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High Glucose Down-regulates Intercellular Communication in Retinal Endothelial Cells by Enhancing Degradation of Connexin 43 by a Proteasome-dependent Mechanism

2004; Elsevier BV; Volume: 279; Issue: 26 Linguagem: Inglês

10.1074/jbc.m400446200

1083-351X

Rosa Fernandes, Henrique Girão, Paulo Pereira,

Advanced Glycation End Products research

Intercellular communication through gap junctions (GJIC) is most likely relevant to maintaining the integrity of the blood-retinal barrier. In this study, we investigated the mechanism whereby high glucose enhances degradation of connexin 43 (Cx43), thus contributing to a decrease in GJIC. The levels of Cx43 in bovine retinal endothelial cells exposed to high glucose (25 mm) decreased about 50% as compared with controls (5.5 mm glucose). Consistently, the half-life of the protein decreased from 2.3 to 1.9 h. The proteasome inhibitors MG132 and lactacystin prevented the loss of Cx43 induced by high glucose and extended Cx43 half-life. The amount of phosphorylated Cx43 increased in high glucose and after proteasome inhibition. Scrape-loading dye transfer experiments show that high glucose is associated to a decrease of 40% in GJIC. Significantly, this reduction can be reversed by proteasome inhibitors. The decrease in GJIC in cells exposed to high glucose is associated with a loss of Cx43 from the plasma membrane, as demonstrated by immunofluorescence and biotinylation of cell-surface proteins. Results indicate that increased phosphorylation of Cx43 under high glucose is the mechanism targeting Cx43 for degradation by a proteasome-dependent mechanism. Increased degradation of Cx43 and reduction of GJIC in high glucose may be of physiological importance by contributing to endothelial cell dysfunction associated with the breakdown of the blood-retinal barrier in diabetic retinopathy. Intercellular communication through gap junctions (GJIC) is most likely relevant to maintaining the integrity of the blood-retinal barrier. In this study, we investigated the mechanism whereby high glucose enhances degradation of connexin 43 (Cx43), thus contributing to a decrease in GJIC. The levels of Cx43 in bovine retinal endothelial cells exposed to high glucose (25 mm) decreased about 50% as compared with controls (5.5 mm glucose). Consistently, the half-life of the protein decreased from 2.3 to 1.9 h. The proteasome inhibitors MG132 and lactacystin prevented the loss of Cx43 induced by high glucose and extended Cx43 half-life. The amount of phosphorylated Cx43 increased in high glucose and after proteasome inhibition. Scrape-loading dye transfer experiments show that high glucose is associated to a decrease of 40% in GJIC. Significantly, this reduction can be reversed by proteasome inhibitors. The decrease in GJIC in cells exposed to high glucose is associated with a loss of Cx43 from the plasma membrane, as demonstrated by immunofluorescence and biotinylation of cell-surface proteins. Results indicate that increased phosphorylation of Cx43 under high glucose is the mechanism targeting Cx43 for degradation by a proteasome-dependent mechanism. Increased degradation of Cx43 and reduction of GJIC in high glucose may be of physiological importance by contributing to endothelial cell dysfunction associated with the breakdown of the blood-retinal barrier in diabetic retinopathy. Hyperglycemia and the consequent exposure of the intracellular milieu of the retinal capillary endothelial cells to elevated blood glucose concentrations have been implicated in the pathogenesis of vascular complications in diabetes, including the breakdown of the blood-retinal barrier (1Winegrad A.I. Diabetes. 1987; 36: 396-406Crossref PubMed Scopus (281) Google Scholar, 2King G.L. Kunisaki M. Nishio Y. Inoguchi T. Shiba T. Xia P. Diabetes. 1996; 45: S105-S108Crossref PubMed Google Scholar). The exact biochemical and molecular mechanisms that transduce chronic hyperglycemia into micro- and macrovascular complications of the retina are not clear. However, it has been suggested that several mechanisms play a role in the pathogenesis of diabetic retinopathy; those include increased nonenzymatic glycation (3Nishikawa T. Edelstein D. Du X.L. Yamagishi S. Matsumura T. Kaneda Y. Yorek M.A. Beebe D. Oates P.J. Hammes H.P. Giardino I. Brownlee M. Nature. 2000; 404: 787-790Crossref PubMed Scopus (3693) Google Scholar), activation of aldose reductase (4Obrosova I.G. Minchenko A.G. Vasupuram R. White L. Abatan O.I. Kumagai A.K. Frank R.N. Stevens M.J. Diabetes. 2003; 52: 864-871Crossref PubMed Scopus (178) Google Scholar), oxidative stress (3Nishikawa T. Edelstein D. Du X.L. Yamagishi S. Matsumura T. Kaneda Y. Yorek M.A. Beebe D. Oates P.J. Hammes H.P. Giardino I. Brownlee M. Nature. 2000; 404: 787-790Crossref PubMed Scopus (3693) Google Scholar), increased production of diacylglycerol, and stimulation of retinal protein kinase C (PKC) 1The abbreviations used are: PKC, protein kinase C; Cx43, connexin 43; LEC, lens epithelial cells; GJIC, intercellular communication through gap junctions; BREC, bovine retinal endothelial cells; DMEM, Dulbecco's modified Eagle's medium; TPA, 12-O-tetradecanoylphorbol 13-acetate; PBS, phosphate-buffered saline; PVDF, polyvinylidene fluoride; RT-PCR, reverse transcription-PCR; P/NP, phosphorylated/nonphosphorylated. (5Koya D. King G.L. Diabetes. 1998; 47: 859-866Crossref PubMed Scopus (1165) Google Scholar). Despite the nature of such mechanisms, early cell dysfunction related to diabetic vascular complications is often associated with abnormalities in cell-cell communication and maintenance of cell homeostasis. Gap junctions are intercellular-channels that permit the passage of small molecules such as small metabolites, ions, and second messengers (6Kumar N.M. Gilula N.B. Cell. 1996; 84: 381-388Abstract Full Text Full Text PDF PubMed Scopus (1652) Google Scholar). These channels consist of two hemi-channels, called connexons, that are located in the plasma membrane of two adjacent cells. Each connexon is composed of six subunits of the protein connexin. Gap junctions have an important role in a variety of cellular processes including homeostasis, morphogenesis, cell differentiation, and growth control (7Simon A.M. Goodenough D.A. Trends Cell. 1998; 8: 477-483Abstract Full Text Full Text PDF PubMed Scopus (347) Google Scholar). Three connexin subtypes are expressed in the endothelium of the blood vessels: Cx37, Cx40, and Cx43 (8Yeh H.I. Rothery S. Dupont E. Coppen S.R. Severs N.J. Circ. Res. 1998; 83: 1248-1263Crossref PubMed Scopus (155) Google Scholar). Endothelial cells rely on a network of gap junctions for intercellular communication (9Little T.L. Beyer E.C. Duling B.R. Am. J. Physiol. 1995; 268: H729-H739PubMed Google Scholar, 10Larson D.M. Wrobleski M.J. Sagar G.D. Westphale E.M. Beyer E.C. Am. J. Physiol. 1997; 272: C405-C415Crossref PubMed Google Scholar). Previous studies have shown that intercellular communication in endothelial cells is reduced under conditions of hyperglycemia (11Sato T. Haimovici R. Kao R. Li A.F. Roy S. Diabetes. 2002; 51: 1565-1571Crossref PubMed Scopus (131) Google Scholar). Such a decrease in intercellular communication is most likely due to a reduction of the abundance of connexin 43 (Cx43) in endothelial cells. One of the most remarkable aspects of gap junction biosynthesis is the exceptional metabolic lability of connexins. Although the half-life of the great majority of plasma membrane proteins exceeds 24 h, connexins present a rapid turnover rate, with half-lives of only 1.5–5 h (12Fallon R.F. Goodenough D.A. J. Cell Biol. 1981; 90: 521-526Crossref PubMed Scopus (225) Google Scholar, 13Beardslee M. Lerner D. Tadros P. Laing J. Beyer E. Yamada K. Kleber A. Schuessler R. Saffitz J. Circ. Res. 2000; 87: 656-662Crossref PubMed Scopus (444) Google Scholar, 14Musil L.S. Le A.C. Van Slyke J.K. Roberts L.M. J. Biol. Chem. 2000; 275: 25207-25215Abstract Full Text Full Text PDF PubMed Scopus (200) Google Scholar). Until the present time, two proteolytic pathways have been implicated in connexin turnover, the lysosome (14Musil L.S. Le A.C. Van Slyke J.K. Roberts L.M. J. Biol. Chem. 2000; 275: 25207-25215Abstract Full Text Full Text PDF PubMed Scopus (200) Google Scholar, 15Laing J.G. Tadros P.N. Westphale E.M. Beyer E.C. Exp. Cell Res. 1997; 236: 482-492Crossref PubMed Scopus (217) Google Scholar) and the proteasome (13Beardslee M. Lerner D. Tadros P. Laing J. Beyer E. Yamada K. Kleber A. Schuessler R. Saffitz J. Circ. Res. 2000; 87: 656-662Crossref PubMed Scopus (444) Google Scholar, 14Musil L.S. Le A.C. Van Slyke J.K. Roberts L.M. J. Biol. Chem. 2000; 275: 25207-25215Abstract Full Text Full Text PDF PubMed Scopus (200) Google Scholar, 15Laing J.G. Tadros P.N. Westphale E.M. Beyer E.C. Exp. Cell Res. 1997; 236: 482-492Crossref PubMed Scopus (217) Google Scholar, 16Laing J.G. Beyer E.C. J. Biol. Chem. 1995; 270: 26399-26403Abstract Full Text Full Text PDF PubMed Scopus (205) Google Scholar, 17Girao H. Pereira P. Mol. Vis. 2003; 9: 24-30PubMed Google Scholar). The mechanisms and upstream events that lead to the choice of one degradation pathway over the other are largely unknown. It has, however, been shown that both pathways coexist and are active in a number of cell types and in a variety of experimental and pathological conditions (18Fuertes G. Martin De Llano J.J. Villarroya A. Rivett A.J. Knecht E. Biochem. J. 2003; 375: 75-86Crossref PubMed Scopus (139) Google Scholar, 19Qin H. Shao Q. Igdoura S.A. Alaoui-Jamali M.A. Laird D.W. J. Biol. Chem. 2003; 278: 30005-30014Abstract Full Text Full Text PDF PubMed Scopus (129) Google Scholar, 20Ward W.F. Prog. Mol. Subcell. Biol. 2002; 29: 35-42Crossref PubMed Scopus (67) Google Scholar). For example, we have previously shown that in response to specific stimuli, proteasome is involved in the degradation of phosphorylated Cx43 in lens epithelial cells (LEC) (17Girao H. Pereira P. Mol. Vis. 2003; 9: 24-30PubMed Google Scholar). It has been widely shown that phosphorylation of Cx43 results in decreased intercellular communication through gap junctions (GJIC), probably because of a reduction in abundance at the plasma membrane (21Matesic D. Rupp H. Bonney W. Ruch R. Trosko J. Mol. Carcinog. 1994; 10: 226-236Crossref PubMed Scopus (170) Google Scholar, 22TenBroek E. Louis C. Jonhson R. Dev. Biol. 1997; 191: 88-102Crossref PubMed Scopus (27) Google Scholar, 23Lampe P.D. TenBroek E.M. Burt J.M. Kurata W.E. Johnson R.G. Lau A.F. J. Cell Biol. 2000; 149: 1503-1512Crossref PubMed Scopus (470) Google Scholar, 24Rivedal E. Opshal H. Carcinogenesis. 2001; 22: 1543-1550Crossref PubMed Scopus (121) Google Scholar). For example, it was shown that in smooth muscle cells, high glucose induced the inhibition of GJIC activity through hyperphosphorylation of Cx43 by PKC (25Kuroki T. Inoguchi T. Umeda F. Ueda F. Nawata H. Diabetes. 1998; 47: 931-936Crossref PubMed Scopus (91) Google Scholar). On the other hand, a recent study has shown that high glucose inhibited GJIC activity by down-regulating Cx43 synthesis in rat microvascular endothelial cells (11Sato T. Haimovici R. Kao R. Li A.F. Roy S. Diabetes. 2002; 51: 1565-1571Crossref PubMed Scopus (131) Google Scholar). We have shown before that Cx43 is remarkably labile and that the ubiquitin proteasome pathway is involved in the degradation of Cx43 in LEC (17Girao H. Pereira P. Mol. Vis. 2003; 9: 24-30PubMed Google Scholar). Further, we have suggested that the combined action of phosphorylation and protein degradation by the proteasome pathway acts as a mechanism of decreasing intercellular communication in the LEC (17Girao H. Pereira P. Mol. Vis. 2003; 9: 24-30PubMed Google Scholar). By analogy, it is thus conceivable that a similar mechanism may occur in retinal endothelial cells. To investigate the mechanism whereby hyperglycemia leads to decreased intercellular communication in endothelial cells, we have hypothesized that hyperglycemia may create the conditions that favor increased degradation of Cx43, presumably involving increased phosphorylation of the protein. A reduction in Cx43 half-life and a decreased abundance of Cx43 at the plasma membrane would thus account for the reduced intercellular communication observed under conditions of hyperglycemia. Cell Cultures—Bovine retinas were the source of capillaries used to isolate cells for primary culture. Cow eyes were obtained from a local slaughterhouse. Primary bovine retinal endothelial cells (BREC) cultures were established from fresh calf eyes. Under sterile conditions, the retinas were isolated and washed in Dulbecco's modified Eagle's medium (DMEM), and pieces of adherent retinal pigment epithelial cells were removed. The retinas were transferred to an enzyme solution containing Pronase (100 μg/ml), collagenase (500 μg/ml), and DNase (70 μg/ml) and incubated with shaking at 37 °C for 20 min. After incubation, the retinal digest was passed through 210- and 50-μm nylon mesh, and the microvessels trapped on top of the 50-μm mesh were collected in DMEM by centrifugation. The fragments were resuspended in DMEM with 15% fetal calf serum, 20 μg/ml endothelial growth supplement (Roche Diagnostics, Mannheim, Germany), heparin (100 μg/ml), and antibiotic-antimycotic solution (Sigma), plated, and grown on fibronectin-coated dishes in low glucose DMEM at 37 °C with 5% CO2. Cultures were passaged every 7 to 10 days. For all experiments, cultures from passages three to five were used. To determine the effect of high glucose on Cx43 expression and GJIC activity, BREC were grown in low (5.5 mm) or high (25 mm) d-glucose medium for 8 days to confluence. Antibodies and Reagents—The rabbit polyclonal and mouse monoclonal anti-Cx43 antibodies were obtained from Zymed Laboratories Inc. (San Francisco, CA). The mouse anti-Cx43 monoclonal antibody was raised against a peptide sequence that represents amino acid residues 360–376 of Cx43. Unless otherwise noted, all other reagents were from Sigma, except MG132, which was obtained from Calbiochem (Darmstadt, Germany). 12-O-tetradecanoylphorbol 13-acetate (TPA) and MG132 were dissolved in Me2SO. Gel Electrophoresis and Western Blotting—Cells exposed to normal and high-glucose medium were washed, collected in phosphate-buffered saline (PBS) solution by centrifugation, and cell pellets were frozen at -80 °C until use. The cells were resuspended in lysis buffer containing 10 mm Tris, pH 7.4, 1 mm EDTA, 1% Triton X-100, and 0.5% sodium deoxycholate, supplemented with protease inhibitor mixture (Roche Diagnostics), 2 mm phenylmethylsulfonyl fluoride, 10 mm iodoacetamide, 10 mm NaF, 500 μm Na3VO4. The lysates were sonicated six times for 3 s to completely disrupt all cells and then centrifuged at 16,000 × g for 15 min. The supernatants were used to determine the protein concentration by BCA reagent (Pierce) and then were denatured with Laemmli buffer. For studies involving total cell lysates, electrophoresis was performed on 50-μg aliquots of each sample on an SDS-12% polyacrylamide gel and transferred to polyvinylidene fluoride (PVDF) membranes. Membranes were probed with rabbit polyclonal or mouse monoclonal antibodies against connexin 43. The signals were detected by ECL system (Amersham Biosciences). Films were scanned and the optical densities of the bands were measured with appropriate software. All results are representative of at least three independent experiments. Metabolic Labeling and Immunoprecipitation—For metabolic labeling with 35S, cells were rinsed with methionine-free medium prior to incubation with [35S]methionine (Amersham Biosciences) 100 μCi/ml for 1 h. The cells were then chased in DMEM supplemented with 0.5 mm unlabelled methionine in the presence or absence of MG132 for 1, 2, or 4 h. The samples were resuspended in lysis buffer (190 mm NaCl, 50 mm Tris-HCl, 6 mm EDTA, 2.5% Triton X-100, 0.2% SDS, pH 8.3) supplemented with protease inhibitor mixture (Roche Diagnostics), protein phosphatase inhibitor set II (Calbiochem, La Jolla, CA), 2 mm phenylmethylsulfonyl fluoride, 10 mm iodoacetamide, 50 mm NaF, 500 μm Na3VO4. Cells were lysed by sonication, and supernatants were used for immunoprecipitation using polyclonal antibodies directed against Cx43. After centrifugation at 16,000 × g, the supernatants were incubated with antibodies directed against Cx43 for 3 h at 4 °C, followed by incubation with protein A-Sepharose for 1 h. The samples were then centrifuged, and the protein A-Sepharose sediments were resuspended in Laemmli buffer and denatured at 37 °C for 30 min. Proteins were resolved by SDS-PAGE, and the gels were dried and autoradiographed. Semi-quantitative Reverse Transcription (RT)-PCR Analyses—RNA extracted from BREC grown in low and high glucose medium was simultaneously determined by semi-quantitative RT-PCR using the forward primer 5′-TTAAGGATCGTGTGAAGGGAAAGAG-3′ and the reverse primer 5′-CTAGATCTCTAGGTCATCAGGCCG-3′ for amplification of Cx43, and the forward primer 5′-AAGGAGAAGCTGTGCTACGTCGCCCTGG-3′ and the reverse primer 5′-GATCTTGATCTTCATTGTGCTGGGTGCC-3′ for amplification of actin. For simultaneous amplification of Cx43 and β-actin, cDNAs were generated in the same RT reaction. To confirm that amplification was in the linear region, separate tubes containing increasing volumes of the RT reaction were used. Amplification products were electrophoresed on a 1% agarose gel and stained with ethidium bromide. Densitometry was performed at nonsaturating exposures, and the Cx43/β-actin ratios were determined. Biotinylation of Cell-surface Proteins—The cell-surface proteins of BREC were biotinylated. Dishes of confluent BREC cells (10-cm diameter) were rinsed twice with 5 ml of ice-cold PBS containing 0.5 mm MgCl2 and 1 mm CaCl2, followed by the addition of 3 ml of the same cold solution containing 1 mg/ml freshly added Sulfo-NHS-SS-biotin (Pierce). After 30 min at 4 °C, the medium was removed, and the plates were washed three times with PBS containing 0.5 mm MgCl2, 1 mm CaCl2, and 100 mm glycine. The cells were scraped in RIPA buffer (50 mm Tris-HCl, 150 mm NaCl, 5 mm EGTA containing 1% Triton, 0.5% deoxycholate, 0.1% SDS and supplemented with protease inhibitor mixture, 2 mm phenylmethylsulfonyl fluoride, 10 mm iodoacetamide, 10 mm NaF, and 500 μm Na3VO4; pH 7.5). After 10–20 min on ice the cells were sonicated, and the homogenates were centrifuged at 16000 × g for 10 min. The protein content of the supernatants was determined, and the same quantity of protein was transferred to 1.5-ml Eppendorf microfuge tubes containing 200 μl of Neutravidin (Pierce). After 2 h of incubation at 4 °C with agitation, the beads were washed four times with RIPA buffer. The resulting pellets were resuspended in 150 μl of 2× Laemmli buffer and incubated for 1 h at 37 °C. The beads were pelleted, and the proteins were resolved by SDS-PAGE, transferred to PVDF membranes, and blotted against Cx43 antibodies. Immunofluorescence—BREC grown on fibronectin-coated glass coverslips were fixed with 4% paraformaldehyde in PBS. The samples were then washed with PBS, permeabilized with 1% (v/v) Triton X-100 in PBS, and blocked with goat serum (1:10) for 20 min prior to incubation with primary mouse monoclonal antibody against connexin (1:25) for 1 h at room temperature. The specimens were rinsed in PBS and mounted with Glycergel (Dako, Carpinteria, CA). All solutions were made up in 0.02% (w/v) bovine serum albumin (Sigma) containing 0.02% sodium azide (Sigma) in PBS. For controls, primary antibodies were omitted. For alkaline phosphatase treatment, the dephosphorylation reactions were carried out in lysis buffer after overnight incubation at 37 °C in the presence of alkaline phosphatase (5 units) from Escherichia coli (Sigma). Cell-cell Communication Assay—BREC grown on fibronectin-coated glass coverslips were assessed for gap junction-mediated intercellular coupling as described by Musil et al. (14Musil L.S. Le A.C. Van Slyke J.K. Roberts L.M. J. Biol. Chem. 2000; 275: 25207-25215Abstract Full Text Full Text PDF PubMed Scopus (200) Google Scholar). Briefly, the culture medium from confluent cells was removed and saved. The cells were rinsed three times with Hanks' balanced salt solution containing 1% bovine serum albumin, after which a 27-gauge needle was used to create multiple scrapes through the cell monolayer in the presence of Dulbecco's phosphate-buffered saline containing 0.5% rhodamine-dextran and 0.5% Lucifer yellow. After 3 min of incubation at room temperature, the culture was rinsed three times with Hanks' balanced salt solution containing 1% bovine serum albumin and then incubated for an additional 8 min in the saved culture medium to allow the loaded dye to transfer to adjoining cells. The cells were then rinsed and fixed with 4% paraformaldehyde and viewed using a fluorescence microscope with a UV light source. Statistical Analysis—Data are expressed as means ± S.D. or S.E. Comparison between groups was performed with a Student's t test. High Glucose Leads to a Decrease in the Amount of Cx43 by a Proteasome-dependent Mechanism—It has previously been shown that hyperglycemia leads to a decrease in total Cx43 in various cell types (11Sato T. Haimovici R. Kao R. Li A.F. Roy S. Diabetes. 2002; 51: 1565-1571Crossref PubMed Scopus (131) Google Scholar, 25Kuroki T. Inoguchi T. Umeda F. Ueda F. Nawata H. Diabetes. 1998; 47: 931-936Crossref PubMed Scopus (91) Google Scholar, 26Malfait M. Gomez P. van Veen T.A. Parys J.B. De Smedt H. Vereecke J. Himpens B. J. Membr. Biol. 2001; 181: 31-40Crossref PubMed Scopus (40) Google Scholar). To investigate the mechanisms whereby high glucose leads to decreased Cx43 in BREC, the amount of total Cx43 was determined by Western blotting (Fig. 1A). The levels of Cx43 decreased about 50% in cells exposed to 25 mm glucose for 8 days, as compared with controls (cells incubated in 5.5 mm glucose; see Fig. 1B). Because the proteasome was reported to be involved in Cx43 degradation (13Beardslee M. Lerner D. Tadros P. Laing J. Beyer E. Yamada K. Kleber A. Schuessler R. Saffitz J. Circ. Res. 2000; 87: 656-662Crossref PubMed Scopus (444) Google Scholar, 14Musil L.S. Le A.C. Van Slyke J.K. Roberts L.M. J. Biol. Chem. 2000; 275: 25207-25215Abstract Full Text Full Text PDF PubMed Scopus (200) Google Scholar, 15Laing J.G. Tadros P.N. Westphale E.M. Beyer E.C. Exp. Cell Res. 1997; 236: 482-492Crossref PubMed Scopus (217) Google Scholar, 16Laing J.G. Beyer E.C. J. Biol. Chem. 1995; 270: 26399-26403Abstract Full Text Full Text PDF PubMed Scopus (205) Google Scholar, 17Girao H. Pereira P. Mol. Vis. 2003; 9: 24-30PubMed Google Scholar), we further evaluated the participation of the proteasome on Cx43 degradation in high glucose by treating BREC with the proteasome inhibitors MG132 (Fig. 1, A and B) or lactacystin (data not shown). Data shown in Fig. 1 clearly indicate that proteasome inhibitors prevent, to a significant extent, the loss of Cx43 induced by high glucose. In fact, the levels of Cx43 in cells exposed to high glucose were restored to about 85% of the initial levels by proteasome inhibitors (Fig. 1B). Cx43 Is Stabilized by Proteasome Inhibitors under High Glucose—Because RT-PCR experiments suggest that the levels of mRNA for Cx43 are not remarkably altered after exposure of BREC to high glucose (data not shown), the decreased amounts of Cx43 observed under high glucose are likely to be related to an increased turnover of the protein. To determine the half-life of Cx43, cells were metabolically labeled with [35S]methionine for 1 h and then chased for 1, 2, or 4 h. The data presented in Fig. 2 shows that the half-life of Cx43 in cells exposed to high glucose decreased from 2.3 h, in control cells, to 1.9 h. To further determine whether the increased turnover of Cx43 in high glucose was associated with increased degradation of the protein by a proteasome-dependent mechanism, proteins in cells were metabolically labeled with [35S]methionine for 1 h and chased with unlabelled medium in the presence of the proteasome inhibitor MG132. Data shows that Cx43 degradation under high glucose is, at least in part, prevented by the proteasome inhibitor MG132 (Fig. 2) and by the more specific inhibitor lactacystin (data not shown). The half-life of Cx43 in cells grown in high glucose increased from 1.9 h to 3.4 h when the proteasome was inhibited. The fact that proteasome inhibitors extended Cx43 half-life beyond the half-life of the protein in controls indicates that proteasome has a role in constitutive degradation of Cx43 and that high glucose may create the conditions that favor increased degradation of the protein by a proteasome-dependent mechanism. Increased Degradation of Cx43 under High Glucose Is Associated with Increased Phosphorylation of the Protein—High glucose was shown to induce PKC-mediated phosphorylation of Cx43, which in turn may stimulate protein degradation (11Sato T. Haimovici R. Kao R. Li A.F. Roy S. Diabetes. 2002; 51: 1565-1571Crossref PubMed Scopus (131) Google Scholar, 25Kuroki T. Inoguchi T. Umeda F. Ueda F. Nawata H. Diabetes. 1998; 47: 931-936Crossref PubMed Scopus (91) Google Scholar, 26Malfait M. Gomez P. van Veen T.A. Parys J.B. De Smedt H. Vereecke J. Himpens B. J. Membr. Biol. 2001; 181: 31-40Crossref PubMed Scopus (40) Google Scholar). The effect of high glucose on phosphorylation of Cx43 induced by PKC was confirmed by incubating cells with staurosporine, an inhibitor of PKC. The decrease in the levels of Cx43 in cells exposed to high glucose was prevented, at least in part, by incubating cells with staurosporine (Fig. 3, A and B). Consistently, incubation with TPA, an activator of PKC, resulted in a decrease of about 85% in the content of Cx43 (Fig. 3B). These results show that high glucose may activate PKC, which, in turn, may hyperphosphorylate Cx43, leading to its increased degradation. Results obtained in our laboratory showed that the phosphorylated forms of Cx43 are preferentially degraded by a mechanism that involves the proteasome (17Girao H. Pereira P. Mol. Vis. 2003; 9: 24-30PubMed Google Scholar). To investigate whether proteasome is the mechanism leading to increased degradation of phosphorylated Cx43 under high glucose, Cx43 was immunoprecipitated from lysates of cells incubated under high glucose in the presence of proteasome inhibitors. Proteins were separated by SDS-PAGE and transferred to PVDF membranes that were probed with antibodies directed against the phosphoserine/phosphothreonine residues (Fig. 4A) or polyclonal antibodies directed against Cx43 (Fig. 4B). The ratio of phosphorylated/nonphosphorylated (P/NP) Cx43 was calculated and plotted in a graph (Fig. 4D). The results show that the ratio P/NP Cx43 increased 2-fold in cells incubated under high glucose and, more importantly, inhibition of the proteasome led to a 3-fold increase in the ratio of P/NP Cx43, as compared with control cells incubated under low glucose. On the other hand, the ratio of P/NP Cx43 was not significantly altered when the PKC inhibitor staurosporine was added to cells exposed to high glucose. These results suggest that phosphorylation of Cx43 in cells exposed to high glucose may act as a signal for degradation of the protein by a proteasome-dependent mechanism.Fig. 4Effect of the proteasome inhibitors on phosphorylation of Cx43. Cx43 was immunoprecipitated from cell lysates of BREC incubated with MG132 or staurosporine using polyclonal antibodies. Immunoprecipitated proteins were separated by SDS-PAGE, transferred to PVDF membranes, and probed with antibodies directed against phosphorylated residues of serine/threonine (A) or polyclonal antibodies to Cx43 (B). C, enzymatic dephosphorylation of Cx43. Cell lysates were incubated in the absence or presence of alkaline phosphatase (AP) from E. coli at 37 °C overnight. The intensity of the bands was determined by laser scanning the films followed by quantitative densitometric analysis. D, the ratio of P/NP Cx43 was calculated and plotted in a graph. Data are means ± S.E. (n = 3 per group). *, p < 0.05, difference from control incubated in low glucose as determined by unpaired two-tailed Student's t test.View Large Image Figure ViewerDownload Hi-res image Download (PPT) High Glucose Leads to Decreased Intercellular Communication by a Proteasome-dependent Mechanism—The functional implications of increased Cx43 degradation in high glucose was evaluated by scrape-loading dye transfer experiments. The intercellular communication was quantified as the distance traveled by the Lucifer yellow dye after scrape-loading (Fig. 5A). The GJIC decreased about 40% in cells exposed to high glucose (Fig. 5B). Conversely, but not surprisingly, proteasome inhibitors had the opposite effect in GJIC, leading to an increase of about 20% in the distance traveled by the dye (Fig. 5B). However, under high glucose, proteasome inhibitors not only restored the GJIC to control levels, but also increased intercellular communication 2-fold, as compared with controls incubated under low glucose. Taken together, these results suggest that high glucose has a direct impact in GJIC by a mechanism that involves increased degradation of Cx43 in a proteasome-dependent manner. Treatment of BREC, grown in high glucose with the PKC inhibitor staurosporine, resulted in an increase of GJIC of about 36%. On the other hand, and as predicted, treatment with TPA resulted in a dramatic inhibition (about 80%) of GJIC. Inhibition of GJIC Is the Direct Result of Decreased Abundance of Cx43 at the Plasma Membrane—Intercellular communication is usually associated with the abundance of functional gap junction plaques, at cell-cell interfaces. Thus, an alteration of intercellular communication is either associated with changes in gap junction activity or with the levels of Cx43 at the plasma membrane available to form gap junctions. To investigate whether the decrease of GJIC in high glucose is related to alterations in the subcellular distribution of Cx43, BREC were immunostained with antibodies directed against Cx43 and imaged by confocal microscopy. In contr