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J. Biol. Chem., Vol. 277, Issue 44, 42188-42196, November 1, 2002

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Inhibition of Glucocorticoid-induced Apoptosis in 697 Pre-B Lymphocytes by the Mineralocorticoid Receptor N-terminal Domain^*

Sonia L. Planey, Assia Derfoul^§, Andrzej Steplewski, Noreen M. Robertson, and Gerald Litwack^¶

From the Department of Biochemistry and Molecular Pharmacology, Jefferson Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania 19107

Received for publication, May 23, 2002, and in revised form, August 20, 2002

	ABSTRACT

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

The glucocorticoid and mineralocorticoid receptors (GR and MR) share considerable structural and functional homology and bind as homodimers to hormone-response elements. We have shown previously that MR and GR can form heterodimers that inhibit transcription from a glucocorticoid (GC)-responsive gene and that this inhibition was mediated by the N-terminal domain (NTD) of MR. In this report, we examined the effect of NTD-MR on GC-induced apoptosis in the GC-sensitive pre-B lymphoma cell line, 697. In GC-treated 697 cells, we demonstrated that stable expression of NTD-MR blocks apoptosis and inhibits proteolytic processing of pro-caspases-3, -8, and -9 and poly(ADP-ribose) polymerase. Importantly, gel shift and immunoprecipitation analyses revealed a direct association between the GR and amino acids 203-603 of NTD-MR. We observed down-regulation of c-Myc and of the anti-apoptotic proteins Bcl-2 and Bfl-1 as well as high levels of the pro-apoptotic proteins Bax and Bid. Conversely, cells stably expressing NTD-MR exhibited increased expression of Bcl-2 and Bfl-1 and diminished levels of Bid and Bax. These data provide a potential mechanism for the observed inhibition of cytochrome c and Smac release from the mitochondria of NTD-MR cells and resultant resistance to GC-induced apoptosis. Thus, NTD-MR may mediate GC effects through heterodimerization with GR and ensuing inhibition of GC-regulated gene transcription.

	INTRODUCTION

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

The glucocorticoid and the mineralocorticoid receptors (GR¹ and MR) are closely related members of the steroid receptor superfamily, with high sequence homology within the DNA binding and ligand binding domains (1). These receptors function as ligand-activated transcription factors that control various aspects of metabolic homeostasis, embryonic development, and physiological stress by binding to specific hormone-response elements in the regulatory regions of target genes (2). In vitro, both the GR and the MR bind to and are activated by the physiological glucocorticoid (GC), cortisol. Although both receptors, when activated, can bind and transactivate glucocorticoid-response elements (GREs) in the promoters of target genes, each has distinct transcriptional activities (3, 4). For instance, the GR, but not the MR, self-synergizes at multimerized hormone-response elements (5, 6), and only the GR can inhibit induction of AP-1-dependent genes by Fos-Jun heterodimers (7). In addition, the ability to mediate apoptosis in susceptible cells is exclusive to the GR (8).

Induction of apoptosis by GCs occurs in numerous cell types including immature lymphocytes and various malignancies of lymphoid origin (9, 10). Evidence that the GR is essential for this process has been provided by studies using GR antagonists, such as RU486, that completely block GC-induced cell death and by experiments involving GR knockout mice (11-13). The effects of mutations in the GR on its ability to cause apoptosis vary among cell lines. In human CEM and Jurkat lymphoid cells, the DNA binding domain and the ligand binding domain of the GR are essential for GC-induced cell death. Specifically, mutations that deleted either of the zinc fingers of the DNA binding domain or substituted amino acids in critical sites within the N-terminal zinc finger completely blocked the lethal response (14). Ligand binding domain mutations also inhibited cell death demonstrating a requirement for hormone binding (15). GR mutants lacking the N-terminal transactivation domain did not prevent apoptosis in these cell lines; however, in S49 mouse lymphoma cells, this region was essential for steroid-induced lethality (16).

Differences in the transcriptional activities of the GR and the MR, including the ability to mediate apoptosis, may be attributed to structural variability within the N-terminal domain (NTD). This region contains a transactivation function, AF-1, which is involved in the transcriptional transactivation of genes, in receptor heterodimerization, and in binding to other transcription factors (17). Moreover, in the absence of a ligand binding domain, this region is constitutively active. The NTDs of GR and MR share only 15% sequence homology and have been shown to have opposite transactivation properties (1). Specifically, chimeric receptor analyses demonstrated that this region of the MR is inhibitory for GR-mediated regulation of the Na/K-ATPase 1 gene promoter when MR and GR are coexpressed (18). In addition, several laboratories (5, 18-20) have shown that GR and MR can form heterodimers capable of inhibiting transcription from a GC-responsive gene.

Although the functional consequences of MR/GR heterodimerization are not well understood, the possible physiological significance stems from the observed co-localization of the receptors in various tissues and cells including the brain, heart, vascular smooth muscle, and leukocytes (21-24). For example, in the brain, the MR is involved in the excitability of neurons, whereas the GR opposes these effects. Moreover, in the dentate gyrus of the hippocampus, there is evidence that MR activation can protect neurons against acute GR ligand-mediated apoptosis (25). A recent study has also demonstrated that heterodimerization of MR and GR mediates direct corticosteroid-induced transrepression of the 5-HT1A receptor promoter (20). These studies have prompted us to examine whether the MR can mediate or abrogate apoptotic cell death in the GC-sensitive pre-B lymphoma cell line, 697.

	EXPERIMENTAL PROCEDURES

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

Materials-- Restriction enzymes and other reagents were obtained from Promega (Madison, WI), Roche Molecular Biochemicals, or New England Biolabs (Beverly, MA). Horseradish peroxidase-conjugated antibodies, ECL reagents, and Hybond membranes were purchased from Biosciences. Triamcinolone acetonide (TA), a synthetic GC analog, was purchased from Sigma. All tissue culture media and supplements were from Invitrogen. All other chemicals were purchased from Fisher.

Cell Lines and Culture Conditions-- The 697 cell line is a cloned human pre-B leukemic cell line derived from childhood acute lymphoblastic leukemia that carries the t(1;19) translocation (26, 27). These cells were cultured with RPMI media supplemented with 10% fetal bovine serum, 2 mM L-glutamine, penicillin at 100 units/ml, and streptomycin at 100 µg/ml at 37 °C under 5% CO₂ in a humidified atmosphere. Exponentially growing cells were used throughout all experiments at a concentration of 5 × 10⁵-1 × 10⁶ cells/ml. The cells were treated with TA at a concentration of 1 µM. After steroid treatment, cells were harvested by centrifugation at 1500 × g for 5 min and washed twice with phosphate-buffered saline (PBS).

Generation of Stably Transfected Cell Lines-- The N-terminal domain of MR (NTD-MR) or of GR (NTD-GR) was subcloned from the original RshMR or RshGR plasmids (gifts from Dr. R. M. Evans), respectively, into the mammalian expression vector pCMV/myc/nuc (Invitrogen) using the SalI/NotI restriction sites. This vector contains a C-terminal c-Myc epitope tag and three tandem nuclear localization signals located downstream of the multiple cloning site. Consequently, the expression of the NTD-MR/c-Myc and NTD-GR/c-Myc fusion proteins, which lack the domains required for translocation, would be efficiently targeted to the nucleus. Following sequence confirmation, these constructs were stably transfected into the 697 cell line. Cells (6 × 10⁶) were transfected with the Effectene reagent (Qiagen, Valencia, CA) and either 1 µg of the NTD-MR plasmid, the NTD-GR plasmid, or the empty vector and selected by G418 resistance. G418-resistant cells were subcloned by limiting dilution, and fusion protein expression was evaluated by Western blot using a c-Myc monoclonal antibody (mAb) (Invitrogen).

The generation of NTD-MR derivatives 1-103, 1-203, 1-303, 1-403, and 1-603 was carried out by PCR amplification of the pRshMR plasmid using the forward primer, MRfor-ATG-SalI, 5'-CCCCGTCGACATGGAGACCAAAGGCTACCAC-3', and the reverse primers MRrev103-NotI, 5'-GGGGGGGGCGGCCGCCTCAGCTACAGTTGCTGA-3', MRrev203-NotI, 5'-GGGGGGGGCGGCCGCCGAAGATGTCATGTTCAG-3', MRrev303-NotI, 5'-GGGGGGGGCGGCCGCAATATTTGCAGGGCTAGA-3', MRrev403-NotI, 5'-GGGGGGGGCGGCCGCATCTGGTTCTGGTTTTAT-3', and MRrev603-NotI, 5'-GGGGGGGGCGGCCGCTTGGGCAAAGGTAAATAC-3'. These constructs were subsequently cloned into the pCMV/myc/nuc vector using SalI/NotI restriction sites and stably transfected into 697 cells as described above.

Determination of Cell Number and Viability-- Cells (1 × 10⁶ cells/ml) were seeded in 24-well plates and incubated at 37 °C for 2 days in the presence or absence of 1 µM TA. Throughout the 48-h time course, cell viability was determined by trypan blue exclusion using a hemocytometer. For TUNEL staining, cells were treated with 1 µM TA for 0, 24, or 48 h and spun onto slides using a cytospin centrifuge. The cells were fixed with 4.0% paraformaldehyde in 0.1 M phosphate buffer (pH 7.4) for 15 min at room temperature and subsequently washed three times with PBS for 5 min. Cells were permeabilized with 0.1% Triton X-100, 0.1% sodium citrate, labeled with TUNEL reaction mixture (Roche Molecular Biochemicals), and incubated in a humidified chamber for 60 min at 37 °C in the dark. After rinsing 3 times with PBS, the cells were mounted in Vectashield with 4,6-diamidino-2-phenylindole counterstain (Vector Laboratories, Burlingame, CA) and examined with a Zeiss Axiovert 405M microscope using epifluorescence microscopy and photographed using a Phase 3 Imaging System with Cool Spot RT digital camera (Phase 3 Imaging Systems, Glen Mills, PA).

Gel Electrophoresis and Western Blotting-- Proteins were electrophoresed in 8, 10, or 12% SDS-polyacrylamide gels and transferred to nitrocellulose for Western blotting. Membranes were blocked overnight with 10% nonfat milk, 1× PBS, 0.1% Tween 20 and incubated with the -active caspase-3 rabbit polyclonal antibody (pAb) (1:1000) (BD Biosciences), -Myc mouse mAb (1:5000) (Invitrogen), -caspase-8 mouse mAb (0.5 µg/ml) (BD Biosciences), -caspase-9 rabbit pAb (1:1000) (BD Biosciences), or the PARP mouse mAb (1:200) (BD Biosciences) in 1× PBS, 5% nonfat milk for 1 h at room temperature, followed by a 1-h incubation with horseradish peroxidase-labeled donkey anti-rabbit or sheep anti-mouse antibodies (1:2500). Proteins were detected using ECL reagent.

Immunofluorescence-- NTD-MR (MR-H7) cells were harvested 1 h after treatment with 1 µM TA, spun onto slides, and fixed with 70% methanol, 30% acetone for 10 min at 20 °C and 5 min at room temperature. Cells were blocked for 30 min with 5% normal goat serum (NGS) in PBS and then incubated with avidin D blocking solution (Vector Laboratories) for 15 min. Slides were washed in PBS, 0.05% Tween 20, incubated with biotin blocking solution (Vector Laboratories) for 15 min, washed again, and incubated overnight at 4 °C with preimmune serum or GR pAb (5 µg/ml). Slides were washed in PBS, 0.05% Tween and incubated for 2 h at room temperature with biotinylated anti-rabbit IgG (5 µg/ml; Vector Laboratories) diluted in 5% NGS/PBS. Slides were washed in PBS 0.05% Tween and incubated with Texas Red avidin (20 µg/ml; Vector Laboratories) diluted in 5% NGS/PBS for 1.5 h at room temperature. Slides were washed in PBS prior to air drying, mounted in Vectashield (Vector Laboratories), and visualized as described for TUNEL analysis.

Electrophoretic Mobility Shift Assay-- A double-stranded oligonucleotide corresponding to a GRE from the human Na/K-ATPase 1 gene ( wt MRE) at position 662 to 628 GGGTTTGGCAATTGTCCTGCTCGAGGTGGTTCAGG was synthesized. 1 wt MRE was filled using the Klenow fragment (Roche Molecular Biochemicals) and labeled by incorporating [-³²P]CTP (PerkinElmer Life Sciences) for use as a probe. Nuclear extracts of TA-treated 697 cells with vector or NTD-MR (3-6 µg) were incubated on ice for 10 min in 10 mM Tris-HCl (pH 7.5), 80 mM KCl, 10% glycerol, 1 mM dithiothreitol, 1 mM of poly(dI-dC), in a total volume of 18 µl. c-Myc mAbs (-Myc) (Invitrogen or CN Biosciences, San Diego, CA) or MR pAbs (MR recognizing the N terminus and hMRsN recognizing a 10-amino acid peptide within the N terminus) (28), as well as preimmune serum and a GR pAb (GR) were included in reaction mixtures where indicated. 0.1 ng of 5' ³²P-end-labeled 1 wt MRE was added to the reaction, and incubation was continued for 10 min at room temperature. Reaction mixtures were applied to a 4% non-denaturing polyacrylamide gel, and DNA-protein complexes were resolved by electrophoresis (250 V) at 4 °C, with buffer recirculation in 1× TAE (6.7 mM Tris-HCl (pH 7.5), 3.3 mM sodium acetate, 1 mM EDTA). The gel was dried under vacuum and autoradiographed at 80 °C.

Immunoprecipitations-- Following a 1-h treatment with 1 µM TA, 2.0 × 10⁷ 697 cells with either vector, NTD-MR, or stably expressed NTD-MR derivatives 1-103, 1-203, 1-303, 1-403, and 1-603 were harvested by low speed centrifugation. Cells were disrupted using ice-cold RIPA buffer (1× PBS, 1% Nonidet P-40, 0.5% sodium deoxycholate, 0.1% SDS) containing fresh protease inhibitors and homogenized with passage through a 21-gauge needle. After incubation on ice, the samples were centrifuged at 10,000 × g, and the resulting cell lysates were precleared for 1 h at 4 °C with agitation using 2 µg of mouse IgG (Vector Laboratories) and 20 µl of protein A/G-agarose conjugate (Santa Cruz Biotechnology, Santa Cruz, CA). The beads were pelleted by centrifugation for 5 min at 2500 rpm at 4 °C, and the supernatants were transferred to a fresh tube. c-Myc mAb (2 µg/ml) was added to 1 ml of each cell extract, and the mixtures were rocked for 1 h at 4 °C. Then 20 µl of protein A/G-agarose conjugate was added to each sample for overnight incubation at 4 °C in a rotating device. Precipitates were collected by centrifuging at 2500 rpm for 5 min at 4 °C, washed 4 times with RIPA buffer and once with PBS, and resuspended in 40 µl of 1× SDS-electrophoresis buffer.

Isolation and Analysis of RNA-- After steroid treatment, cells were harvested by centrifugation and then frozen immediately on dry ice. Total cell RNA was isolated from frozen samples using the RNeasy® kit from Qiagen. RNA concentrations were determined by measuring the absorbance of each sample at 260 and 280 nm. Analysis of RNA for repression of c-Myc expression was carried out using RT-PCR and Northern blot analyses. RT-PCR was performed on 1 µg of each RNA sample using the TITANIUM^TM One-step RT-PCR Kit (BD Biosciences) and c-Myc- or GAPDH-specific primer pairs (c-Myc forward, 5'-ATGCCCCTCAACGTTAGCTTCACCAACAGG-3', c-Myc reverse, 5'-TTACGCACAAGAGTTCCGTAGCTGTTCAAG-3'; GAPDH forward, 5'-CCACCCATGGCAAATTCCATGGCA-3', GAPDH reverse 5'-TCTAGACGGCAGGTCAGGTCCACC-3'). The amplification was performed as follows: 50 °C/1 h, 94 °C/5 min, 30 cycles of 94 °C/30 s, 65 °C/30 s, 68 °C/1 min, and then 68 °C/2 min. PCR products were separated by electrophoresis in a 1.0% agarose gel and visualized by ethidium bromide staining. Band intensities were quantitated using Kodak 1D Imaging Software (Eastman Kodak Co.), and fold induction of mRNA expression was normalized to the level of glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

For Northern blot analysis, RNA samples (15 µg each) containing 0.2 µg/ml ethidium bromide were fractionated in a 1.2% formaldehyde-agarose gel. The gel was photographed, rinsed in 10× SSC, and transferred by blotting to Hybond-N nylon membrane (Amersham Biosciences) with 20× SSC. Accuracy of RNA loading and transfer was confirmed by fluorescence under ultraviolet light after staining with ethidium bromide. The RNA was UV cross-linked to the membrane, prehybridized, and hybridized at 42 °C in 50% formamide, 5× SSC, 0.5% SDS, 0.3 mg/ml salmon sperm DNA, 1× Denhardt's solution. Radioactive human c-Myc DNA probe (100 ng) (Geneka Biotechnology Inc., Montreal, Quebec, Canada) was used at a concentration of 0.5-1 × 10⁶ cpm/ml and was prepared by the random primer labeling method with [-³²P]dCTP. After hybridization, the membranes were washed in 0.1-0.5× SSC, 0.1% SDS at 42-68 °C and exposed to x-ray film.

Isolation of Mitochondria-- 697 cells with vector or NTD-MR were treated with 1 µM TA for 0, 24, and 48 h and harvested by centrifugation at 600 × g for 10 min at 4 °C. The cell pellets were washed once with ice-cold PBS and resuspended with 5 volumes of buffer A (20 mM Hepes-KOH (pH 7.5), 10 mM KCl, 1.5 mM MgCl₂, 1 mM sodium EDTA, 1 mM sodium EGTA, 1 mM dithiothreitol, and 0.1 mM phenymethylsulfonyl fluoride) containing 250 mM sucrose. The cells were homogenized for 15 s, and the homogenates were centrifuged twice at 750 × g for 10 min at 4 °C. The supernatants were centrifuged at 10,000 × g for 15 min at 4 °C, and the resulting mitochondrial pellets were resuspended in buffer A containing 250 mM sucrose and frozen in multiple samples at 80 °C. The supernatants of the 10,000 × g spin were further centrifuged at 100,000 × g for 1 h or more at 4 °C, and the resulting cytosolic fractions were concentrated through a Microcon YM-10 Centrifugal Filter Device (Millipore, Bedford, MA). Mitochondrial and cytosolic fractions were used for Western blot analysis.

	RESULTS

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

We have demonstrated previously (18, 29) that the NTD of MR is inhibitory for GR-mediated gene transcriptional regulation. To examine the ability of this region to modulate GR-induced apoptosis, the NTD of MR (NTD-MR) composed of amino acids 1-516, or the NTD of GR (NTD-GR), encompassing amino acids 1-421, was stably expressed in 697 cells. These cells provide a model system for this study because we have shown previously (30, 31) that they express GR, and that they are exquisitely sensitive to GC-induced cell death. More importantly, immunoblot and RT-PCR analyses of 697 whole cell extracts and of RNA, respectively, have demonstrated that these cells do not express MR (data not shown). As shown in Fig. 1, expression of the NTD-MR/c-Myc or NTD-GR/c-Myc fusion proteins was evaluated by Western blot analysis using a c-Myc mAb (Fig. 1). The predicted 59-kDa recombinant NTD-MR protein was detected in 5 of 6 clones examined (Fig. 1A, lanes 1-6), although no c-Myc-tagged NTD-MR was expressed in the cells transfected with the control vector (lane 7). Expression of the 51-kDa recombinant NTD-GR protein was also detected in stably transfected cells (Fig. 1C, lanes 1-6). Following evidence of expression, the clones with the highest level of NTD-MR (MR-H7 or -A2) or NTD-GR (GR-D6) were used for further experimentation.

View larger version (20K): [in this window] [in a new window]   Fig. 1.   A and C, detection of recombinant NTD-MR and NTD-GR in stably transfected 697 cells. Samples containing whole cell extracts prepared from 1 × 106 cells transfected with vector alone (pCMV), NTD-MR/c-Myc, or with NTD-GR/c-Myc were subjected to SDS-PAGE followed by immunoblotting with a c-Myc mAb. Molecular mass markers are indicated (kDa). B and D, kinetics of 697 cell survival following GC treatment. At time 0, 697 cells stably transfected with either vector alone, NTD-GR (clone D6), or NTD-MR (clones H7 and A2) were cultured in the presence or absence of 1 µM TA, and survival was analyzed over time by trypan blue exclusion. Data shown are means and standard deviations for three experiments in which each was performed in triplicate.

NTD-MR Inhibits Glucocorticoid-induced Apoptosis in 697 Cells-- To examine the effects of NTD-MR or NTD-GR on the kinetics of GC-induced cell death, cells were treated with 1 µM TA for a 48-h time course. Fig. 1D shows that 697 cells with vector and NTD-GR cells exhibit declining viability within the first 24 h of treatment, with complete cell death occurring by 48 h. Importantly, stable transfection of the NTD-MR in these cells resulted in a strong inhibition of GC-induced cell death (Fig. 1B). To confirm that overexpression of the MR N terminus protects 697 cells from GC-induced apoptosis, DNA isolated from cells at the indicated time points following treatment with 1 µM TA (0, 24, and 48 h) was examined for nuclear fragmentation using the TUNEL assay. As shown in Fig. 2, 697 cells with vector, treated with TA for 24 h, exhibited the typical morphologic changes associated with apoptosis such as shrinkage and nuclear blebbing, compared with untreated cells (Fig. 2, A and B). Moreover, the nuclei of these cells exhibited fluorescence indicating the presence of the labeled 3'-OH ends characteristic of apoptotic cells. In contrast, cells stably expressing NTD-MR, which had been treated with TA for the same time period, retained their viability (Fig. 2, C and D).

View larger version (33K): [in this window] [in a new window]   Fig. 2.   Stable expression of NTD-MR inhibits GC-induced apoptosis in 697 cells. 697 cells with vector or NTD-MR (MR-H7) were incubated in the presence or absence of 1 µM TA. At the 24-h time point, aliquots of cell suspensions were processed using the TUNEL assay (green) and counterstained with 4,6-diamidino-2-phenylindole (blue) to detect changes in nuclear morphology.

NTD-MR Does Not Affect GR Expression or Nuclear Translocation-- To explore the mechanism of inhibition of GC-induced apoptosis by NTD-MR at the receptor level, we first examined GR protein levels by Western blot and GR subcellular localization by immunofluorescence. To compare GR protein levels in 697 and MR-H7 cells, whole cell extracts were prepared from cells harvested at 0, 3, 8, 12, 18, 24, 36, and 48 h of treatment with 1 µM TA. As shown in Fig. 3A, overexpression of NTD-MR did not alter endogenous levels of GR protein, which remained steady over the 48-h time course and comparable with those levels detected in 697 cells. Immunocytochemical analysis in Fig. 3B revealed that endogenous GR expression in cells stably transfected with NTD-MR (MR-H7) is cytoplasmic. Following treatment of cells with 1 µM TA for 1 h, the GR was detected primarily in the nucleus. These data suggest that the expression of NTD-MR in 697 cells does not prevent translocation of the GR into the nucleus upon hormone binding.

View larger version (31K): [in this window] [in a new window]   Fig. 3.   Subcellular localization and expression levels of endogenous GR in MR-H7 cells treated with GC. A, 697 cells with vector or NTD-MR were treated with 1 µM TA over a 48-h time course, harvested at designated time points, and subjected to SDS-PAGE followed by immunoblotting with a GR pAb. Accuracy of protein loading and transfer was confirmed by stripping and reprobing with a -actin pAb (Santa Cruz Biotechnology). B, untreated MR-H7 cells (T0) or cells treated with 1 µM TA for 1 h (T1) were processed for immunofluorescence using a GR pAb and confocal microscopy.

NTD-MR Does Not Affect the Ability of GR to Bind DNA-- To determine whether the expression of NTD-MR interferes with the ability of GR to bind DNA, EMSA was performed using a GR/MR-specific response element as a probe and nuclear extracts from 697 cells with vector or MR-H7 cells treated for an hour with 1 µM TA. In extracts of 697 cells, we detected protein binding to the 1 MRE/GRE corresponding to endogenous GR (Fig. 4A, lane 1). This binding was reduced when a GR antibody was included in the gel shift reaction (Fig. 4A, lane 2) and was unaffected in the presence of nonspecific serum (Fig. 4A, lane 3) or c-Myc mAb (Fig. 4A, lane 4). In extracts of MR-H7 cells, binding of endogenous GR to the 1 MRE/GRE was similar to that seen for 697 cells (Fig. 4B, lanes 1 and 2). To determine whether the protein-DNA complexes contained the N-terminal MR, we used two different c-Myc mAbs and MR pAbs. In all cases, the protein-DNA complexes were either ablated or shifted to a higher position when these antibodies were used (Fig. 4B, lanes 3-6) but remained unchanged when a preimmune serum was included in the reaction (Fig. 4B, lane 7). These results indicate that the N terminus of MR is present with the GR in the protein-DNA complex, suggesting the possibility of MR-GR heterodimer formation.

View larger version (46K): [in this window] [in a new window]   Fig. 4.   NTD-MR physically associates with endogenous GR. EMSA was performed using a GR/MR-specific response element as a probe and nuclear extracts from 697 cells with vector or NTD-MR (MR-H7) treated with 1 µM TA for 1 h. A, GR pAb (GR) or c-Myc mAb (myc) was incubated with nuclear extracts 10 min prior to the addition of probe (lanes 2 and 4, respectively). Lane 1 contained a buffer control and lane 3 a preimmune nonspecific serum (NSS). The asterisk denotes GR-specific binding, and the arrow indicates the antibody-mediated shifts on DNA-protein complexes. Ab, antibody. B, MR (lane 4) or hMRsN (lane 6) pAb was incubated with nuclear extracts 10 min prior to the addition of probe. Similarly, a c-Myc mAb (myc) from Invitrogen or from CN Biosciences was incubated with samples in lanes 3 and 5, respectively. Lane 1 contained a buffer control, lane 2 GR, and lane 7 a preimmune nonspecific serum (NSS). C, schematic representation of NTD-MR derivatives 103, 203, 303, 403, MR-H7, and 603 cloned into the pCMV/myc/nuc vector. D, 697 cells with vector, NTD-MR, or stably expressed NTD-MR derivatives 103, 203, 303, 403, and 603 were treated with 1 µM TA and harvested after 3 h. Cellular lysates were subjected to immunoprecipitation with c-Myc mAb and analyzed by Western blot using a GR pAb (top) or a c-Myc mAb (bottom) as a control for the amount of immunoprecipitated protein. In lane 3, lysate from cells transfected with full-length GR served as a positive control.

Interaction between GR and Amino Acids 203-603 of NTD-MR-- We have shown previously (18, 29) that when co-expressed, the MR and the GR are able to form heterodimers. To determine whether the inhibitory effects of NTD-MR on GR function are the result of a direct interaction with the GR, we performed immunoprecipitation analysis. 697 cells stably expressing NTD-MR (MR-H7) or NTD derivatives (1-103, 1-203, 1-303, 1-403, and 1-603) (Fig. 4C) were treated with 1 µM TA for 3 h. Cell lysates were subjected to immunoprecipitation using a c-Myc mAb. As shown in Fig. 4D (top), Western blot analysis with a GR pAb demonstrated that endogenous GR physically associates with the NTD of the MR. Specifically, this interaction occurred within the N-terminal region encompassing amino acids 203-603 (lanes 5-9), because no binding was detected with the deletion derivative 1-103 (lane 4). As a control for the amount of immunoprecipitated protein, the membrane was stripped and successively reprobed with a c-Myc mAb (bottom).

Effect of NTD-MR on GR Transcriptional Activity-- To test the effect of GR/NTD-MR heterodimers on GR transcriptional activity in 697 and MR-H7 cells, we evaluated the effect of TA on GR-mediated regulation of the endogenous c-myc gene. Suppression of c-Myc mRNA has been reported previously (31) when GR-sensitive cells were treated with GC. To examine the expression of c-Myc at the mRNA level, 697 cells with vector or NTD-MR were cultured in the presence of 1 µM TA for 48 h, and RNA was prepared from cells harvested at time 0, 4, 16, 24, and 48 h. As determined by semi-quantitative RT-PCR, treatment of 697 cells with GC caused a 7-fold repression of c-Myc transcription by 24 h as compared with untreated cells (time 0) (Fig. 5A). This repression was blocked by NTD-MR in MR-H7 cells as shown in Fig. 5A. GAPDH levels were unaffected by TA treatment in both cell lines. These data were confirmed by Northern blot analysis using a c-Myc-specific cDNA probe in Fig. 5B, which shows that expression of c-Myc mRNA was dramatically reduced in 697 cells treated with TA after 4 h. Within the period of the experiment, the level of the c-Myc mRNA reached its lowest point at 24 h after TA treatment. However, in the MR-H7 cells, c-Myc mRNA levels remained constant throughout the time course.

View larger version (67K): [in this window] [in a new window]   Fig. 5.   Effect of TA on the expression of c-Myc mRNA in 697 and MR-H7 cells. A, gel electrophoresis of semi-quantitative RT-PCR using 1 µg of total cellular RNA from 697 cells with vector or NTD-MR (MR-H7) harvested at indicated time points throughout a 48-h incubation with 1 µM TA. GAPDH was included as an internal control. Fold induction (FI) of c-Myc mRNA expression is indicated. B, total cellular RNA was isolated from 697 cells with vector (lanes 1-5) or NTD-MR (MR-H7) (lanes 6-10) at 0-48 h after TA (1 µM) treatment. Equal amounts of RNA (15 µg/lane) were fractionated on an agarose-formaldehyde gel (top) and transferred by blotting onto Hybond-N nylon membranes as described under "Experimental Procedures." The c-Myc mRNA was identified by hybridization using a 1-kb 32P-labeled human c-Myc probe (bottom). The locations of the 28 S and 18 S rRNAs are indicated. The periods of TA treatment (h) are indicated at the top of each lane.

NTD-MR Inhibits Proteolytic Processing of Caspases and PARP-- A common end point to apoptosis is a network of caspases whose activation is required for the irreversible commitment to cell death. To determine whether NTD-MR expression inhibits caspase activation in 697 cells, enzymatic cleavage of endogenous caspases during GC-induced apoptosis was assessed. 697 cells stably expressing NTD-MR (MR-H7) or vector alone were cultured in the presence or absence of 1 µM TA during a 48-h time course, and whole cell lysates were examined by Western blot analysis. As shown in Fig. 6A, proteolytic processing of the proform of the apical caspases-8 (55 kDa) and -9 (46 kDa) and the downstream effector caspase-3 (32 kDa) was observed in 697 cells treated with TA. In contrast, in MR-H7 cells treated with TA, the inactive proenzyme forms of caspases-8, -9, and -3 remained intact, revealing that GC-induced caspase cleavage was abolished. Further evidence of this inhibition was seen when a downstream target of activated caspase-3, PARP, was examined for enzymatic degradation. Immunoblot analysis in Fig. 6B shows that following treatment of 697 cells with TA, the "death substrate" PARP (116 kDa) was proteolyzed with generation of its signature 85-kDa cleavage product, although in MR-H7 cells, PARP cleavage was inhibited.

View larger version (42K): [in this window] [in a new window]   Fig. 6.   Stable expression of NTD-MR inhibits caspase activation and PARP cleavage during GC-induced apoptosis. Western blot analysis of caspase-8, caspase-9, caspase-3, and PARP status after treatment with TA. A, 697 cells with vector or NTD-MR (MR-H7) were treated with 1 µM TA for a 48-h time course. Samples containing whole cell extracts from 1 × 106 cells were subjected to SDS-PAGE followed by immunoblotting with a mAb to caspase-8 and pAbs to caspase-9 and active caspase-3. B, for PARP analysis, samples (50 µg) were electrophoresed on an 8% SDS-polyacrylamide gel, transferred to nitrocellulose membrane, and probed with anti-PARP mAb. Molecular mass markers are indicated (kDa).

Effect of NTD-MR on Bcl-2 Family Members-- It has been shown that GC-induced apoptosis is regulated by members of the Bcl-2 family upstream of caspase activation (32-34). To address potential mechanisms involved in N-terminal MR inhibition of GC-induced apoptosis, we evaluated the expression levels of the anti-apoptotic proteins, Bcl-2 and Bfl-1. As determined by semi-quantitative RT-PCR, treatment of 697 cells with 1 µM TA caused an 18-fold repression of Bcl-2 transcription by 16 h; however, in MR-H7 cells, Bcl-2 mRNA levels increased nearly 2-fold over the 48-h time course (Fig. 7A). We also observed a 6-fold down-regulation of Bfl-1 mRNA in 697 cells within 4 h of treatment, whereas Bfl-1 mRNA expression in MR-H7 cells was up-regulated 8-fold (Fig. 7A). These results were corroborated by Western blot analyses of cytosolic and mitochondrial extracts. Following GC treatment of 697 cells, mitochondrial levels of Bcl-2 were decreased, although cytosolic levels increased slightly (Fig. 7B). In contrast, mitochondrial Bcl-2 levels were dramatically increased in MR-H7 cells (Fig. 7B). Furthermore, mitochondrial and cytosolic Bfl-1 expression levels were non-detectable in 697 cells following GC treatment, whereas in MR-H7 cells, the expression levels of Bfl-1 in the mitochondrial fraction increased slightly at 24 h and in the cytosolic fraction were increased at 48 h (Fig. 7B).

View larger version (51K): [in this window] [in a new window]   Fig. 7.   Effect of GC on Bcl-2 and Bfl-1 mRNA expression and protein levels in 697 and MR-H7 cells. A, gel electrophoresis of semi-quantitative RT-PCR using 1 µg of total cellular RNA from 697 cells with vector or (NTD-MR) MR-H7 harvested at indicated time points throughout a 48-h incubation with 1 µM TA. RT-PCR was performed as described under "Experimental Procedures" using the following primer pairs: Bcl-2 forward, 5'-ATGGCGCACGCTGGGAGAACGGGGTACGAC-3', and Bcl-2 reverse, 5'-TCACTTGTGGCTCAGATAGGCACCCAGGGT-3'; Bfl-1 forward, 5'-ATGACAGACTGTGAATTTGGATATATTTAC-3', and Bfl-1 reverse 5'-TCAACAGTATTGCTTCAGGAGAGATAGCAT-3'. GAPDH was included as an internal control. Fold induction (FI) of Bcl-2 and Bfl-1 mRNA expression is indicated. B, mitochondrial and cytosolic extracts from 697 cells with vector or NTD-MR (MR-H7) treated with 1 µM TA for a 48-h time course were subjected to SDS-PAGE followed by immunoblotting with a mAb to Bcl-2 (BD Biosciences) and a pAb to Bfl-1 (Santa Cruz Biotechnology). To ensure that the same content of mitochondrial and cytosolic protein was loaded in each case, the membrane was stripped and successively reprobed with a VDAC pAb (Santa Cruz Biotechnology) as a marker for the mitochondrial fraction and a -actin pAb as a marker for the cytosolic fraction.

A recent study (35) has demonstrated that Bfl-1 can prevent the formation of a pro-apoptotic complex by sequestering BH3 domain-only proteins like Bid and blocking its collaboration with Bax or Bak in the plane of the mitochondrial membrane. Thus, we examined the localization and protein levels of the pro-apoptotic proteins Bid and Bax in 697 and MR-H7 cells treated with 1 µM TA. Western blot analysis in Fig. 8A shows that in 697 cells, both cytosolic and mitochondrial levels of Bid were dramatically higher than in MR-H7 cells. Moreover, in MR-H7 cells, Bid was located primarily within the mitochondria, whereas in 697 cells it was detected in the cytosol as well. Bax protein levels did not seem to be significantly different between the two cell lines; however, Bax was only faintly detectable in the cytosol of MR-H7 cells at 48 h (Fig. 8A).

View larger version (57K): [in this window] [in a new window]   Fig. 8.   A, localization of Bid, Bax, Cyt c, and Smac in GC-treated 697 and MR-H7 cells. Mitochondrial and cytosolic extracts from 697 cells with vector or NTD-MR (MR-H7) treated with 1 µM TA for a 48-h time course were subjected to SDS-PAGE followed by immunoblotting with a pAb to Bid (BIOSOURCE), a pAb to Bax (Santa Cruz Biotechnology), a mAb to Cyt c (BD Biosciences), and a pAb to Smac/DIABLO (Upstate Biotechnology, Inc.). To ensure that the same content of mitochondrial and cytosolic protein was loaded in each case, the membrane was stripped and successively reprobed with a VDAC pAb as a marker for the mitochondrial fraction and a -actin pAb as a marker for the cytosolic fraction. B, NTD-MR inhibits degradation of XIAP after treatment with TA. Cytosolic extracts from 697 cells with vector or NTD-MR (MR-H7) treated with 1 µM TA for a 48-h time course were subjected to SDS-PAGE followed by immunoblotting with a mAb to XIAP (Stressgen). Accuracy of protein loading and transfer was confirmed by stripping and reprobing with a -actin pAb.

NTD-MR Inhibits Cytochrome c and Smac Release from the Mitochondria-- Bcl-2 has been shown to inhibit cytochrome c (Cyt c) release from mitochondria in pre-apoptotic cells (36). Because we observed reduced expression of Bcl-2 in GC stimulated 697 cells and increased expression in MR-H7 cells, we sought to examine whether Cyt c was released from the mitochondria. As shown in Fig. 8A, GC induced a time-dependent release of Cyt c from the mitochondria with a concomitant increase of Cyt c into the cytosolic fraction of 697 cells. In contrast, Cyt c was retained in the mitochondria of MR-H7 cells (Fig. 8A). Because Smac/DIABLO is known to promote caspase activation in the Cyt-c/Apaf-1/caspase-9 pathway, we examined whether inhibition of Smac release from the mitochondria plays a role in NTD-MR-mediated inhibition of GC-induced apoptosis. As demonstrated in Fig. 8A, the expression level of Smac in the mitochondrial fraction of 697 cells was dramatically reduced within 48 h following treatment with 1 µM TA. This loss of Smac from the mitochondria was accompanied by its presence in the cytosol within 24 h, an effect that was inhibited in the presence of NTD-MR (Fig. 8A). These results demonstrate that GC-induced apoptosis in 697 cells is accompanied by the release of Cyt c and Smac from the mitochondria into the cytosol and that the expression of NTD-MR inhibits this process.

Smac/DIABLO, when released from mitochondria into the cytosol, functions by eliminating the inhibitory effects of inhibitor of apoptosis proteins (IAPs), particularly XIAP, on caspases (37-39). We examined the cytosolic fractions from GC-treated 697 and MR-H7 cells for the presence of XIAP. As shown in Fig. 8B, XIAP levels were relatively low in 697 cells and completely diminished by 48 h. However, in MR-H7 cells, levels of XIAP were much higher and remained constant throughout the 48-h time course (Fig. 8B). These data are important because they support a model in MR-H7 cells that by inhibiting the release of Smac from the mitochondria, XIAP is able to maintain its association with caspases and inhibit their activity as well as cell death.

	DISCUSSION

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

GC-induced lymphocytic cell death is one of the earliest recognized forms of apoptosis (8), yet progress in understanding this process has lagged behind significant advances in understanding other forms of apoptosis, such as that induced by death receptors (40). In this report, we examined the ability of the NTD of MR to modulate GR-induced apoptosis in the GC-sensitive cell line, 697, based on our previous findings that this region is inhibitory for GR-mediated gene transcriptional regulation (18, 29). Our data show that when treated with the GC analog, TA, parental 697 cells undergo apoptosis. However, in 697 cells stably expressing the NTD-MR, GC-induced apoptosis was dramatically inhibited, indicating that the N-terminal region of MR induces a dominant negative effect and potently inhibits GR function.

Inhibition of GC-induced apoptosis in 697 cells by NTD-MR may reflect interactions occurring at the receptor level. In its inactivated form, the GR exists in the cytoplasm of cells complexed with heat-shock proteins, immunophilins, and other inhibitory proteins (41). Upon binding ligand, the GR sheds these proteins and translocates to the nucleus, where it can regulate the transcription of GC-responsive genes by binding to specific glucocorticoid-response elements (GREs) within DNA, either enhancing or repressing gene transcription (42). We show that overexpression of NTD-MR does not prevent translocation of the GR into the nucleus upon hormone binding nor does it alter endogenous GR protein levels. However, EMSA and immunoprecipitation analyses demonstrate that there is a direct interaction between the GR and amino acids 203-603 of the NTD-MR. An evaluation of GR transcriptional activity in both 697 and MR-H7 cells further revealed that NTD-MR expression interfered with the GR-mediated suppression of endogenous c-Myc. These results suggest that the observed inhibitory activity of NTD-MR on GR-mediated transcription and ensuing apoptosis in 697 cells is likely mediated through heterodimerization of the NTD-MR with GR. Importantly, these data are in agreement with several studies (18-20, 43) substantiating the potential for transcriptional regulation via heteromeric complexes of the GR and MR.

In mammals, the initiation of apoptosis is controlled by the following two major signaling pathways: the receptor-mediated "extrinsic" pathway and the mitochondrial-mediated "intrinsic" pathway. Caspase-8 is the key initiator of the extrinsic pathway where it is activated in response to death receptor engagement by ligands belonging to the tumor necrosis factor superfamily (44, 45). The intrinsic pathway involves mitochondrial disruption by pro-apoptotic Bcl-2 family members and consequent release of factors such as cytochrome c that promote caspase-9 activation (46-49). Both pathways culminate in the activation of downstream effector caspases-3, -6, and -7 and can cooperate to enhance apoptosis through caspase-8-mediated cleavage of Bid (50-52). Here we provide evidence that treatment of 697 cells with GC mediates the efficient proteolytic processing of caspases-8, -9, and -3 as well as cleavage of the death substrate, PARP. Remarkably, this processing is completely abolished in 697 cells expressing NTD-MR, suggesting that the survival function of NTD-MR is upstream of caspase activation. Our observation that GC-induced apoptosis in 697 cells is accompanied by the cleavage of caspases-9 and -3 as well as the release of Cyt c from the mitochondria provides strong evidence that apoptosis in pre-B lymphocytes proceeds mainly through the intrinsic cell death pathway.

Members of the Bcl-2 family, including death repressor (e.g. Bcl-2, Bcl-x_L, and Bfl-1) and death inducer (e.g. Bax, Bcl-x_S, and Bak) proteins, are major regulators of mitochondrial apoptotic events and act in part by controlling Cyt c release from the mitochondria (53). For example, expression of Bcl-2 and Bcl-x_L prevents the redistribution of Cyt c in response to multiple death-inducing stimuli (54-56), whereas Bid, Bax, and Bak promote Cyt c release (36, 57, 58). Bcl-2 family members also form homo- or heterodimers with one another and, depending on the ratio of inhibitor to activator, can either inhibit or activate cell death (59, 60). In the present study, we observed that stimulation of 697 cells with GC triggered the loss of Bcl-2 and Bfl-1 expression and the release of cytochrome c and Smac from the mitochondria. Moreover, levels of the pro-apoptotic proteins Bax and Bid remained elevated, supporting destructive alterations in the mitochondria. In sharp contrast, 697 cells stably expressing NTD-MR exhibited increased expression levels of Bcl-2 and Bfl-1 and inhibition of Cyt c and Smac release from the mitochondria. The protein levels of Bid and Bax in these cells were either significantly reduced or not sustained over the 48-h treatment period with TA, supporting the inhibition of mitochondrial disruption in these cells. Furthermore, the elevated levels of XIAP observed in MR-H7 cells suggest that XIAP would be allowed to maintain its association with caspases and prevent apoptosis.

The observed up-regulation of the anti-apoptotic proteins, Bcl-2 and Bfl-1, in MR-H7 cells sheds light not only on the mechanism by which NTD-MR inhibits the pro-apoptotic action of GCs but also on the process by which GCs induce apoptosis in pre-B lymphocytes. Recent findings indicate that Bcl-2 family members function upstream of caspase activation to inhibit commitment to cell death. Bcl-2 is thought to act on the outer mitochondrial membrane to prevent mitochondrial permeability transition pore opening and the subsequent release of apoptogenic proteins from the mitochondria (53, 61). Bcl-2 can also inhibit the action of Bax/Bak by forming inactivating heterodimers (57). More recently, it has been shown that overexpression of Bcl-2 in dexamethasone-treated thymocytes inhibits proteasome activation (62). Involvement of the proteasome in the induction of apoptosis is a distinguishing characteristic of the corticosteroid-induced death pathway versus the Fas-mediated cell death pathway where the proteasome appears dispensable (62). Degradation of the cell cycle proteins, Cdk2 and p27Kip1 (33, 63), the pro-survival transcription factors, c-Fos and NF-B (34, 64), and the IAPs, c-IAP1 and XIAP (60), by the proteasome have been described. Hence, higher levels of Bcl-2 in MR-H7 cells may act not only to preserve mitochondrial function but may also function by regulating proteasome-mediated degradation of cell cycle and pro-survival proteins.

Bfl-1 is an anti-apoptotic Bcl-2 family member whose preferential expression in hematopoietic cells and endothelium is controlled by inflammatory stimuli. Cellular expression of Bfl-1 has been shown to confer protection against CD95- and Trail receptor-induced Cyt c release as well as p53- and etoposide-induced apoptosis (65-67). However, a protective function of Bfl-1 in GC-induced apoptosis has not been documented. We observed localization of Bfl-1 and Bid primarily to the mitochondria in MR-H7 cells but not in 697 cells undergoing apoptosis. Bfl-1 has been shown to prevent the formation of a pro-apoptotic complex by sequestering BH3 domain-only proteins at the mitochondria. Thus, up-regulation of Bfl-1 in MR-H7 cells may serve to bind and sequester tBid at the mitochondria and prevent its association with Bax, thereby inhibiting mitochondrial disruption and Cyt c release.

A possible mechanism for the inhibitory effect of NTD-MR on GC-induced apoptosis may involve the disruption of an interaction between GR and a specific cellular factor or competition between the GR and NTD-MR for limited amounts of mutual coactivators. A coactivator that clearly distinguishes between the GR and MR has not been identified; however, it is likely that coactivators interacting differentially with the AF-1 transactivation domain of these receptors may play an important role in conferring specific glucocorticoid/mineralocorticoid-mediated regulation. A recent study by Sadar and co-workers (68) has demonstrated that interleukin-6 mediates activation of the androgen receptor NTD by a mechanism dependent upon mitogen-activated protein kinase and STAT3 signal transduction pathways in LNCaP prostate cancer cells. Furthermore, STAT3 was shown to interact specifically with fragments of the androgen receptor NTD containing all or part of the AF-1 site.

In summary, we have demonstrated that in GC-induced apoptosis of 697 cells, the NTD of MR inhibited apoptosis prior to commitment to cell death by interfering with GR-mediated changes in gene transcription. Specifically, we show that GR-mediated repression of c-Myc and of the anti-apoptotic proteins Bcl-2 and Bfl-1 is abrogated in cells expressing NTD-MR. The up-regulation of these anti-apoptotic proteins in MR-H7 cells as well as the diminished levels of Bax and Bid provide a potential mechanism for the observed inhibition of Cyt c and Smac release from the mitochondria and resultant resistance to GC-induced apoptosis. Thus, in normal physiology, in cells where MR and GR are coexpressed, the MR may function to counteract the role of activated GR by increasing the ratio of anti-apoptotic molecules relative to pro-apoptotic molecules. Indeed, such a scenario has been observed in the rat hippocampus where the opposing actions of MR and GR on neuronal survival were shown to result from their ability to differentially influence the expression of members of the bcl-2 gene family (69). Further studies are underway to identify GR-induced pro-apoptotic genes that are repressed by NTD-MR and pro-survival genes that are up-regulated by NTD-MR. The elucidation of GR-regulated apoptotic genes may offer a molecular basis for the treatment of inflammatory diseases and cancer.

	ACKNOWLEDGEMENTS

We are grateful to R. M. Evans for providing the expression plasmids for the human MR and the human GR. We also thank Dr. Jim Zangrilli and Dr. Annette Hastie for critical review of the manuscript and members of the Litwack laboratory for helpful discussions.

	FOOTNOTES

^* This work was supported in part by National Institutes of Health Grant AI/HL 40976 (to G. L.) and American Lung Association Grant RG-034N (to N. R.).The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

Supported by National Institutes of Health Training Grant 5T32 DK07705.

^§ Present address: NIAMS, National Institutes of Health, Rm. 3W17, 13 South Dr., MSC5755, Bethesda, MD 20892.

^¶ To whom correspondence should be addressed: Thomas Jefferson University, 233 S. 10th St., BLSB 350, Philadelphia, PA 19107. Tel.: 215-503-4634; Fax: 215-503-5393; E-mail: Gerry.Litwack@mail.tju.edu.

Published, JBC Papers in Press, August 22, 2002, DOI 10.1074/jbc.M205085200

	ABBREVIATIONS

The abbreviations used are: GR, glucocorticoid receptor; Cyt c, cytochrome c; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; GC(s), glucocorticoid(s); GRE, glucocorticoid-response element; IAP, inhibitor of apoptosis protein; mAb, monoclonal antibody; MR, mineralocorticoid receptor; NGS, normal goat serum; NTD, N-terminal domain; NTD-MR, N-terminal domain of MR; pAb, polyclonal antibody; PARP, poly(ADP-ribose) polymerase; PBS, phosphate buffered saline; TA, triamcinolone acetonide; wt, wild type; EMSA, electrophoretic mobility shift analysis; TUNEL, terminal dUTP nick-end labeling; RT, reverse transcriptase.

	REFERENCES

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES