Cleavage of bleomycin hydrolase by caspase-3 during apoptosis

  • Authors:
    • Yang Chen
    • Rong Xu
    • Jianguo Chen
    • Xiaoyu Li
    • Qiyang He
  • View Affiliations

  • Published online on: May 23, 2013     https://doi.org/10.3892/or.2013.2484
  • Pages: 939-944
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Abstract

Bleomycin hydrolase (BLH) affects bleomycin chemotherapy through inactivation of bleomycin with deamination. As a neutral cysteine protease, it also plays various roles in physiological conditions and diseases. However, its mechanism of degradation remains unclear. In the present study, we showed that the levels of BLH were significantly reduced during apoptosis induced by the antitumor agents bleomycin, etoposide and hydroxycamptothecin, and inhibited by the caspase inhibitors Q-VD-oph and Z-DEVD-FMK. Furthermore, the caspase-dependent cleavage of BLH was confirmed by cleavage of partly-purified human BLH with caspase-3 and caspase-9 in vitro. The stability of BLH at normal culture conditions was analyzed with the protein synthesis inhibitor cycloheximide and the proteasome inhibitor MG132. BLH was degraded at a rate lower than that of cyclin D1. This is the first report to demonstrate that BLH is cleaved by caspase-3 during apoptosis.

Introduction

Bleomycin hydrolase (BLH), a member of the papain family of cysteine proteases, is metabolically inactivated antitumor antibiotic bleomycin (BLM) by deamination (1). It functions as a tumor suppressor gene in hepatocellular carcinoma (2). Accumulating data show that BLH plays multifaceted roles under different physiological and pathological conditions, including preparation of peptides for antigen presentation (3), involvement in the pathogenesis of Alzheimer’s disease (4,5), detoxification of homocysteine thiolactone (6), N-terminal proteolysis of mutant huntingtin (7) and breakdown of deiminated filaggrin into amino acids (8). Analysis of the human BLH gene indicates that its features are shared by those characteristic of housekeeping genes (9,10). For example, BLH is expressed at high levels in human tissues except for the kidneys and lungs (11,12). We recently demonstrated that BLH serves as a biomarker for predicting the efficacy of treatment of tumors with BLM (13).

The level of BLH in tumor cells affects the efficacy of BLM (1316). Therefore, it is necessary to understand how BLH is regulated to facilitate the development of new antibiotics structurally related to BLM and to demonstrate the pathological roles in the diseases. Therefore, in the present study we determined the stability of BLH in human tumor cells.

Materials and methods

Drugs and chemicals

BLM was purchased from Nippon Kayaku (Tokyo, Japan) and was dissolved in phosphate-buffered saline (PBS) at 5 mg/ml and stored at −20°C prior to use. Hydroxycamptothecin (HCPT) was purchased from Shenzhen Wanle Pharmaceutical Co., Ltd., (Guangzhou, China) and was dissolved in PBS at 2 mg/ml. Caspase inhibitors Q-VD-oph and Z-DEVD-FMK were purchased from R&D Systems Inc. (Minneapolis, MN, USA) and dissolved in dimethyl sulfoxide (DMSO) before use. Cycloheximide (CHX) was purchased from Millipore (Billerica, MA, USA) and dissolved in ethanol at 100 mg/ml. Etoposide (VP-16), Z-Leu-Leu-Leu-al (MG132), and all the chemicals except for those specifically mentioned were purchased from Sigma-Aldrich Inc. (St. Louis, MO, USA). VP-16 and MG132 were dissolved in DMSO at 50 mM.

Cell lines and cell culture

The HeLa human cervical cancer cell line was purchased from the American Type Culture Collection (ATCC; Rockville, MD, USA) and the human colon carcinoma HCT-116 cell line was a gift from Bert Vogelstein (Johns Hopkins University, Baltimore, MD, USA). The cell lines were cultured in Dulbecco’s modified Eagle’s medium supplemented with 10 % fetal bovine serum (Thermo Fisher Scientific Inc., Waltham, MA, USA). All cultures were maintained in an incubator at 37°C in a humidified atmosphere with 5% CO2.

Western blotting

The method was performed according to the protocol previously published (13). The sources of primary antibodies were as follows: rabbit-anti-cleaved/total PARP-1 (9532), rabbit-anti-cleaved caspase-3 (9661) and cleaved caspase-9 (9501), all from Cell Signaling Technology, Inc. (Danvers, MA, USA). The rabbit-anti-BLH (sc-68888), mouse-anti-His tag (sc-804) and mouse-anti-actin (sc-1616) were from Santa Cruz Biotechnology, Inc. (Santa Cruz, CA, USA). All primary antibodies were diluted to 1:1,000.

Detection of apoptotic cells by Annexin V-FITC/propidium iodide

To quantify apoptosis, cells were stained with Annexin V and propidium iodide (PI) using an Annexin V-FITC/PI Apoptosis kit (BD Biosciences, San Jose, CA, USA), following the protocol provided by the manufacturer. The fluorescence intensity was measured using a BD FACSCalibur flow cytometer.

Heterologous expression and purification of recombinant human BLH

Human BLH gene was cloned using RT-PCR with the forward primer 5′-CGCGGATCCATGAGCAGCT CGGGACTGAATTCG-3′ and the reverse primer 5′-CCG CTCGAGTCACTCAGCCAAAGCTCCCATG-3′, which contain the initiator methionine and termination codons and the BamHI and XhoI restriction sites, respectively, as indicated by the underlined bases. cDNA of the template was isolated from 293T cells. The cDNA was amplified for 25 cycles as follows: denaturing for 15 sec at 98°C, annealing for 90 sec at 60°C, and primer extension for 30 sec at 72°C. PCR was carried out using PrimeSTAR HS DNA polymerase kit from Takara Bio Inc. The product was cloned into the BamHI and XhoI restriction sites of cDNA3.1 (Invitrogen) and completely sequenced in both directions. E. coli BL21 (DE3) expressing recombinant BLH was generated as described above, following cloning of BLH cDNA into the BamHI and XhoI site of the pET32a (Novagen, Darmstadt, Germany). Expression of recombinant BLH was induced with 1 mM IPTG. Bacterial cells were sonicated and lysates were cleared by centrifugation at 12,000 × g at 4°C for 15 min. The supernatants were used for affinity purification on a column containing Ni-NTA-agarose. Protein concentrations of cell lysates were determined using the Bio-Rad Protein Assay. The BLH content was determined in comparison with BSA using SDS-PAGE.

Assay of BLH activity by high performance liquid chromatography

The metabolism of bleomycin was assessed using high performance liquid chromatography (HPLC), which separates bleomycin A2 and B from their inactive metabolites. Briefly, partially-purified BLH (2 mg/ml) was incubated with 5 μg BLM in 40 μl of reaction buffer (20 mM Tris, pH 7.5), at 37°C for 1 h. The reaction was stopped by the addition of 10 μl of methanol, the mixture was centrifuged, and the resulting supernatant fractions were injected into a ZORBAX Eclipse Plus C18 column (4.6 × 250 mm; Agilent Technology Inc., Santa Clara, CA, USA). The mixtures were eluted at 1 ml/min with 6% methanol, 6% acetonitrile and 88% acetic acid (pH 4.2) and were detected by their absorbance at 254 nm.

Assays of BLH cleavage in vitro

Partially-purified BLH (50 ng) was incubated with 0.1 unit caspase-6, -8, -9 and-10 (BioVision, Mountain View, CA, USA), respectively, in 20 μl reaction buffer (50 mM HEPES, pH 7.2, 0.1% CHAPS, 10 mM EDTA, 5% glycerol, 10 mM DTT, 50 mM NaCl and 100 mg/ml BSA) at 37°C for 1 h, or with 150 ng caspase-3 (Sigma-Aldrich) in 20 μl reaction buffer (10 mM HEPES, pH 7.0, 5 mM MgCl2, 5 mM EDTA, 10% glycerol, 1 mM DTT, 50 mM NaCl and 100 mg/ml BSA) at 30°C for 1 h. The inhibition of BLH cleavage by caspases was confirmed using 20 μM Q-VD-oph. The resulting mixtures were separated by SDS-PAGE and detected by western blotting.

Statistical analysis

SPSS 17.0 software was used for statistical analysis. Student’s t-test was applied for comparing the means of 2 groups and a P-value of <0.05 was considered to indicate a statistically significant difference.

Results

Reduction of BLH levels during apoptosis

To verify whether the expression level of BLH was affected during apoptosis, HCT-116 cells were treated for 48 h with lethal concentrations of BLM or HCPT. The results showed that the level of BLH was markedly reduced by treatment with high concentrations of drug (Fig. 1A and B). Similar results were obtained within 48 h when HeLa cells were exposed to BLM and VP-16 (Fig. 1C and D).

The presence of apoptotic cells was confirmed by Annexin V/PI staining after HCT-116 cells were treated with 2 μM HCPT for different times (Fig. 1E). Approximately 53% of cells showed apoptotic features after exposure to HCPT for 24 h. The levels of BLH and activation of the caspase pathway were monitored after exposure to 2 μM HCPT (Fig. 1F). Upregulation of BLH expression was detected after treatment with 2 μM HCPT for 8 h. The reduction of BLH levels began at 24 h. Activation of caspase-3 and caspase-9 was observed within 8–12 h. The times at which BLH was degraded were similar to those for cleavage of PARP-1. The data suggest that the degradation of BLH was triggered by the intrinsic apoptotic pathway.

Cleavage of BLH by caspases during apoptosis

To identify the mechanism for the reduction of the levels of BLH due to cleavage by caspase during apoptosis, the broad-spectrum pan-caspase inhibitor Q-VD-oph was used. The cleavage of PARP-1 and the levels of BLH were reduced after exposure to 1 μM HCPT by treatment of HCT-116 cells with 20 μM Q-VD-oph (Fig. 2A, lanes 3, 4 and B), indicating that cleavage of BLH was caspase dependent. We compared the sequence of BLH with recognition consensus of caspases. Only 1 potential cleavage site for caspase-3 was found. It localizes to Asp39 in the N-terminus of BLH (DLLD), a caspase-3 specific consensus recognition sequence (17). The reduction in the level of BLH was significantly inhibited by the caspase-3-specific inhibitor Z-DEVD-FMK (Fig. 2C and D), consistent with the predicted presence of a caspase-3 recognition site. Similar results were also observed during apoptosis of HeLa cells induced by BLM and VP-16 (data not shown).

Hydrolysis of BLM by recombinant BLH

The findings described above that degradation of BLH is caspase-dependent prompted us to further characterize the cleavage of BLH in vitro. Human recombinant BLH was expressed in E. coli BL21 and partially purified using a Ni-NTA-agarose column. The concentration of the resultant recombinant protein was estimated to be ~2 mg/ml. The activity of recombinant BLH was confirmed by its ability to hydrolyze BLM, and the resultant reaction mixtures were analyzed using reversed phase chromatography monitored at 254 nm. The results showed that the recombinant BLH converted BLM-A2 and B2 to its known metabolites, and the hydrolysis of BLM-B2 was faster than that of BLM-A2, with most B2 hydrolyzed at 20 min and only approximately two-thirds of A2 at 60 min (Fig. 3).

Cleavage of BLH by caspase-3 and caspase-9 in vitro

We incubated recombinant BLH in vitro with caspase-3, -6, -8, -9 and -10, respectively. Recombinant BLH was only cleaved detectably by caspase-3 and caspase-9. When the recombinant BLH was incubated with purified caspase-3 at 37°C, both its degradation product and cleaved band were detected over a period of 12 h (Fig. 4A). The caspase-3-specific inhibitor Z-DEVD-FMK inhibited degradation of BLH (Fig. 4B). The small amount of BLH cleavage by caspase-9 was also detected using an anti-His Tag antibody but not by an anti-BLH antibody (Fig. 4C). This cleavage reaction was inhibited by Q-VD-oph (Fig. 4D).

Lower rate of BLH degradation at normal culture conditions

To determine whether the degradation of BLH is involved in the ubiquitin-proteasome pathway, de novo protein synthesis was blocked with the protein synthesis inhibitor CHX under normal culture conditions. The stability of short-lived cyclin D1 was monitored for comparison. Treatment of HCT-116 cells with 20 μg/ml CHX resulted in a time-dependent reduction of the cyclin D1 levels, and only 50% of its initial level remained after exposure to CHX for 1 h. By contrast, the level of BLH remained constant initially and was then reduced by ~20% after treatment with CHX for 4 h (Fig. 5A and B). A small amount of the cleaved PARP fragment was observed at 4 h, suggesting induction of apoptosis by CHX. This prevented us from further calculations of the half-life of BLH degradation using this method. These same results were obtained using HeLa cells (Fig. 5C and D).

To verify whether BLH is degraded via the ubiquitin-proteasome pathway, HCT-116 cells were treated with CHX plus 50 μM MG132, a specific inhibitor of the ubiquitin-proteasome pathway. The degradation of cyclin D1 was completely suppressed, and degradation of BLH was also inhibited (Fig. 6), indicating that BLH is degraded via the ubiquitin-proteasome pathway.

Discussion

In the present study, we investigated the degradation of BLH under different conditions. To the best of our knowledge, this is the first report showing that degradation of BLH is caspase-dependent during apoptosis and that BLH can be cleaved by caspase-3 and caspase-9 in vitro. In apoptotic pathways, caspases act as signal transducers, directing the cell toward death by cleaving numerous substrates (18). We identified a caspase-3 recognition site at Asp39 in the N-terminus of BLH (DLLD), but no site for caspase-9. This could be explained by the requirement for a tertiary structure, as caspases can cleave at ‘non-canonical’ sites, such as the viral caspase inhibitor p35 bound to caspase-8 (19).

Our present results are consistent with data of others showing that the half-life of BLH is greater than 6 h (20). However, we could not determine the half-life of BLH precisely, as CHX treatment led to apoptotic degradation of BLH. Protein stability plays a role in the abundance of cellular proteins, and several housekeeping proteins tend to have stable mRNAs and proteins to improve energy efficiency (21). The function of BLH is evolutionarily conserved from yeasts to humans and the yeast homologue of BLH metabolizes BLM in mammalian cells (22). The features of BLH are characteristic of housekeeping genes (9). The relationship between stability of BLH and its function is being investigated in our laboratory.

BLH can hydrolyze the bleomycin to generate the inactive deamino form. The mice with knockout of BLH gene are very sensitive to bleomycin (15). The patients with homozygous variant G/G of BLH gene SNP (A1450G) are associated with reduced survival in testicular germ cell cancer (16). The expression of BLH increased after exposure to low concentrations of bleomycin (13). All data indicate that the BLH level plays an important roles in bleomycin action. The present results provide new evidence for the regulation of BLH level that may aid in the translational development of new bleomycin-related antibiotics.

Loss of BLH leads to astrogliosis and behavioral changes in mice (23), suggesting its importance in the functions of neurons. Although it has not been confirmed that genetic polymorphisms of BLH are involved in the genesis of Alzheimer’s disease, regulation of the secretion of amyloid precursor protein by BLH plays a function (5). Accumulating data show that apoptosis of neurons is involved in the genesis of Alzheimer’s disease (24). Furthermore, the levels of BLH activity are reduced in patients with Alzheimer’s disease (4). This finding might be explained by the degradation of BLH during the apoptosis of neurons by a mechanism similar to that demonstrated here.

In summary, the degradation of BLH can occur through the caspase-3 and ubiquitin-proteasome pathways. The results presented here facilitate further studies of BLH functions under different physiological and pathological conditions.

Acknowledgements

The present study was supported by grants from the National Scientific Foundation of China (81273553) and the National S&T Major Special Project on Major New Drug Innovation (2012ZX09301002-001-015).

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Chen Y, Xu R, Chen J, Li X and He Q: Cleavage of bleomycin hydrolase by caspase-3 during apoptosis. Oncol Rep 30: 939-944, 2013.
APA
Chen, Y., Xu, R., Chen, J., Li, X., & He, Q. (2013). Cleavage of bleomycin hydrolase by caspase-3 during apoptosis. Oncology Reports, 30, 939-944. https://doi.org/10.3892/or.2013.2484
MLA
Chen, Y., Xu, R., Chen, J., Li, X., He, Q."Cleavage of bleomycin hydrolase by caspase-3 during apoptosis". Oncology Reports 30.2 (2013): 939-944.
Chicago
Chen, Y., Xu, R., Chen, J., Li, X., He, Q."Cleavage of bleomycin hydrolase by caspase-3 during apoptosis". Oncology Reports 30, no. 2 (2013): 939-944. https://doi.org/10.3892/or.2013.2484