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The immunological synapse (IS), a highly organized structure that forms at the point of contact between a T cell and an antigen presenting cell, is essential for the proper development of signaling events including the Ca2+ response. Kv1.3 channels control Ca2+ homeostasis in human T cells and move into the IS upon antigen presentation. However, the process involved in channel accumulation in the IS and the functional implications of this localization are not yet known. Here we define the movement of Kv1.3 into the IS and study whether Kv1.3 localization into the IS influences Ca2+ signaling in Jurkat T cells. Crosslinking of the channel protein with an extracellular antibody limits Kv1.3 mobility and accumulation at the IS. Moreover, Kv1.3 recruitment to the IS does not involve the transport of newly synthesized channels and it does not occur through recycling of membrane channels. Kv1.3 localization in the IS modulates the Ca2+ response. Blockade of Kv1.3 movement into the IS by crosslinking significantly increases the amplitude of the Ca2+ response triggered by anti-CD3/anti-CD28 coated beads which induce the formation of the IS. On the contrary, the Ca2+ response induced by TCR stimulation without the formation of the IS with soluble anti-CD3/anti-CD28 antibodies is unaltered. The results presented herein indicate that, upon antigen presentation, membrane-incorporated Kv1.3 channels move along the plasma membrane to localize in the IS. This localization is important to control the amplitude of the Ca2+ response and disruption of this process can account for alterations of downstream Ca2+-dependent signaling events.
Ion channels are important modulators of T cell function as they regulate the membrane potential and Ca2+ influx during T cell activation. T cell activation is initiated by the presentation of the antigen to the T cells through antigen presenting cells (APC) such as B lymphocytes and dendritic cells. The initial recognition phase is followed by a cascade of signaling events. An increase in intracellular Ca2+ concentration ([Ca2+]i) occurs very early upon T cell activation and this increase is essential for cytokine release and proliferation (1). Indeed Ca2+ is a key regulator of the activity of important transcription factors in T lymphocytes (1, 2). The increase in [Ca2+]i upon T cell activation depends on various membrane channels and transporters.
The main ion channels expressed in human T lymphocytes are the voltage-dependent Kv1.3 channel, the Ca2+-sensitive KCa3.1 channel and the Ca2+-release activated Ca2+ channel (CRAC) (3, 4). These channels act in concert to regulate the onset and development of the Ca2+ response upon encounter with an antigen. The sequence of events triggered upon activation of the T cell receptor (TCR) can be summarized as follows: TCR stimulation induces the release of Ca2+ from the endoplasmic reticulum (ER) via phospholipase C γ (PLC-γ) activation and production of inositol-3-phosphate (IP3). Once ER Ca2+ stores are sufficiently depleted, stromal interaction molecule 1 (STIM1) in the ER moves into proximity to, and activates, Orai1 (a pore-forming subunit of the CRAC channel) and Ca2+ influx begins (4, 5). The activity of CRAC channels is facilitated by membrane hyperpolarization which increases the total driving force for Ca2+ entry. Kv1.3 and KCa3.1 channels regulate membrane potential. Thus, opening of Kv1.3 and KCa3.1 channels enhances Ca2+ entry by hyperpolarizing the cell membrane, while their inhibition suppresses the Ca2+ response (6, 7). Along with allowing initiation of the Ca2+ influx, the crosstalk between these and other channels/transporters determines the amplitude and duration of the Ca2+ response (1).
Recent evidence indicates that Kv1.3, KCa3.1 and CRAC channels are redistributed in the immunological synapse (IS) (8-11). The IS is a tight and highly organized interactive signaling zone localized at the point of contact between T cell and APC, containing membrane proteins (e.g., TCR, CD3 and LFA-1) and signaling molecules (12, 13). The structure of the IS is dynamic and different configurations are achieved with time. Initially, small TCR clusters form and the activation response begins. Eventually, these clusters organize into a mature structure characterized by its “bull’s eye” configuration with a central TCR cluster (cSMAC) and a peripheral adhesion molecule ring (pSMAC) (12, 14). Functionally, IS formation is thought to fine-tune the outcome of TCR engagement. It has been shown that the mature synapse functions as a signal terminator by facilitating TCR degradation and reducing the Ca2+ response (15, 16). Mossman et al. have shown that disruption of the formation of a mature synapse is associated with an increased Ca2+ response (15). Quintana et al. showed that the redistribution of mitochondria to the IS upon TCR activation guarantees Ca2+ uptake at this site and maintenance of Ca2+ influx (17). We have also shown that Kv1.3 channels are rapidly recruited to the IS upon T cell activation and herein persist for a long time (9). Furthermore, this process is altered in T cells from patients with the autoimmune disease Systemic Lupus Erythematosus (SLE) (9). Since SLE T cells display abnormalities in the Ca2+ response to TCR stimulation, Kv1.3 trafficking to the IS may be essential for the proper Ca2+ signaling (9, 18).
These findings suggest the importance of localization and regionalized function of Kv1.3 channels in the IS. Yet, the mechanisms mediating the channel localization to the IS and the functional significance of this rearrangement are not understood. Herein we performed studies to elucidate the movement of Kv1.3 channels to the IS and its functional consequence on Ca2+ signaling.
Jurkat T cells (American Tissue Culture Collection, Masassas, VA) were maintained in RPMI medium supplemented with 10% fetal bovine serum (FBS) (Fisher Scientific, Pittsburgh, PA), 100 U/ml penicillin, 100 μg/ml streptomycin and 1 mM Hepes as previously described (19).
Surface Kv1.3 proteins were immobilized by antibody complexes with rabbit anti-Kv1.3 antibody and secondary anti-rabbit antibody. Briefly, Jurkat cells were incubated on ice for one hour with polyclonal anti-Kv1.3 antibody against an extracellular epitope (EC-Kv1.3, Sigma-Aldrich cat # P4497, St. Louis, MO) at 100:1 ratio of antibody:Kv1.3 α subunit (0.8 ug antibody/10 ml cell suspension of 2 million cells/ml), unless otherwise indicated. This concentration was determined considering, on average, the expression of ca. 400 Kv1.3 channels/cell and the fact that each channel is formed by four α subunits. The incubation with Kv1.3 antibody was followed by a 30-minute incubation with anti-rabbit IgG. Control cells underwent the same experimental steps with either isotype IgG or without antibody, as specified in the text.
Jurkat cells were loaded with 1 μM Fura-2/AM and the experiments were performed on a Cyt-Im2 Ca2+ imaging system (Intracellular Imaging, Cincinnati, OH) as previously described (20). Experiments were performed at 34.3 ± 0.2°C (n=29). Fura-2 loaded cells were recorded while bathed in 0.5 mM Ca2+ Ringer solution for 2 min before addition of either anti-CD3/CD28 coated beads (Invitrogen) or soluble anti-CD3 antibody (OrthoBiotech Products) or a mixture of soluble anti-CD3 and anti-CD28 antibodies (BD Pharmigen). Visual inspection showed formation of stable bead/T cell conjugates in the bath. Absolute intracellular Ca2+ concentrations ([Ca2+]i) were obtained using the formula: [Ca2+]i = Kd (R-Rmin)/(Rmax-R) * F380min/F380max, where Kd= effective fura-2 dissociation constant, R= 340/380 ratio, Rmin= R at 0 Ca2+, Rmax= R of maximum saturating Ca2+ and F380min/F380max is the ratio of the 380 nm intensity of Fura-2 at minimum and maximum saturating Ca2+. The Kd was empirically derived using human CD4+ T cells and calibration buffers with estimated free [Ca2+]i of 0-30 μM (Molecular Probes, Inc., Eugene, OR). We measured a Kd of 250 ± 7 nM (n=2) at 34.7 ± 0.1 °C which is in agreement with previous reports (21). Rmin was measured after every experiment using 0 mM Ca2+ Ringer solution in the presence of 3 μM ionomycin. Rmax was also measured after every experiment using 2.5 mM Ca2+ Ringer solution. We observed no difference in Rmax when using 10 mM Ca2+ Ringer solution. The Ca2+ response is expressed as changes in [Ca2+]i (Δ[Ca2+]i) elicited upon TCR stimulation and it was determined by subtracting the baseline [Ca2+]i from the peak and steady-state (5 min from onset of the Ca2+ response) [Ca2+]i. To obtain the average [Ca2+]i response we included only cells that showed a significant increase of [Ca2+]i after stimulation and these cells were synchronized to reflect initiation of Ca2+ influx as previously described (10). Briefly, we considered cells with a significant increase in Ca2+ those cells that had an increase in 340/380 ratio ≥0.1 ratio units. We have previously established that this value is well above two standard deviations of the average background noise (10). We excluded cells that display [Ca2+]i oscillation before stimulation and did not respond to TCR engagement. Cells that did not respond, but showed an increase in [Ca2+]i with ionomycin (1-2 uM), added at the end of the experiment, were considered non-responding cells. To determine the distribution of Ca2+ responses we defined as transient responses brief [Ca2+]i increases that return to baseline within the 15 min duration of the experiment; sustained responses as Ca2+ responses that are followed by a sustained plateau that is maintained for the whole duration of the experiment; oscillatory as Ca2+ responses that include three or more peaks in [Ca2+]i during the 15 min recording. The number of cells displaying a specific response was reported as % of total responding cells. We also measure the frequency of oscillations as previously described (22). The data analysis was performed using the program Microcal Origin 5.0 (Microcal Software Inc., Northampton, MA) and Microsoft Office Excel with home-written macros. When beads were added in the bath they made contact with T cells at various time points. To allow for direct comparison, time points prior to 50 sec before the first oscillation were excluded. The data were fitted using a third order polynomial function. Next, the data were analyzed using the fast fourier transform (FFT) algorithm and the FFT data were then used to determine the power spectral density (PSD), which provides information regarding oscillation frequency. For each cell the frequency was determined by using the PSD maximum value.
Kv1.3 currents were induced in whole-cell configuration by depolarizing voltage steps from -80 mV holding potential (HP) to +50 mV applied every 30 s, as previously described (19). The external solution had the following composition (in mM): 150 NaCl, 5 KCl, 2.5 CaCl2, 1.0 MgCl2, 10 glucose and 10 HEPES, pH 7.4. The pipette solution was composed of (mM): 134 KCl, 1 CaCl2, 10 EGTA, 2 MgCl2, 5 ATP-sodium, and 10 HEPES, pH 7.4.
T cell activation with anti-CD3/CD28 coated beads (Invitrogen) and immunocytochemistry have been previously described (9). CD3ε was visualized with anti-CD3ε antibody (Santa Cruz Biotechnology, Inc., Santa Cruz, CA) and F-actin with Alexa Fluor 546 phalloidin (Invitrogen). Kv1.3 was visualized with either EC-Kv1.3 antibody or anti-Kv1.3 antibody against an intracellular epitope (Kv1.3 ab, Sigma, cat#P9107) as specified in the text or figure legends. Images were acquired using either a Nikon Microphot FXA or a Zeiss Axioplan Imaging 2 infinity-corrected upright scope coupled to an Orca-ER cooled camera (Axioscope, Carl Zeiss, Microimaging Inc.), Plan-Apochromat 60X-100X oil immersion objectives and the appropriate filters. Proteins’ accumulation at the bead/T cell point of contact was analyzed as follows: boxes of equal area were drawn around the IS and in the area most representative of the membrane outside the IS (9). The mean fluorescence ratio (MFR) was then calculated as follows: MFR = [Mean Fluorescence Intensity (MFI) at the IS-background]/[MFI outside the IS-background]. Based on our previous experiments, T cell/bead conjugates that displayed a MFR ≥1.5 were scored positive for protein polarization in the IS (9). The data were analyzed using the Metamorph computer software with home-written macros.
All data are presented as means ± SEM. Statistical analyses were performed using Student’s t-test (paired or unpaired); p≤0.05 was defined as significant. The Wilcoxon Signed Rank Test was used for non-normal distribution and/or unequal variances.
We tested whether native Kv1.3 channels accumulate in the IS by lateral movement along the plasma membrane. We hypothesized that, if indeed this was the case, crosslinking of surface Kv1.3 channels should prevent their recruitment to the IS. We took advantage of the availability of an antibody against an extracellular epitope located in the loop between the membrane spanning domains S1 and S2 of the Kv1.3 polypeptide, far from the conducting pore (EC-Kv1.3 antibody) (23). Live Jurkat cells were incubated with EC-Kv1.3 antibody followed by secondary antibody to crosslink the surface channel proteins. This intervention was designed to entrap the Kv1.3 membrane proteins in an antibody network that limits the channel mobility upon encounter with an APC. This antibody is specific for Kv1.3 as pre-adsorption to the antigen peptide eliminates the fluorescent signal (Fig. 1A) (9). More importantly, the binding of this antibody to the channel protein and subsequent application of secondary anti-rabbit antibody did not alter Kv1.3 activity (Fig. 1B-D). Kv1.3 crosslinking results in the formation of clusters/puncta of Kv1.3 proteins in the membrane, but other proteins that are recruited at the IS such as CD3ε remain uniformly distributed (Fig. 2A). The crosslinked cells were then exposed to CD3/CD28 beads and the degree of Kv1.3 accumulation in the IS determined. Microscopy experiments showed that Kv1.3 crosslinking prevents the translocation of channel proteins to the IS (Fig. 2B and D). No inhibition of Kv1.3 recruitment into the IS was observed with isotype IgG instead of anti-Kv1.3 antibody. The Kv1.3 recruitment in the IS with rabbit IgG was 54.7±5.4 (SD)% (n=2 experiments, on average 64 conjugates/experiment). Kv1.3 crosslinking did not affect the formation of the IS, as F-actin and CD3ε accumulation to the bead/T cell contact site were preserved (Fig. 2B-D). Overall, the crosslinking of membrane-incorporated Kv1.3 channels reduced the accumulation of channel proteins in the IS by 90±5% (Fig. 2D).
To test if Kv1.3 recruitment involves the transport of newly synthesized channels, further experiments were conducted in the presence of the protein synthesis inhibitor cycloheximide (CHX) (Fig. 3A) (24). Jurkat cells were pre-treated overnight with CHX (10 uM) and then exposed to CD3/CD28 beads. The degree of Kv1.3 polarization in the IS was then determined in these cells by fluorescent microscopy and compared to untreated cells. CHX treatment, which deprives cells of newly synthesized proteins, did not affect the extent of Kv1.3 recruitment in the IS indicating that the accumulation of Kv1.3 in the IS reflects the movement of mature channel proteins present at the plasma membrane. Overall these data support the hypothesis that the recruitment of Kv1.3 at the IS results from the lateral movement of membrane-incorporated channels. Further experiments were conducted to determine whether Kv1.3 localization into the IS occurs by endocytosis of membrane incorporated channels and their subsequent re-insertion in the plasma membrane at the IS. It has been shown that Kv channels can undergo the rapid recycling shuffle between endosomes and the cell surface (25). We studied if inhibition of either endocytosis or exocytosis by dynamin inhibitor peptide (DIP) and low temperature (20°C), respectively, prevented Kv1.3 translocation to the IS (Fig. 3B). DIP blocks dynamin, which is responsible for the clipping of nascent endocytotic vesicles from the membrane, while a 20°C temperature is sufficient to allow normal internalization of endocytotic vescicles, but it is not compatible with recycling to the plasma membrane (26). Specifically, we exposed Jurkat T cells to either DIP (50 uM) or equal concentrations of DIP scramble control overnight and after that we measured the degree of Kv1.3 localization into the IS and compared. For the exocytosis experiments, we compared the degree of Kv1.3 polarization in T cells at 20°C to that of cells maintained at 37°C. These same experimental conditions were used to study how retrograde trafficking regulates surface expression of Kv1.5 (26). We observed that neither intervention inhibits Kv1.3 localization indicating that Kv1.3 recruitment into the IS occurs by lateral movement in the plane of the membrane.
The functional implications of Kv1.3 localization in the IS are still not known. It has been speculated that the recruitment of ion channels in this signalosome may be important to regulate Ca2+ signaling (9, 11, 27). A direct way to prove this is to prevent the channel trafficking to the IS and determine if this intervention alters TCR-mediated Ca2+ response. The previous section established that Kv1.3 crosslinking can be used to “mechanically” disrupt the movement of Kv1.3 to the IS, thus providing a simple and convenient experimental tool for trapping Kv1.3 outside the synapse. We used this approach to study the functional consequences of Kv1.3 trafficking to the IS.
Fura-2 experiments were performed to measure the Ca2+ response to antigen stimulation in Kv1.3 crosslinked (XL) and untreated (CTR) Jurkat cells (Fig. 4). Antigen stimulation was produced by exposure to CD3/CD28 beads as surrogate APCs (9). A large fraction of XL and CTR cells responded to antigen presentation with an increase in [Ca2+]i. The percentages of responding cells were 74±7% in CTR and 84±4% in XL (n=8; p=0.1). The CD3/CD28 beads elicited a variety of Ca2+ responses (Fig. 4A). However, the average Ca2+ response triggered by beads differed between CTR and XL responding cells. We found that crosslinking and blockade of Kv1.3 translocation to the IS significantly increased the peak [Ca2+]i by 1.8±0.2 folds (n=8, p=0.002) (Fig. 4B top and D). This effect was not associated with a change in the rate of Ca2+ rise. We have fitted the Ca2+ rise with a Boltzmann equation and compared the time at 50% [Ca2+]i (t1/2) and the slope in control and crosslinked cells. The t1/2 were 199.1±12.3 s in CTR and 192.3±11.1 s in XL (n=8; p=0.228). The slopes in CTR and XL were 11.7±1.8 and 13.1±1.5 nM/s, respectively (n=8; p=0.348). We also observed that in all but one experiment crosslinking on average increased steady-state [Ca2+]i by 1.7 ±0.3 folds (n=7; p=0.018) (Fig. 4B, bottom). On the contrary, the Ca2+ response induced by TCR stimulation without the formation of the IS with either soluble anti-CD3 or anti-CD3/anti-CD28 antibodies was the same in CTR and XL cells (Fig. 4C-D). The average fold increase in [Ca2+]i by CD3/CD28 antibody in XL experiments was 1.0±0.1 folds (n=6, p=0.47, Fig. 4D), and that by CD3 antibody was 1.0±0.3 folds (n=5, p=0.70, Fig. 4D). No significant difference in baseline [Ca2+]i was seen between XL and CTR cells: the [Ca2+]i baselines in CTR and XL were 112.7±33.5 nM and 93.6±36.5 nM (n=19 experiments, 30-80 cells/experiment, p=0.114), respectively. Overall, the Ca2+ signal in the Kv1.3-crosslinked cells was significantly higher than in control cells only when activated by the stimulus that induced the formation of an IS (with CD3/CD28 beads) (Fig. 4D). These findings indicate that the accumulation of Kv1.3 channels at the IS regulates the Ca2+ response to antigen stimulation.
Further detailed analysis was done to determine whether Kv1.3 localization in the IS affects the kinetic of the Ca2+ response. At the single cell level Jurkat T cells stimulated with beads display three characteristic Ca2+ responses: oscillatory, sustained and transient (Fig. 5A). We found no difference in distribution of Ca2+ responses of CTR and XL cells stimulated with beads (Fig. 5B). Similarly, there was no difference in the frequency of oscillations. The oscillation pattern in XL cells closely mirrored that of CTR cells with a median frequency response of 3.4 mHz. The detailed distribution for CTR and XL cells is shown in the frequency histogram in Fig. 5C. Overall, in Jurkat T cells blockade of Kv1.3 localization in the IS affects the magnitude, but not the kinetics, of [Ca2+]i.
In this study we have shown that the recruitment of Kv1.3 to the IS occurs by lateral movement of surface channels along the plasma membrane. Furthermore, we found that Kv1.3 localization in the IS regulates the amplitude of the Ca2+ response that develops upon encounter with an APC. Thus, the dynamic recruitment of the plasma membrane-embedded Kv1.3 channels to the IS constitutes a part of the physiological function of the IS.
It has been shown that ion channels accumulate in the IS (8-11). Yet, the mechanisms and functional consequences of the channel targeting remain unknown. We have observed that antibody-based Kv1.3 crosslinking blocks the translocation of endogenous channels to the IS and the inhibition of protein synthesis did not influence the accumulation of channels to the IS (Figs (Figs22 and and3).3). Furthermore, we found that Kv1.3 relocation into the IS does not involve a recycling process with endocytosis of membrane incorporated channels and their subsequent re-insertion in the plasma membrane. These observations strongly support the idea that the localization of native Kv1.3 channels in the IS occurs by lateral movement of surface channels along the plasma membrane. Other membrane proteins such as TCR and the integrin LFA-1 have been reported to move along the plasma membrane and accumulate at the IS via an actin-mediated process (28-30). Others suggested that a “diffusion trapping” process may be involved in the synapse formation (24, 31, 32). Molecular diffusion of proteins into the IS is initially random, although limited by various constraints such as the molecule size and association with other molecules. Once at the IS, diffusion is slowed, or even arrested, because new interactions occur with anchoring proteins. In neuronal and epithelial cells clustering and retention of ion channels within a particular plasma membrane domain involve, in part, the actin-cytoskeleton and scaffolding proteins that serve as a link between the channel and the cytoskeleton (33). In neurons the human homolog of the Drosophila discs large tumor suppressor protein (hDlg1), a PDZ protein of the membrane-associated guanylate kinase protein (MAGUK) family, acts as an anchor for voltage-gated K+ channels to allow specific subcellular localization (34). In immune cells, hDlg1 accumulates in the IS and coordinates actin polymerization and IS assembly (35, 36). Immunoprecipitation studies in Jurkat T cells have shown that Kv1.3 exists in association with hDlg1 (37). Thus, it is possible that hDlg1 and the actin cytoskeleton may play a key role in Kv1.3 recruitment to the IS.
While the Kv1.3 crosslinking was useful to define the process by which Kv1.3 channels move into the IS, this procedure also provided us an experimental tool to study the functional relevance of Kv1.3 localization in the IS. We have compared the Ca2+ responses triggered upon formation of an IS (with CD3/CD28 beads) to the treatment with soluble CD3/CD28 antibodies. The latter intervention does not induce the formation of an IS. In agreement with a previous report, we observed different kinetics of the average Ca2+ response with two stimuli: a more sustained increased in [Ca2+]i with formation of the IS and transient changes in [Ca2+]i with soluble antibodies (17). This difference has been attributed to the redistribution of mitochondria to the IS which results in reduced local accumulation of Ca2+ and prolongation of Ca2+ entry through CRAC channels (17). Interestingly, we observed that prevention of Kv1.3 trafficking to the IS by crosslinking results in an exaggerated Ca2+ response only with CD3/CD28 beads. The Kv1.3 crosslinking neither affected the IS formation, as measured by F-actin and CD3ε accumulation to the IS (Fig. 2), nor altered Kv1.3 activity (Fig. 1D). Moreover, soluble anti-CD3/CD28 antibody produced identical Ca2+ response in the crosslinked and control cells. Thus, the observed change in Ca2+ response is not due to altered channel activity, general disarrangement of the IS or non-functional Ca2+ reserves, but it correlates with the disrupted localization of Kv1.3 channels in the IS. However, we cannot exclude the possibility that Kv1.3 crosslinking might immobilize other factors important for the Ca2+ response. The crosslinking generated clusters/puncta of Kv1.3 proteins (Fig. 2 A and B). Although CD3ε does not appear to be driven into this configuration, it is possible that other membrane and signaling molecules tightly associated to the Kv1.3 proteins and clustered in these puncta might participate in the altered Ca2+ response.
Overall these results provide compelling evidence that Kv1.3 accumulation in the IS is necessary for the development of a proper Ca2+ response. Furthermore, they suggest that the IS may constitute a site for regulation of the Kv1.3 channel activity. Many signaling molecules recruited at the IS such as Lck, PKCθ and PKA have been shown to modulate the activity of Kv1.3 (38-44). Kv1.3 has multiple potential phosphorylation sites and it is likely that Kv1.3 localization in the IS is important to guarantee channel downregulation by signaling molecules accumulating at this site thus providing a feedback regulation of Ca2+ signaling (38, 39, 45). Thus Kv1.3 inhibition at the IS would result in membrane depolarization that prevents, in normal conditions, the development of an exaggerated Ca2+ response. Although blockade of Kv1.3 in the IS was not associated with altered Ca2+ kinetics, defective permanence of the channel in the IS could affect the kinetics of the Ca2+ response. If, for ex., the Kv1.3 channel enters in the IS, but it moves out prematurely, what would have normally being a transient Ca2+ response could instead become more sustained because the channel downregulation is removed.
Overall altered Kv1.3 localization in the IS could have important patho-physiological consequences. Ca2+ is a key regulator of the activity of transcription factors which control cytokine production and proliferation in T cells. It is well established that amplitude and duration of the Ca2+ response determine the specificity of transcription factor activation and, consequently, the pattern of gene expression (46). We have reported that the movement of Kv1.3 is altered in T cells from patients with SLE and that a long-lasting localization in the IS, like the one that occurs in normal individuals, is instead short-lived in SLE (9). SLE T cells have been also reported to have more pronounced and sustained Ca2+ signaling as well as increased NF-AT nuclear translocation than normal T cells (18, 47). The data presented here indicate that defective Kv1.3 localization in the IS could indeed contribute to the Ca2+ defect in these patients. Overall our studies raise the possibility that defects in ion channel trafficking to the IS could be involved in disease-associated abnormalities in Ca2+ signaling.
1This work was supported by NIH grants #CA95286, #AI083076 and AHA Ohio Affiliate Grant-in-aid #0855457D to LC. SAN was supported by a AHA Ohio Affiliate Fellowship #0615213B and AS by a fellowship of the NSF-REU program #0647677.
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