Oxidative Medicine and Cellular Longevity

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Research Article | Open Access

Volume 2019 |Article ID 8535163 | https://doi.org/10.1155/2019/8535163

Sander Bekeschus, Clarissa S. Schütz, Felix Nießner, Kristian Wende, Klaus-Dieter Weltmann, Nadine Gelbrich, Thomas von Woedtke, Anke Schmidt, Matthias B. Stope, "Elevated H2AX Phosphorylation Observed with kINPen Plasma Treatment Is Not Caused by ROS-Mediated DNA Damage but Is the Consequence of Apoptosis", Oxidative Medicine and Cellular Longevity, vol. 2019, Article ID 8535163, 15 pages, 2019. https://doi.org/10.1155/2019/8535163

Elevated H2AX Phosphorylation Observed with kINPen Plasma Treatment Is Not Caused by ROS-Mediated DNA Damage but Is the Consequence of Apoptosis

Guest Editor: Rizwan Wahab
Received24 May 2019
Revised23 Jul 2019
Accepted26 Aug 2019
Published19 Sep 2019


Phosphorylated histone 2AX (γH2AX) is a long-standing marker for DNA double-strand breaks (DSBs) from ionizing radiation in the field of radiobiology. This led to the perception of γH2AX being a general marker of direct DNA damage with the treatment of other agents such as low-dose exogenous ROS that unlikely act on cellular DNA directly. Cold physical plasma confers biomedical effects majorly via release of reactive oxygen and nitrogen species (ROS). In vitro, increase of γH2AX has often been observed with plasma treatment, leading to the conclusion that DNA damage is a direct consequence of plasma exposure. However, increase in γH2AX also occurs during apoptosis, which is often observed with plasma treatment as well. Moreover, it must be questioned if plasma-derived ROS can reach into the nucleus and still be reactive enough to damage DNA directly. We investigated γH2AX induction in a lymphocyte cell line upon ROS exposure (plasma, hydrogen peroxide, or hypochlorous acid) or UV-B light. Cytotoxicity and γH2AX induction was abrogated by the use of antioxidants with all types of ROS treatment but not UV radiation. H2AX phosphorylation levels were overall independent of analyzing either all nucleated cells or segmenting γH2AX phosphorylation for each cell cycle phase. SB202190 (p38-MAPK inhibitor) and Z-VAD-FMK (pan-caspase inhibitor) significantly inhibited γH2AX induction upon ROS but not UV treatment. Finally, and despite γH2AX induction, UV but not plasma treatment led to significantly increased micronucleus formation, which is a functional read-out of genotoxic DNA DSBs. We conclude that plasma-mediated and low-ROS γH2AX induction depends on caspase activation and hence is not the cause but consequence of apoptosis induction. Moreover, we could not identify lasting mutagenic effects with plasma treatment despite phosphorylation of H2AX.

1. Introduction

γH2AX is a recognized marker for DNA double-strand breaks (DSBs) in radiation biology [1]. Phosphorylation at serine139 of the histone 2AX occurs rapidly, and approximately 1% of all H2AX proteins are phosphorylated per gray irradiation via a molecular machinery [2]. Based on these findings in radiobiology, γH2AX has been used as direct surrogate and correlate of DNA DSBs in a variety of studies testing chemical and physical treatments, for example, in the field of oncology [3]. One novel physical treatment modality for the treatment of cancer is cold physical plasma [4]. Its antitumor effects on several types of tumor cells such as skin cancer have been shown in vitro and in vivo [57], and to a limited extent also in small patient cohorts [8]. Medical plasmas are multicomponent systems consisting of, e.g., electrons and ions, electric fields, and a multiplicity of different reactive oxygen and nitrogen species (ROS) [9].

ROS are the major component mediating biomedical effects of plasma treatment, at least in vitro [1012]. Concomitant with plasma-induced cell death, many studies reported a phosphorylation of H2AX with different kinds of plasma sources and (tumor) cell types [1319]. This lead to the conclusion that plasma-derived ROS directly induce DNA damage. Yet, there are several pitfalls of this assumption. Firstly, plasma-derived ROS are not generated within the cells but reach them from the outside. Due to the charge as well as short lifetime of some of these species detected and quantified in plasma-treated liquids, and hence possibly in the vicinity of cells [2022], only a fraction of the ROS is able to diffuse or being transported through the cell membrane directly. Secondly, once in the cytosol, there are abundant reaction partners including, for instance, peroxiredoxins (PRDX) to scavenge the ROS [23]. Thirdly, the remaining ROS would have to cross several membranes of the endoplasmic reticulum (ER) and ultimately the nucleus membrane to directly act on cellular DNA after—again—passing by several antioxidant proteins such as PRDX2 [24]. In the light of large distances (2-10 μm) that ROS would have to travel from the membrane to the nucleus, the direct action of plasma-derived ROS on cellular DNA denies the nature of ROS being reactive and short-lived. This also questions the conclusion that γH2AX is an indicator of DNA DSBs arising from primary ROS derived from plasma treatment. Rather, a role of γH2AX might be in marking DNA DSBs secondary to plasma treatment (e.g., due to apoptosis). γH2AX was originally identified as an early event after the direct formation of DSBs. Now, γ-H2AX is considered to occur after the indirect formation of DSBs caused by cellular process such as DNA repair, replication, and/or transcription at sites of initial DNA damage such as oxidative bases, DNA adducts, single-strand breaks, cross-linking, and DNA photoproducts [25, 26].

In general, γH2AX seems to fulfill pleiotropic roles in cell biology. For instance, low levels of γH2AX are not associated with DNA DSBs [27]. Untreated cells are found to be positive for γH2AX in the M phase of the cell cycle without being exposed to a DNA-damaging agent [28]. Decreased expression of the H2AX primarily leads to damage in the mitochondria [29]. The amount of γH2AX in apoptotic cells also exceeds that of nonapoptotic cells by a factor of ten [30]. γH2AX also seems dispensable for the initial recognition of DNA breaks [31]. Finally, there is evidence that not only DNA DSBs but also ROS may be responsible for γH2AX induction [32]. Mechanistically, it is known that while the serine/threonine kinase ataxia telangiectasia mutated (ATM) forms γH2AX at DNA DSBs [33], the serine/threonine kinase ataxia telangiectasia and Rad3-related protein (ATR) have been also implicated in this process [34]. Interestingly, ATM does so by redox-sensitive thiols, so ATM activation is a marker of both oxidative stress and DNA DSBs [35].

In the light of these studies, we sought to study the role of plasma-derived ROS in γH2AX induction. The lymphocyte cell line TK6 was treated with an atmospheric pressure argon plasma jet (kINPen) as ROS-source. The γH2AX expression along with the amount of ROS, ROS scavengers, cell viability, and an OECD- (Organization for Economic Co-operation and Development-) accredited genotoxicity (micronucleus) assay were investigated. We found that plasma but not UV-induced γH2AX induction was dependent on apoptosis and caspase activation, making DNA damage marked via γH2AX rather a consequence than the cause for plasma-induced cell death.

2. Materials and Methods

2.1. Cell Culture

Lymphocytes are the cell type most often used when investigating DNA damage [36]. Especially the human TK6 lymphocyte cell line has been widely utilized in genotoxicity studies [37, 38]. For this reason, we used TK6 (ATCC CRL-8015) cells, a p53-competent, human lymphoblast cell line. Cells were cultured in Roswell Park Memorial Medium without phenol red (RPMI1640; PanBioTech) supplemented with 10% fetal bovine serum, 2% glutamine, and 1% penicillin/streptomycin (all Sigma). All incubations were performed in cell culture conditions (CB210; Binder) at 37°C, 95% humidity, and 5% carbon dioxide. As ROS scavengers, catalase (cat; 20 μg/ml), glutathione (GSH; 1 mM), or superoxide dismutase (SOD; 100 U/ml) was used (all Sigma). As enzyme or signaling inhibitors, Z-VAD-FMK (R&D Biosciences), SB202190 (Sigma), KU55933 (SelleckChem), Ly294002 (Cell Signaling Technologies), wortmannin (InvivoGen), or SP600125 (Santa Cruz Biotechnology) was used at different concentrations and incubated with cells for 1 h prior ROS or UV treatment. Final concentrations for a selected choice of inhibitors were 1 μM for KU55933, 1 μM for SB202190, and 25 μM for Z-VAD-FMK.

2.2. Exposure of Cells to ROS, Cold Physical Plasma, or UV

For all procedures, TK6 cells in 500 μl of fully supplemented cell culture medium were added to wells of a 24-well plate (Sarstedt). For hydrogen peroxide (H2O2; Sigma) treatment, the stock was diluted in double-distilled water, and a range of concentrations was tested initially. Final concentration for subsequent assays was 10 μM. For hypochlorous acid (HOCl; Roth), the stock was diluted in double-distilled water, and a range of concentrations was tested initially. Final concentration for subsequent assays was 500 μM. Plasma treatment was done using the atmospheric pressure argon plasma jet kINPen (neoplas tools) that expels various reactive agents (Figure 1(a)) as reported before [9]. Its biomedical effects were summarized recently [39]. The plasma source was operated at two standard liters per minute of argon gas (Air Liquide, purity 99.999%). Plasma treatment was performed in a highly standardized manner as shown previously [40]. Briefly, the plasma jet was attached to a computer-controlled -table (CNC step), which hovered the plasma exactly over the center of each well for a predefined time and height. A range of treatment times was initially tested. Immediately after treatment, a predetermined amount of double-distilled water was added to the wells after plasma treatment to compensate for evaporation effects and to maintain isoosmolality. A treatment time of 10 s was used for subsequent experiments if not indicated otherwise. For exposure to UV light, a range of exposure times was tested, and 120 s was used for experiments if not indicated otherwise. The wells of the plate that were not intended to be exposed to UV light were covered with aluminum foil. A broadband UVB (20-160 Jeff m−2) light source (Philips TL12 fluorescent lamp) emitting radiation between 290 and 315 nm was used. UVB exposure modifies DNA directly by forming cyclobutane pyrimidine dimers (CPD) and 6-4 photoproducts. Indirect effects of UVB on DNA occur due to photolysis and generation of hydroxyl radicals, leading to formation of 8-hydroxy-2-deoxyguanosine (8-OhdG) [41].

2.3. Intracellular Oxidation

To assess intracellular oxidation, TK6 cells were stained with chloromethyl 2,7-dichlorodihydrofluorescein diacetate (CM-H2DCF-DA; final concentration 2.5 μM; Thermo Fisher) in phosphate-buffered saline (PBS), washed, and resuspended in fully supplemented cell culture medium (in the presence or absence of antioxidants). Cells were seeded into plates and treated as described above. Immediately after, cells were added to tubes (Sarstedt) containing 4,6-diamidin-2-phenylindol (DAPI; final concentration 1 μM; Sigma), and samples were acquired by multicolor flow cytometry (Gallios, equipped with 405 nm, 488 nm, and 638 nm laser; Beckman Coulter). Sample analysis was performed using Kaluza 2.1.1 software (Beckman Coulter) and analyzing the mean fluorescent intensity (MFI) of DCF within the viable (DAPI-) cell fraction.

2.4. Metabolic Activity, Mitochondrial Mass, and Viability

Metabolic activity was investigated by incubating the cells for 4 h with resazurin (final concentration 100 μM; Alfa Aesar) after two hours of incubation posttreatment. Metabolically active cells transform nonfluorescent resazurin into fluorescent resorufin, which can be quantified using a multiplate reader (F200; Tecan) at ex 560 nm and em 590 nm. Absolute sample values were normalized to that of untreated To quantify mitochondrial mass, cells were incubated for 15 min with chloromethyltetramethylrosamine, also called MitoTracker Orange (MTO; final concentration 1 μM; Thermo Fisher), at 6 h after plasma treatment. The cationic rosamine probe only binds to mitochondrial membranes with intact potential. Sample acquisition was performed using flow cytometry. To quantify nonterminally dead (alive) and terminally dead cells, DAPI was used to discriminate the percentage of either population using flow cytometry. For some experiments, the amount of cells active for caspase 3 and 7 was investigated to quantify the amount of apoptotic cells. For this, cells were incubated for 30 min with CellEvent dye (final concentration 2.5 μM; Thermo Fisher). Samples were analyzed by flow cytometry.

2.5. Analysis of Cell Cycle and γH2AX

Flow cytometry is the most sensitive, quantitative, and informative method of analyzing and quantifying γH2AX in cells, as it can be related to cell cycle and other cellular populations stained with additional markers [36]. To prepare the cells for DNA and γH2AX staining, cells were harvested 2 h after exposure to agents into tubes. In an initial kinetic experiment, 2 h was shown to be optimal. Cells were washed with PBS and fixed with -20°C methanol for 30 min at 4°C. Cells were washed and incubated with murine phosphor-specific anti-γH2AX antibodies (BioLegend) for 20 min. The optimal antibody dilution was determined experimentally. Cells were washed and incubated with DAPI (10 μM) and an anti-mouse IgG1 antibody conjugated to Alexa Fluor 647 (Thermo Fisher) for 20 min in permeabilization wash buffer (BioLegend) in the dark. Cells were washed and resuspended in PBS and acquired by flow cytometry. Gating of cells was performed as shown. Appropriate gating of the DAPI-area vs. DAPI-width parameters for cell cycle analysis was confirmed with Michael H. Fox algorithm integrated into Kaluza analysis software. If the algorithm could not calculate G1, S, and G2 phase properly, the gating was adjusted accordingly. This way, γH2AX induction could be accurately calculated in relation to mathematical modeling for each cell cycle phase. A total of more than 1.800 single FACS measurements was prepared, stained, and individually acquired in this study. Each measurement contained at least 20,000 single cells, yielding quantitative single cell data. To analyze γH2AX foci via laser scanning confocal microscopy (TP5; Leica), cells were stained as described above and added to 8-well glass slides (Ibidi). Fluorescence was acquired using excitation at 405 nm for DAPI and 640 nm for Alexa Fluor 647.

2.6. Quantification of Micronuclei

The cytokinesis-block micronucleus (MN) assay requires quantification of micronuclei in binucleated cells (BNCs) only [42]. Cells were treated as described above with minor changes and incubated for 24 h. As additional genotoxic positive control, the DNA-damaging agent methyl methanesulfonate (MMS; final concentration 20 ng/ml; Sigma) was added. The plasma treatment time was reduced from 10 s to 2.5 s as the plasma treatment acted synergistically toxic together with cytochalasin B, leading to insufficient cell counts. Similar observations were made for UV treatment, which was reduced from 120 s to 24 s. Ten wells were pooled into T75 flasks (Sarstedt) per condition, and cytochalasin B (final concentration 5 μg/ml; Sigma) was added. Flasks were incubated for another 24 h. Cells were collected into 15 ml tubes (Sarstedt), washed, fixed with 4% fixation buffer (BioLegend) for 20 min, and washed and stored at 4°C in PBS until staining. For staining, cells were washed and stained in permeabilization wash buffer (BioLegend) containing draq5 (final concentration 50 μM; BioLegend) for 20 min at room temperature in the dark. Other DNA staining dyes were also compared (SYTOX green, final concentration 1 μM, Thermo Fisher; DAPI, final concentration 10 μM, Sigma; Hoechst 33342, final concentration 10 μg/ml, Sigma) but found to be less suitable. Cells were washed in permeabilization wash buffer and resuspended in PBS in siliconized 1.5 ml tubes. Speed beats (Merck Millipore) were used to operate the imaging fluids of an ImageStream ISX Mark II (Merck Millipore), which was used for sample acquisition. Up to 2 × 105 cells (images) were acquired per sample. The digital MN analysis was in main parts similar as reported before [43], with some minor modifications in mask design and gating steps. A total of more than 40 Mio single cells—each represented by at least two individual images of about pixels in size—were acquired and partly analyzed in this study.

2.7. Statistical Analysis

Data were analyzed and graphed using Prism 8.1 (GraphPad software). Mean and standard error (S.E.) were given if not indicated otherwise. Statistical analysis was performed either using one-way analysis of variances or -test.

3. Results

3.1. Viability and Oxidation upon Exposure to Plasma, H2O2, HOCl, and UV Light

In order to obtain ROS concentrations and UV exposure times as well as plasma treatment times that were neither too toxic nor failed to show effects on cells, dilution and treatment time series were performed, respectively. From these, we concluded to use 10 s of plasma treatment (Figure 1(b)), 10 μM of H2O2 (Figure 1(c)), 500 μM of HOCl (Figure 1(d)), and 120 s of UV treatment (Figure 1(e)) in viability experiments assayed 6 h after exposure for subsequent experiments. Data for metabolic activity were in principal similar for longer incubation times (Supplementary Figure S1a). Terminally dead cells at 6 h posttreatment were also quantified (Supplementary Figure S1b). Next, it was tested whether antioxidant agents and enzymes protected cells 6 h postagent-induced toxicity (Figure 1(f)). While catalase (cat) and glutathione (GSH) conferred protection, superoxide dismutase (SOD) did not. To confirm that this finding was related to protection from ROS, cells were stained with CM-H2DCF-DA, which after intracellular modifications fluoresces upon oxidation with, e.g., plasma treatment (Figure 1(g)). Indeed, GSH and cat significantly protected cells from oxidation with plasma, H2O2, and HOCl treatment (Figure 1(h)). For UV exposure, only cat but not GSH conferred protection. This might be due to UV radiation directly oxidizing DCFH-DA. In lymphocytes, ROS-induced toxicity leads to depolarization of the mitochondrial membrane potential [44], which allows the quantification of mitochondria with intact using appropriate dyes (Figure 1(i)). The agents decreased the total amount of mitochondria with intact , while cat and GSH but not SOD protected from insult (Figure 1(j)). Presence of cat even led to higher values, suggesting the growth-supporting activity of antioxidant enzymes. In summary, the ROS agents and UV radiation oxidized the cells leading to mitochondrial damage and reduction of metabolic activity and viability.

3.2. Induction of γH2AX Depended on ROS but Not of Cell Cycle Phase

To quantify γH2AX in cells, a rigid flow cytometric gating strategy was set up. Cells were gated based on time (Figure 2(a)) and forward and side scatter properties (Figure 2(b)) followed by exclusion of doublets, aggregates, and subG1 cells (Figure 2(c)). γH2AX was quantified in singlets (Figure 2(d)). Alternatively, γH2AX was determined per cell cycle phase, which was validated using Michael H. Fox algorithms (Figure 2(e)). For each phase, a separate gating was applied (Figure 2(f)), from which the number (% gated) and intensity (mean fluorescence intensity of % gated) was calculated (Figure 2(g)). Staining was performed using appropriate antibody dilutions (Supplementary Figure S1c) at 2 h posttreatment (Supplementary Figure S1d) and was confirmed using confocal laser scanning microscopy (Figure 2(h)). γH2AX foci are formed within seconds, but since they are initially quite small, reliably quantification is recommend earliest at 30 min after initial insult [45]. A prominent γH2AX induction was observed with plasma and UV treatment and to a lesser extent with H2O2 and HOCl exposure (Figure 2(i)). This difference may be explained by slight (H2O2) and larger (HOCl) differences of the oxidants to induce cytotoxic effects as compared to those seen with plasma (Figures 1(f) and 1(j)). The reason might have been a change of TK6 sensitivity between the initial titration (Figures 1(b) and 1(c)) and subsequent experiment due to passage number. Strikingly, antioxidants (GSH and cat) significantly reduced γH2AX induction for plasma and H2O2 treatment. For UV treatment, it was significantly enhanced. Similar observations were made when analyzing γH2AX induction for each phase of the cell cycle (Figure 2(j)). In general, G1 cells gave lower signals compared to S and G2 phase cells, and the increase observed with antioxidants in UV conditions was evenly proportional for each cell cycle phase. Notably, cat and GSH had no effect on γH2AX induction in resting (untreated) cells for each cell cycle phase (Supplementary Figure S1e). By contrast, the antioxidant N-acetylcysteine (NAC) increased γH2AX induction in untreated as well as treated cells (Supplementary Figure S1f). With reference to cell cycle phase-dependent γH2AX intensity (Figure 2(j)), another question was whether there was a relatively higher increase in proliferating (S and G2 phase) cells. These cells have intrinsically more DSBs and unwinded DNA, which could make them more prone to ROS-induced DNA damage. It was observed that the opposite was the case, as γH2AX intensity in S over G1 and G2 over G1 was overall significantly lower compared to those of untreated control cells (Supplementary Figure 1g). Altogether, γH2AX showed a major increase in plasma-treated cells, which was almost fully abrogated in presence of cat or GSH during the treatment.

3.3. Intracellular Signaling and Apoptosis Govern Plasma-Induced γH2AX

The next question was to investigate intracellular signaling events upon plasma-induced H2AX phosphorylation. Many pathways leading to γH2AX have been unraveled [36], and we used several inhibitors in preliminary tests (Supplementary Figure S2af). One promising candidate was SB202190, a p38-MAPK inhibitor, which gave a significant decrease in γH2AX induction for all ROS but not for UV treatment (Figure 3(a)). Similar results were achieved with Z-VAD-FMK, a pan-caspase inhibitor (Figure 3(b)), but only a no-significant reduction was observed with KU59933 for plasma conditions (Supplementary Figure 2g), an ataxia telangiectasia mutated (ATM) inhibitor. This suggests that plasma-induced γH2AX induction is a result of apoptosis induction rather than of plasma-derived ROS directly traveling through the cells and eventually to the nucleus to confer DNA damage. To confirm functionality of Z-VAD-FMK on inhibiting apoptosis, we measured caspase 3 and 7 activity (Figure 2(c)). Quantification at 4 h (Figure 2(d)) and 24 h (Figure 2(e)) revealed a significant increase in nonapoptotic cells with all treatment modalities. The fact that UV-induced apoptosis but not H2AX phosphorylation was abrogated with Z-VAD-FMK suggests that γH2AX induction was regulated by pathways not related to apoptosis, which was not the case for ROS conditions. Finally, using confocal laser scanning microscopy, we confirmed that γH2AX foci were majorly present in apoptotic cells showing fragmented nuclei (Figure 3(f)). Taken together, plasma and ROS but not UV-induced γH2AX was largely dependent on stress (p38-MAPK) and apoptosis (caspase) signaling pathways.

3.4. Plasma-Mediated γH2AX Induction Does Not Correlate to DNA DSB-Related Micronuclei

To confirm that plasma and ROS-induced γH2AX foci were a consequence of ROS-induced stress signaling and apoptosis-induced DNA DSBs rather than markers of direct ROS-induced DNA DSBs, we performed a functional assay on DNA DSBs, the cytokinesis-block micronucleus (MN) assay. Sufficient numbers of DNA DSBs lead to replication errors during DNA synthesis in G2 phase cells, which converts into micronuclei formation as genotoxic endpoint measurement [46]. The addition of cytochalasin B blocks cytoplasmic division due to inhibition of network formation of actin filaments. The result is an enrichment of binucleated (G2 phase) cells (BNCs) that can be quantitatively assessed with different DNA stains (Supplementary Figure 3a). Imaging (Supplementary Figure 3b) and quantification of BNCs (Supplementary Figure 3c) confirmed this principle, and we decided to use draq5 for subsequent experiments. Another observation was that the plasma and UV treatment time utilized in experiments were too toxic in combination with cytochalasin B, leaving only few cells to analyze at 48 h posttreatment. Therefore, plasma and UV treatment time was reduced to 2.5 s and 24 s, respectively, which still generated significantly more γH2AX signal compared to untreated control (Figures 4(a) and 4(b)). By applying customized mathematical operands, several masks were develop to clearly identify and quantify BNCs as well as MN within the population of BNCs in an algorithm-based, unbiased fashion (Figure 4(c)) across millions of cells. Final analysis showed a significant increase in MN formation with UV but not plasma treatment. A chemical genotoxic agent (MMS) was installed as additional control in this experiment, which differed significantly from untreated cells (Figure 4(d)). As additional quality control, the average number of cells analyzed in these experiments was quantified and was similar among all conditions (Supplementary Figure 3d). In sum, MN formation correlated with γH2AX induction for UV treatment, which directly acts on cellular DNA, but not for plasma treatment, which acts on cells by generating exogenous ROS that subsequently diffuse to cells to exert their stress and apoptosis-inducing but not directly DNA-damaging function.

4. Discussion

DNA damage and the DNA damage response are important elements in medical treatment modalities, such as radiation therapy and chemotherapeutic drugs in several medical fields including in oncology [3]. For example, the anticancer drug doxorubicin can both induce DNA DSBs and generate ROS, leading to γH2AX induction [4749]. Cell metabolism, oxidative stress, and DNA damage are often intertwined and difficult to study independently, leading to the general assumption of γH2AX foci being a hallmark of DNA DSBs and damage. We here provide evidence that exogenous ROS added experimentally or generated with cold physical plasmas led to γH2AX induction only in case of apoptosis, and without long-term genotoxic effects. In such setting, the presence of γH2AX may be a consequence of low oxidative stress rather than an indicator of DNA damage. Recent data suggest γH2AX to even play in pivotal role in antioxidant defense signaling [50]. H2AX-knockout cells showed increase endogenous ROS levels and failed to activate the antioxidant response elements through nuclear factor E2-related factor 2, Nrf2 [51], along with mitochondrial damage [29].

In our study, we used UV-B radiation as positive control for γH2AX and micronuclei induction. In contrast to exogenous ROS (plasma, H2O2, or HOCl), occurrence of γH2AX was independent of the use of antioxidants and maximum in S-phase cells. The latter corroborates previous findings, where also a repression of γH2AX induction with PI3K inhibition using 5 mM of caffeine was found [52]. We did not find such decrease with PI3K inhibitors wortmannin and Ly294002, which may be due to different cell types and concentrations tested. Another study found ATR kinase to be the crucial determinant for UV-induced H2AX phosphorylation and confirmed our findings of maximum γH2AX induction at 2 h after treatment prior to onset of intermediate stages of apoptosis where γH2AX dramatically increases [53]. The ability of UV-B enhancing the frequency of MN in cells has been reported before [54, 55]. Interestingly, catalase decreased oxidation in UV-treated cells but not H2AX phosphorylation. UV generates ROS in the intracellular as well as extracellular compartment [56]. As the experimentally added catalase only acts in the extracellular compartment, a partial protection from oxidation was observed without protecting the DNA (intracellular compartment) from UV-mediated ROS and damage.

With exogenous ROS (plasma, H2O2, HOCl), we observed a strong dependence on p38-MAPK signaling and caspase activation in TK6 cells. This is in line with previous findings using oxaliplatin, an antitumor tumor drug leading to DNA DSBs, where pretreatment of cells with SB202190 (p38-MAPK inhibitor) and Z-VAD-FMK (caspase inhibitor) abrogated oxaliplatin-induced γH2AX induction and apoptosis in HCT116 cells [57]. In leukemia cells, it was reported that γH2AX (or blockage of H2AX phosphorylation by SB202190) expression sensitizes cells to apoptosis, suggesting a pivotal role of γH2AX in cell death signaling [58]. This is supported by findings with H2AX-knockout fibroblasts, which upon UV treatment activates caspase 3 but cannot activate caspase-activated DNAse (CAD), a crucial step in DNA fragmentation required for apoptosis [59]. Another form of regulated cell death (RCD) leading to widespread DNA fragmentation is parthanatos, but this mode of RCD is independent of apoptotic caspases [60]. Hence, parthanatos is not a main mechanism in our study because we observed apoptosis-induced and caspase-dependent DNA fragmentation. Hence, γH2AX is heavily intertwined in cell death signaling and our study supports this notion as caspase inhibition abrogated both H2AX phosphorylation and apoptosis.

Heavy H2AX phosphorylation indicates toxic numbers of DNA DSBs in, e.g., ionizing radiation, UV treatment, replication, and apoptosis. Contrasting radiation-induced DNA DSBs, we found γH2AX to be a consequence of ROS-induced apoptosis rather than its cause. T lymphocytes are very sensitive towards (plasma-induced) oxidative stress [6164]. This is due to (low-dose) ROS acting as proapoptotic and redox-signaling agents and not as toxic molecules per se [65]. In our study, e.g., few micromolar H2O2 on 250,000 cells were sufficient to induce cell death. The concentrations of, e.g., H2O2 used in many genotoxicity studies are 10-50-fold higher at lower absolute cell numbers [6668]. So far, only few studies in plasma medicine investigated genotoxicity in cells and tissues using non-γH2AX assays, and the once that have did not report mutagenic effects of plasma treatment. Using the hypoxanthine-guanine phosphoribosyl-transferase (HPRT) assay and the MN assay in V79 cells, plasma treatment failed to induce mutagenic effects when exposing cells to the plasma of the kINPen or its products [69], or when using another plasma source designed for medical application at microbicidal concentrations [70, 71]. Modulation of the feed gas composition of the kINPen yielded similar results [43]. Micronuclei have also been quantified in vivo in the hen’s egg model after treatment with cyclophosphamide or methotrexate (as positive control), or cold physical plasma generated with the kINPen. Results showed the absence of genotoxicity-indicating MN with plasma treatment compared to positive controls [72]. In human tissue exposed to cold physical plasma at short, intermediate, and long treatment times, an increase of γH2AX was not observed when compared to untreated control tissue [73]. Moreover, in a one-year follow-up of mice (human equivalent of 65 years) treated six times with plasma within 2 weeks, no occurrence of malignant lesions was observed anywhere in the body as shown by immunohistochemistry and PET-CT and MRI scan [74].

ROS can also induce lipid peroxidation [75], which can contribute to DNA damage. However, for H2O2—which gave large γH2AX signals—concentration reported for lipid peroxidation exceeds the one used in our study by 50-fold [76]. For lipid vesicles, H2O2 is ineffective in the absence of the Fenton reaction [77], even at concentration 5000 times of that used in our work [78]. For H2O2 treatment in our study, caspase inhibition decreased H2O2-incuded γH2AX to background levels, which argues against H2O2-induced lipid peroxidation as major mechanism for DNA DSBs. Moreover, if lipid peroxidation would have contributed to plasma-induced DNA damage, e.g., via UV-mediated photolysis and hydroxyl radical generation, addition of catalase would not have abrogated the increase observed in γH2AX.

Our results are of relevance for medical plasmas, while findings may be different for industrial plasma applications. Atmospheric and room temperature plasma (ARTP) has been recently described as tool for mutation breeding in microorganisms [7981]. Its efficacy seemed greater than that of several conventional methods, e.g., chemicals and UV radiation [82], and ARTP can also be combined with such methods [83]. As result, ARTP was found to increase production of, for instance, α-ketoglutaric acid [84], biofuel [85], polysaccharides [86, 87], arachidonic acid [88], erythritol [89], l-arginine [90], alkaline α-amylase [91, 92], d-lactic acid [93], lycopene [94], and carotenoids and lipids [95] in different types of microorganisms. However, it is important to mention that these plasma sources are not intended for medical applications. Hence, they may differ substantially in their geometry and power consumption, leading to enhanced UV radiation, ROS generation, and electrical discharges. In our study, we used a low-energy [96] and clinically effective [8, 97, 98] plasma jet complying to European regulations (e.g., generation of ozone, UV, and leak currents), which is not true for the majority of other plasma devices reported in experimental studies.

A limitation of our study is the lack of short-term kinetic measurements of γH2AX and (onset of) apoptosis. Moreover, γH2AX foci expand over time [99], making it difficult to distinguish between many foci with low intensity vs. few foci with high intensity (and anything in between) in our flow cytometry data. Additionally, other proteins including Nbs1, 53BP1, and Brca1 are recruited to and hence mark DNA DSBs [31], which may be investigated in future studies.

5. Conclusion

Cold physical plasma-induced γH2AX marks DNA DSBs as a consequence of oxidative stress and apoptosis in vitro. Upon blocking apoptosis and p38 MAPK signaling, increased γH2AX with plasma treatment was abolished, arguing that H2AX phosphorylation is a secondary event in redox or apoptotic signaling rather than a primary consequence of direct ROS-mediated DNA damage. In contrast to UV treatment, exposure to plasma did not correlate with long-lasting genotoxic effects as indicated using the micronucleus assay. Hence, γH2AX measurements in plasma medical research should be interpreted with care, keeping in mind the pleiotropic roles of this molecule in redox sensing and apoptotic pathways.

Data Availability

The data used to support the findings of this study are available from the corresponding author upon request.

Conflicts of Interest

The authors declare that there is no conflict of interest regarding the publication of this paper.


This work was funded by the German Federal Ministry of Education and Research (BMBF), grant numbers 03Z22DN11 and 03Z22DN12. C.S.S. received funding from the Gerhard-Domagk Foundation.

Supplementary Materials

Supplementary Figure S1: (a) metabolic activity in TK6 cells at 24 h, 48 h, and 72 h after exposure to γH2AX-inducing agents; (b) quantification of nonterminally dead (DAPI-) TK6 cells at 6 h after exposure to different concentrations or treatment times of γH2AX-inducing agents; (c) dilution series of anti-γH2AX antibody in control and UV-treated TK6 cells to obtain optimal antibody concentration; (d) kinetic experiment of γH2AX intensity in control or plasma and UV-treated TK6 cells; (e) γH2AX intensity in each cell cycle phase of untreated cells incubated with vehicle, catalase, and GSH; (f) incubation with antioxidant NAC increased γH2AX intensity with all treatments as well as in untreated cells and therefore was not used in this study. Supplementary Figure S2: serial dilutions of inhibitors. (a) SB202190 (p38-MAPK inhibitor) was used in the study (Figure 3(a)); (b) SP600125 (JNK inhibitor) disqualified due to the increase of γH2AX in untreated cells upon incubation with the drug; (c) Ly294002 (PI3K inhibitor) did not decrease γH2AX in plasma-treated cells; (d) wortmannin (PI3K inhibitor) disqualified due to the increase of γH2AX in untreated cells upon incubation with the drug; (e) Z-VAD-FMK (pan-caspase inhibitor) was used in the study (Figure 3(b)); (f) KU55933 (ATM-kinase inhibitor) showed a small decrease in γH2AX, which (g) was not significant with any treatment in three independent repeats. Supplementary Figure S3: optimization of the micronucleus assay. (a) cell cycle analysis of untreated and treated (cytochalasin B for 24 h) TK6 cells with different DNA-binding dyes; (b) representative images of cells in brightfield (Ch05 or Ch01) and DNA-binding dye (Ch1 or Ch5) showing binucleated cells (BNCs); (c) quantification of binucleated cells stained with four different DNA-binding dyes via a complex software algorithm designed to create a specific set of masks to BNCs as described before [1], we aimed at a low amount of BNCs to obtain a high specificity for micronuclei leading to the choice of draq5 for main experiments; (d) mean total count of cells in samples from each condition. (Supplementary Materials)


  1. S. H. Macphail, J. P. BanÁth, T. Y. Yu, E. H. M. Chu, H. Lambur, and P. L. Olive, “Expression of phosphorylated histone H2AX in cultured cell lines following exposure to X-rays,” International Journal of Radiation Biology, vol. 79, no. 5, article 12943243, pp. 351–359, 2003. View at: Publisher Site | Google Scholar
  2. E. P. Rogakou, D. R. Pilch, A. H. Orr, V. S. Ivanova, and W. M. Bonner, “DNA double-stranded breaks induce histone H2AX phosphorylation on serine 139,” Journal of Biological Chemistry, vol. 273, no. 10, pp. 5858–5868, 1998. View at: Publisher Site | Google Scholar
  3. L.-J. Mah, A. El-Osta, and T. C. Karagiannis, “γH2AX: a sensitive molecular marker of DNA damage and repair,” Leukemia, vol. 24, no. 4, pp. 679–686, 2010. View at: Publisher Site | Google Scholar
  4. D. Yan, J. H. Sherman, and M. Keidar, “Cold atmospheric plasma, a novel promising anti-cancer treatment modality,” Oncotarget, vol. 8, no. 9, pp. 15977–15995, 2017. View at: Publisher Site | Google Scholar
  5. S. Bekeschus, K. Rodder, B. Fregin et al., “Toxicity and immunogenicity in murine melanoma following exposure to physical plasma-derived oxidants,” Oxidative Medicine and Cellular Longevity, vol. 2017, Article ID 4396467, 12 pages, 2017. View at: Publisher Site | Google Scholar
  6. A. Lin, Y. Gorbanev, J. de Backer et al., “Non-thermal plasma as a unique delivery system of short-lived reactive oxygen and nitrogen species for immunogenic cell death in melanoma cells,” Advanced Science, vol. 6, no. 6, p. 1802062, 2019. View at: Publisher Site | Google Scholar
  7. G. Pasqual-Melo, R. K. Gandhirajan, I. Stoffels, and S. Bekeschus, “Targeting malignant melanoma with physical plasmas,” Clinical Plasma Medicine, vol. 10, pp. 1–8, 2018. View at: Publisher Site | Google Scholar
  8. H.-R. Metelmann, C. Seebauer, V. Miller et al., “Clinical experience with cold plasma in the treatment of locally advanced head and neck cancer,” Clinical Plasma Medicine, vol. 9, pp. 6–13, 2018. View at: Publisher Site | Google Scholar
  9. S. Reuter, T. von Woedtke, and K. D. Weltmann, “The kINPen—a review on physics and chemistry of the atmospheric pressure plasma jet and its applications,” Journal of Physics D: Applied Physics, vol. 51, no. 23, p. 233001, 2018. View at: Publisher Site | Google Scholar
  10. S. Bekeschus, J. Kolata, C. Winterbourn et al., “Hydrogen peroxide: a central player in physical plasma-induced oxidative stress in human blood cells,” Free Radical Research, vol. 48, no. 5, pp. 542–549, 2014. View at: Publisher Site | Google Scholar
  11. K. P. Arjunan, G. Friedman, A. Fridman, and A. M. Clyne, “Non-thermal dielectric barrier discharge plasma induces angiogenesis through reactive oxygen species,” Journal of The Royal Society Interface, vol. 9, no. 66, pp. 147–157, 2012. View at: Publisher Site | Google Scholar
  12. D. B. Graves, “The emerging role of reactive oxygen and nitrogen species in redox biology and some implications for plasma applications to medicine and biology,” Journal of Physics D: Applied Physics, vol. 45, no. 26, p. 263001, 2012. View at: Publisher Site | Google Scholar
  13. S. Arndt, E. Wacker, Y. F. Li et al., “Cold atmospheric plasma, a new strategy to induce senescence in melanoma cells,” Experimental Dermatology, vol. 22, no. 4, pp. 284–289, 2013. View at: Publisher Site | Google Scholar
  14. J. W. Chang, S. U. Kang, Y. S. Shin et al., “Non-thermal atmospheric pressure plasma induces apoptosis in oral cavity squamous cell carcinoma: Involvement of DNA-damage-triggering sub-G1 arrest via the ATM/p53 pathway,” Arch Biochem Biophys, vol. 545, pp. 133–140, 2014. View at: Publisher Site | Google Scholar
  15. F. Judée, C. Fongia, B. Ducommun, M. Yousfi, V. Lobjois, and N. Merbahi, “Short and long time effects of low temperature plasma activated media on 3D multicellular tumor spheroids,” Scientific Reports, vol. 6, no. 1, 2016. View at: Publisher Site | Google Scholar
  16. N. Kaushik, N. Uddin, G. B. Sim et al., “Responses of solid tumor cells in DMEM to reactive oxygen species generated by non-thermal plasma and chemically induced ROS systems,” Scientific Reports, vol. 5, no. 1, 2015. View at: Publisher Site | Google Scholar
  17. J. M. Plewa, M. Yousfi, C. Frongia et al., “Low-temperature plasma-induced antiproliferative effects on multi-cellular tumor spheroids,” New Journal of Physics, vol. 16, no. 4, 2014. View at: Publisher Site | Google Scholar
  18. S. K. Sagwal, G. Pasqual-Melo, Y. Bodnar, R. K. Gandhirajan, and S. Bekeschus, “Combination of chemotherapy and physical plasma elicits melanoma cell death via upregulation of SLC22A16,” Cell Death & Disease, vol. 9, no. 12, 2018. View at: Publisher Site | Google Scholar
  19. R. Sensenig, S. Kalghatgi, E. Cerchar et al., “Non-thermal plasma induces apoptosis in melanoma cells via production of intracellular reactive oxygen species,” Annals of Biomedical Engineering, vol. 39, no. 2, pp. 674–687, 2011. View at: Publisher Site | Google Scholar
  20. H. Jablonowski, J. Santos Sousa, K. D. Weltmann, K. Wende, and S. Reuter, “Quantification of the ozone and singlet delta oxygen produced in gas and liquid phases by a non-thermal atmospheric plasma with relevance for medical treatment,” Scientific Reports, vol. 8, no. 1, p. 12195, 2018. View at: Publisher Site | Google Scholar
  21. H. Jablonowski, A. Schmidt-Bleker, K. D. Weltmann, T. von Woedtke, and K. Wende, “Non-touching plasma-liquid interaction - where is aqueous nitric oxide generated?” Physical Chemistry Chemical Physics, vol. 20, no. 39, pp. 25387–25398, 2018. View at: Publisher Site | Google Scholar
  22. H. Jablonowski and T. von Woedtke, “Research on plasma medicine-relevant plasma–liquid interaction: what happened in the past five years?” Clinical Plasma Medicine, vol. 3, no. 2, pp. 42–52, 2015. View at: Publisher Site | Google Scholar
  23. M. B. Hampton and K. M. O'Connor, “Peroxiredoxins and the regulation of cell death,” Molecules and Cells, vol. 39, no. 1, pp. 72–76, 2016. View at: Publisher Site | Google Scholar
  24. C. Gu, J. Luo, X. Lu et al., “REV7 confers radioresistance of esophagus squamous cell carcinoma by recruiting PRDX2,” Cancer Science, vol. 110, no. 3, pp. 962–972, 2019. View at: Publisher Site | Google Scholar
  25. W. M. Bonner, C. E. Redon, J. S. Dickey et al., “γH2AX and cancer,” Nature Reviews Cancer, vol. 8, no. 12, pp. 957–967, 2008. View at: Publisher Site | Google Scholar
  26. O. A. Sedelnikova, C. E. Redon, J. S. Dickey, A. J. Nakamura, A. G. Georgakilas, and W. M. Bonner, “Role of oxidatively induced DNA lesions in human pathogenesis,” Mutation Research/Reviews in Mutation Research, vol. 704, no. 1-3, pp. 152–159, 2010. View at: Publisher Site | Google Scholar
  27. P. Rybak, A. Hoang, L. Bujnowicz et al., “Low level phosphorylation of histone H2AX on serine 139 (γH2AX) is not associated with DNA double-strand breaks,” Oncotarget, vol. 7, no. 31, pp. 49574–49587, 2016. View at: Publisher Site | Google Scholar
  28. Y. Ichijima, R. Sakasai, N. Okita, K. Asahina, S. Mizutani, and H. Teraoka, “Phosphorylation of histone H2AX at M phase in human cells without DNA damage response,” Biochemical and Biophysical Research Communications, vol. 336, no. 3, pp. 807–812, 2005. View at: Publisher Site | Google Scholar
  29. J. H. Jeong, Y. Cheol Kang, Y. Piao, S. Kang, and Y. K. Pak, “miR-24-mediated knockdown of H2AX damages mitochondria and the insulin signaling pathway,” Experimental & Molecular Medicine, vol. 49, no. 4, p. e313, 2017. View at: Publisher Site | Google Scholar
  30. T. Tanaka, X. Huang, H. D. Halicka et al., “Cytometry of ATM activation and histone H2AX phosphorylation to estimate extent of DNA damage induced by exogenous agents,” Cytometry Part A, vol. 71A, no. 9, pp. 648–661, 2007. View at: Publisher Site | Google Scholar
  31. A. Celeste, O. Fernandez-Capetillo, M. J. Kruhlak et al., “Histone H2AX phosphorylation is dispensable for the initial recognition of DNA breaks,” Nature Cell Biology, vol. 5, no. 7, pp. 675–679, 2003. View at: Publisher Site | Google Scholar
  32. M. A. Kang, E. Y. So, A. L. Simons, D. R. Spitz, and T. Ouchi, “DNA damage induces reactive oxygen species generation through the H2AX-Nox1/Rac1 pathway,” Cell Death & Disease, vol. 3, no. 1, p. e249, 2012. View at: Publisher Site | Google Scholar
  33. S. Burma, B. P. Chen, M. Murphy, A. Kurimasa, and D. J. Chen, “ATM phosphorylates histone H2AX in response to DNA double-strand breaks,” Journal of Biological Chemistry, vol. 276, no. 45, pp. 42462–42467, 2001. View at: Publisher Site | Google Scholar
  34. B. Mukherjee, C. Kessinger, J. Kobayashi et al., “DNA-PK phosphorylates histone H2AX during apoptotic DNA fragmentation in mammalian cells,” DNA Repair, vol. 5, no. 5, pp. 575–590, 2006. View at: Publisher Site | Google Scholar
  35. Z. Guo, R. Deshpande, and T. T. Paull, “ATM activation in the presence of oxidative stress,” Cell Cycle, vol. 9, no. 24, pp. 4805–4811, 2010. View at: Publisher Site | Google Scholar
  36. A. Sharma, K. Singh, and A. Almasan, “Histone H2AX phosphorylation: a marker for DNA damage,” Methods in Molecular Biology, vol. 920, pp. 613–626, 2012. View at: Publisher Site | Google Scholar
  37. M. Lukamowicz, M. Kirsch-Volders, W. Suter, and A. Elhajouji, “In vitro primary human lymphocyte flow cytometry based micronucleus assay: simultaneous assessment of cell proliferation, apoptosis and MN frequency,” Mutagenesis, vol. 26, no. 6, pp. 763–770, 2011. View at: Publisher Site | Google Scholar
  38. M. Lukamowicz, K. Woodward, M. Kirsch-Volders, W. Suter, and A. Elhajouji, “A flow cytometry based in vitro micronucleus assay in TK6 cells-Validation using early stage pharmaceutical development compounds,” Environmental and Molecular Mutagenesis, vol. 52, no. 5, pp. 363–372, 2011. View at: Publisher Site | Google Scholar
  39. S. Bekeschus, A. Schmidt, K.-D. Weltmann, and T. von Woedtke, “The plasma jet kINPen – a powerful tool for wound healing,” Clinical Plasma Medicine, vol. 4, no. 1, pp. 19–28, 2016. View at: Publisher Site | Google Scholar
  40. S. Bekeschus, A. Schmidt, F. Niessner, T. Gerling, K. D. Weltmann, and K. Wende, “Basic research in plasma medicine - a throughput approach from liquids to cells,” Journal of Visualized Experiments, no. 129, 2017. View at: Publisher Site | Google Scholar
  41. A. Budiyanto, N. U. Ahmed, A. Wu et al., “Protective effect of topically applied olive oil against photocarcinogenesis following UVB exposure of mice,” Carcinogenesis, vol. 21, no. 11, pp. 2085–2090, 2000. View at: Publisher Site | Google Scholar
  42. M. Kirsch-Volders, G. Plas, A. Elhajouji et al., “The in vitro MN assay in 2011: origin and fate, biological significance, protocols, high throughput methodologies and toxicological relevance,” Archives of Toxicology, vol. 85, no. 8, pp. 873–899, 2011. View at: Publisher Site | Google Scholar
  43. S. Bekeschus, A. Schmidt, A. Kramer et al., “High throughput image cytometry micronucleus assay to investigate the presence or absence of mutagenic effects of cold physical plasma,” Environmental and Molecular Mutagenesis, vol. 59, no. 4, pp. 268–277, 2018. View at: Publisher Site | Google Scholar
  44. S. Bekeschus, T. von Woedtke, A. Kramer, K.-D. Weltmann, and K. Masur, “Cold physical plasma treatment alters redox balance in human immune cells,” Plasma Medicine, vol. 3, no. 4, pp. 267–278, 2013. View at: Publisher Site | Google Scholar
  45. M. Lobrich, A. Shibata, A. Beucher et al., “γH2AX foci analysis for monitoring DNA double-strand break repair: Strengths, limitations and optimization,” Cell Cycle, vol. 9, no. 4, pp. 662–669, 2010. View at: Publisher Site | Google Scholar
  46. G. P. Watters, D. J. Smart, J. S. Harvey, and C. A. Austin, “H2AX phosphorylation as a genotoxicity endpoint,” Mutation Research/Genetic Toxicology and Environmental Mutagenesis, vol. 679, no. 1-2, pp. 50–58, 2009. View at: Publisher Site | Google Scholar
  47. E. U. Kurz, P. Douglas, and S. P. Lees-Miller, “Doxorubicin activates ATM-dependent phosphorylation of multiple downstream targets in part through the generation of reactive oxygen species,” Journal of Biological Chemistry, vol. 279, no. 51, pp. 53272–53281, 2004. View at: Publisher Site | Google Scholar
  48. S. Zhang, X. Liu, T. Bawa-Khalfe et al., “Identification of the molecular basis of doxorubicin-induced cardiotoxicity,” Nature Medicine, vol. 18, no. 11, pp. 1639–1642, 2012. View at: Publisher Site | Google Scholar
  49. P. K. Singal and N. Iliskovic, “Doxorubicin-induced cardiomyopathy,” New England Journal of Medicine, vol. 339, no. 13, pp. 900–905, 1998. View at: Publisher Site | Google Scholar
  50. A. Schmidt, S. Bekeschus, K. Jarick, S. Hasse, T. von Woedtke, and K. Wende, “Cold physical plasma modulates p53 and mitogen-activated protein kinase signaling in keratinocytes,” Oxidative Medicine and Cellular Longevity, vol. 2019, Article ID 7017363, 16 pages, 2019. View at: Publisher Site | Google Scholar
  51. U. Weyemi, B. D. Paul, A. M. Snowman et al., “Histone H2AX deficiency causes neurobehavioral deficits and impaired redox homeostasis,” Nature Communications, vol. 9, no. 1, 2018. View at: Publisher Site | Google Scholar
  52. H. D. Halicka, X. Huang, F. Traganos, M. A. King, W. Dai, and Z. Darzynkiewicz, “Histone H2AX phosphorylation after cell irradiation with UV-B: relationship to cell cycle phase and induction of apoptosis,” Cell Cycle, vol. 4, no. 2, pp. 338–344, 2004. View at: Publisher Site | Google Scholar
  53. S. Hanasoge and M. Ljungman, “H2AX phosphorylation after UV irradiation is triggered by DNA repair intermediates and is mediated by the ATR kinase,” Carcinogenesis, vol. 28, no. 11, pp. 2298–2304, 2007. View at: Publisher Site | Google Scholar
  54. D. Bettega, P. Calzolari, L. Doneda, F. Belloni, L. Tallone, and J. L. Redpath, “Differential effectiveness of solar UVB subcomponents in causing cell death, oncogenic transformation and micronucleus induction in human hybrid cells,” International Journal of Radiation Biology, vol. 79, no. 3, pp. 211–216, 2003. View at: Publisher Site | Google Scholar
  55. A. Ferahbas, H. Donmez-Altuntas, Z. Hamurcu, E. Aktas, and S. Utas, “Micronucleus evaluation in mitogen-stimulated lymphocytes of narrow-band (311 nm TL01) UVB-treated patients,” Photodermatology, Photoimmunology and Photomedicine, vol. 20, no. 2, pp. 81–85, 2004. View at: Publisher Site | Google Scholar
  56. T. Herrling, K. Jung, and J. Fuchs, “Measurements of UV-generated free radicals/reactive oxygen species (ROS) in skin,” Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, vol. 63, no. 4, pp. 840–845, 2006. View at: Publisher Site | Google Scholar
  57. S. J. Chiu, J. I. Chao, Y. J. Lee, and T. S. Hsu, “Regulation of gamma-H2AX and securin contribute to apoptosis by oxaliplatin via a p38 mitogen-activated protein kinase-dependent pathway in human colorectal cancer cells,” Toxicology Letters, vol. 179, no. 2, pp. 63–70, 2008. View at: Publisher Site | Google Scholar
  58. Y. Dong, M. Xiong, L. Duan et al., “H2AX phosphorylation regulated by p38 is involved in Bim expression and apoptosis in chronic myelogenous leukemia cells induced by imatinib,” Apoptosis, vol. 19, no. 8, pp. 1281–1292, 2014. View at: Publisher Site | Google Scholar
  59. C. Lu, F. Zhu, Y. Y. Cho et al., “Cell apoptosis: requirement of H2AX in DNA ladder formation, but not for the activation of caspase-3,” Molecular Cell, vol. 23, no. 1, pp. 121–132, 2006. View at: Publisher Site | Google Scholar
  60. L. Galluzzi, I. Vitale, S. A. Aaronson et al., “Molecular mechanisms of cell death: recommendations of the Nomenclature Committee on Cell Death 2018,” Cell Death & Differentiation, vol. 25, no. 3, pp. 486–541, 2018. View at: Publisher Site | Google Scholar
  61. L. Bundscherer, K. Wende, K. Ottmuller et al., “Impact of non-thermal plasma treatment on MAPK signaling pathways of human immune cell lines,” Immunobiology, vol. 218, no. 10, pp. 1248–1255, 2013. View at: Publisher Site | Google Scholar
  62. S. Bekeschus, J. Kolata, A. Muller et al., “Differential viability of eight human blood mononuclear cell subpopulations after plasma treatment,” Plasma Medicine, vol. 3, no. 1-2, pp. 1–13, 2013. View at: Publisher Site | Google Scholar
  63. L. Bundscherer, S. Bekeschus, H. Tresp et al., “Viability of human blood leukocytes compared with their respective cell lines after plasma treatment,” Plasma Medicine, vol. 3, no. 1-2, pp. 71–80, 2013. View at: Publisher Site | Google Scholar
  64. S. Bekeschus, K. Rödder, A. Schmidt et al., “Cold physical plasma selects for specific T helper cell subsets with distinct cells surface markers in a caspase-dependent and NF-κB-independent manner,” Plasma Processes and Polymers, vol. 13, no. 12, pp. 1144–1150, 2016. View at: Publisher Site | Google Scholar
  65. P. S. Hole, J. Zabkiewicz, C. Munje et al., “Overproduction of NOX-derived ROS in AML promotes proliferation and is associated with defective oxidative stress signaling,” Blood, vol. 122, no. 19, pp. 3322–3330, 2013. View at: Publisher Site | Google Scholar
  66. D. Slamenova, K. Kozics, L. Hunakova, M. Melusova, J. Navarova, and E. Horvathova, “Comparison of biological processes induced in HepG2 cells by tert-butyl hydroperoxide (t-BHP) and hydroperoxide (H2O2): the influence of carvacrol,” Mutation Research/Genetic Toxicology and Environmental Mutagenesis, vol. 757, no. 1, pp. 15–22, 2013. View at: Publisher Site | Google Scholar
  67. N. M. Machado, A. B. Ribeiro, H. D. Nicolella et al., “Usnic acid attenuates genomic instability in Chinese hamster ovary (CHO) cells as well as chemical-induced preneoplastic lesions in rat colon,” Journal of Toxicology and Environmental Health, Part A, vol. 82, no. 6, pp. 401–410, 2019. View at: Publisher Site | Google Scholar
  68. J. Feruszova, P. Imreova, K. Bodnarova et al., “Photoactivated hypericin is not genotoxic,” General physiology and biophysics, vol. 35, no. 02, pp. 223–230, 2016. View at: Publisher Site | Google Scholar
  69. K. Wende, S. Bekeschus, A. Schmidt et al., “Risk assessment of a cold argon plasma jet in respect to its mutagenicity,” Mutation Research/Genetic Toxicology and Environmental Mutagenesis, vol. 798-799, pp. 48–54, 2016. View at: Publisher Site | Google Scholar
  70. V. Boxhammer, Y. F. Li, J. Koritzer et al., “Investigation of the mutagenic potential of cold atmospheric plasma at bactericidal dosages,” Mutation Research/Genetic Toxicology and Environmental Mutagenesis, vol. 753, no. 1, pp. 23–28, 2013. View at: Publisher Site | Google Scholar
  71. T. Maisch, A. K. Bosserhoff, P. Unger et al., “Investigation of toxicity and mutagenicity of cold atmospheric argon plasma,” Environmental and Molecular Mutagenesis, vol. 58, no. 3, pp. 172–177, 2017. View at: Publisher Site | Google Scholar
  72. S. Kluge, S. Bekeschus, C. Bender et al., “Investigating the mutagenicity of a cold argon-plasma jet in an HET-MN model,” PLoS One, vol. 11, no. 9, 2016. View at: Publisher Site | Google Scholar
  73. S. Hasse, O. Hahn, S. Kindler, T. von Woedtke, H.-R. Metelmann, and K. Masur, “Atmospheric pressure plasma jet application on human oral mucosa modulates tissue regeneration,” Plasma Medicine, vol. 4, no. 1-4, pp. 117–129, 2014. View at: Publisher Site | Google Scholar
  74. A. Schmidt, T. Woedtke, J. Stenzel et al., “One year follow-up risk assessment in SKH-1 mice and wounds treated with an argon plasma jet,” International Journal of Molecular Sciences, vol. 18, no. 4, p. 868, 2017. View at: Publisher Site | Google Scholar
  75. E. E. Farmer and M. J. Mueller, “ROS-mediated lipid peroxidation and RES-activated signaling,” Annual Review of Plant Biology, vol. 64, no. 1, pp. 429–450, 2013. View at: Publisher Site | Google Scholar
  76. K. Kannan and S. K. Jain, “Effect of vitamin B6 on oxygen radicals, mitochondrial membrane potential, and lipid peroxidation in H2O2-treated U937 monocytes,” Free Radical Biology and Medicine, vol. 36, no. 4, pp. 423–428, 2004. View at: Publisher Site | Google Scholar
  77. G. Minotti and S. D. Aust, “The requirement for iron (III) in the initiation of lipid peroxidation by iron (II) and hydrogen peroxide,” J Biol Chem, vol. 262, pp. 1098–1104, 1987. View at: Google Scholar
  78. M. Iqbal, Y. Okazaki, and S. Okada, “In vitro curcumin modulates ferric nitrilotriacetate (Fe-NTA) and hydrogen peroxide (H2O2)-induced peroxidation of microsomal membrane lipids and DNA damage,” Teratogenesis, Carcinogenesis, and Mutagenesis, vol. 23, no. S1, pp. 151–160, 2003. View at: Publisher Site | Google Scholar
  79. X. Zhang, X. F. Zhang, H. P. Li et al., “Atmospheric and room temperature plasma (ARTP) as a new powerful mutagenesis tool,” Applied Microbiology and Biotechnology, vol. 98, no. 12, pp. 5387–5396, 2014. View at: Publisher Site | Google Scholar
  80. C. Ottenheim, M. Nawrath, and J. C. Wu, “Microbial mutagenesis by atmospheric and room-temperature plasma (ARTP): the latest development,” Bioresources and Bioprocessing, vol. 5, no. 1, 2018. View at: Publisher Site | Google Scholar
  81. M. Fang, L. Jin, C. Zhang et al., “Rapid mutation of Spirulina platensis by a new mutagenesis system of atmospheric and room temperature plasmas (ARTP) and generation of a mutant library with diverse phenotypes,” PLoS One, vol. 8, no. 10, p. e77046, 2013. View at: Publisher Site | Google Scholar
  82. X. Zhang, C. Zhang, Q. Q. Zhou et al., “Quantitative evaluation of DNA damage and mutation rate by atmospheric and room-temperature plasma (ARTP) and conventional mutagenesis,” Applied Microbiology and Biotechnology, vol. 99, no. 13, pp. 5639–5646, 2015. View at: Publisher Site | Google Scholar
  83. B. Zhao, Y. Li, C. Li, H. Yang, and W. Wang, “Enhancement of Schizochytrium DHA synthesis by plasma mutagenesis aided with malonic acid and zeocin screening,” Applied Microbiology and Biotechnology, vol. 102, no. 5, pp. 2351–2361, 2018. View at: Publisher Site | Google Scholar
  84. W. Zeng, G. Du, J. Chen, J. Li, and J. Zhou, “A high-throughput screening procedure for enhancing α-ketoglutaric acid production in Yarrowia lipolytica by random mutagenesis,” Process Biochemistry, vol. 50, no. 10, pp. 1516–1522, 2015. View at: Publisher Site | Google Scholar
  85. F. Qi, Y. Kitahara, Z. Wang, X. Zhao, W. Du, and D. Liu, “Novel mutant strains ofRhodosporidium toruloidesby plasma mutagenesis approach and their tolerance for inhibitors in lignocellulosic hydrolyzate,” Journal of Chemical Technology & Biotechnology, vol. 89, no. 5, pp. 735–742, 2014. View at: Publisher Site | Google Scholar
  86. B. Liu, Z. Sun, X. Ma et al., “Mutation breeding of extracellular polysaccharide-producing microalga Crypthecodinium cohnii by a novel mutagenesis with atmospheric and room temperature plasma,” International Journal of Molecular Sciences, vol. 16, no. 12, pp. 8201–8212, 2015. View at: Publisher Site | Google Scholar
  87. L. Zhu, D. Wu, H. Zhang et al., “Effects of atmospheric and room temperature plasma (ARTP) mutagenesis on physicochemical characteristics and immune activity in vitro of Hericium erinaceus polysaccharides,” Molecules, vol. 24, no. 2, p. 262, 2019. View at: Publisher Site | Google Scholar
  88. X. Li, R. Liu, J. Li et al., “Enhanced arachidonic acid production from Mortierella alpina combining atmospheric and room temperature plasma (ARTP) and diethyl sulfate treatments,” Bioresource Technology, vol. 177, pp. 134–140, 2015. View at: Publisher Site | Google Scholar
  89. X. Liu, J. Lv, J. Xu et al., “Erythritol production by Yarrowia lipolytica mutant strain M53 generated through atmospheric and room temperature plasma mutagenesis,” Food Science and Biotechnology, vol. 26, no. 4, pp. 979–986, 2017. View at: Publisher Site | Google Scholar
  90. G. Cheng, J. Xu, X. Xia et al., “Breeding L-arginine-producing strains by a novel mutagenesis method: atmospheric and room temperature plasma (ARTP),” Preparative Biochemistry and Biotechnology, vol. 46, no. 5, pp. 509–516, 2016. View at: Publisher Site | Google Scholar
  91. Y. Ma, H. Yang, X. Chen et al., “Significantly improving the yield of recombinant proteins in Bacillus subtilis by a novel powerful mutagenesis tool (ARTP): Alkaline α-amylase as a case study,” Protein Expression and Purification, vol. 114, pp. 82–88, 2015. View at: Publisher Site | Google Scholar
  92. Y. Ma, W. Shen, X. Chen et al., “Significantly enhancing recombinant alkaline amylase production in Bacillus subtilis by integration of a novel mutagenesis-screening strategy with systems-level fermentation optimization,” Journal of Biological Engineering, vol. 10, no. 1, 2016. View at: Publisher Site | Google Scholar
  93. J. Sun, Y. Wang, B. Wu, Z. Bai, and B. He, “Enhanced production of d-lactic acid by Sporolactobacillus sp.Y2-8 mutant generated by atmospheric and room temperature plasma,” Biotechnology and Applied Biochemistry, vol. 62, no. 2, pp. 287–292, 2015. View at: Publisher Site | Google Scholar
  94. W. Qiang, F. Ling-ran, W. Luo et al., “Mutation breeding of lycopene-producing strain Blakeslea trispora by a novel atmospheric and room temperature plasma (ARTP),” Applied Biochemistry and Biotechnology, vol. 174, no. 1, pp. 452–460, 2014. View at: Publisher Site | Google Scholar
  95. C. Zhang, H. Shen, X. Zhang et al., “Combined mutagenesis of Rhodosporidium toruloides for improved production of carotenoids and lipids,” Biotechnology Letters, vol. 38, no. 10, pp. 1733–1738, 2016. View at: Publisher Site | Google Scholar
  96. J. Winter, R. Brandenburg, and K. D. Weltmann, “Atmospheric pressure plasma jets: an overview of devices and new directions,” Plasma Sources Science and Technology, vol. 24, no. 6, p. 064001, 2015. View at: Publisher Site | Google Scholar
  97. C. Ulrich, F. Kluschke, A. Patzelt et al., “Clinical use of cold atmospheric pressure argon plasma in chronic leg ulcers: a pilot study,” Journal of Wound Care, vol. 24, no. 5, pp. 196–203, 2015. View at: Publisher Site | Google Scholar
  98. M. Schuster, C. Seebauer, R. Rutkowski et al., “Visible tumor surface response to physical plasma and apoptotic cell kill in head and neck cancer,” Journal of Cranio-Maxillofacial Surgery, vol. 44, no. 9, pp. 1445–1452, 2016. View at: Publisher Site | Google Scholar
  99. D. M. S. Pinto and A. Flaus, “Structure and function of histone H2AX,” in Subcellular Biochemistry, vol. 50, Springer, Dordrecht, 2010. View at: Publisher Site | Google Scholar

Copyright © 2019 Sander Bekeschus et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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