; Sigma, St. Louis, MO), followed by iron loading with ferric ammonium citrate as described previously (Barroso and Sztul, 1994). Alexa488 (donor) or Alexa555 (acceptor) bound to human Tfn were purchased from Invitrogen and preloaded with iron. Previously, we have shown that MDCK cells expressing only pIgA-R (MDCK-PWE cells) bound iron-loaded human Tfn at very low levels because of the inability of dog TFR to recognize human Tfn (Barroso and Sztul, 1994). Furthermore, iron-loaded dog Tfn was internalized at low levels into MDCK cells in a TFR-dependent and pIgA-R-independent manner (Barroso and Sztul, 1994). Significant apical re-endocytosis upon release of ligands into the apical media does not happen under our internalization conditions (Barroso and Sztul, 1994; Wallrabe et al., 2003a).

Internalization of Fluorophore-labeled Ligands
Inserts with a fully polarized MDCK-PTR cell monolayer were washed with PBS²⁺, equilibrated with MEM/HEPES/BSA at 37°C, and pretreated 15 min with or without 10 µM BFA. Then, these cells were internalized for 30 min at 37°C with different amounts of Alexa488-pIgA-R ligands and/or Cy3-Tfn/Alexa555-Tfn (40–100 µg/ml) from the basolateral and/or apical PM in the presence or absence of 10 µM BFA. High concentrations of pIgA-R ligand and Tfn helped minimize the presence of empty receptors. Cells were washed and fixed with 4% paraformaldehyde/phosphate-buffered saline (PBS), as described previously (Barroso and Sztul, 1994; Wallrabe et al., 2003a,b, 2006). For live cells, the protocol was exactly the same, except that each insert followed the regimen individually and was imaged immediately at room temperature. As a positive control for random distribution of substrate-bound proteins, Alexa488-Tfn and Alexa555-Tfn were incubated for 30 min at room temperature onto polylysine-coated glass coverslips, fixed with 4% paraformaldehyde, washed in PBS, and imaged within 48 h using confocal microscopy. As a positive control for membrane protein clustering, Alexa488-Tfn and Alexa555-Tfn were internalized for 30 min at 37°C into polarized MDCK-PTR cells, as described previously (Wallrabe et al., 2006).

For FRET assay purposes (filter-bound cells or polylysine-bound coverslips), three different samples were used: double-labeled specimens, containing D- and A-labeled ligands (pIgA-R and/or Tfn) and two single-label specimens containing either D- or A-labeled ligands; the single-label reference samples were used to establish spectral-bleedthrough (SBT) levels.

Immunofluorescence of Polarized Cells
Polarized MDCK-PTR cells were internalized from the basolateral PM with Alexa555-Tfn for 30 min at 37°C and treated with or without BFA, as described above. Then, cells were washed, fixed with 4% paraformaldehyde, and processed for immunofluorescence, as described previously (Andrade et al., 2004). Monoclonal antibodies against EEA1 (BD Biosciences, San Jose, CA) and rabbit polyclonal against Rab11 (Invitrogen/Zymed, South San Francisco, CA) were used at 1:100 and 1:40 dilutions, respectively. Cells were visualized using a Zeiss 510META LSM microscope (Thornwood, NY, as described below), and Z-series with a 0.5-mm interval were collected. Image analysis of confocal images was performed using Adobe Photoshop 5.5 (San Jose, CA). To allow intensity comparisons, we used similar conditions to collect and manipulate images within each antibody experiment.

Laser Scanning FRET Microscopy
For data collection, the specimen was positioned in a small chamber created by a coverslip between two metal rings, filled with a small amount of PBS (fixed cells) or MEM/HEPES/BSA media (live cells) and placed on the microscope stage. Nikon PCM 2000 (Melville, NY) or Bio-Rad Radiance 2100 laser scanning confocal microscopes (Richmond, CA), respectively, mounted on a Nikon TE200 or TE300 epifluorescence microscopes and equipped with Argon (488 nm) and Green HeNe (543 nm) lasers and emission filters, 515/30 nm and LP590 nm, were used with a 60x water immersion lens, 1.2 NA to collect images for FRET processing. For image acquisition and processing, SimplePCI software (Compix, Cranberry Township, PA) was used to drive the Nikon hardware, and LaserSharp2000 was used for the Bio-Rad microscope.

Data Collection
Two-color Z-series with a 0.5-µm vertical step were collected to check cell height (10–15 µm) and to select focal planes at different cell heights. Optimal PMT and accumulation settings and laser power levels were established in this pre-FRET-acquisition phase. With the zoom setting at 2x, images of the double-labeled specimen were taken with the Green HeNe laser, 543-nm excitation, i.e., acceptor excitation, and the acceptor emission channel (LP590 nm) followed by imaging with the argon laser 488-nm excitation, i.e., donor excitation, and the donor (515/30 nm) or the acceptor (LP590 nm) emission channels. The single-labeled acceptor specimen followed the same protocol. The image of the single-labeled donor specimen at acceptor excitation wavelength was collected to verify the instrument cross-talk in both channels. Images of all three types of specimen were taken under identical imaging conditions; PMT gain and black-level were set at identical values to collect data simultaneously in both channels into 1024 x 1024- or 512 x 512-pixel eight-bit images. Bleaching was undetectable during the short exposure to collect the final image. The Bio-Rad Radiance 2100 confocal system was used for live cell image acquisition. A custom macro was used to toggle between donor and acceptor excitation lasers and thus minimize the delay in switching lasers. The Nikon PCM2000 microscopes were used to collect images from fixed cells.

Postacquisition Data Generation
First, images were background-subtracted and processed by the PFRET software, which removed donor and acceptor SBT pixel-by-pixel on the basis of matched fluorescence levels between the double-label specimen and single-label reference specimens, using seven images: two single-label donor reference images (donor excitation/donor channel and acceptor channel); two single-label acceptor reference images (donor and acceptor excitation, both in the acceptor channel); three double-label images (donor excitation/donor and acceptor channel, acceptor excitation/acceptor emission; Elangovan et al., 2003; Wallrabe et al., 2003a, b). The three double-labeled images were named as follows: quenched donor (qD), i.e., the donor excitation/donor emission; acceptor (A), i.e., acceptor excitation/acceptor emission; and uncorrected FRET (uFRET), i.e., donor excitation/acceptor emission. The pixel-by-pixel correction used to generate the processed FRET (PFRET) image was actually based on the average value of narrow fluorescence ranges, for more efficient running of the correction algorithm (Elangovan et al., 2003). In our case, we chose the average of 12 fluorescence units per range, i.e., 0–12, 13–24, etc., continuing to the highest fluorescent units in the image. Using the average of even narrower ranges did not improve the sensitivity.

Postacquisition Data Analysis
Our measurements fall into the category of "apparent" E%, which is dependent on Förster-type energy transfer E (Wouters et al., 1998; Lakowicz et al., 1999), but is also influenced by the concentrations of those donor or acceptor molecules that are not involved in energy transfer; for brevity we will use E%, instead of "apparent" E%. E% is an expression of the energy transfer as a percentage of the unquenched donor, d = qD + ·PFRET, as described in the following equation: E% + 100·(·PFRET)/D, i.e., E% = 100·1 – (qD/D) (Elangovan et al., 2003; Wallrabe et al., 2003a, 2006; Bonamy et al., 2005; Wallrabe and Barroso, 2005). The factor, which is a function of the quantum yield of the fluorophores and the spectral sensitivity of the detection setup, plays a crucial role in recording precise E% and distances between fluorophores. Because the excitation efficiencies (), quantum yields of the fluorophore molecules and the detection efficiencies (Q) remain constant throughout the experiments, and the factor does not affect the answers that FRET-based clustering analysis seeks. Therefore, for simplicity we used = 1, as described previously (Elangovan et al., 2003; Wallrabe et al., 2003a,b, 2006). Nevertheless, different microscopes using different imaging collection instruments and settings will by definition have distinct factors. Therefore, the relative E% values differ for data collected using distinct microscope systems. Such a case is demonstrated when comparing the perinuclear data set collected using different microscopic settings (cf. Figures 4C vs. 6B). Thus, different data sets can only be compared when collected using identical microscopy settings, for example, Figures 4, C and D, and 5D or Figures 6, A and B, 7, C and D, and 8, A and B.

A custom-written analysis program was able to select pixels of the eight-bit gray-scale fluorescence intensities of uFRET, A and qD images ranging between 0 at the lower bound and at the higher bound one below [255 minus background value] to exclude any saturated pixels. Under our imaging conditions, there were very few saturated pixels (Wallrabe et al., 2003a, 2006). Then, appropriate regions of interest (ROIs) were visually selected from the uFRET image. These ROIs were subsequently applied to the other images to extract the fluorescence values. The values which include PFRET (actual energy transfer levels as per the PFRET SBT correction algorithm), qD and A levels were transferred to an Excel spreadsheets (Microsoft, Redmond, WA) for calculation of additional parameters such as E%, D, and D/A ratios. These values were averaged over ROIs containing 50–500 pixels. For further FRET clustering analysis, E% values that correspond to A or D values of 10–80 Gy-scale units per pixel were selected to avoid the noise of very high or very low A or D fluorescence intensities on E% and to exclude outlier values (<5%), i.e., individual values that lie outside the overall observed range (Bhatia et al., 2005; Wallrabe et al., 2006).

Statistical Analysis
To provide insights as to whether E% is affected by increasing levels of A at specific D/A ranges, the data were arranged into several D/A and A ranges. For D/A ranges, we used the following ranges: D/A 1 [1/] and D/A 2 [], which corresponds to categories with a twofold increase, centered around 1 and 2, respectively. Thus, D/A 1 ranged from D/A values of 0.7–1.4, whereas D/A 2 ranged from values of 1.4–2.8. In bar charts, the gray-scale intensity cohorts for A were defined by splitting in three the range defined by the lowest and highest value of A (Low = [20;40], Medium = [40;60], High = [60;80]). This approach can only be used to compare E% values for different data sets that show overlap between the high, medium and high ranges of A (Figures 3E and 8B).

To statistically analyze whether or not E% was dependent of the level of A at specific D/A ranges, we used the correlation coefficients (r value) and the slope (s values) as indicators (Table 1). The closer the r values are to 0, the less E% is dependent on A levels; the closer r values are to 1, the more E% depends on A levels. Another important parameter to determine whether E% depends on A levels is the slope of the linear regression, because a slope close to zero may have a high correlation, but suggest that E% does not depend on A. To analyze whether the E% cohorts at different A levels (10–19, 20–29, 30–39, 40–49, etc.) were significantly different or not, we used the ANOVA with a single-factor analysis from the Excel data analysis software package to establish p values between groups; significance of the statistic differences between the groups was indicated by p < 0.001.

	RESULTS

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

Morphology-based Assay To Discriminate between Different Polarized Endosomes
A strategy based on cell morphology has been developed to identify distinct endocytic compartments in polarized epithelial cells using FRET confocal microscopy (Barroso and Sztul, 1994; Brown et al., 2000; Wang et al., 2000, 2001; Maxfield and McGraw, 2004; Rodriguez-Boulan et al., 2005). A two-step approach was used: Various endocytic compartments were identified in the polarized MDCK-PTR cell system in the presence or absence of BFA by determining their "geographical" localization in comparison to two well-known endocytic markers, Rab11, a well-characterized ARE marker (Casanova et al., 1999; Leung et al., 2000; Wang et al., 2001), and EEA1, an effector of Rab5 function that has been associated with early endosomes (Mu et al., 1995; Simonsen et al., 1998b; Leung et al., 2000), in particular the AEE (Leung et al., 2000). A selection criterion based on the relationship between basolateral, perinuclear, and apical endocytic structures located at different cell heights and subcellular regions and different polarized compartments, such as AEE/BEE, CE and ARE, was applied to a ROI-based quantitative FRET approach to assign FRET values to specific endocytic compartments. The main objective is to assay FRET events located at different endocytic regions while avoiding the technical challenges that may arise from introducing an additional fluorescent endocytic marker into a FRET-based assay in view of potential spectral overlap and/or availability of laser lines.

To identify various polarized endocytic compartments by colocalization with well-known markers, MDCK-PTR cells were basolaterally internalized with Alexa555-Tfn for 30 min at 37°C in the presence or absence of BFA, which missorts Tfn to the apical PM (Wang et al., 2001). Because Tfn remains attached to TFR during its intracellular trafficking, detectable fluorescence staining indicates the presence of Tfn-TFR receptor-ligand complexes; referred to, for simplicity, as TFR complexes. Then, cells were fixed and immunofluorescence was performed using anti-Rab11 or anti-EEA1 and Alexa488-secondary antibodies. Cells were imaged using a Zeiss 510META LSM confocal microscope and z-series of double-label images were collected at 0.5-µm intervals. Finally, the distribution of Rab11 and EEA1 was overlaid with that of Tfn-TFR complexes, and three images were selected at different cell heights: 2–4 µm (basolateral region), 6–7 µm (perinuclear region), and 10–9 µm (apical region) above the insert filter (Figure 2).

As shown previously (Wang et al., 2001), TFR complexes undergo a dramatic shift in distribution upon treatment with BFA. In untreated cells, TFR complexes accumulate in punctate structures predominantly at the basolateral and perinuclear regions, with a reduced amount found in the apical region (Figure 2, a–e). In BFA-treated cells, TFR complexes redistribute mainly to the apical and perinuclear regions, with few punctate structures found in the basolateral region (Figure 2, i–k). Although the distribution of TFR complexes remain the same in the presence or absence of BFA in the basolateral (periphery) and perinuclear (dispersed throughout) regions, in the apical region it shifts from a dispersed peripheral pattern in the absence of BFA to a more centralized distribution in the presence of BFA. In untreated cells, Rab11's centralized apical distribution shows a reduced colocalization with the weak Tfn staining (Figure 2c; Wang et al., 2001). In contrast, in the apical region of BFA-treated cells, the TFR distribution pattern shows a significant overlap with the Rab11 staining (Figure 2h). These results suggest that BFA induces the movement of TFR complexes into the ARE as it is being delivered to the apical PM via the transcytotic pathway (Wang et al., 2001).

Our results also confirm previous data showing that basolaterally internalized TFR complexes are delivered to the AEE (Leung et al., 2000), because colocalization is detected between them and that of EEA1, predominantly in the cell periphery of the perinuclear and apical regions (Figure 2, d and e). These results suggest that AEE may play a role in the basolateral recycling of TFR complexes (Leung et al., 2000). Interestingly, in BFA-treated cells, only a reduced level of colocalization is detected between the peripherally disperse EEA1 punctate structures and the TFR complexes concentrated in the central area of the apical region (Figure 2k). These results suggest that in the absence of BFA, the TFR complexes participating in the basolateral recycling pathway have access to the BEE, CE, and AEE at the basolateral, perinuclear, and apical regions, respectively. In contrast, in the presence of BFA, the TFR complexes are shifted to the basolateral-to-apical transcytotic pathway in which they are mainly delivered to the BEE, CE, and ARE at the basolateral, perinuclear, and apical regions, respectively.

To develop a morphology- and ROI-based quantitative imaging approach to localize FRET signal to different endocytic compartments in polarized MDCK-PTR cells, Alexa488-pIgA-R ligands and/or Cy3-Tfn were internalized jointly from the basolateral surface for 30 min at 37°C in the absence or presence of BFA (Figure 3A) and imaged at different cell heights using confocal microscopy (Figures 1 and 2). As mentioned above, detectable fluorescence staining indicates the presence of pIgA-R and/or TFR receptor-ligand complexes, referred to, for simplicity, as pIgA-R and TFR complexes. Our preparation of [Fab]₂ derived from affinity-purified polyclonal antibodies against secretory component shows significantly higher transcytotic ability than monovalent Fabs (50–60 vs. 25–30%; Breitfeld et al., 1989; Barroso and Sztul, 1994) but lower than dIgA (50–60 vs. 70–80%; Apodaca et al., 1994; Brown et al., 2000) and does not accumulate intracellularly (Breitfeld et al., 1989; Barroso and Sztul, 1994). This difference in transcytotic/recycling behavior is probably due to the fact that the binding of dIgA induces the dimerization of pIgA-R (Singer and Mostov, 1998; Rojas and Apodaca, 2002; Van IJzendoorn et al., 2002; Mostov et al., 2003), resulting in the stimulation of the receptor transcytosis, at least threefold (Song et al., 1994; Luton et al., 1999; Luton and Mostov, 1999; Giffroy et al., 2001). [Fab]₂ may partially cross-link pIgA-R, thus mimicking the ligand-induced receptor dimerization and allowing the partial induction of pIgA-R transcytosis. However, there is no abnormal cross-linking between [Fab]₂ and the pIgA-R because that process would generate large complexes that would mask the FRET signal and be directed to the lysosomes. This targeting to the lysosomes would result in high levels of degradation (Weissman et al., 1986), which does not occur under our experimental conditions (Barroso and Sztul, 1994; Wallrabe et al., 2003a). Here, we show that there is significant colocalization between basolaterally internalized TFR and pIgA-R ligand complexes in BFA treated or untreated cells (Figure 3B, a–d) as well as between TFR complexes and Rab11 in BFA-treated cells (Figure 2h). These results suggest that TFR and pIgA-R complexes are part of the recycling/transcytotic pathway and not of the late endosome/lysosomal pathway.

A wide variety of ROIs were collected using a selection criterion based on their subcellular location in relationship to: 1) insert surface, i.e., the basal surface of the cells; 2) the nucleus; and 3) the cell center or periphery (Figures 1–3). In Figure 1B, a schematic representation of the different endocytic morphologies of cross sections at the basolateral, perinuclear, and apical locations is shown to help understand the ROI selection; basolateral ROIs are collected at the periphery of the cell across the lower part of the nucleus, whereas perinuclear ROIs are collected at the upper part of the nucleus away from the PM and the apical ROIs at the center of the cell above the nucleus. Finally, the ROI fluorescence intensities were subjected to a quantitative analysis to determine the response of these three endosome groups to BFA (Figure 3C). On the basis of the TFR/Rab11 and TFR/EEA1 colocalization distribution pattern (Figure 2), we propose the following: The basolateral ROIs represent the BEE and the perinuclear ROIs the CE. The apical region contains both the AEE and the ARE. In the nontreated cells, apical TFR complexes colocalize with EEA1 and a weak colocalization with Rab11. In contrast, in the BFA-treated cells, the TFR complexes exhibit a weak corelation with EEA1 distribution and high levels of colocalization with Rab11, clearly identifying the ARE.

View larger version (80K): [in this window] [in a new window]   Figure 1. Endocytic/transcytotic membrane trafficking pathways in polarized MDCK-PTR cells. (A) Arrows indicate natural endocytic/transcytotic membrane trafficking pathways available to fluorescently labeled pIgA-R ligand and Tfn in MDCK-PTR polarized cells. pIgA-R ligand and Tfn bind pIgA-R and TFR, respectively, at the basolateral PM and those receptor-ligand complexes are delivered to the BEE (arrows 1), and then to the CE (arrows 2b). Whereas TFR complexes are recycled back to the basolateral PM together with a minor fraction of pIgA-R complexes (arrow 2a), the majority of pIgA-R complexes are transcytosed to the apical PM via the CE and ARE (arrows 3b and 6). On internalization from the apical PM, pIgA-R complexes are delivered to the AEE (arrow 4) and CE (arrow 5b) and recycled back to the cell surface (arrows 5a and 6). Cell images (Figure 2B) are collected using confocal microscopy at different cell heights: the basolateral (blue rectangle), perinuclear (green rectangle), and apical (red rectangle) regions. Cy3- or Alexa555-labeled Tfn-TFR complexes, red arrows; Alexa488-labeled pIgA-R-ligand complexes, green arrows. AEE, apical early endosome; ARE, apical recycling endosome; BEE, basolateral early endosome; CE, common endosome; PM, plasma membrane; TJ, tight junction. (B) Cross sections of the polarized endocytic morphology show that the majority of the BEE localizes at the periphery of the cell in the basolateral region, whereas the CE localizes predominantly in the perinuclear region and the ARE above the nucleus and below the apical PM. This model also shows the potential contamination of perinuclear and apical endosomes with peripherally localized BEE and AEE, respectively.

View larger version (104K): [in this window] [in a new window]   Figure 2. Characterization of polarized endocytic compartments. Alexa555-Tfn (red staining) was cointernalized for 30 min at 37°C into the basolateral surface of polarized MDCK cells in the presence [Treatment (+BFA), f–k] or absence [Control (-BFA), a–e] of BFA. Then, immunofluorescence was performed using anti-Rab11 (a–c and f–h), a ARE marker, or anti-EEA1 (d–e and i–k), an early endosomal marker, and secondary antibodies labeled with Alexa488 (green staining). Then, confocal imaging was performed and images were collected at different cell regions. Apical, 10–9 µm above the insert filter (a, d, f, and i); perinuclear, 6–7 µm above the insert filter (b, d, g, and j); and basolateral, 2–4 µm above the insert filter (c, e, h, and k). Bar, 5 µm. Yellow staining indicates overlap between the TFR and the Rab11 or EEA1 distribution patterns.

View larger version (76K): [in this window] [in a new window]   Figure 3. A morphology-based system to discriminate between polarized endosomes. (A) Basolateral-to-apical endocytic/transcytotic pathway of basolaterally cointernalized TFR and pIgA-R complexes in the presence (+) or absence (–) of BFA, which missorts TFR to the apical PM, as shown by the red arrows 3b, 5a, and 6. (B) Alexa488-pIgA-R ligand (green staining) and Cy3-Tfn (red staining) were cointernalized for 30 min at 37°C into the basolateral surface of polarized MDCK cells in the presence (+BFA, b, d, and f) or absence (–BFA, a, c and e) of BFA. Then, confocal imaging was performed and images were collected at different cell regions. Apical, 10 µm above the insert filter (a and b); perinuclear, 7.5 µm above the insert filter (c and d); and basolateral, 3 µm above the insert filter (e and f). Bar, 5 µm. Yellow staining indicates overlap between the pIgA-R ligand and TFR distribution patterns. (C) BFA effect on basolateral, perinuclear, and apical endosomes containing TFR-Tfn and pIgA-R-ligand complexes. The relative amount of fluorescently labeled pIgA-R ligand and Tfn is evaluated by the average fluorescence intensity of a wide variety of ROIs that were collected and discriminated into basolateral, perinuclear, and apical endocytic regions according to the morphology-based system based on their location versus the filter insert, PM, and nucleus (Figure 1B). ROIs include endocytic punctate structures and contain 50–500 pixels. In the presence of BFA, a significant portion of TFR complexes redistributes to the apical region (+BFA, TFR bars), due to the elimination of their basolateral polarized sorting, which is clearly detected in the absence of BFA (–BFA, TFR bars). Error bars, 95% confidence interval.

In Figure 3C, three groups of endosomes (basolateral, perinuclear, and apical) are distinguishable based on their location, relative amount of TFR and pIgA-R and response to BFA, confirming the qualitative results of Figures 2 and 3B. This quantitative fluorescence analysis is consistent with previous reports indicating that BFA disrupts polar sorting (Hunziker et al., 1991; Wan et al., 1992; Prydz et al., 1992; Barroso and Sztul, 1994; Futter et al., 1998; Wang et al., 2001) and supports our morphology-based approach.

FRET To Discriminate Clustered and Random Protein Distributions
Mathematical models have been used to discriminate a clustered from a random membrane protein organization based on the relationship between E% and A levels at specific ranges of D/A ratios, which are experimentally determined using quantitative FRET (Zimet et al., 1995; Kenworthy and Edidin, 1998; Kenworthy et al., 2000; Zacharias et al., 2002; Wallrabe et al., 2003a,b, 2006; Wallrabe and Barroso, 2005). In a random situation, the likelihood of an acceptor colocalizing with a given donor is positively correlated with A levels and leads to an increase in E% (Figure 4A). Conversely, in a clustered scenario where molecules by definition are in proximity either in dimer or higher-order oligomeric complexes, E% is largely independent of A levels, and it does not decrease to zero when A trends to zero (Kenworthy and Edidin, 1998; Kenworthy et al., 2000; Pentcheva and Edidin, 2001; Spiliotis et al., 2002; Figure 4C). Furthermore, E% versus D/A is used to provide further insights into the tightness of the cluster organization (Wallrabe et al., 2003a,b, 2006). An overall negative dependency between E% and D/A at high and low A levels suggests a tight cluster organization (Figure 4C), whereas a general independency, highlights a random organization (Figure 4A). In a mixed random/clustered organization, where an assortment of clusters and randomly distributed proteins are found, E% may be positively correlated to A levels, but at a given A level it may be negatively dependent on D/A (Pentcheva and Edidin, 2001; Bhatia et al., 2005).

As a positive control for randomly organized proteins, different ratios of donor-Tfn and acceptor-Tfn bound to polylysine-coated coverslips were subjected to FRET confocal imaging (Figure 4B). A strong positive relationship between E% and A levels at both D/A 1 and D/A 2 is detected for Tfn-bound to polylysine-covered coverslips (Figures 4, B and E), with E% values trending to zero with decreasing A levels and correlation coefficients of r = 0.72 (slope s = 0.5) at D/A 1 and r = 0.85 at D/A 2 (Table 1). ANOVA test on E% at different A levels at D/A 1 yields a p value indicating significant evidence that the means are not equal (p < 0.001; Table 1). Furthermore, the E% versus A relationship behaves independently of D/A, i.e., at both low and high A levels E% values are not dependent on D/A (Figure 4B). These results indicate that donor-Tfn and acceptor-Tfn show a random organization upon binding to polylysine-coated coverslips.

View larger version (40K): [in this window] [in a new window]   Figure 4. FRET-based assay distinguishes between clustered and random membrane protein distributions. (A) A random organization model, E% is dependent on acceptor levels but not on D/A ratios. (B) Alexa488- and Alexa555-Tfn are bound to polylysine-covered coverslips, imaged by confocal microscopy and processed for FRET analysis. The Acceptor, D/A and E% values were extracted for a wide variety of ROIs and plotted against Acceptor levels at D/A 1 (squares) or D/A 2 (triangles). E% shows a clear dependency on Acceptor levels and independency from D/A. (C) In a clustered organization model, E% is independent from acceptor levels but rises with decreasing D/A ratios. (D) Alexa488- and Alexa555-Tfn are bound to TFR at the basolateral PM and internalized for 30 min at 37°C, imaged by confocal microscopy and processed for FRET analysis. The Acceptor, D/A and E% values were extracted for a wide variety of ROIs and plotted against Acceptor levels as described for B. In B and D, trendlines are shown as visual helpers (D/A 1, dotted line; D/A 2, dashed line). E% is largely independent from Acceptor levels and decreases with increasing D/A ratios. (E) Acceptor values at D/A 1 were split into three groups (low, medium, and high), and the respective average E% values were plotted for these Acceptor groups. Although the E% values from polylysine-bound Tfn samples positively correlated to A levels, E% from TFR-bound Tfn remains similar at all Acceptor levels, as expected for random and clustered distributions, respectively. Error bars, 95% confidence interval.

pIgA-R and TFR Complexes Show Distinct Organizations in Basolateral versus Perinuclear Endosomes. To test whether pIgA-R and TFR complexes cluster together along the endocytic pathway, we have used FRET to assay the organization of pIgA-R and TFR complexes at the basolateral and perinuclear endosomes. Live-cell FRET confocal microscopy is performed on images collected at 2–4 µm above the filter (basolateral; blue rectangle) upon cointernalization of donor-pIgA-R ligand and acceptor-Tfn for 30 min at 37°C into the basolateral surface of polarized epithelial MDCK-PTR cells (Figure 5A). Pseudocolor images depict D/A, A, and E%, respectively, in a pixel-by-pixel manner, showing the morphology patterns of these parameters. The typical basolateral morphology with peripherally localized punctate endocytic structures and a centrally located nucleus (N) is clearly detected across all images (Figure 5B, d–f). E% images show significant energy transfer between TFR and pIgA-R complexes in the basolateral region (Figure 5Bf).

View larger version (62K): [in this window] [in a new window]   Figure 5. pIgA-R and TFR complexes form clusters in perinuclear, but not in basolateral endosomes. (A) The organization and distribution of pIgA-R and TFR complexes in endosomes that are localized at the basolateral (blue rectangle) and perinuclear (green rectangle) regions was assayed using FRET confocal microscopy after cointernalization of Cy3-Tfn and Alexa488-pIgA-R ligand from the basolateral PM. (B) Live-cell confocal FRET imaging was performed on polarized MDCK-PTR cells basolaterally cointernalized with Alexa488-pIgA-R ligand and Cy3-Tfn. Pseudocolor images, processed using the PFRET correction algorithm, depict the pixel-by-pixel distribution of Acceptor (b and e), D/A (a and d), and E% (c and f) levels at the basolateral (d–f) and perinuclear (a–c) regions. Examples of selected ROIs that were selected according to the definitions of basolateral and perinuclear endocytic regions are shown as white squares. Bar, 5 µm. (C and D) E%, D/A and Acceptor levels were calculated for a wide range of ROIs (white squares). E% values were plotted as a function of Acceptor levels for D/A 1 () and for D/A 2 (). In C and D, trendlines are shown as visual helpers (D/A 1, dotted line; D/A 2, dashed line). (C) E% is largely independent of Acceptor levels and increases with decreasing D/A ratios, suggesting a clustered organization of TFR and pIgA-R complexes in perinuclear endosomes. (D) E% shows a variable dependency on Acceptor levels depending on D/A, indicating a mixed/random organization of TFR and pIgA-R complexes in basolateral endosomes.

To determine whether pIgA-R and TFR show a random or clustered distribution in perinuclear endosomes, quantitative confocal FRET is performed on images collected from the same live cells at 6.0–8.0 µm above the filter under identical imaging settings (Figure 5A, green rectangle). The typical perinuclear shape of irregular and punctate endocytic structures surrounding the upper region of the nucleus (N) is detected across all images (Figure 5B, a–c). Significant energy transfer levels are also detected between TFR and pIgA-R complexes in the perinuclear region (Figure 5Bc). Again, a broad set of ROIs is selected from these structures (Figure 5B, a–c, white squares). To avoid potential contamination with basolateral endosomes, perinuclear ROIs are not collected at the cell periphery (Figure 1B). At both D/A ranges, E% shows a clear independence from A levels (Figure 5C). Correlation analysis substantiates these conclusions with values of r = –0.22 (slope s = –0.13) and r = –0.31, respectively, for D/A 1 and D/A 2 (Table 1). ANOVA single-factor comparing E% values at different A levels within the D/A 1 range yields a nonsignificant p value (p > 0.001; Table 1). Furthermore, E% displays a negative dependence on D/A at both high and low A levels (Figure 5C). These results clearly suggest that pIgA-R and TFR complexes are organized in a clustered distribution in perinuclear endosomes.

Perinuclear Distribution Investigated in the Presence of BFA by Internalizing pIgA-R and TFR Complexes from Opposite PMs
A caveat of the studies described above is the potential contamination of the perinuclear region with basolateral endosomes, which may occur upon the cointernalization of pIgA-R and TFR complexes from the basolateral surface. To address this potential problem, we have investigated the perinuclear organization of these receptor-ligand complexes, cointernalized from opposite PMs in the presence of BFA (Figure 6A, green rectangle), because the majority of the pIgA-R and TFR complexes colocalizes at the perinuclear and apical regions (Figure 6B).

View larger version (50K): [in this window] [in a new window]   Figure 6. Perinuclear TFR and pIgA-R complexes show a clustered organization upon internalization from opposite PMs in the presence of BFA. (A) The organization of pIgA-R and TFR complexes cointernalized from opposite PMs in the presence of BFA was assayed at the perinuclear region (green rectangle) using FRET confocal microscopy. (B) Live-cell confocal FRET imaging was performed at the perinuclear region of polarized MDCK-PTR cells upon internalization of Cy3-Tfn and Alexa488-pIgA-R ligand from the basolateral and apical surfaces, respectively, in the presence of BFA. Pseudocolor images depict the pixel-by-pixel distribution of D/A (a) Acceptor (b), and E% (c) levels at the perinuclear region. Examples of selected ROIs are shown as white squares. Bar, 5 µm. (C) E%, D/A and Acceptor levels were calculated for a wide range of perinuclear ROIs. E% values were plotted as a function of Acceptor levels for D/A 1 () and for D/A 2 (). Trendlines are shown as visual helpers (D/A 1, dotted line; D/A 2, dashed line). E% is largely independent of Acceptor levels and increases with decreasing D/A ratios, suggesting that TFR and pIgA-R complexes show a clustered organization in perinuclear endosomes, independently of BFA and internalization protocols. (D) Perinuclear E% using cointernalization from basolateral PM in the absence of BFA (; Figure 4C) or from opposite surfaces in the presence of BFA () were plotted as a function of Acceptor levels for D/A 1. Trendlines are shown as visual helpers (–BFA Bas. PM inter., dotted line; +BFA Opp. PM inter., dashed line). These two data sets are not significantly different (p > 0.001) using an ANCOVA statistical analysis (Table 2).

To analyze the impact or otherwise of BFA on the organization of pIgA-R and TFR complexes in perinuclear endosomes, we compared above FRET data obtained upon internalization from opposite PMs in the presence of BFA (Figure 6C) with that obtained upon internalization from the basolateral surface in the absence of BFA (Figure 5C). As shown in Figure 6D, perinuclear E% at D/A 1 behaves in a largely independent manner from increasing A levels in the presence and absence of BFA using different internalization protocols. Furthermore, an ANCOVA analysis comparing the perinuclear E% data obtained using different internalization protocols in the presence and absence of BFA yields a nonsignificant p value, p > 0.001, at all the A ranges (Figure 6D; Table 2).

pIgA-R and TFR Clusters Are Differentially Affected by BFA in Polarized Endosomes
To assay whether BFA affects the organization of pIgA-R and TFR complexes in different endocytic regions, we have compared FRET data collected at the basolateral and perinuclear regions upon cointernalization of pIgA-R and TFR complexes into the basolateral surface for 30 min at 37°C in the absence or presence of BFA. Although basolateral E% at D/A 1 rises with increasing A levels in the presence and absence of BFA with correlation coefficients and slope values of r = 0.40, s = 0.40 and r = 0.48, s = 0.39, respectively (Figure 7A), perinuclear E% at D/A 1 behaves in a largely independent manner from increasing A levels in the presence and absence of BFA with correlation coefficients and slope values of r = 0.01, s = 0.01 and r = 0.06, s = 0.04, respectively (Figure 7B). Interestingly, an ANCOVA analysis comparing the E% data in the presence and presence of BFA shows a significant p value for basolateral endosomes (p < 0.001) and a nonsignificant p value (p > 0.001) for perinuclear endosomes (Table 2).

View larger version (36K): [in this window] [in a new window]   Figure 7. BFA affects receptor organization in basolateral endosomes but not in perinuclear endosomes. (A) E% values at D/A 1 were plotted as a function of Acceptor levels for basolateral ROIs collected from images generated upon internalization from basolateral PM in the presence (diamonds) or absence (circles) of BFA. Trendlines are shown as visual helpers (–BFA, dotted line; +BFA, dashed line). As expected, E% is dependent of Acceptor levels in basolateral endosomes. These two data sets are significantly different (p > 0.001) using an ANCOVA statistical analysis (Table 2) with +BFA E% levels slightly higher than –BFA E% levels. (B) E% values at D/A 1 were plotted as a function of Acceptor levels for perinuclear ROIs collected from images generated upon internalization from basolateral PM in the presence (diamonds) or absence (circles) of BFA. Trendlines are shown as visual helpers (–BFA, dotted line; +BFA, dashed line). As expected, E% is independent of Acceptor levels in perinuclear endosomes. These two data sets are not significantly different (p > 0.001) using an ANCOVA statistical analysis (Table 2).

pIgA-R and TFR Complexes Show Different Clustered Organizations in Apical and Perinuclear Endosomes
Here, we compare the perinuclear and apical organization of pIgA-R and TFR complexes internalized from basolateral PMs in the presence of BFA. Images are collected at 6–8 µm above the basal substrate for perinuclear localization and at 9–11 µm for apical localization (Figure 8A; green and red rectangles, respectively). Comparing FRET events at the perinuclear and apical endosomes is only possible in the presence of BFA, whereas TFR complexes are redistributed to the apical region showing strong colocalization with ARE's Rab11 as well as with transcytosing pIgA-R; in contrast, in untreated cells, the apical TFR complexes colocalize mainly with the AEE's EEA1 and not with Rab11. As expected, in the apical region of untreated cells, FRET between TFR and pIgA-R complexes is undetectable, i.e., <5% (data not shown) because they are found in different compartments, AEE and ARE, respectively. With BFA, perinuclear endosomes show a typical perinuclear distribution surrounding the upper nuclear region (Figure 8B, d–f), whereas the apical endocytic punctate structures are localized in the center of the cell, above the nucleus (a–c). Again, a large number of ROIs are selected to compare perinuclear and apical endosomes, considering the selection criteria described in Figure 1B (Figure 8B, white squares). The dependency or otherwise of E% on A levels for a range of apical and perinuclear ROIs is plotted on Figure 8, C and D. Both perinuclear and apical regions demonstrate a low r at D/A 1 (r = 0.01 and 0.13, respectively) with also low slope values, s = 0.01–0.09, and at D/A 2 (r = 0.03 and 0.43, respectively; Table 1), indicating that E% is not dependent on A levels for both perinuclear and apical endosomes. Single-factor ANOVA comparing E% values at D/A 1, yields nonsignificant p values (p > 0.001) for both perinuclear and apical receptor clusters corroborating the r and slope analysis (Table 1). Furthermore, perinuclear and apical E% show a clear negative dependency on D/A at both high and low A levels (Figure 8, C and D), all parameters indicating a highly clustered organization.

View larger version (71K): [in this window] [in a new window]   Figure 8. Perinuclear and apical TFR and pIgA-R complexes show a clustered organization. (A) The organization of pIgA-R and TFR complexes cointernalized from basolateral PMs in the presence of BFA was assayed at the apical (red rectangle) and perinuclear (green rectangle) regions using FRET confocal microscopy. (B) Live-cell confocal FRET imaging was performed at the perinuclear and apical regions of polarized MDCK-PTR cells upon internalization of Cy3-Tfn and Alexa488-pIgA-R ligand from the basolateral PM, in the presence of BFA. Pseudocolor images depict the pixel-by-pixel distribution of Acceptor (b and e), D/A (a and d), and E% (c and f) levels at the apical (a–c) and perinuclear (d–f) regions. Examples of selected ROIs are shown as white squares. Bar, 5 µm. (C and D) E%, D/A and Acceptor levels were calculated for a wide range of ROIs. E% values were plotted as a function of Acceptor levels for D/A 1 () and for D/A 2 (). Trendlines are shown as visual helpers (D/A 1, dotted line; D/A 2, dashed line). E% is largely independent of Acceptor levels and increases with decreasing D/A ratios, suggesting that TFR and pIgA-R complexes present a clustered organization in perinuclear and apical endosomes.

View larger version (31K): [in this window] [in a new window]   Figure 9. Perinuclear and apical E% show significant differences. (A) E% values at D/A 1 were plotted as a function of Acceptor levels for perinuclear (circles) versus apical (diamonds) ROIs collected from images generated upon internalization from basolateral PM in the presence of BFA. Trendlines are shown as visual helpers (perinuclear, dotted line; apical, dashed line). As expected, E% is independent of Acceptor levels in perinuclear and apical endosomes. These two data sets are significantly different (p > 0.001) using an ANCOVA statistical analysis (Table 2) with perinuclear E% levels slightly higher than apical E% levels. (B) Perinuclear + BFA (light grey bars) and apical + BFA (dark grey bars) E% averages were plotted versus different groups of Acceptor (low, medium, and high) upon cointernalization from basolateral PM in the presence of BFA are shown to be significantly different (p < 0.001) by an ANOVA single-factor statistical analysis. The presence of significantly higher E% levels in the perinuclear endosomes at the same D/A 1 suggests a different overall organization of the receptor-ligand complexes in the perinuclear versus the apical endosomes in the presence of BFA. Error bars, 95% confidence interval.

	DISCUSSION

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

Intracellular Localization of the FRET Signal
To localize the intensity-based FRET signal within polarized cells, we have developed a method to differentiate the basolateral, perinuclear, and apical endosomal locations, representing the BEE, CE, and ARE compartments, respectively (Apodaca et al., 1994