Heat shock protein 90 is an essential molecular chaperone for CB2 cannabinoid receptor–mediated signaling in trabecular meshwork cells

Materials

Penicillin/Streptomycin mixture and Dulbecco’s Modification of Eagle’s Medium (DMEM) were purchased from Fisher Scientific (Pittsburg, PA). JWH 015 was purchased from Tocris (Baldwin, MO). SR144528 was obtained from the National Institute of Drug Abuse (Rockville, MD). Geldanamycin was from BIOMOL Research Laboratories (Plymouth Meeting, PA). PD98059, fibronectin, and fatty acid-free BSA (BSA) were bought from Sigma-Aldrich (St. Louis, MO). Alexa Fluor 488-conjugated phalloidin was purchased from Molecular Probes, Inc. (Eugene, OR). Rabbit polyclonal anti-CB2 antibody was purchased from Cayman Chemicals (Ann Arbor, MI). Mouse monoclonal anti-Hsp90 antibody was purchased from BD Bioscience (San Jose, CA). Rabbit anti-mouse immunoglobulin G was purchased from Chemicon (Temecula, CA). His-Tag monoclonal antibody was from EMD Bioscience (Madison, WI). Polyclonal anti-ERK1/2 antibody and monoclonal antiphospho-ERK1/2 (Thr202/Tyr204) antibody were purchased from Cell Signaling Technology (Beverly, MA). Horseradish peroxidase–conjugated goat anti-rabbit secondary antibody and anti-mouse secondary antibody, and enhanced chemiluminescence (ECL) kit were purchased from GE Healthcare (Piscataway, NJ).

Trabecular meshwork cell culture

The TM was isolated from fresh porcine eyes by blunt dissection. Culture of TM cells was performed according to previously published methods [22,23]. Explants of dissected trabecular tissue were placed in Dulbecco's modified Eagle's medium (DMEM) supplemented with 10% (v/v) fetal bovine serum, 100 U/ml penicillin, 100 mg/ml streptomycin, and 20 mM L-glutamine, and incubated at 37° under a 10% CO₂ atmosphere. The tissue explants were left undisturbed for 2 weeks. During this period, they attached to the culture dish, and cells migrated spontaneously from all areas of the explants. After 2 weeks of plating, the tissue explants were removed, and the cells were passed. The identity of TM cells was established by their morphology and their ability to take up acetylated low-density lipoprotein and to secrete tissue plasminogen activator.

Membrane preparation and solubilization

For membrane preparations, cells were washed twice with cold phosphate-buffered saline (PBS; 137 mM NaCl, 2.7 mM KCl, 10 mM Na₂HPO₄•2H₂O, 2 mM KH₂PO₄, pH 7.4), scraped off the tissue culture plates, and collected by centrifugation at 1000 × g for 5 min at 4 °C. Subsequently, the cells were homogenized in membrane buffer (50 mM Tris–HCl, 5 mM MgCl₂, and 2.5 mM EDTA, pH 7.4) with a Polytron homogenizer (Kinematica, Basel, Switzerland). After the homogenate was centrifuged at 32,000 × g for 20 min at 4 °C, the pellet was resuspended in membrane buffer containing 1% dodecyl maltoside and the sample was incubated with rotation for 2 h at 4 °C. The solubilized samples were then centrifuged for 20 min at 100,000 × g for 20 min at 4 °C, and the protein content in the supernatant was determined using a Broadford protein assay kit from Bio-Rad (Hercules, CA).

Immunoprecipitation

For coimmunoprecipitation experiments, 500 μg proteins from solubilized membrane preparations were incubated with 20 μg primary antibody and 80 μl protein G-Sepharose beads. After overnight incubation at 4 °C, the resins were washed with 10 volumes of solubilization buffer with increasing concentrations of NaCl, and proteins were eluted from beads in sample loading buffer.

Western blot analysis

Samples were incubated with 2X Laemmli buffer under reducing conditions at room temperature for 20 min, and proteins were resolved on a 10% sodium dodecyl sulfate (SDS)–polyacrylamide gel using an Invitrogen Mini Gel electrophoresis system (Grand Island, NY). Proteins were transferred onto a nitrocellulose membrane for immunodetection with the indicated antibodies. The nitrocellulose membranes were blocked with 5% nonfat dry milk in Tris-buffered saline/Tween-20 (TBS-T; 20 mM Tris, 137 mM NaCl, and 0.1% Tween-20, pH 7.6) for 1 h and then incubated overnight at 4 °C with the primary antibody. Thereafter, the membranes were washed twice for 10 min each time with TBS-T buffer and incubated with horseradish peroxidase-conjugated secondary antibody for 1 h at room temperature. The membranes were then washed three times with TBS-T buffer for 10 min each time, and the antibody-recognized protein bands were visualized using an enhanced chemiluminescence kit from GE Healthcare (Piscataway, NJ).

Extracellular-signal-regulated kinases 1/2 (ERK1/2) phosphorylation assay

The TM cells were seeded into six-well plates at a density of 2 × 10⁵ cells per well and were grown to confluence. TM cells were maintained in serum-free medium overnight, and then the TM cells were treated with drugs for 15 min. For antagonism experiments, the cells were pretreated with vehicle, antagonist, or inhibitor for 15 min. The cells were then treated with agonist for 15 min. At the end of the treatment period, cells were washed with ice-cold PBS, and 100 µl of ice-cold lysis buffer containing 50 mM β-glycerophosphate, 20 mM EGTA, 15 mM MgCl₂, 1 mM NaVO₄, 1 mM dithiothreitol (DTT), 1 mM phenylmethylsulfonyl fluoride, and 1 µg/ml of a protease inhibitor cocktail (Roche Diagnostics, Indianapolis, IN) were added. The whole cell lysate was clarified with centrifugation at 14,000 × g for 10 min, the supernatants were collected, and total protein concentration was measured using the Bradford protein assay reagent (Bio-Rad, Hercules, CA). About 50 µg of proteins were mixed with 4X Laemmli sample buffer, and after boiling for 5 min, proteins were separated on a 10% sodium dodecyl sulfate–polyacrylamide gel. Subsequently, the proteins were transferred onto a nitrocellulose membrane, and the membranes were blocked with 3% non-fat milk. The blots were probed with a monoclonal antiphospho-ERK1/2(Thr202/Tyr204) antibody. Antibody binding was visualized with enhanced chemiluminescence western blotting detection reagents (GE Healthcare, Piscataway, NJ). The membranes were then stripped and reprobed for total ERK1/2 using a rabbit polyclonal anti-ERK1/2 antibody.

Phalloidin staining of actin cytoskeleton

TM cells were allowed to grow to confluence on sterile glass coverslips precoated with 5 μg/ml fibronectin and were starved in DMEM for 48 h. TM cells were then treated with JWH 015 for 3 h. Subsequently, cells were washed twice with PBS, fixed with freshly prepared 4% paraformaldehyde for 15 min, washed twice with PBS, permeabilized with 0.5% Triton-X100/PBS for 10 min, washed twice again with PBS, and then blocked for 1 h with 1% BSA/PBS. For actin cytoskeleton staining, Alexa Fluor 488–conjugated phalloidin was added onto permeabilized and BSA-blocked cells at a concentration of 0.7 units/ml for 1 h. Finally, coverslips were mounted with Vectashield (Vector Laboratories, Burlingame, CA) and viewed with a fluorescence microscope (model IX50; Olympus, Lake Success, NY).

Data analysis

For ERK1/2 phosphorylation assay, the bands on X-ray films were scanned (Personal Densitometer SI; Molecular Dynamics, Sunnyvale, CA) and were quantified using the ImageQuant software (Molecular Dynamics). The bar graphs were generated with GraphPad Prism software (La Jolla, CA), and the data were expressed as mean±standard error of the mean (SEM). One-way ANOVA (ANOVA) with the Newman–Keuls post-test was used to compare the data points of the different treatment groups. The level of significance was chosen as p<0.05.

Identification of heat shock protein 90 as a CB2 receptor interacting protein in trabecular meshwork cells

As the first step to test the hypothesis that Hsp90 is essential for CB2-mediated signaling to actin cytoskeleton changes in TM cells, we identified the interactions of Hsp90 with the CB2 receptor in TM cells with coimmunoprecipitation experiments and western blot analyses. The CB2 receptor protein complex was immunoprecipitated by using an anti-CB2 antibody and then immunoblotted with an anti-Hsp90 antibody. To ensure the specificity of the results, equal amounts of solubilized membrane proteins from TM cells were incubated with a non-relevant antibody as negative control. As shown in Figure 1A, the Hsp90 band was detected in TM cell membrane preparations, and Hsp90 was coimmunoprecipitated with the CB2 receptor in solubilized TM cell membrane preparation, whereas the Hsp90 signal was absent when membrane proteins were incubated with the non-relevant antibody.

To further confirm the interactions of Hsp90 with the CB2 receptor, coimmunoprecipitation and immunoblotting experiments were performed in reverse order, i.e., anti-Hsp90 was used for immunoprecipitation to see if the CB2 receptor could be coimmunoprecipitated. As shown in Figure 1B, the CB2 band was detected in TM cell membrane preparations, and the CB2 receptor was coimmunoprecipitated with Hsp90 from the solubilized membrane preparations. However, the CB2 band was not detected when the solubilized membrane preparations were incubated with a non-relevant antibody. These data clearly demonstrated the specific interactions between Hsp90 and the CB2 receptor in TM cells expressing the endogenous CB2 receptor.

The effect of geldanamycin on the interaction between heat shock protein 90 and the CB2 receptor in trabecular meshwork cells

Geldanamycin, a small molecule that specifically binds to the ATP–binding pocket in Hsp90, but not other chaperone proteins, alters the tertiary structure of Hsp90, and prevents Hsp90 from interacting with target proteins [24]. In this study, the effect on geldanamycin on the interaction between Hsp90 and the CB2 receptor in TM cells was investigated. As shown in Figure 2, geldanamycin treatment did not significantly affect the amount of CB2 receptor and Hsp90 in TM cell membrane preparations. However, treatment with geldanamycin markedly reduced the amount of Hsp90 pulled down by the anti-CB2 antibody in the coimmunoprecipitation experiments. Since geldanamycin specifically inhibits the interaction of Hsp90 with its client proteins, these data provided further evidence for the specific interactions between Hsp90 and the CB2 receptor in TM cells.

The effects of geldanamycin on CB2 receptor–mediated extracellular signal-regulated kinase 1/2 activation in trabecular meshwork cells

CB2 receptor activation leads to the stimulation of the ERK1/2 pathway. Previously, we have shown that JWH 015, a CB2 selective cannabinoid agonist, activates ERK1/2 in TM cells [14]. In this study, we hypothesized that the interaction between the CB2 receptor and Hsp90 might be crucial for CB2 receptor–mediated ERK1/2 activation. To test this hypothesis, geldanamycin was used in the ERK1/2 phosphorylation assay. As shown in Figure 3, treatment of trabecular meshwork cells with 100 nM JWH 015 for 15 min activated ERK1/2, as represented by increased phosphorylation of ERK1/2. This effect of JWH 015 was antagonized by SR144528, a selective CB2 antagonist. Treatment of TM cells for 15 min with geldanamycin by itself had no measurable effect on ERK1/2 phosphorylation. However, pretreatment of TM cells with geldanamycin significantly inhibited JWH 015–induced ERK1/2 phosphorylation. The total ERK1/2 protein levels did not change with all the treatments. These data indicated that through interaction with the CB2 receptor, Hsp90 plays an important role in CB2 receptor–mediated ERK1/2 activation.

The effects of PD98059 on CB2 receptor–mediated actin cytoskeleton changes in trabecular meshwork cells

Previously, we found that treatment of TM cells with the CB2 receptor agonist JWH 015 results in cytoskeleton rearrangement, which can be blocked by the CB2 selective antagonist SR144528 [15]. In addition, we have reported that by acting on CB2 receptors, JWH 015 activates ERK1/2 in TM cells [14]. In the current study, PD98059, an inhibitor of the ERK1/2 pathway, was used to test the hypothesis that ERK1/2 activation is involved in JWH 015–induced actin cytoskeleton rearrangement. As shown in Figure 4A, vehicle-treated (control) TM cells exhibited a well organized actin cytoskeleton with F-actin fibers crossing the body of the cells and forming a dense filamentous network. Cells treated with CB2 agonist JWH 015 showed a significant reduction in the number of stress fibers and a different pattern of these stress fibers, i.e., they are distributed more in the periphery of the cells (Figure 4B). TM cells treated with PD98059 by itself (Figure 4C) exhibited morphology and actin stress fibers similar to that of the control cells. Importantly, as shown in Figure 4D, pretreatment with PD98059 blocked the effects of JWH 015 on the actin cytoskeleton—the cells exhibited most of the cytoskeletal features associated with control cells. These results indicated that ERK1/2 activation plays a key role in the TM cell actin cytoskeleton changes induced by JWH 015.

The effects of geldanamycin on CB2 receptor–mediated actin cytoskeleton changes in trabecular meshwork cells

Having shown that in TM cells geldanamycin can specifically inhibit the interaction of Hsp90 with CB2 and CB2 receptor–mediated ERK1/2 phosphorylation, we next examined the possible role of Hsp90 in CB2 receptor–mediated actin cytoskeleton changes using geldanamycin. Treatment of TM cells with geldanamycin alone (Figure 4E) had no visible effects on the distribution of actin stress fibers, compared to control TM cells. However, pretreatment of TM cells with geldanamycin for 2 h significantly inhibited JWH 015–induced changes of actin stress fibers, i.e., compared with control group, there was no visible changes in actin stress fiber appearance in the geldanamycin plus JWH 015 group (Figure 4F). Collectively, these data indicated that the interaction of Hsp90 with the CB2 receptor is crucial for CB2 receptor–mediated remodeling of the actin cytoskeleton in TM cells.