- Open Access
Disrupted ADP-ribose metabolism with nuclear Poly (ADP-ribose) accumulation leads to different cell death pathways in presence of hydrogen peroxide in procyclic Trypanosoma brucei
Parasites & Vectors volume 9, Article number: 173 (2016)
Poly(ADP-ribose) (PAR) metabolism participates in several biological processes such as DNA damage signaling and repair, which is a thoroughly studied function. PAR is synthesized by Poly(ADP-ribose) polymerase (PARP) and hydrolyzed by Poly(ADP-ribose) glycohydrolase (PARG). In contrast to human and other higher eukaryotes, Trypanosoma brucei contains only one PARP and PARG. Up to date, the function of these enzymes has remained elusive in this parasite. The aim of this work is to unravel the role that PAR plays in genotoxic stress response.
The optimal conditions for the activity of purified recombinant TbPARP were determined by using a fluorometric activity assay followed by screening of PARP inhibitors. Sensitivity to a genotoxic agent, H2O2, was assessed by counting motile parasites over the total number in a Neubauer chamber, in presence of a potent PARP inhibitor as well as in procyclic transgenic lines which either down-regulate PARP or PARG, or over-express PARP. Triplicates were carried out for each condition tested and data significance was assessed with two-way Anova followed by Bonferroni test. Finally, PAR influence was studied in cell death pathways by flow cytometry.
Abolition of a functional PARP either by using potent inhibitors present or in PARP-silenced parasites had no effect on parasite growth in culture; however, PARP-inhibited and PARP down-regulated parasites presented an increased resistance against H2O2 treatment when compared to their wild type counterparts. PARP over-expressing and PARG-silenced parasites displayed polymer accumulation in the nucleus and, as expected, showed diminished resistance when exposed to the same genotoxic stimulus. Indeed, they suffered a necrotic death pathway, while an apoptosis-like mechanism was observed in control cultures. Surprisingly, PARP migrated to the nucleus and synthesized PAR only after a genomic stress in wild type parasites while PARG occurred always in this organelle.
PARP over-expressing and PARG-silenced cells presented PAR accumulation in the nucleus, even in absence of oxidative stress. Procyclic death pathway after genotoxic damage depends on basal nuclear PAR. This evidence demonstrates that the polymer may have a toxic action by itself since the consequences of an exacerbated PARP activity cannot fully explain the increment in sensitivity observed here. Moreover, the unusual localization of PARP and PARG would reveal a novel regulatory mechanism, making them invaluable model systems.
Trypanosoma brucei is the etiological agent of the sleeping sickness in humans and Nagana in cattle, in the region of Sub-Saharan Africa. According to the World Health Organization, African trypanosomosis is endemic in 24 African countries, with approximately 30,000 cases in 2010 (WHO, 2010). Current treatments depend on the stage of the affliction and the disease is typically diagnosed only after it has already advanced.
Poly(ADP-ribose)polymerases (PARPs) catalyze the formation of ADP-ribose polymer chains (PAR) by transferring the ADP-ribose region from NAD+ to certain residues in target proteins or to a nascent chain (PAR). Most of these enzymes also typically carry out an auto-modification reaction. The superfamily of human PARP comprises 17 proteins . Among the functions they carry out, the participation of human PARP-1 (hPARP-1) in signalling and repair of harmed DNA has been the center of most of the research carried out in the field [2–8].
Poly(ADP-ribose) glycohydrolase (PARG) hydrolyzes the glycosidic bonds present in the polymer synthesized by PARP enzymes, re-establishing basal levels of PAR [3, 4, 9]. One PARG gene is encoded in the human genome and is expressed as several isoforms which occur in different cellular organelles . It has been shown that the depletion of all such isoforms is lethal in embryonic mice stages . On the other hand, cell-based models evidenced that the lack of PARG isoforms has no consequences on cell viability. However, PARG-deficient cells failed to amend strand breaks after genomic harm augmenting cell death; an outcome that points out the importance of PARG involvement in DNA damage response [12–14]. Illuzi et al.  highlighted that PARG tightly regulates the polymer levels produced upon genomic harm, avoiding injurious cell consequences caused by PAR over-accumulation. Trypanosoma brucei has only one PARG of 531 amino acids, sharing high sequence identity and similarity with the orthologous sequence in Trypanosoma cruzi . To date, no functional studies for PARG in trypanosomatids have been reported.
Our earlier studies on PAR metabolism in trypanosomatids showed that the inhibition of TcPARP negatively impacts on T. cruzi growth . This result encouraged us to analyze the only PARP protein identified in T. brucei (TbPARP). Here we describe the activity requirements for the enzyme and identify potent TbPARP inhibitors. The most potent compounds were tested in T. brucei cultures to assess their effect on parasite growth and their ability to inhibit the polymer synthesis after a genotoxic stimulus. We have also tested the sensitivity of PARP over-expressing parasites, as well as PARP or PARG silenced parasites in oxidative stress conditions. Furthermore, we determined the cell death pathways involved in every case.
TbPARP was cloned into a pET-22b + expression vector . For expression, the pET-22b + vector bearing the TbPARP gene was transformed to E. coli Rosetta2 (DE3) strain. Cells were grown in baffled flasks containing 750 mL of Terrific Broth (TB) auto-induction media with antibiotics (50 μg/mL ampicillin and 34 μg/mL chloramphenicol), glycerol 8 g/L and trace elements. Cell pellet was stored at -20 °C in lysis buffer (0.1 M HEPES pH 7.5, 500 mM Sodium Chloride, 10 % glycerol, 0.01 M imidazole, 500 μM TCEP, 0.05 % IGEPAL).
Lysozyme 0.25 mg, benzonase 250 U (both compounds from Sigma-Aldrich), a protease inhibitor tablet (Roche), and 3-AB 1 mM (Alexis Biochemicals) were added to the thawed cells and samples were sonicated with 50 % duty cycle for 30 min (BRANSON 250 Sonifier). After centrifugation, the supernatant was filtered through a 0.45 μm syringe filter. Samples were loaded in HisTrap HP column (GE Healthcare) and washed with 10 mL of binding buffer (20 mM HEPES pH 7.5, 0.5 M NaCl, 10 mM imidazole, 10 % glycerol, 500 μM TCEP) using a peristaltic pump at 4 °C. The column was washed at room temperature with 25 mM imidazole binding buffer and eluted with 250 mM imidazole binding buffer. Elute was divided into four and each sample was further purified by size exclusion chromatography using a Superdex 200 High Load 10/30 column (GE Healthcare) with binding buffer. Fractions with higher activity were pooled and flash frozen as small aliquots to be stored at -70 °C.
Activity assay optimization
The optimal conditions for the activity of purified recombinant TbPARP, were determined by using a fluorometric activity assay . Incubation at 25 °C with shaking at 300 rpm was placed in propylene plates of 96 wells (Greiner BioOne). To terminate the reaction 2 M KOH (20 μL) and 20 % acetophenone in ethanol (20 μL) were added to each well. After incubating for 10 min at 4 °C, 90 μl of 88 % formic acid was added and incubated in an oven at 110 °C for 5 min. This reaction converts remaining NAD+ to a fluorescent derivative. After incubation, the plate was allowed to cool down for 15 min and fluorescence was measured using excitation wavelengths of 372 nm and 444 nm for excitation and emission, respectively (Varioskan Flash 4.00.53, Thermo Scientific). Consumption of NAD+ was detected by the decrease in fluorescence. Experiments were done in triplicates. The activity in control wells were kept under 25 % by optimizing the protein concentration and the incubation time, in order to get a robust signal without slowing down the enzyme activity.
Different assay buffers were tested (Additional file 1) and the buffering agent was found to have a large impact on enzymatic activity. The optimal activity was obtained with phosphate (Na) or phosphate (K) buffer at pH 7. Importantly, TbPARP activity increases as a function of nicked DNA (activated DNA) concentration. Maximum TbPARP activation was achieved at 25 μg/mL (Additional file 1) causing an 18-fold increase in TbPARP activity. A small set of cations was also tested in order to verify whether the enzymatic activity would depend on them. Most divalent cations resulted in decreased TbPARP activity, with Ni2+, Mn2+,Ca2+, and Zn2+ showing the greatest inhibition, while Mg2+, a known co-factor of enzymes that participate in DNA metabolism, increased TbPARP activity in vitro 2-fold (Additional file 1). As stabilizing agents were tested, we observed that the addition of BSA was beneficial to maintain TbPARP activity when enzyme concentration was in nM range. Notably, the addition of both BSA and Mg2+ showed no increase in TbPARP activity when compared to the addition of BSA alone and therefore Mg2+ was not added in the reaction buffer for further experiments. The final assay buffer was 100 mM Na2HPO4/NaH2PO4 pH 7, 500 μM TCEP, 1 μg/μL BSA, and 0.025 mg/mL activated DNA (Sigma Aldrich) and 500 nM NAD+ (Sigma Aldrich).
Screening of TbPARP inhibitors
Thirty - one compounds were tested. Dilutions from DMSO stocks were made (100 μM, 10 μM and 1 μM) and aliquots of those were used in the enzymatic reaction with 10-fold dilution. Inhibitor solutions were added in triplicates to the plate, followed by the addition of the NAD+. Reactions were initiated by addition of TbPARP diluted in the same buffer (10 nM). The plate was incubated at 25 °C with shaking (300 rpm, Biosan PST-100 HL) for 45 min. This resulted in consumption of 50 % of the NAD+ and signal to background ratio of 2. To detect any potential fluorescence inherent in the compounds, control reactions were carried out separately with compound alone at 10 μM final concentration. The possible fluorescence quenching properties were controlled using wells within the experimental plate containing the compound with 500 nM NAD+ in the assay buffer. Wells with only NAD+ present were considered as 100 % inhibition and wells with NAD+ and PARP present were considered as 0 % inhibition.
Homogenous assay results were confirmed for the best inhibitors using biotinylated NAD+ as a substrate (bioNAD+, Trevigen). Incubation mixture consisted of TbPARP (120 nM), bioNAD+ (1 μM) and nicked DNA (25 μg/mL) (Sigma Aldrich) in 0.1 M sodium phosphate buffer (pH 7) at room temperature. The assay was performed in absence (positive control) or in presence of 1 μM inhibitors, after which SDS sample buffer was added to stop the reaction by heating at 98 °C for 5 min. TbPARP (120 nM) was also added to the reaction immediately before stopping it (negative control). PAR-biotinylated proteins were identified with streptavidin-conjugated horseradish peroxidase (PerkinElmer) after each reaction mix was run on SDS-PAGE and transferred onto a membrane of nitrocellulose.
Potency of inhibitors
The half maximal inhibitory concentration (IC50) was obtained for the most potent TbPARP inhibitors: Veliparib (ABT-888, Alexis Biochemicals), 4-ANI (Alexis Biochemicals), EB-47 (Alexis Biochemicals), 1,5-Isoquinolinediol (Alexis Biochemicals), NU1025 (Alexis Biochemicals), PJ-34 (Alexis Biochemicals), Olaparib (JS Research Chemicals Trading), RF03876 (Maybridge), and Rucaparib (Selleck Biochemicals). The IC50 value for 3-AB (Alexis Biochemicals) was also determined to be used as a reference. Briefly, reaction mix together with the inhibitors at half log dilutions were added to a 96-well plate (10 data points). Reactions were incubated for 11 min at 25 °C after initiating the reaction with the addition of 5 nM TbPARP at a final volume of 50 μL. Measurement of the remaining NAD+ is described in section Screening of TbPARP inhibitors. All reactions were performed in triplicates and three independent dose response curves were fitted for each inhibitor. Control wells with only NAD+ or NAD+ and enzyme were used in the curve fitting, as detailed in our previous work .
TbPARP homologues [UniProt:Q0PW89] were searched from Protein Data Bank. hPARP-1 [PDB: 3GJW] , hPARP-2 [PDB:3KJD]  and hPARP-3 [PDB:3C4H]  crystal structures were chosen based on homology and the quality of the structures, and aligned to TbPARP with ClustalW . Aline  was used for the analysis of the sequence alignment. TbPARP regulatory and catalytic domains were modelled with Modeller , based on hPARP-1 structure. SSM superposition algorithm implemented in COOT [26, 27] was utilized for structural superpositions. Structural figures were made with CCP4mg .
Parasite cultures and in culture inhibition of TbPARP
T. brucei procyclic strain 29–13  was cultured at 28 °C in SDM-79 (Bioscience) containing 10 % (v/v) FCS and 0002 % hemin. T. brucei bloodstream strain 427 90-13  was cultured at 37 °C in HMI-11 (Iscore’s Modified Dulbecco’s Medium (Invitrogen), 100 mg/L sodium pyruvate, 136.1 mg/L hypoxantine, 38.7 mg/L thymidine, 28.22 mg/L bathocuproinedisulfonic acid, 181.8 mg/L L-cysteine, 3.024 mg/L sodium carbonate, 196 μM β-mercaptoethanol) containing FCS (10 % v/v). Parasite viability was analyzed by microscopy.
For in culture inhibition assays, parasites of the procyclic form of Trypanosoma brucei were grown for 48 h up to a density of 5×106 parasites/mL. Parasites of the bloodstream form were grown for 24 h up to a density of 5×105 parasites/mL. In both cases, cells were harvested and preincubated for 30 min or 10 min in PBS-Glucose 2 % with inhibitors added, after which the parasites were treated with 500 μM or 250 μM hydrogen peroxide for procyclic and bloodstream forms, respectively, for 10 min. Protein extracts were prepared as indicated in our previous work , and 3 μg of total protein were manually spotted onto a membrane of nitrocellulose (GE Healthcare) for Dot blot analysis revealed with by commercial PAR antibody (BD).
Effect of the inhibitors on parasite growth
Trypanosoma brucei procyclic parasites were grown in SDM-79 medium for 48 h until reaching a density of 5×106 cells/mL. Aliquots of 200 μl were distributed in 96-well plates and inhibitors were present at different final concentrations, as indicated in the figures. Nifurtimox (NFX) was used as a positive control in concentrations ranging from 0.25–25 μM. Culture density was checked by OD600 after 48 h.
Trypanosoma brucei bloodstream parasites were grown in HMI-11 medium for 24 h until reaching a density of 5×105 cells/mL. Aliquots of 100 μL were distributed in 96-well plates and inhibitors were added at different concentrations as indicated in the figures. After an incubation period of 24 h, the parasite number was counted with a Neubauer chamber.
In all experiments, triplicates were done for each condition tested and data significance was assessed by one-way Anova (GraphPad Prism5.03 version Software).
PARP and PARG down-regulated T. brucei lines and PARP over-expressing T. brucei line
A fragment of the TbPARP cDNA (nucleotides 1030 to 1445) [GenBank:DQ679800, Tb927.5.3050] and a fragment of the TbPARG cDNA (nucleotides 593 to 979) [Tb927.9.12810] were sub-cloned into the tetracycline-inducible expression vector p2T7TI-177  to down-regulate the genes of interest. In addition, whole TbPARP cDNA sequence was sub-cloned into the expression vector p2216  (PCR primer sequences available upon request) to over-express the PARP-eYFP fusion gene.
Not I-linearized RNAi-TbPARP and RNAi-TbPARG constructs and the over-expression construct (10 μg) were transfected into procyclic parasites by electroporation, as described by Downey et al. . The selection of the transfectants was carried out with 20 μg/mL zeocin, and dsRNA and over-expression of the fusion protein was induced with 1.0 μg/mL tetracycline for 3 days.
Gene expression knock- down was confirmed by Northern-blot and Western-blot analysis and gene over-expression was confirmed by Western blot with specific antibodies.
Effect of hydrogen peroxide (H2O2) in cell survival
Cell survival was determined by incubating 500 μL of 1 × 106 parasites/mL culture in 24-well cell culture plates (Cellstar) for 6 h with different concentrations of H2O2 (30 μM, 95 μM, 300 μM and 950 μM) and counting motile parasites over the total number using a Neubauer chamber. Each condition was tested in triplicates. Statistical significance was assessed with two-way Anova followed by Bonferroni test (version 5.03 of GraphPad Prism for Windows).
Wild type procyclic culture was preincubated for 30 min with Olaparib at 29 nM concentration in order to measure cell survival, compared to the culture with no inhibitor added (control). The addition of DMSO in the same concentration as it is present in Olaparib experiment did not show any difference compared to the control culture.
Transgenic RNAi-TbPARP (p2T7-TbPARP), RNAi-TbPARG (p2T7-TbPARG) and TbPARP over-expressing (p2216-TbPARP) procyclic cultures induced for 3 days with tetracycline (1 μg/mL) were also challenged with H2O2 and compared to the non-induced cultures.
Analysis of PAR formation after hydrogen peroxide (H2O2) treatment by Western blot
Parasites were treated for 10 min with 1 mM H2O2. Western blot analysis was carried out as it is detailed in our previous work  with 1:5.000 polyclonal anti-PAR antibody (BD) made in rabbit. As a loading control we used α-tubulin antibody.
Immunolocalization of poly(ADP-ribose)
Immunolocalization experiments were carried out as detailed in our previous work  with 1:500 polyclonal anti- PAR antibody (BD) made in rabbit to detect PAR and 1:100 polyclonal anti-TbPARP antibody (GenScript) made in rabbit to detect TbPARP. Nuclear and kinetoplast DNA were stained with DAPI (2 μg/mL) (Sigma).
Nucleus Fluorescence Measurement
Nucleus fluorescence measurement was obtained following ImageJ instructions. The area of interest was selected and parameters such as integrated density, area and mean grey value were measured by the software. Three different regions next to the nucleus were also selected as the background. Finally, corrected nucleus fluorescence was calculated with the formula: CTCF = Integrated Density - (Area of selected nucleus × Mean fluorescence of background readings).
Annexin V flow cytometric analysis
Parasites were treated with 1 mM H2O2 for different time intervals and the cell death pathway involved was assessed as it has been detailed in our previous work . The exposure of wild type procyclic parasites for 6 and 12 h to 10 μg/mL Concanavalin A type IV (Sigma-Aldrich) confirmed the apoptosis-like death pathway (positive control) [35, 36]. Transgenic TbPARP over-expressing (p2216-TbPARP) and RNAi-TbPARG (p2T7-TbPARG) procyclic cultures were previously induced for 3 days with tetracycline (1 μg/mL). Results were analyzed with Cyflogic v 1.2.1 software.
In vitro screening of compounds that inhibit TbPARP
Thirty one compounds, most of them previously reported to inhibit PARP enzymes, were tested to assess their ability to abrogate TbPARP activity in vitro (Additional file 2: Table S1) . The compounds were analyzed by the described activity assay at concentrations of 1 and 10 μM (Fig. 1a). DMSO concentration was kept under 1 % in all experiments described below. Compounds that demonstrated to have apparent IC50 values higher than 1 μM were retested at a lower concentration (100 nM) (Fig. 1b) and the results were corroborated by Western Blot, in which inhibitors were added to the reaction at 1 μM concentration together with the biotinylated NAD+ substrate (bioNAD+) (Fig. 1c). Afterwards, IC50 values were experimentally measured for the best inhibitors (Table 1). The compounds with the most potent inhibiting ability were Olaparib (IC50 2.9 nM), EB -47 (IC50 6.5 nM), 4-ANI (IC50 23 nM), and Veliparib (IC50 49 nM) (Table 1). These same inhibitors had previously been demonstrated to be the most potent inhibitors for the orthologous enzyme in T. cruzi .
Homology modeling and inhibitor selectivity
Inhibitor binding to TbPARP was evaluated by generating a homology model based on human PARP crystal structures. Sequence alignment included PARP regulatory (REG) and ADP-ribosyl transferase (CAT) domains as they are conserved in hPARP1-3 and in TbPARP . Importantly, the donor NAD+ binding site is highly conserved between these proteins. The nicotinamide subsite (NI) contains the common interactions utilized by many PARP inhibitors, as the inhibitors form a π-stacking interaction with Tyr907 and hydrogen bonds to Gly863 and to Ser904 (Fig. 2). This is demonstrated with the superposition of chicken PARP-1 in complex with 4-ANI (PDB accession code 2PAX) and TbPARP homology model. However, there are a few differences between the REG domains of the hPARP-1 and TbPARP that may affect the binding of larger inhibitors that extend out of the NI pocket, such as PJ-34 and Rucaparib, which show selectivity towards hPARP-1 (Fig. 2).
In culture inhibition of PARP from Trypanosoma brucei
The compounds that were identified as the best inhibitors of TbPARP in vitro were tested for their effectiveness to inhibit in culture PAR synthesis on both procyclic and bloodstream forms of T. brucei. The parasites were challenged with hydrogen peroxide, a DNA damaging agent [18, 34]. The inhibitors were tested in culture at a concentration 10-fold higher than the in vitro IC50 value. The compounds and concentrations were the following: 0.23 μM 4-ANI; 65 nM EB-47; 29 nM Olaparib and1.5 μM Rucaparib. 3-AB at 580 μM was also tested since it is a well-known PARP inhibitor. In the case of procyclic parasites, Olaparib and Rucaparib inhibited PAR formation in culture while 4-ANI scarcely inhibited the enzyme and EB-47 did not inhibit TbPARP at all (Fig. 3a). Most of the inhibitors diminished, but didn’t inhibit completely PAR formation in the bloodstream stage of T. brucei at the indicated concentrations (Fig. 3b).
PARP is not essential for T. brucei growth
Olaparib and Rucaparib, which demonstrated to inhibit PAR formation in culture more effectively than the rest of the compounds, were selected to be evaluated on their ability to affect procyclic parasite growth in a series of concentrations ranging from the in vitro IC50 value up to two orders of magnitude higher. 3-AB, the inhibitor reported to diminish T. cruzi growth, was also tested. Nifurtimox was also included in the panel of compounds as a positive control due to its extensively proven trypanocidal activity [37, 38]. None of the PARP inhibitors tested were able to negatively affect parasite growth in culture (Fig. 3c), except for Rucaparib, which caused a 20 % decrease in growth at the highest 15 μM concentration. Nifurtimox, in contrast, slowed down procyclic parasite growth already at a 2.5 μM concentration. Growth curves were measured for the bloodstream form parasites in the presence of Olaparib (29 nM) and Rucaparib (1.5 μM), and despite that they were able to inhibit PAR formations in culture they were not able to significantly affect T. brucei growth or survival (Fig. 3b). Incubation in the presence of 3-AB or Nifurtimox, however, did provoke a decrease on bloodstream parasite growth; although only the effect of 3-AB was significant when compared to the control (Fig. 3d).
As these results are in contrast with our previous results on T. cruzi , we set out to verify them by knocking down the enzyme of interest by interference RNA. The experiments performed with transgenic RNAi-TbPARP procyclic parasites indeed indicate that the lack of TbPARP does not alter the culture growing rate (Additional file 3). Since the protein was not completely silenced and the low PARP amount remaining could be enough for survival in regular growth conditions, we evaluated Tet induced RNAi-TbPARP procyclic parasites in the presence of 290 nM Olaparib. A similar result was obtained, with no change in growth rate (Additional file 3). Overall, the experiments suggest that TbPARP would not be indispensable for the procyclic form of T. brucei under standard conditions.
Sensitivity of procyclic Trypanosoma brucei to oxidative stress
Given that TbPARP is not crucial for the survival of the procyclic form, we next tried to determine the possible role of TbPARP in genomic harm signaling and repair processes. As a parameter of the sensitivity of T. brucei procyclic parasites to the oxidative stress, we determined the response to the genotoxic compound hydrogen peroxide (H2O2). We estimated the parasite survival by measuring motility 6 h after the treatment with this agent in parasites with no functional PARP. Olaparib was chosen due to its inhibitory potency towards TbPARP (Table 1). When low doses of hydrogen peroxide (30 μM) were used, there was no difference in parasite viability in presence or absence of Olaparib at a concentration that has been proven to inhibit effectively PAR formation in culture (29 nM). However at 95 μM H2O2, a concentration that diminishes the number of motile parasites, the presence of Olaparib in the medium reduced the loss of viability induced by the oxidant and cultures became more resistant to this genotoxic agent (Fig. 4a). At a lethal H2O2 concentration (300 μM) there was a significant decrease in parasite motility both in absence or presence of Olaparib, however a slight protective effect could be observed in the presence of this compound, though not statistically significant. A similar result could be observed when we compared the effect of H2O2 on 3 day-induced transgenic RNAi-TbPARP procyclic cultures to the non-induced ones subjected to the same treatment (Fig. 4b). Altogether, these experiments demonstrate that the lack of a functional TbPARP leads to an increase in the resistance against hydrogen peroxide in procyclic T. brucei parasites.
PARGs are responsible for the break-down of PAR. We have identified only one protein that belongs to the PARG family in T. brucei (TbPARG), which expresses in both stages of the parasite (Additional file 4B). This enzyme has an expected molecular weight of 60 kDa. Moreover, it is always located in the nucleus in procyclic cultures, independently of the occurrence of genomic harm (Additional file 4A). This is similar to what we observed earlier for T. cruzi PARG (TcPARG) .
In order to test the importance of PAR on the sensitivity towards oxidative stress we down- regulated PARG expression by RNAi and also obtained parasites over expressing TbPARP (Additional file 5 A, B and C). PARG silencing or increased PARP expression did not cause morphological alterations but culture growth rate was slightly diminished in both cases (data not shown). Nevertheless, when we analyzed cell death by FACS, there was no difference in distribution of population between wild type, RNAi-TbPARG or PARP over-expressing parasites in fresh cultures, as it will be shown in the next sections. In a similar experiment as the one described in Fig. 4a and b, we analyzed the effect of H2O2 on RNAi-TbPARG and PARP over-expressing parasites, induced for 3 days. Both transgenic cells showed increased sensitivity to hydrogen peroxide treatment, as compared with the control (Fig. 4c, PARP over-expressing and 4D, PARG silenced parasites). In the case of the transgenic line over-expressing the PARP-eYFP fusion protein, we confirmed that this outcome is specific of an augmented expression of PARP, since transgenic eYFP over-expressing parasites presented a milder effect compared to the PARP over-expressing counterparts (Additional file 6).
Nuclear PAR mediates apoptosis-like to necrosis switch in severe oxidative stress
Based on these results we decided to examine the consequence of PAR metabolism alteration on H2O2-induced cell death. We treated parasites with 500 μM H2O2 and, as shown in Fig. 5a, the amount of PAR in wild type parasites increased after 10 min, diminished partially within the first 90 min and then increased again, probably due to DNA damage still present in the nucleus. When we examined the dynamics of PAR synthesis and degradation in PARP-over expressing or PARG-silenced procyclic forms of T. brucei, we observed a different pattern in the amount of PAR 90 and 120 min after a genotoxic stimulus, compared to wild type cultures (Fig. 5a). Intracellular PAR levels in wild type parasites are usually high (Fig. 5a 0 min) and located in the cytoplasm (Fig. 5b). After a genotoxic stimulus, an extensive quantity of PAR was synthesized in the nucleus and PARP translocated to this organelle (Fig. 5b and c). PAR signal in the nucleus was further quantified and it was shown that the difference between treated and control parasites was significant. Moreover, it is worth noting that both TbPARG-silenced and TbPARP-over expressing parasites showed PAR accumulation in the nucleus even in the absence of a genotoxic stimulus (Fig. 5d and e, and Additional file 7). TbPARP-eYFP fusion protein was also recruited to the nucleus; supporting these results (Fig. 5d, Additional file 5).
We further investigate the mode in which hydrogen peroxide induces cell death in these parasites. Wild type and transgenic cultures were analyzed for phospholipid redistribution and PI incorporation by flow cytometry. Concanavalin A is well known to cause an apoptotic-like death in T. brucei [35, 36] and control cultures exposed to this lectin (10 μg/mL) showed the typical apoptosis response with an increment in Annexin incorporation (Fig. 6b). A similar pattern to apoptosis control was observed in wild type cells 6 h after H2O2 injury (Fig. 6c). However, when cells with modified PAR metabolism were treated, a pattern with an earlier incorporation of PI was obtained in both transgenic cultures, displaying a necrotic death signal. It should be taken into account that PARP-over expressing parasites display an apparent basal apoptosis-like pattern at time 0 h that is caused by the intrinsic eYFP fluorescence from the fusion protein; however, the overall process shows a necrotic-like death pathway (Fig. 6c).
Previously, we have demonstrated that T. brucei presents only one PARP protein (TbPARP) . Here, in an attempt to describe its enzymatic requirements, we proved TbPARP is highly activated by damaged DNA, in agreement with our previous report for the trypanosomatids C. fasciculata  and T. cruzi , and this is also in-line with the behaviour described for hPARP-1 and 2 . The N-terminus of T. brucei PARP is abundant in basic amino acids and probably the region responsible for DNA strand break-detection and activity modulation . TbPARP does not require any metal ions to carry out its activity. The divalent cations such as Mn2+, Ni2+or Zn2+ resulted in an inhibitory effect probably because these ions could bind to important sulphydryl groups.
The optimization of the reaction conditions allowed the use of an activity assay based on the fluorescence [17, 19] and helped us to identify specific inhibitors towards TbPARP from a library of PARP inhibitors. Similarly to TcPARP, the most potent TbPARP inhibitors identified were Olaparib, EB-47, 4-ANI, Veliparib, and Rucaparib. Mostly, the similarities in the IC50 values among TbPARP, TcPARP, and hPARP-1 can be explained by the conservation of the donor NAD+ binding pocket, as evidenced by the homology model (Table 1, Fig. 2). Rucaparib binds to the nicotinamide binding pocket of PARPs  and lower potency of Rucaparib towards TbPARP (150 nM) compared to TcPARP (25 nM)  and hPARP-1 (1 nM) can be explained by the amino acid difference as a conserved alanine is replaced by a serine (Ser461) in TbPARP, leading to unfavorable interactions. EB-47 and 4-ANI have been previously reported to inhibit PAR synthesis in human cells [41, 42] and presented 10-fold selectivity for TbPARP over hPARP-1. However, despite the displayed in vitro enzymatic inhibition they were not able to reduce PAR synthesis in the parasite. Only Olaparib and Rucaparib were able to reduce PAR formation in both procyclic and bloodstream forms. This might be explained by variations in the capability of these drugs to penetrate the parasites external membrane or by other mechanisms that allow metabolic detoxification of these inhibitors by the parasite . Surprisingly, only Rucaparib at the highest concentration (15 μM) rendered a visible impact on the growth rate of procyclic parasites in the conditions tested here. This concentration was in a range similar to that exerted by Nifurtimox, a compound that has been recently incorporated as a combination therapy against Sleeping Sickness [37, 38].
On the other hand, the absence of an active TbPARP in procyclic parasites has no consequences on viability, which has also been proved by our RNAi experiments. This evidence is in agreement with those results reported by an RNAi target sequencing study . The result obtained here differs from the one reported for T. cruzi epimastigotes in culture where Olaparib at 25 nM concentration led to a 50 % decrease in growth of the parasites , indicating different roles of PARP enzymes in these trypanosomatids.
PARP down-regulation did not interfere with normal cell growth but the cytotoxicity induced by H2O2 was reduced both by PARP down-regulation and by Olaparib. Cell death can be achieved through an apoptotic or a necrotic pathway, which depends on the type of cell and the concentration of the H2O2 involved. There is evidence that PAR acts as a switch not only between survival pathways but also between cell death signalling, mediating a particular cellular response against a specific DNA damage . This mechanism was described by us for the trypanosomatid T. cruzi  where PARP carries out a differential function in genomic damage-response. Despite DNA repair mechanisms are not totally clarified in these parasites, many pieces of this puzzle are available in the literature [44, 45]. Here we have demonstrated that TbPARP is activated under a genotoxic stimulus and migrates to the nucleus. This phenomenon of translocation has also been demonstrated in T. cruzi by our group . An antagonic role can be assigned to PARP function under stress conditions. When the levels of genomic harm are low, PARP activation plays a protective role. Otherwise, substantial genotoxic stimulus induces loss of viability and cell death. PAR is therefore the molecular switch between different cell death pathways . In this regard, PARP inhibition could prevent the massive reduction of NAD+ and thus prevent the energy store depletion  that leads to the loss of viability induced by high doses of H2O2. Our results obtained with Olaparib, PARP- silenced and PARP over-expressing parasites are in line with this reasoning.
The real function of PARG regarding cell death is controversial and some authors have reported that PARG inhibition provides protection to oxidative-stressed neuronal cells . Studies based on PARG-silenced cells show conflicting results ranging from protection to lack of effect using different cytotoxic agents [13, 46]. PARG suppression would lead to PARP inhibition by auto-PARylation. Although we have demonstrated auto-PARylation in T. cruzi, this mechanism was not established in T. brucei yet. On the other hand, cell death is augmented in PARG-deficient cells which are impaired to repair breaks in one and both strands, pointing out the PARG critical role in DNA damage response [12–14]. Although a function for PARG in regulation of oxidative stress-induced cell death has not been clarified, alteration of PAR cycle would lead to a delay in DNA repair and would explain the increased sensitivity to genotoxic stimuli.
PARP over-expressing and PARG-silenced cells evidenced PAR accumulation in the nucleus, even in absence of oxidative stress. Increased nuclear PAR in parasites with abrogated PARG demonstrates an active polymer synthesis in procyclic parasites and indicates that PARG is the main PAR cycling enzyme. After a cytotoxic stimulus, both transgenic parasites presented a different pattern in the PAR levels. Moreover, these parasites with an altered PAR metabolism demonstrated an increased sensitivity towards oxidative stress, and the changes obtained in the pattern of membrane permeability and PI incorporation indicate that PARP and PARG would mediate apoptosis-like to necrosis death switch. The duality of PAR being a molecular switch between both life and cell death has been proposed by many authors. PAR is involved in DNA damage response. However, an augmented PAR formation could deplete NAD+ and consequently remove ATP from the cell, inducing cell death. We showed that not only the quantity of the synthesized PAR might have an effect on parasite survival, but also its particular nuclear localization. Andrabi and colleagues described that PAR could be toxic by itself studying the effect of the presence of in vitro synthesized PAR delivered inside the cells with a system based on lipids .
Cells die by different mechanisms and this is a subject of many investigations. Among them, “parthanatos” happens when hPARP-1 is over activated; and is mainly related to synthesis of PAR and accumulation, mitochondrial depolarization, AIF translocation to the nucleus and caspases activation; although the latter is not mandatory . Very little is known about the regulation and the type of parasite death in trypanosomatids. Moreover, caspases, calpains and cathepsins, as well as serine proteases and important mediators such as AIF, have not been identified yet; making the characterization of different death pathways even harder.
Summing up, disrupted PAR metabolism with accumulated polymer in the nucleus has deleterious consequences to the parasites when exposed to genotoxic stimulus.
Trypanosoma brucei, like Trypanosoma cruzi, has only one enzyme PARP. However, unlike T. cruzi, protein inhibition or the lack of PARP in T. brucei has no consequences on normal replication. This finding shows substantial dissimilarity regarding PARP role in different trypanosomatids’ cell cycle.
TbPARP activity seems to be very dynamic, even in standard conditions. However, after genotoxic stimulus PAR accumulation in the nucleus is observed. Our results demonstrate that TbPARP down regulation reduced cytotoxicity induced by H2O2; and, accordingly, TbPARP over expression led to a higher sensitivity against the mentioned agent.
PARG, the main PAR hydrolyzing enzyme, has an important function in maintenance of PAR levels and in regulation of cell death following a genotoxic insult. Our results have shown that in undamaged parasites PARG deficiency does not result lethal; however PAR accumulation in the nucleus conferred an increased sensitivity towards oxidative stress. In all cases, the presence of high levels of nuclear PAR constituted a signal leading to a different cell death pattern. This confirms that the PAR polymer is cytotoxic by itself.
Overall we have demonstrated the importance of PAR metabolism in cell death induced by oxidative stress, although further investigation needs to be done to clarify the mechanisms involved.
- T. brucei :
- T. cruzi :
Trypanosoma brucei Poly(ADP-ribose)glycohydrolase
Trypanosoma brucei Poly(ADP-ribose)polymerase
Trypanosoma cruzi Poly(ADP-ribose)polymerase
Ame JC, Spenlehauer C, de Murcia G. The PARP superfamily. Bioessays. 2004;26(8):882–93.
Burkle A, Virag L. Poly(ADP-ribose): PARadigms and PARadoxes. Mol Aspects Med. 2013;34(6):1046–65.
D’Amours D, Desnoyers S, D’Silva I, Poirier GG. Poly(ADP-ribosyl)ation reactions in the regulation of nuclear functions. Biochem J. 1999;342(Pt 2):249–68.
Diefenbach J, Burkle A. Introduction to poly(ADP-ribose) metabolism. Cell Mol Life Sci. 2005;62(7-8):721–30.
Krishnakumar R, Kraus WL. The PARP side of the nucleus: molecular actions, physiological outcomes, and clinical targets. Mol Cell. 2010;39(1):8–24.
Schreiber V, Dantzer F, Ame JC, de Murcia G. Poly(ADP-ribose): novel functions for an old molecule. Nat Rev Mol Cell Biol. 2006;7(7):517–28.
Virag L. 50Years of poly(ADP-ribosyl)ation. Mol Aspects Med. 2013;34(6):1043–5.
Virag L, Robaszkiewicz A, Rodriguez-Vargas JM, Oliver FJ. Poly(ADP-ribose) signaling in cell death. Mol Aspects Med. 2013;34(6):1153–67.
Bonicalzi ME, Haince JF, Droit A, Poirier GG. Regulation of poly(ADP-ribose) metabolism by poly(ADP-ribose) glycohydrolase: where and when? Cell Mol Life Sci. 2005;62(7-8):739–50.
Meyer-Ficca ML, Meyer RG, Coyle DL, Jacobson EL, Jacobson MK. Human poly(ADP-ribose) glycohydrolase is expressed in alternative splice variants yielding isoforms that localize to different cell compartments. Exp Cell Res. 2004;297(2):521–32.
Koh DW, Lawler AM, Poitras MF, Sasaki M, Wattler S, Nehls MC, Stoger T, Poirier GG, Dawson VL, Dawson TM. Failure to degrade poly(ADP-ribose) causes increased sensitivity to cytotoxicity and early embryonic lethality. Proc Natl Acad Sci U S A. 2004;101(51):17699–704.
Ame JC, Fouquerel E, Gauthier LR, Biard D, Boussin FD, Dantzer F, de Murcia G, Schreiber V. Radiation-induced mitotic catastrophe in PARG-deficient cells. J Cell Sci. 2009;122(Pt 12):1990–2002.
Erdelyi K, Bai P, Kovacs I, Szabo E, Mocsar G, Kakuk A, Szabo C, Gergely P, Virag L. Dual role of poly(ADP-ribose) glycohydrolase in the regulation of cell death in oxidatively stressed A549 cells. Faseb J. 2009;23(10):3553–63.
Fisher AE, Hochegger H, Takeda S, Caldecott KW. Poly(ADP-ribose) polymerase 1 accelerates single-strand break repair in concert with poly(ADP-ribose) glycohydrolase. Mol Cell Biol. 2007;27(15):5597–605.
Illuzzi G, Fouquerel E, Ame JC, Noll A, Rehmet K, Nasheuer HP, Dantzer F, Schreiber V. PARG is dispensable for recovery from transient replicative stress but required to prevent detrimental accumulation of poly(ADP-ribose) upon prolonged replicative stress. Nucleic Acids Res. 2014;42(12):7776-92.
Alonso GDVL SC, Fernández Villamil SH. Metabolism of Poly-ADP-ribose in Trypanosomatids. In: Peeters ODBS, editor. Parasitology research trends. New York: Nova Science Publishers, Inc; 2010. p. 119–41.
Vilchez Larrea SC, Haikarainen T, Narwal M, Schlesinger M, Venkannagari H, Flawia MM, Villamil SH, Lehtio L. Inhibition of poly(ADP-ribose) polymerase interferes with Trypanosoma cruzi infection and proliferation of the parasite. PLoS One. 2012;7(9):e46063.
Fernandez Villamil SH, Baltanas R, Alonso GD, Vilchez Larrea SC, Torres HN, Flawia MM. TcPARP: A DNA damage-dependent poly(ADP-ribose) polymerase from Trypanosoma cruzi. Int J Parasitol. 2008;38(3-4):277–87.
Putt KS, Hergenrother PJ. An enzymatic assay for poly(ADP-ribose) polymerase-1 (PARP-1) via the chemical quantitation of NAD(+): application to the high-throughput screening of small molecules as potential inhibitors. Anal Biochem. 2004;326(1):78–86.
Miyashiro J, Woods KW, Park CH, Liu X, Shi Y, Johnson EF, Bouska JJ, Olson AM, Luo Y, Fry EH, et al. Synthesis and SAR of novel tricyclic quinoxalinone inhibitors of poly(ADP-ribose)polymerase-1 (PARP-1). Bioorg Med Chem Lett. 2009;19(15):4050–4.
Karlberg T, Markova N, Johansson I, Hammarstrom M, Schutz P, Weigelt J, Schuler H. Structural basis for the interaction between tankyrase-2 and a potent Wnt-signaling inhibitor. J Med Chem. 2010;53(14):5352–5.
Lehtio L, Jemth AS, Collins R, Loseva O, Johansson A, Markova N, Hammarstrom M, Flores A, Holmberg-Schiavone L, Weigelt J, et al. Structural basis for inhibitor specificity in human poly(ADP-ribose) polymerase-3. J Med Chem. 2009;52(9):3108–11.
Larkin MA, Blackshields G, Brown NP, Chenna R, McGettigan PA, McWilliam H, Valentin F, Wallace IM, Wilm A, Lopez R, et al. Clustal W and Clustal X version 2.0. Bioinformatics. 2007;23(21):2947–8.
Bond CS, Schuttelkopf AW. ALINE: a WYSIWYG protein-sequence alignment editor for publication-quality alignments. Acta Crystallogr D Biol Crystallogr. 2009;65(Pt 5):510–2.
Sali A, Blundell TL. Comparative protein modelling by satisfaction of spatial restraints. J Mol Biol. 1993;234(3):779–815.
Emsley P, Cowtan K. Coot: model-building tools for molecular graphics. Acta Crystallogr D Biol Crystallogr. 2004;60(Pt 12 Pt 1):2126–32.
Krissinel E, Henrick K. Secondary-structure matching (SSM), a new tool for fast protein structure alignment in three dimensions. Acta Crystallogr D Biol Crystallogr. 2004;60(Pt 12 Pt 1):2256–68.
McNicholas S, Potterton E, Wilson KS, Noble ME. Presenting your structures: the CCP4mg molecular-graphics software. Acta Crystallogr D Biol Crystallogr. 2011;67(Pt 4):386–94.
Wirtz E, Leal S, Ochatt C, Cross GA. A tightly regulated inducible expression system for conditional gene knock-outs and dominant-negative genetics in Trypanosoma brucei. Mol Biochem Parasitol. 1999;99(1):89–101.
Wickstead B, Ersfeld K, Gull K. Targeting of a tetracycline-inducible expression system to the transcriptionally silent minichromosomes of Trypanosoma brucei. Mol Biochem Parasitol. 2002;125(1-2):211–6.
Kelly S, Reed J, Kramer S, Ellis L, Webb H, Sunter J, Salje J, Marinsek N, Gull K, Wickstead B, et al. Functional genomics in Trypanosoma brucei: a collection of vectors for the expression of tagged proteins from endogenous and ectopic gene loci. Mol Biochem Parasitol. 2007;154(1):103–9.
Downey N, Hines JC, Sinha KM, Ray DS. Mitochondrial DNA ligases of Trypanosoma brucei. Eukaryotic Cell. 2005;4(4):765–74.
Vilchez Larrea SC, Schlesinger M, Kevorkian ML, Flawia MM, Alonso GD, Fernandez Villamil SH. Host Cell Poly(ADP-Ribose) Glycohydrolase Is Crucial for Trypanosoma cruzi Infection Cycle. PLoS One. 2013;8(6):e67356.
Vilchez Larrea SC, Alonso GD, Schlesinger M, Torres HN, Flawia MM, Fernandez Villamil SH. Poly(ADP-ribose) polymerase plays a differential role in DNA damage-response and cell death pathways in Trypanosoma cruzi. Int J Parasitol. 2011;41(3-4):405–16.
Welburn SC, Dale C, Ellis D, Beecroft R, Pearson TW. Apoptosis in procyclic Trypanosoma brucei rhodesiense in vitro. Cell Death Differ. 1996;3(2):229–36.
Welburn SC, Barcinski MA, Williams GT. Programmed cell death in trypanosomatids. Parasitol Today. 1997;13(1):22–6.
Dethoua M, Nzoumbou-Boko R, Truc P, Daulouede S, Courtois P, Bucheton B, Cuny G, Semballa S, Vincendeau P. Evaluation of trypanocidal drugs used for human African trypanosomosis against Trypanosoma lewisi. Parasite. 2013;20:39.
Priotto G, Kasparian S, Mutombo W, Ngouama D, Ghorashian S, Arnold U, Ghabri S, Baudin E, Buard V, Kazadi-Kyanza S, et al. Nifurtimox-eflornithine combination therapy for second-stage African Trypanosoma brucei gambiense trypanosomiasis: a multicentre, randomised, phase III, non-inferiority trial. Lancet. 2009;374(9683):56–64.
Podesta D, Garcia-Herreros MI, Cannata JJ, Stoppani AO, Fernandez Villamil SH. Purification and properties of poly(ADP-ribose)polymerase from Crithidia fasciculata. Automodification and poly(ADP-ribosyl)ation of DNA topoisomerase I. Mol Biochem Parasitol. 2004;135(2):211–9.
Haikarainen T, Narwal M, Joensuu P, Lehtio L. Evaluation and Structural Basis for the Inhibition of Tankyrases by PARP Inhibitors. ACS Med Chem Lett. 2013;5(1):18–22.
Jagtap PG, Southan GJ, Baloglu E, Ram S, Mabley JG, Marton A, Salzman A, Szabo C. The discovery and synthesis of novel adenosine substituted 2,3-dihydro-1H-isoindol-1-ones: potent inhibitors of poly(ADP-ribose) polymerase-1 (PARP-1). Bioorg Med Chem Lett. 2004;14(1):81–5.
Schlicker A, Peschke P, Burkle A, Hahn EW, Kim JH. 4-Amino-1,8-naphthalimide: a novel inhibitor of poly(ADP-ribose) polymerase and radiation sensitizer. Int J Radiat Biol. 1999;75(1):91–100.
Alsford S, Turner DJ, Obado SO, Sanchez-Flores A, Glover L, Berriman M, Hertz-Fowler C, Horn D. High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome. Genome Res. 2011;21(6):915–24.
Badjatia N, Nguyen TN, Lee JH, Gunzl A. Trypanosoma brucei harbours a divergent XPB helicase paralogue that is specialized in nucleotide excision repair and conserved among kinetoplastid organisms. Mol Microbiol. 2013;90(6):1293–308.
Machado-Silva A, Teixeira SM, Franco GR, Macedo AM, Pena SD, McCulloch R, Machado CR. Mismatch repair in Trypanosoma brucei: heterologous expression of MSH2 from Trypanosoma cruzi provides new insights into the response to oxidative damage. Gene. 2008;411(1-2):19–26.
Blenn C, Althaus FR, Malanga M. Poly(ADP-ribose) glycohydrolase silencing protects against H2O2-induced cell death. Biochem J. 2006;396(3):419–29.
Ying W, Sevigny MB, Chen Y, Swanson RA. Poly(ADP-ribose) glycohydrolase mediates oxidative and excitotoxic neuronal death. Proc Natl Acad Sci U S A. 2001;98(21):12227–32.
Andrabi SA, Kim NS, Yu SW, Wang H, Koh DW, Sasaki M, Klaus JA, Otsuka T, Zhang Z, Koehler RC, et al. Poly(ADP-ribose) (PAR) polymer is a death signal. Proc Natl Acad Sci U S A. 2006;103(48):18308–13.
Fatokun AA, Dawson VL, Dawson TM. Parthanatos: mitochondrial-linked mechanisms and therapeutic opportunities. Br J Pharmacol. 2014;171(8):2000-16.
Banasik M, Komura H, Shimoyama M, Ueda K. Specific inhibitors of poly(ADP-ribose) synthetase and mono(ADP-ribosyl)transferase. J Biol Chem. 1992;267(3):1569–75.
Penning TD, Zhu GD, Gandhi VB, Gong J, Liu X, Shi Y, Klinghofer V, Johnson EF, Donawho CK, Frost DJ, et al. Discovery of the Poly(ADP-ribose) polymerase (PARP) inhibitor 2-[(R)-2-methylpyrrolidin-2-yl]-1H-benzimidazole-4-carboxamide (ABT-888) for the treatment of cancer. J Med Chem. 2009;52(2):514–23.
Jagtap P, Szabo C. Poly(ADP-ribose) polymerase and the therapeutic effects of its inhibitors. Nat Rev Drug Discov. 2005;4(5):421–40.
Griffin RJ, Srinivasan S, Bowman K, Calvert AH, Curtin NJ, Newell DR, Pemberton LC, Golding BT. Resistance-modifying agents. 5. Synthesis and biological properties of quinazolinone inhibitors of the DNA repair enzyme poly(ADP-ribose) polymerase (PARP). J Med Chem. 1998;41(26):5247–56.
Menear KA, Adcock C, Alonso FC, Blackburn K, Copsey L, Drzewiecki J, Fundo A, Le Gall A, Gomez S, Javaid H, et al. Novel alkoxybenzamide inhibitors of poly(ADP-ribose) polymerase. Bioorg Med Chem Lett. 2008;18(14):3942–5.
Thomas HD, Calabrese CR, Batey MA, Canan S, Hostomsky Z, Kyle S, Maegley KA, Newell DR, Skalitzky D, Wang LZ, et al. Preclinical selection of a novel poly(ADP-ribose) polymerase inhibitor for clinical trial. Mol Cancer Ther. 2007;6(3):945–56.
Ruf A, de Murcia G, Schulz GE. Inhibitor and NAD+ binding to poly(ADP-ribose) polymerase as derived from crystal structures and homology modeling. Biochemistry. 1998;37(11):3893–900.
This work was supported by Agencia Nacional de Promoción Científica y Tecnológica (Argentina), Consejo Nacional de Investigaciones Científicas y Técnicas (Argentina), Universidad de Buenos Aires (Argentina) and EMBO Short Term Fellowship, Europe. MS is a fellow of the CONICET. SCVL, MMF and SHFV form part of the Scientific Researcher Career of CONICET. The work was also funded by Biocenter Oulu (LL) and the Academy of Finland (TH; grant No. 266922).
The authors declare that they have no competing interests.
MS obtained the parasite transgenic lines and performed the experiments. She participated in the conception and experiment design, acquisition, analysis and interpretation of data. She was also involved in drafting the manuscript. SCVL carried out all TbPARP activity assay optimization experiments and screening of inhibitors. TH generated the homology model and inhibitor binding modes of TbPARP, and revised the manuscript. MN helped to carry out the screening of TbPARP inhibitors. HV carried out the western blot to evaluate the effect of inhibitors on TbPARP. MMF participated in revising the manuscript and with critical contributions. LL and SHFV conceived the study, participated in its design, and coordinated and helped to draft the manuscript. All authors read and approved the final manuscript.
Optimization of assay conditions for TbPARP in vitro activity. NAD+ consumption was measured by a decrease in fluorescence in a 96-well plate. Triplicates were obtained for every data point, and expressed as means and standard deviations. A) NAD+ consumption by TbPARP was measured as a function of pH using a variety of buffering agents as indicated on the x-axis. B) NAD+ consumption was determined in 100 mM Na2HPO4/NaH2PO4 buffer at pH 7 at different concentrations of activated DNA. C) NAD+ consumption by TbPARP (10 nM) was determined in 100 mM Na2HPO4/NaH2PO4 buffer at pH 7 supplemented with 25 μg/mL activated DNA in the presence of chloride salts of different divalent cations (2 mM). (TIF 3064 kb)
PARP inhibitor like compounds tested. (XLSX 12 kb)
Transgenic RNAi-TbPARP procyclic parasites. A) Representative growth curve shows cell density of tetracycline 3 day-induced (+Tet) and non-induced (− Tet) RNAi-TbPARP procyclic parasites of two different clones, 1 and 2, monitored for 11 and 9 days, respectively. B) Representative growth curve shows cell density of tetracycline 3 day-induced (+Tet) and non-induced (− Tet) RNAi-TbPARP procyclic parasites in presence or in absence of 290 nM Olaparib, monitored for 6 days. C) Northern blot analysis of RNAi-TbPARP procyclic parasites on days 3, 6, 9 and 11 post-induction (p.i.) compared to non-induced cells at identical time points. 30 μg of total RNA was loaded on every lane. Hybridization was performed with a [32P]dCTP-labelled TbPARP fragment made by random priming the same PCR product used as insert in the p2T7-177 vector. Ribosomal RNA levels confirmed total RNA equal amounts in each lane. The band corresponding to TbPARP mRNA is shown by an arrow and it is also present in wild type parasites (WT). D) Western blot analysis of 2 × 106 three day-induced (+ Tet) and non-induced (- Tet) RNAi-TbPARP cell equivalents revealed with specific 1:100 anti-TbPARP polyclonal antibody (GeneScript). The membrane stained with Red Ponceau was used as a loading control. (TIF 888 kb)
TbPARG in Trypanosoma brucei. A) TbPARG localization in untreated (control) and in procyclic cultures exposed to 500 μM H2O2 for 10 min. IFI was carried out as reported in our previous work . TbPARG was identified with our home-made antibody against TcPARG ; and PAR was identified with a commercial antibody against PAR (BD). White bar represents 50 μm. B) Western blot analysis of 40 μg protein per lane revealed with a commercial anti-PARG antibody (Antibody Verify) in T. brucei procyclic (PC) and bloodstream (BST) forms. The arrow indicates the band with the expected molecular weight (approximately 60 kDa). The membrane stained with Red Ponceau was used as a loading control. (TIF 4272 kb)
Transgenic TbPARP over-expressing and TbPARG down-regulated procyclic parasites. A) Western blot analysis of 3 day-induced (Tet+) and non-induced (Tet-) TbPARP over-expressing (p2216-TbPARP-eYFP) parasites. 2 × 106 cell equivalents were revealed with specific 1:500 mouse monoclonal antibody directed against GFP (Santa Cruz) (Arrow). Staining of the membrane with Red Ponceau was used as a loading control. B) Over-expression of TbPARP-eYFP fusion protein in a 3 day-induced culture (p2216 TbPARP) was also assessed by IFI, detecting eYFP fluorescence. C) Western blot assessment of 3 day-induced (Tet+) and non-induced (Tet-) RNAi-TbPARG (p2T7 TbPARG) parasites. 2 × 106 cell equivalents were revealed with commercial 1:500 rabbit antibody directed against PARG proteins (Antibody Verify) (Arrow). The same membrane revealed with anti-Tubulin antibody was used as a loading control. (TIF 18,172 kb)
Cell survival in eYFP over-expressing (p2216) cultures subjected to hydrogen peroxide (H2O2) treatment. As a control of the experiment carried out with TbPARP-eYFP over-expressing (p2216-TbPARP) cultures (Fig. 4c), cell survival of 3 day-induced (Tet+) and non-induced (Tet -) eYFP over-expressing (p2216) cultures was studied by measuring parasite motility 6 h after treatment with different hydrogen peroxide concentrations. Statistical significance of three independent experiments was assessed in comparison to the control group (* p < 0.05). (TIF 700 kb)
Nuclear PAR signal quantification in TbPARP-eYFP over-expressing and TbPARG down-regulated procyclic parasites. PAR and DAPI (control) fluorescence was measured following ImageJ instructions. Nuclear area was selected from ten to fifteen parasites and integrated density (IntDen) was calculated. Three different regions per parasite were also selected next to the nuclei as a background. CTCF was obtained as described in Fig. 5b. A and B) TbPARP-eYFP over-expressing parasites. C and D) RNAi-TbPARG parasites. Student’s Test was performed and significance of the nuclear signal in (Tet +) versus (Tet -) parasites is indicated (*** p < 0.001; **, p < 0.01). (TIF 5373 kb)
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Schlesinger, M., Vilchez Larrea, S.C., Haikarainen, T. et al. Disrupted ADP-ribose metabolism with nuclear Poly (ADP-ribose) accumulation leads to different cell death pathways in presence of hydrogen peroxide in procyclic Trypanosoma brucei . Parasites Vectors 9, 173 (2016) doi:10.1186/s13071-016-1461-1
- Trypanosoma brucei
- Genotoxic damage
- Cell death