Topological DNA damage, telomere attrition and T cell senescence during chronic viral infections
Immunity & Ageingvolume 16, Article number: 12 (2019)
T cells play a key role in controlling viral infections; however, the underlying mechanisms regulating their functions during human viral infections remain incompletely understood. Here, we used CD4 T cells derived from individuals with chronic viral infections or healthy T cells treated with camptothecin (CPT) - a topoisomerase I (Top 1) inhibitor - as a model to investigate the role of DNA topology in reprogramming telomeric DNA damage responses (DDR) and remodeling T cell functions.
We demonstrated that Top 1 protein expression and enzyme activity were significantly inhibited, while the Top 1 cleavage complex (TOP1cc) was trapped in genomic DNA, in T cells derived from individuals with chronic viral (HCV, HBV, or HIV) infections. Top 1 inhibition by CPT treatment of healthy CD4 T cells caused topological DNA damage, telomere attrition, and T cell apoptosis or dysfunction via inducing Top1cc accumulation, PARP1 cleavage, and failure in DNA repair, thus recapitulating T cell dysregulation in the setting of chronic viral infections. Moreover, T cells from virally infected subjects with inhibited Top 1 activity were more vulnerable to CPT-induced topological DNA damage and cell apoptosis, indicating an important role for Top 1 in securing DNA integrity and cell survival.
These findings provide novel insights into the molecular mechanisms for immunomodulation by chronic viral infections via disrupting DNA topology to induce telomeric DNA damage, T cell senescence, apoptosis and dysfunction. As such, restoring the impaired DNA topologic machinery may offer a new strategy for maintaining T cell function against human viral diseases.
T cells play a crucial role in defending the host from pathogenic infections; however, the precise mechanisms dampening their responses during chronic viral infections remain incompletely understood. In studying the role of T cell dysregulation in viral persistence in humans, we and others have previously shown that chronic viral infections can cause premature T cell aging and immune senescence, as evidenced by the overexpression of aging markers, such as p16ink4a, p21cip1, killer cell lectin-like receptor superfamily G 1 (KLRG1), and dual specific phosphatase 6 (DUSP6), the decline of aging-associated microRNA181 (miR181), and the particularly shortened telomeres, indicating excessive cell proliferative turnover or inadequate telomere maintenance during chronic viral infections [1,2,3,4,5,6,7,8,9,10,11,12,13]. Telomeres are repeating hexameric DNA sequences (TTAGGG) that are found at the chromosome ends in association with a complex of shelterin proteins . Telomere integrity is a key feature of linear chromosomes that preserve genome stability and function. Conversely, telomere attrition is a hallmark of cell senescence that drives cell dysfunction and apoptosis [15,16,17].
The intertwined nature of two complementary DNA structures is a unique feature of chromosomes to ensure the storage and transmission of valuable genetic codes. However, almost all types of DNA activities, including gene replication, transcription, and recombination, lead to topological entanglements that must be resolved to ensure normal DNA transactions and subsequent cell functions . In order to prevent and correct these types of topological problems, topoisomerases (enzymes that modulate the topology of DNA) bind to DNA and cut the phosphate backbone of either one or both DNA strands by creating transient breaks in the chromosomes . This intermediate break allows the DNA to be untangled or unwound so as to exert genetic activities, and, at the end of these processes, the DNA backbone is resealed.
There are three main types of DNA topology: supercoiling, knotting, and catenation. Correspondingly, the human genome encodes three types of topoisomerases to resolve such DNA entanglements: type IA (Top3α and Top3β), type IB (nuclear Top1 and mitochondrial Top1), and type IIA (Top2α and Top2β) . Topoisomerases cleave and rapidly reseal one (type I) or two (type II) DNA or RNA strands, generating a transient break through which topological modifications can occur . This catalytic process is rather “dangerous” in that it generates an intermediate in which the topoisomerase becomes covalently linked to the 3′ (type IB) or 5′ (type IA and IIA) terminus of nucleic acids through a phosphotyrosine linkage, designated as the topoisomerase cleavage complex (TOPcc). Failure to complete this catalytic cycle results in trapping of topoisomerase on DNA termini, generating protein-linked DNA breaks (PDB) – a frequent event that causes cell death [20,21,22,23]. Notably, the insertion of viral or bacterial DNA into host chromosomes and other forms of recombination also requires the action of topoisomerases. Many drugs, such as broad-spectrum fluoroquinolone antibiotics and chemotherapy drugs, operate through disrupting or interfering with the function of bacterial or cancer cell topoisomerases to create breaks in chromosomal DNA and to lead cell apoptosis or dysfunction [24, 25]. Thus, although DNA topology is crucial for normal cell function, its disruption may lead to DNA damage response (DDR) and cell dysfunction or death.
While catalytic inhibition of topoisomerases has been widely exploited to kill bacterial or cancer cells [24, 25], the role and mechanisms of topoisomerases in reprogramming telomeric DDR and remodeling the function of T lymphocytes during chronic viral infections remain largely unknown. In this study, we explored the role of topoisomerase I (Top 1) in telomeric DDR, T cell senescence and dysfunction in a translational approach. We provide evidence showing that T cells derived from patients with chronic hepatitis C virus (HCV), hepatitis B virus (HBV), or human immunodeficiency virus (HIV) infection exhibit significantly inhibited Top 1 protein expression and enzyme activity, accompanied by Top1cc accumulation and trapping in genomic DNA. Using camptothecin (CPT, a Top 1 inhibitor)-treated primary T cells as a model, we demonstrate that disruption of telomeric DNA topology promotes T cell senescence, apoptosis, and dysfunction via enhancing DDR as a consequence of Top1cc being formed and trapped at the DNA break site. Importantly, T cells from virally infected subjects with inhibited Top 1 activity were more vulnerable to CPT-induced cell apoptosis, indicating an important role for Top 1 in maintaining DNA integrity and securing cell survival. These results suggest that immunocompromising viruses (HCV, HBV, and HIV) may disrupt this T cell DNA topological processes as a mechanism to dysregulate host immunity and establish chronic viral infection. Thus, restoring the impaired DNA topologic machinery may serve as a novel strategy to protect T cells from unwanted DNA damage and maintain immune competency.
Materials and methods
The study subjects were composed of four populations: 37 chronically HCV-infected patients prior to antiviral therapy; 29 chronically HBV-infected patients on antiviral treatment with undetectable viremia (HBV-DNA); 28 latently HIV-infected patients on antiretroviral therapy (ART) with undetectable viremia (HIV-RNA); and 144 age-matched healthy subjects (HS), which were obtained from Physicians Plasma Alliance (PPA), Gray, TN, and negative for HBV, HCV and HIV infection. The characteristics of the subjects included in this study are described in Table 1.
Cell isolation and culture
Peripheral blood mononuclear cells (PBMCs) were isolated from whole blood by Ficoll (GE Heathcare, Piscataway, NJ) density centrifugation. CD4 T cells were isolated from PBMCs using the CD4 T Cell Negative Isolation Kit and a MidiMACS™ Separator (Miltenyi Biotec Inc., Auburn, CA). The isolated T cells were cultured in RPMI 1640 medium containing 10% FBS (Atlanta Biologicals, Flowery Branch, GA), 100 IU/ml penicillin and 2 mM L-glutamine (Thermo Scientific, Logan, UT) at 37 °C and 5% CO2 atmosphere.
Intracellular IL-2 and IFN-γ cytokine production, DNA damage marker γH2AX expression, PKH26-label CD4 T cell proliferation, telomere length measured by florescence in-situ hybridization (Flow-FISH), and cell apoptosis assay for Av/7AAD expression were analyzed by flow cytometry, as described previously [26, 27]. The following reagents were used in the assays: PE-labelled Av, IL-2, IFN-γ, γH2AX (BD Biosciences, San Jose, CA), CD4-Alexa-647 (BioLegend, San Diego, CA), telomere probe TelC (CCCTAACCCTAACCCTAA)-FITC (0.25 μg probe/mL, PNA Bio, Newbury Park, CA).
RNA isolation and real-time RT-PCR
Total RNA was extracted from 1 × 106 CD4 T cells using PureLink RNA Mini Kit (Invitrogen, Carlsbad, CA), and cDNA was synthesized using High Capacity cDNA Reverse Transcription Kit (Applied Bio systems, Foster city, CA) per the manufacturer’s instructions. Quantitative real-time polymerase chain reaction (PCR) was performed in triplicate as described previously . Gene expression was determined using the 2-ΔΔct method and normalized to GAPDH levels, and is presented as fold changes. The PCR primer sequences are shown in Table 2.
CD4 T cells (2 × 106) purified from HCV, HBV, or HIV patients and HS were used for western blot as described previously [26, 27]. Primary and secondary antibodies included Top1, PARP1, γH2AX, TRF1, TRF2, TPP1, TIN2, RAP1, POT1, ATM, pATM, CHK2, ATR, GAPDH, β-actin, and horseradish peroxide-conjugated antibodies (Cell Signaling). Images were captured using ChemiDoc™ XRS+ System (Bio-Rad). Protein band intensity was quantitated by the Image Lab software (Bio-Rad).
Top 1 activity assay
The activity of Top 1 was measured by Topoisomerase 1 Assay Kit (Topogen, Inc., Cal No: TG1015–1, Buena Vista, CO). Briefly, CD4 T cells were purified from patients and HS, and cell extracts were isolated from the purified cells according to the instructions of the kit. Samples were mixed with plasmid DNA substrate and reaction buffer for 30 min at 37 °C, then loaded onto a 1% agarose gel with loading dye, and electrophoresed for about 2 h at 5~10 V/cm before illuminating with a UV transilluminator. The intensity of supercoiled DNA substrate was measured by densitometry.
Top1cc was detected using the Human Topoisomerase ICE Assay Kit (Topogen, Inc., Cal No: TG1020–1, Buena Vista, CO 81211). The DNA purification protocol was modified by combining ICE Assay Kit and PureLink™ Genomic DNA Mini Kit (Thermo Fisher Scientific, Catalog number: K182001, Waltham, MA 02451). Briefly, genomic DNA sample were isolated from cell pellets using the extraction buffers of ICE assay kit and then purified by the column of PureLink™ Genomic DNA Mini Kit. The DNA samples were loaded onto NC membranes by a vacuum pump, which was incubated with primary anti-Top1cc antibody from ICE assay kit, followed by western blotting as described above.
CD4 T cells were isolated and treated as described above, followed by immunofluorescence staining using a method described previously . Rabbit anti-53BP1, anti-Ku70, anti-RAD51 or anti-Top1cc (Cell Signaling) and mouse TRF1 (Thermo Fisher) were used as primary antibodies and anti-rabbit IgG-Alexa Fluor 488 and anti-mouse IgG-Alexa Fluor 555 (Invitrogen) were used as secondary antibodies. The cells were washed and mounted with DAPI Fluoromount-G (SouthernBiotech, Birmingham, AL). Images were acquired with a confocal laser-scanning inverted microscope (Leica Confocal, Model TCS sp8, Germany).
The data were analyzed using Prism 7 software, and are presented as mean ± SEM or median with interquartile range. Comparisons between two groups were made using unpaired Student’s t test, or paired T test. P-values < 0.05, < 0.01, or < 0.001 were considered statistically significant or very significant, respectively.
Top 1 expression and activity are inhibited in CD4 T cells from individuals with chronic viral infections
Chronic viral (HCV, HBV, HIV) infections are characterized by T cell exhaustion, senescence, and cellular dysfunction [1,2,3,4,5,6,7,8,9,10,11,12,13], but the underlying mechanisms remain incompletely understood. We have recently discovered that these dysfunctional, senescent T cells exhibit pronounced DNA damage and telomere erosion [26, 27]. Given the crucial role of DNA topology in securing genomic integrity and cell survival [20,21,22,23], we used a translational approach to explore the mechanisms of DNA damage and T cell dysregulation by examining the expression level of Top 1 in CD4 T cells derived from individuals with chronic viral (HCV, HBV, HIV) infection and HS. As shown in Fig. 1a, chronically HCV, HBV, or HIV-infected patients exhibited a significantly lower level of Top 1 protein expression in their CD4 T cells compared to age-matched HS, as determined by western blotting. To determine whether Top 1 inhibition occurs at the transcriptional or translational level, we measured Top 1 mRNA levels by real-time RT-PCR in CD4 T cells derived from these subjects. As shown in Fig. 1b, the mRNA levels of Top 1 in CD4 T cells isolated from these patients showed little changes compared to age-matched HS, suggesting that Top 1 inhibition during chronic viral infections primarily occurs at the translational level.
Human Top 1 is a type 1B topoisomerase that can relax (change DNA linking in step one) either positive or negative supercoiled DNA . Thus, we employed a plasmid (pHOT1)-based Top 1 Assay Kit (TopoGEN, Inc.) to measure Top 1 activity in CD4 T cells derived from patients with chronic viral infection. As shown in Fig. 1c (left to right), where the Top 1-relaxed linear plasmid DNA (pHOT1) served as positive control (+), the untreated supercoiled plasmid DNA served as negative control (−), and an escalated amount of nuclear extract-treated plasmid DNA exhibited a pattern from supercoiled DNA substrate to linear DNA topoisomers in 1% agarose gel in a dose-dependent manner. Based on this result, we used 1.6 μg of nuclear extracts, which can resolve > 50% supercoiled DNA substrate, to compare the Top 1 enzyme activity in virus-infected patients versus HS. While the HS-derived nuclear extracts efficiently relaxed the supercoiled plasmid DNA, the nuclear extracts derived from HCV-, HBV- and HIV-infected patients failed to completely relax the plasmid DNA (Fig. 1d).
Top 1 is a prototypical eukaryotic enzyme that relaxes supercoiled DNA without the need for cellular energy (ATP). During the course of its normal catalytic cycle, Top 1 nicks one DNA strand and allows rotation around the intact strand, and then reseals the DNA backbone. This DNA relaxation activity plays an important role in restoring DNA topology, replication, transcription, and viral integration [18,19,20,21,22,23,24,25]. Collisions of this catalytic cycle with the Top1cc formed during DNA nicking are thought to produce further DNA damage, ultimately leading to cell death [20,21,22,23]. To determine if Top1 inhibition resulted in Top1cc buildup and trapping in their T cell chromosomes, we measured Top1cc in genomic DNA isolated from CD4 T cells of virus-infected patients and HS using a monoclonal antibody that specifically recognizes covalent Top 1-DNA complexes, but not free Top 1 or DNA, using immunoblotting . As shown in Fig. 1e, a significant amount of Top1cc was detected in CD4 T cells isolated from HCV, HBV, HIV-infected patients compared to HS. These results, in conjunction with our previous findings of T cell exhaustion and senescence with poor cellular functions during chronic viral infections [1,2,3,4, 26, 27], suggest that these dysfunctional, senescent T cells from chronically virus-infected individuals have topological aberrancies, i.e., Top 1 inhibition, leading to Top1cc accumulation.
Top 1 inhibition by CPT in healthy T cells induces telomeric DNA damage, cell apoptosis and dysfunction
Top 1 is targeted by a class of widely utilized anticancer drugs [18, 19]. CPT intercalates into DNA at the Top 1 catalytic site, inhibiting the reseal step and shifting the equilibrium toward Top1cc accumulation . To explore the role of Top 1 inhibition in DNA damage and T cell dysregulation, we employed CPT-treated primary CD4 T cells as a model. Since Top1cc can be selectively trapped by CPT, which binds at the Top 1-DNA interface, leading to potent transcription- and replication-blocking DNA lesions causing cytotoxicity . To this end, CD4 T cells were isolated from HS and exposed to varying concentrations of CPT (0, 1, 2.5, 5, 10 μM) for different time points (24, 48, 72 h), followed by the measurement of cell apoptotic death by flow cytometry. As shown in Fig. 2a, CPT-treated healthy T cells exhibited a dose- and time-dependent increases in Annexin V (Av, left panel) and 7-Aminoactinomycin D (7AAD, right panel) levels compared to cells treated with dimethyl sulfoxide (DMSO) control. We also measured T cell functions by flow cytometric analysis of intracellular cytokine production and cell proliferation following T cell receptor (TCR) stimulation and with or without CPT treatment. As shown in Fig. 2b, intracellular IL-2 and IFN-γ cytokine productions were significantly inhibited in human T cells exposed to CPT compared to DMSO control in the presence of anti-CD3/CD28 (1 μg/ml) stimulation for 3 days. Moreover, a significantly inhibited T cell proliferation, as evidenced by the delayed PKH26 dye dilution, was observed in human T cells exposed to CPT compared to control, in the presence of TCR stimulation for 5 days (Fig. 2c).
To determine whether CPT-induced DNA damage might be a primary reason for T cell dysfunction, we treated CD4 T cells with CPT or control for 3 days, followed by measuring the phosphorylated histone H2AX (γH2AX), a marker for DNA damage. As shown in Fig. 2d, a significant γH2AX upregulation was detected in CPT-treated CD4 T cells compared to the control, as determined by flow cytometry. Notably, these findings (CPT-induced T cell apoptosis, cytokine or proliferation inhibition via DDR in vitro) recapitulate the T cell dysregulation due to exhaustion and senescence we and others have observed in chronic viral infections in vivo [1,2,3,4,5,6,7,8,9,10,11,12,13, 26, 27]. Therefore, CPT-treated T cells could serve as a model to study the role and mechanisms of Top 1-mediated DNA topological aberrancies in T cell dysregulation.
Human T cell telomeres shorten at a rate of 50~100 base pairs per cell division, acting as a molecular clock to control the replicative capacity before entering cell cycle arrest, senescence, or apoptosis . Since mammalian telomeres consist of triple guanine repeats (TTAGGG) that are very sensitive to oxidative DNA damage [30, 31], we speculated that CPT-induced DNA damage may extend to the telomeres that we have shown to have telomeric DNA damage in T cells derived from chronically virus-infected individuals [26, 27]. Notably, following genotoxic insult, 53BP1 is recruited to the DNA damage site on chromosomes as well as telomeres and acts as a docking station for other mediator or adaptor proteins to form microscopically visible nuclear foci (DNA damage foci) [32, 33]. A single 53BP1-formed focus represents hundreds to thousands of 53BP1 proteins that are recruited around at least one DNA strand break . Thus, identifying damaged telomere induced foci (TIF) is typically regarded as a hallmark of telomeric DNA damage . To determine telomeric DNA damage in CPT-treated T cells, we compared the number of TIFs per nucleus and the percentages of cells with > 3 TIFs, by examining the co-localization of 53BP1/TRF1 (telomeric repeat-binding factor 1) using confocal microscopy. As shown in Fig. 2e, the numbers of TIF per nucleus were significantly higher in CD4 T cells exposed to CPT vs. DMSO-treated control. The percentage of T cells with > 3 TIFs was also higher in CPT-treated cells compared to the control. Taken together, these results suggest that CPT-induced topological DNA damage may cause cell apoptosis and T cell dysfunction, thus emphasizing the role of telomere integrity in securing T cell survival and providing a robust model to study Top 1-mediated telomere topological DNA damage and repair machinery.
CPT-induced DNA damage involves Top1cc accumulation, PARP-1 cleavage, and transcription-dependent, ubiquitin-mediated top 1 proteolysis
Physiologically, Top 1 relaxes intertwined DNA by producing transient Top1cc during DNA transcription. After DNA relaxation, Top1cc reverses rapidly and Top 1 is released as the DNA re-ligates. However, Top1cc can be trapped under pathological conditions, and a consequence of transcription-blocking Top1cc is the production of Top1-lined PDBs . To determine whether CPT-induced T cell inhibition is primarily due to Top 1 suppression, we examined Top 1 protein expression in CD4 T cells treated with CPT by western blot. As shown in Fig. 3a, Top 1 protein expression was significantly inhibited in CD4 T cells exposed to CPT. In addition, Top 1 enzyme activity was also inhibited in CD4 T cells treated by CPT compared to the control (Fig. 3b). To determine whether Top1cc accumulated during DNA nicking in T cells exposed to CPT, we treated primary CD4 T cells with a high dose of CPT (50 μM) for a short period of time (45 min), followed by genomic DNA isolation and immunoblotting . Of note, Top1cc was found to be trapped at genomic DNA in CPT-treated T cells compared to the DMSO control (Fig. 3c). These observations recapitulated the Top 1 inhibition seen in patients with chronic viral infections (Fig. 1).
Trapped Top1cc can cause DNA strand breaks [34, 35], and removal of these breaks depends on the tyrosyl-DNA phosphodiesterase-1 (TDP1) excision pathway [22, 36,37,38,39,40]. Notably, Top1cc excision by TDP1 requires Poly ADP-Ribose Polymerase 1 (PARP1), an enzyme that catalyzes the transfer of ADP-ribose onto target proteins and plays an important role in cell apoptosis, DNA damage repair and chromosomal stability [40,41,42]. PARP1 binds to TDP1, leading to TDP1 stabilization and its recruitment at the sites of Top1cc-induced PDB to initiate the repairing process. To determine whether CPT-induced DNA damage in T cells involves PARP1 cleavage, we measured PARP1 in CPT-treated CD4 T cells. As shown in Fig. 3d, while the total PARP1 level was reduced, the cleaved form of PARP1 was significantly induced by the CPT treatment, which correlated with DNA damage and cell apoptosis.
Since PARP1 binding to TDP1 is crucial for Top1cc removal [40,41,42], we then assessed whether inhibition of PARP1 would increase DNA damage in CPT-treated T cells. As shown in Fig. 3e, compared to the DMSO-treated control (1), CPT treatment (2) significantly inhibited Top 1 level but increased PARP1 cleavage and γH2AX expression. Whereas the PARP1 inhibitor ABT-888 (also known by its trade name, Veliparib, as a chemotherapeutic)  did not block (but feedback increased) Top 1 expression, it augmented the levels of PARP1 and γH2AX in DMSO (3) as well as CPT-treated (4) CD4 T cells (4), indicating that PARP1 is a down-stream molecule acting together with CPT in the Top 1 signaling pathway.
Collisions of transcription complexes with CPT-induced Top1cc are thought to produce DNA damage and cell apoptosis. Consistent with this model, we speculated that inhibition of transcription would diminish the DNA damage of Top 1 poisons. To test whether CPT-induced, Top 1-mediated DNA damage is transcription-dependent, we examined Top 1, PARP1, and γH2AX levels in CD4 T cells treated with CPT in the presence or absence of the transcription inhibitor flavopiridol (FLV). As shown in Fig. 3f, compared to DMSO-treated control (1), CPT treatment (2) inhibited Top 1, but increased PARP1 cleavage and γH2AX expression. As expected, while FLV inhibited Top 1 and significantly boosted PARP1 cleavage and γH2AX expressions (3), inhibition of transcription prevented CPT-induced Top 1 suppression and further induction of PARP1 or γH2AX levels in CD4 T cells (4). These results indicate that CPT induces a transcription-dependent DDR in human T lymphocytes.
As we have shown above, Top 1 inhibition primarily occurs at the protein level (Fig. 1). Indeed, Top1cc-mediated transcription blockade triggers Top 1 degradation by the ubiquitin/proteasome system . Thus, we further examined whether the protein degradation machinery could contribute to the observed Top 1 protein inhibition and occurrence of transcription-dependent DNA damage. As shown in Fig. 3g, compared to the DMSO-treated control (1), CPT treatment inhibited Top 1 level, but induced PARP1 and γH2AX levels (2). Intriguingly, inhibition of ubiquitin by isopeptidase inhibitor (G5), which causes depletion of free nuclear ubiquitin , prevented Top 1 degradation in CPT-treated T cells (4). We then assessed whether inhibiting the ubiquitin system could prevent DDR signaling. Notably, the ubiquitin inhibitor G5 could induce PARP1 cleavage and γH2AX expression in primary CD4 T cells (3); however, G5 treatment prevented further induction of PARP1 and γH2AX levels in CPT-exposed cells (4). Similarly, inhibition of proteolysis by a proteasome inhibitor (MG132), which prevented CPT-induced Top 1 degradation, also prevented CPT-induced accumulation of PARP1 and γH2AX (Fig. 3h), suggesting that topological DNA damage depends upon Top 1 ubiquitination and proteasome degradation. Taken together, these results indicate that the CPT-induced topological DNA damage involves the transcription-dependent, ubiquitin-mediated Top 1 proteolysis.
CPT-induced top 1 inhibition induces telomere attrition via disruption of telomerase activity and shelterin protection
We and others have recently shown that T cell exhaustion and senescence during chronic viral infections are associated with accelerated telomere erosion, a hallmark of cell aging or immune senescence [4,5,6,7, 26, 27]. To determine whether CPT-treated T cells mirror the telomere loss seen in patients with viral infections, we measured the telomere length in CPT-treated T cells by Flow-FISH. As shown in Fig. 4a, significant telomere attrition was observed in CD4 T cells exposed to CPT compared to the DMSO-treated control. Notably, telomeres are replenished by telomerase that comprises telomerase RNA (TR) and human telomerase reverse transcriptase (hTERT) - the catalytic unit of telomerase . Telomerase regulation has been studied extensively in malignant cells, and recently, hTERT measurement has also been employed to study T cells that have a high rate of turnover, especially during pathogenic infections [47, 48]. We have recently measured telomerase expression and activities in CD4 T cells derived from patients with chronic HCV and/or HIV infection, and found that hTERT expression remained unchanged, but its activity was significantly suppressed and failed to be recruited onto telomeres to maintain telomere integrity (unpublished observations). Here, we further measured hTERT expression by real-time RT-PCR and telomerase activities by TRAP assay in CPT-treated CD4 T cells. As shown in Fig. 4b and c, CPT-treated T cells exhibited an unchanged hTERT expression but remarkably inhibited telomerase activity when compared to the DMSO-treated control, which recapitulates the observations in T cells from patients with HCV and HIV infection.
It is well-known that telomeres are protected by shelterin complexes. To explore the mechanisms of telomere erosion in CPT-treated T cells, we examined the integrity of the telomeric shelterin complex, which comprises six telomere-associated proteins, including telomeric repeat-binding factors 1 and 2 (TRF1 and TRF2), repressor/activator protein 1 (RAP1), telomere protection protein 1 (TPP1), protection of telomere 1 (POT1), and TRF1-interacting nuclear protein 2 (TIN2), where they act together in shaping and safeguarding telomeres from erosion [49, 50]. As shown in Fig. 4d, TRF1 and pTRF2 levels were significantly lower than control levels. TPP1 and TIN2 levels were slightly downregulated, whereas RAP1 and POT1 remained unchanged or slightly upregulated, in CD4 T cells after the CPT treatment. However, the mRNA expression of these shelterin proteins remained essentially unchanged, except TPP1, by this treatment (Fig. 4e). These results recapitulate the data we observed in CD4 T cells derived from HCV and/or HIV-infected patients versus HS  (unpublished observations). Since the primary functions of TRF1/TRF2/TPP1/TIN2 sub-complexes are to protect telomeres from unwanted DNA damage and to recruit telomerase to telomeres, their inhibition would lead to telomere uncapping or deprotection, and a telomerase that is unable to access or function at telomeres.
CPT-mediated top 1 inhibition and DDR involves dynamic activation and depletion of DNA repair kinases
Accumulation of DNA damage activates the protein kinase ataxia telangiectasia mutated (ATM), an enzyme critically involved in repairing DNA damage for cell survival [51, 52]. ATM, along with ataxia telangiectasia Rad3-related (ATR), is the pinnacle kinase of the DNA repair signaling cascade, which is important for DNA reprogramming and T cell rearrangement [53, 54]. To investigate the involvement of DNA repair enzymes in CPT-mediated Top 1 inhibition and topological DDR, we examined the kinetic expressions of ATM and ATR, in conjunction with DNA damage and repair markers, γH2AX and PARP1, in CD4 T cells following CPT treatment for different time points (1 h, 3 h, 6 h, 1 d, 3 d, 5 d). As shown in Fig. 5a, an increase in PARP1 cleavage was seen in CPT-treated T cells at all time points. Also, γH2AX was increased in the early phase (1~6 h) of CPT treatment; however, it decreased and eventually could not be detected in CD4 T cells at later times after CPT treatment (3~5 d), which is consistent with a previous report indicating that CPT treatment promotes DDR and activates DNA protein kinase c (DNA-PKc), and that ATM enhances phosphorylation of H2AX at an early phase and then triggers the ubiquitination cascade and proteasome degradation of γH2AX at double strand break (DSB) sites at later stages . Indeed, ATM and pATM were increased in response to DDR in the early phase (1~6 h) and then gradually became deficient in the later phase of CPT treatment (3~5 d). Correspondingly, the downstream checkpoint kinase 2 (CHK2) was also upregulated in the early phase and became progressively depleted in the late phase of CPT treatment. Likewise, ATR exhibited the same pattern as ATM in response to the acute and persistent DDR induced by CPT treatment. In conjunction with our recent findings of ATM insufficiency in CD4 T cells in chronic HCV and HIV infection  (unpublished observations), these data indicate that CPT-induced, Top1-mediated topological DDR involves a dynamic activation and depletion of DNA repair kinases.
Next, we studied the role of these DNA repair kinases (ATM/ATR) in T cell topological DDR to gain insight into their functional relevance. To identify which of these kinases induces γH2AX in topological DDR, we assessed whether γH2AX phosphorylation is prevented by the specific inhibitors of these kinases in CPT-induced TOP 1 inhibition. Since γH2AX induction was primarily observed in the early phase (3~6 h) of CPT treatment (Fig. 5a), we chose to measure its level in CD4 T cells after 3 h of CPT treatment. As shown in Fig. 5b, CPT treatment inhibited Top 1 expression. Correspondingly, the expression of γH2AX was increased by the CPT-induced topological DDR (2 vs.1). ATMi (KU60019) did not affect TOP 1 level, but significantly reduced γH2AX level (3 vs.1). Interestingly, ATMi reduced the CPT-mediated γH2AX induction (4 vs. 2), suggesting that ATMi inhibits DDR. In addition, while ATRi did not affected TOP 1 level as well, it reduced the level of γH2AX (5 vs.1), which is consistent with the ATMi treatment, suggesting that these kinase inhibitors inhibit DDR. However, ATRi treatment further reduced the CPT-mediated Top 1 downregulation and, concurrently, further induced the γH2AX expression (6 vs.2). We observed similar results in repeated experiments, and these are consistent with previous reports , suggesting that ATM, but not ATR, is implicated in the induction of γH2AX in CPT-treated cells.
CPT induces Top1cc accumulation to prevent DNA repair molecule recruitment to the DNA damage sites
We have recently found that the non-homologous end joining (NHEJ) pathway, rather than the homologous recombination (HR) pathway of DNA repair, participates in the ATM-mediated telomeric DNA damage repair (unpublished data). However, how DSBs accumulate in cells despite the presence of DNA repair proteins remains unknown. It is well-known that Ku70 and Ku80 make up the Ku heterodimer, which binds to DNA-DSB ends and is required for the NHEJ pathway of DNA repair. It is also required for V(D)J recombination, which utilizes the NHEJ pathway to promote antigen diversity in the mammalian immune system. In addition to its role in NHEJ, Ku is involved in telomere length maintenance . It has been reported that mutant mice with deficient Ku70 exhibit premature aging , suggesting that Ku70 plays an important role in longevity assurance and that the reduced ability to repair DNA-DSB causes early aging. To determine the role of the NHEJ pathway in repairing CPT-induced telomeric DNA damage, we measured the Ku70-dependent, damaged telomere induced foci (TIF) in CD4 T cells exposed to CPT or DMSO for 6 or 72 h using confocal microscopy. Surprisingly, we could not identify any Ku70/TRF1 co-localization in cells treated with CPT or DMSO control (Fig. 5c), suggesting that Ku 70 failed to be recruited to the damaged telomeres. We also examined possible involvement of the HR pathway in the CPT-induced DSB repair. Since RAD51 is involved in the search for homology and strand pairing stages of the process [58, 59], we used confocal microscopy to examine the RAD51/TRF1 co-localization in CD4 T cells exposed to CPT or DMSO for 6 or 72 h. Again, we did not find any difference between control and treatment (Fig. 5d).
Since CPT induces cytotoxicity by trapping Top1cc at the Top 1-DNA covalent sites, which in turn interacts with advancing replication or transcription complexes to generate lethal DNA lesions, we further hypothesize that Top1cc may accumulate and occupy the DSB ends, preventing the recruitment of DNA repair molecules to the damaged sites in T cells. To test this possibility, we examined the CPT-induced, Top1cc-mediated dysfunctional telomere foci using a monoclonal antibody that specifically recognizes covalent Top 1-DNA complexes, but not free Top 1 or DNA, using confocal microscopy . We found a significant increase in Top1cc/TRF1-formed TIFs in T cells exposed to CPT compared to the DMSO-treated control (Fig. 5e). Also, we observed Top1cc accumulation at damaged telomeres in T cells treated with KML001 (a telomere-targeting drug that can inhibit Top 1 expression and induce Top1cc), but not in cells treated with the ATM inhibitor (KU60019)-induced telomeric DNA damage, which is not involving in Top1cc induction but via the NHEJ pathway for DNA damage repair; unpublished observations). Taken together, these results suggest that CPT induces Top1cc accumulation and trapping at the DSB sites, which may prevent DNA repair molecule recruitment and inhibit DNA damage repair.
T cells from individuals with chronic viral infection are more vulnerable to CPT-induced cell apoptosis
Since chronically virus-infected patients suffer from deficiency in the Top 1 enzyme and exhibit more DNA damage within their CD4 T cells, we hypothesized that these T cells were more vulnerable to CPT-mediated cell apoptosis. We thus examined the apoptotic susceptibility of CD4 T cells derived from virus-infected patients versus age-matched HS upon CPT treatment. Indeed, CD4 T cells isolated from HCV-, HBV-, and HIV-infected patients exhibited higher rates of cell apoptosis (Av expression) than those from HS (Fig. 6a). Correspondingly, a higher rate of cell death (7-AAD expression) was observed in CD4 T cells from virally infected patients versus HS (data not shown). These results, in conjunction with our previous in vivo findings of T cell exhaustion and senescence in virus-infected individuals [26, 27], suggest that Top1-mediated topological DNA damage, if left unrepaired, can trigger both cell apoptosis and cell death.
T cells play a pivotal role in controlling pathogenic infection and vaccine responses. In chronic viral infections, particularly in immunosuppressive HCV, HBV, and HIV infections; T cells are however essentially always dysfunctional and vaccine responses are often blunted . We and others have previously shown that T cells from chronically virus-infected individuals are prematurely aged or senescent due to telomere attrition and erosion [1,2,3,4,5,6,7,8,9,10,11,12,13, 26, 27], but the underlying mechanisms for T cell telomeric DNA damage and repair remain unclear. Since Top 1 is required to remove DNA supercoiling generated during cell overexpansion, and TOP1cc can become trapped during gene transcription to cause Top 1-linked PDB [20,21,22,23], we hypothesized that T cell DNA topology may be altered during viral infections to cause DDR as a mechanism of virus-mediated immune dysregulation.
In this study, we employed T cells isolated from virus-infected individuals and primary T cells treated with CPT as a model to specifically induce transcription-blocking Top1cc in order to obtain insights into the molecular mechanisms underlying both DNA damage and repair processes. We demonstrate that: 1) CD4 T cells derived from chronically HBV, HCV, and HIV-infected individuals with immune dysfunction exhibit an inhibition of Top 1 enzyme expression and activity, leading to accumulation of Top1cc and DNA damage, including telomere erosion; 2) CPT-induced Top 1 inhibition, Top1cc accumulation, topological DNA damage, telomere uncapping and erosion, T cell apoptosis and dysfunctions recapitulate what we observe in T cells during chronic viral (HCV, HBV, HIV) infections, emphasizing the role of Top 1 in maintaining telomeric DNA integrity and securing T cell survival and function; 3) CPT-induced topological DDR is achieved via transcription-dependent, ubiquitin-mediated Top 1 proteolysis, involving dynamic ATM activation followed by deficiency - Top1cc accumulation at the DSB sites may block the recruitment of DNA repair proteins and inhibit DNA damage repair; and 4) T cells from virally infected subjects with lower Top 1 activity are more vulnerable to CPT-induced topological DNA damage and cell apoptosis, indicating an important role for Top 1 in preventing unwanted DNA damage and securing cell survival.
Although accumulation of DNA damage and failure to be repaired may affect cell survival and function, the molecular signaling pathways in T lymphocytes in the context of chronic viral infections remain largely unknown. Our results support a model, as depicted in Fig. 6b, in which Top 1 inhibition and Top1cc accumulation block transcription elongation, which triggers ubiquitin-mediated Top 1 proteolysis and the generation of Top1cc-linked PDBs. Defective repair of these PDBs can further give rise to DDR, which leads to ATM activation and phosphorylation of its downstream substrates such as CHK2 and p53. ATM also activates 53BP1 and γH2AX assembling into nuclear DNA damage foci and promotes ubiquitination of multiple signaling molecules in the process of DNA damage and repair. Notably, several E3 ligases have been reported for γH2AX (RNF2, RNF8, RNF168) and for Top 1 (Cullin3, Cullin4A/4B, BRCA1) ubiquitination and proteasomal degradation [45, 61]. Our findings that Top 1 inhibition and γH2AX production in CPT-treated T cells depend both on transcription and on Top 1 ubiquitination suggest that they arise during the repair of Top1cc and that this pathway feedback to enhance Top1cc repair after Top 1-linked PDB induction. Moreover, inhibition of PARP1, which is required for TDP1 excision of Top1cc [40,41,42], also increases transcription-dependent Top 1-PDB and γH2AX induction following Top1cc stabilization. This model is supported by our recent findings showing that ATM deficiency  and TRF2 uncapping  increases DNA damage, telomere attrition, T cell senescence and apoptosis, likely due to increased Top1cc levels, as demonstrated in this study in both T cells isolated from chronic viral infections or treated with CPT, leading to T cell dysfunction.
While the mechanisms that lead to Top 1 inhibition during chronic viral infections remain unclear, multiple factors may play a role in this process. Topological DNA damage might occur spontaneously in replicating T cells under physiological conditions, but Top1cc can be trapped under a broad range of pathological conditions, including Top 1 inhibition by immunomodulating viruses (HCV, HBV, HIV, and coinfection with CMV or EBV), by oxidative base damage, by alkylation with carcinogenic compounds or antiviral agents, or by ribonucleotide misincorporations during genetic activities in over-proliferating T cells in response to low grade, chronic inflammatory stimuli [20,21,22,23,24,25]. Therefore, these transcriptional Top 1-linked PDBs may have a marked impact on senescent T cells, leading to reprogramming DDR and remodeling of the T cell fate that arise from i) defective removal of Top1cc, ii) deprotection of telomeres by shelterins , iii) failure of telomere elongation by telomerase dysfunction, and iv) deficiency of DNA damage repair by ATM . T cells might be particularly prone and vulnerable to Top 1-mediated topological DNA damage and cell apoptosis as a result of high rates of oxygen consumption, which produces large amounts of reactive oxygen species (ROS), which we have recently found to be significantly increased in T cells of virus- (HCV and HIV)-infected individuals. Indeed, ROS can stabilize Top1cc to cause topological DNA damage and activate the ATM signaling pathway [28, 29, 62, 63]. Hence, our findings suggest a new paradigm in which topological DNA damage contributes to the T cell senescence, apoptosis and immune evasion occurring during chronic viral infections.
This study focuses on the major blood-borne pathogens, HBV, HCV, and HIV. It would be noteworthy to investigate whether topological DNA damage and premature T cell aging also occur in the setting of other chronic viral infections, such as CMV and EBV. These infections often display similar phenotypic characteristics to those observed in HIV, HBV and/or HCV infection, such as exhausted and senescent T cells, and this would be especially relevant in immunocompromised hosts. Our investigation in CD4 T cells is informative because they represent the lymphocyte helper subsets of the immune system, aiding in CD8 T cell and B cell responses, and their survival critically affects the process of immune aging. We expect to see the same topological DNA damage in CD8 T cells, which often display more prominent dysfunctions with exhaustion and senescence phenotype. It should be pointed out that while Top 1 inhibition and Top1cc accumulation explain both telomeric DNA damage and cell apoptosis, they may function as a double-edged sword, resulting in both overwhelming cell death in acute infection and immune tolerance or immune suppression in chronic infection. Nevertheless, these findings provide the first demonstration of a pivotal role for Top 1 in DDR and new molecular insights into immunomodulation during chronic viral infections through disruption of Top 1 to induce telomeric DDR, T cell senescence, apoptosis, and dysfunction. Most importantly, it provides a potential strategy to restore impaired DNA topological machinery as a means to improve T cell functions and vaccine responses during human viral infections.
We and others have previously shown that chronic viral infections could cause premature T cell aging or immune senescence with accelerated telomere erosion, but the mechanisms underlying DNA damage and telomere loss remain unclear. For the first time to our knowledge, here we report that Top 1 was inhibited, and TOP1cc was trapped in genomic DNA, in T cells from patients with chronic HBV, HCV, and HIV infection. We then used healthy T cells treated with CPT as a model to investigate the role and mechanisms of DNA topology in reprogramming telomeric DDR and T cell functions. We demonstrated that Top 1 inhibition caused topological DNA damage, telomere attrition, and T cell apoptosis or dysfunction by inducing Top1cc accumulation and failure in DNA repair, thus recapitulating T cell dysregulation in the setting of chronic viral infections. This study reveals a novel mechanism for immunomodulation by viral infections via disrupting DNA topology, telomere integrity, and T cell biology. Therefore, restoring the impaired DNA topologic machinery may offer a new strategy to maintain T cell function against human viral diseases.
Availability of data and materials
The data and material are available upon request.
Ataxia telangiectasia mutated
Ataxia telangiectasia Rad3-related
DNA damage responses
DNA protein kinase c
Double strand break
Dual specific phosphatase 6
Florescence in-situ hybridization
Hepatitis B virus
Chronic hepatitis C virus
Human immunodeficiency virus
Human telomerase reverse transcriptase
Killer cell lectin-like receptor superfamily G 1
Non-homologous end joining
Poly ADP-Ribose Polymerase 1
Peripheral blood mononuclear cells
Polymerase chain reaction
Protein-linked DNA breaks
Protection of telomere 1
Repressor/activator protein 1
T cell receptor
TRF1-interacting nuclear protein 2
- Top 1:
Top 1 cleavage complex
Telomere protection protein 1
Telomeric repeat-binding factor 1/2
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We acknowledge and appreciate the NIH AIDS Reagent Program for providing key reagents. This publication is the result of work supported with resources and use of facilities at the James H. Quillen Veterans Affairs Medical Center. The contents in this publication do not represent the views of the Department of Veterans Affairs or the United States Government.
Ethic approval and consent to participate
The study protocol was approved by the institutional review board (IRB) of East Tennessee State University and James H. Quillen VA Medical Center (ETSU/VA IRB), Johnson City, TN. All subjects were adults. Written informed consent was obtained from each patient included in this study.
This work was supported by National Institutes of Health (NIH) grants to Z.Q.Y: R01AI114748, R21AI138598, VA Merit Review Award 1I01BX002670, 1I01BX004281, and DoD Award W81XWH-18-1-0327.
Consent for publication
The consent forms of all participants are held by the authors’ institute and are available for review by the Editor-in-Chief. The data in this work have not been published elsewhere. All authors agree to submit this manuscript for publication in this journal.
The authors declare that they have no competing interests.
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