Spectrum emitted by the Cleo Natural 100-W (warm white) lamp (Philips, Eindhoven, the Netherlands).
Expression of apoptosis-regulating proteins, expressed as the median of the mean fluorescent intensity (MFI) before and after repeated UV irradiation in group A (A) and group B (B) subjects who demonstrated an increased apoptotic response. The medians and standard deviations of the 2 groups are shown. *Significant difference.
Narbutt J, Cebula B, Lesiak A, Sysa-Jedrzejowska A, Norval M, Robak T, Smolewski P. The Effect of Repeated Exposures to Low-Dose UV Radiation on the Apoptosis of Peripheral Blood Mononuclear Cells. Arch Dermatol. 2009;145(2):133-138. doi:10.1001/archdermatol.2008.574
To investigate whether repeated exposures to low-dose UV or solar-simulated radiation induce apoptosis of peripheral blood mononuclear cells.
Cohort study in a healthy population.
Departments of Dermatology and Hematology, Medical University of Lodz, Lodz, Poland.
Ninety-eight healthy volunteers were divided into the following 4 groups: group A, whole-body irradiated with a 0.7–minimal erythema dose (MED) of UV-B daily on 10 consecutive days followed by a single dose of 3 MEDs on a small body area 24 hours later; group B, whole body irradiated with 120 J/m2 solar-simulated radiation (10 consecutive days, then single-dose UV-B exposure of 3 MEDs on a small body area after 24 hours); group C, irradiated with a single UV-B dose of 3 MEDs on a small body area; and group D, irradiated with a single UV-B dose of 4 MEDs on a small body area.
Main Outcome Measure
Apoptosis of peripheral blood mononuclear cells as well as expression of several apoptosis-regulating proteins in response to irradiation.
Ten daily whole-body suberythemal exposures to UV-B or solar-simulated radiation enhanced the apoptosis of peripheral blood mononuclear cells, while the single erythemal doses on the small body area, either on their own or following the repeated exposures, did not increase the level significantly. Increase in Bax and p73 protein expression and down-regulation of Mcl-1 and Bcl-2 correlated with enhanced apoptosis.
Repeated suberythemal UV exposures enhance the apoptosis of peripheral blood mononuclear cells in healthy subjects.
Apoptosis, also called programmed cell death, is a physiological process essential for the maintenance of homeostasis by the elimination of damaged or mutated cells. Multiple pathways and a variety of signals (environmental, extracellular, and internal) are responsible for the activation and regulation of this process.1Classic apoptosis requires the activation of caspases. These serine proteases are responsible for proteolysis of several proteins important for the cell survival, such as caspase-dependent DNase, poly(ADP-ribose) polymerase (PARP), and cytoskeleton proteins, thus leading to DNA fragmentation and subsequent cell death.2 Caspase-dependent apoptosis is activated through either receptor (external) or mitochondrial (internal) pathways. The former is triggered via the tumor necrosis factor family receptors, including Fas/Apo1 receptor, with an initial activation of caspase 8. The latter is activated through mitochondria-associated mechanisms, with the collapse of mitochondrial potential, release of cytochrome c into the cytoplasm, and activation of the caspase 9 complex. The main regulator of this pathway is the family of Bcl-2 proteins, consisting of both apoptosis inhibitors, such as Bcl-2 and Mcl-1, and proapoptotic proteins, such as Bax, Bak, and Bad. The ratio of Bax to Bcl-2 determines the death or life of the cells.3 Both initiator caspase pathways activate effector caspases subsequently, mainly caspase 3 and to a lesser extent caspases 6 and 7.4 In addition, one of the signals leading to apoptosis is DNA damage, inducing cell death by the pathway orchestrated by members of the p53 (p53 and p73) and Bcl-2 families.5
Abnormal activation of apoptosis and disturbances in apoptotic cell clearance may result in decreasing immunological tolerance and, as a consequence, the production of autoantibodies and the development of autoimmune diseases.6 However, pathological inhibition of cell apoptosis is believed to play a crucial role in carcinogenesis.7,8
Exposure to solar UV radiation (UVR) is the most important environmental factor in skin carcinogenesis. It is recognized to suppress cell-mediated immune responses in both animal models and human beings by a complex process initiated by chromophores located in the skin and ending with the generation of T regulatory cells.9- 11 For example, we have shown previously that the contact hypersensitivity response is suppressed in subjects exposed to repeated suberythemal doses of solar-simulated radiation (SSR) or UV-B.12,13 In addition, short-term UV-B irradiation can induce the apoptosis of keratinocytes.14 This results in the formation of scattered dyskeratotic keratinocytes with condensed or absent nuclei and eosinophilic cytoplasm, termed sunburn cells. They can be detected in vivo 24 hours after the exposure.15 Several pathways can lead to the formation of sunburn cells, such as p53 protein up-regulation or signaling through the Fas/Apo1 death receptor.16- 18
Our previous studies demonstrated that repeated exposures to both low-dose UV-B and SSR are able to influence the number of circulating blood dendritic cells19 and alter the serum concentrations of interleukin 8 and tumor necrosis factor in healthy human subjects.20 These observations raised the question of whether similar exposures could induce apoptosis in circulating peripheral blood mononuclear cells (PBMCs). The present study was designed to test such a possibility using the TUNEL (TdT-mediated dUTP-biotin nick-end labeling) method and the PARP cleavage assay.
The study group consisted of 98 healthy volunteers aged 19 to 51 (median, 27.5) years, with either skin phototype II or III, as assessed by the Fitzpatrick classification.21 They were without any skin or other diseases and were not receiving any medication. Before the study, blood tests (blood cell counts) and urinalysis were performed. People exposed to excessive sunlight or sunlamps within 2 months before the study began were excluded. To decrease the influence of natural solar radiation, all the procedures were performed in winter months. Each volunteer gave written informed consent before entry into the study, and the experimental plan was approved by the local ethics committee. The study was performed in accordance with the Helsinki declaration. The subjects received a thorough physical examination and blood cell count. The clinical characteristics of the volunteers are given in Table 1.
Phototesting (UV-B radiation) of each volunteer to determine their personal minimum erythema dose (MED) was undertaken approximately 1 week before the experiment began using a Waldmann Medizintechnik UV 109 device (Waldmann Medizintechnik, Villingen-Schwenningen, Germany) containing B12 lamps (Philips, Eindhoven, the Netherlands) emitting 58.6% UV-B and 41.4% UV-A, with an incremental dose series on 6 squares (1 × 1 cm) on the inner surface of the forearm. The initial lowest dose varied between 0.05 and 0.09 J/cm2, depending on skin phototype, and each increment was approximately 20%. The MED was defined as a just-perceptible erythema filling the irradiated site as assessed visually 24 hours later.
The volunteers were divided into 4 groups, as given in Table 1: group A contained 30 individuals who were whole-body irradiated (excluding the genital area) with 0.7-MED UV-B for 10 consecutive days, followed by a single dose of 3-MED UV-B on a small body area (left buttock, 10 × 10 cm) 24 hours later; group B contained 29 subjects who were irradiated with a 1.2–standard erythema dose (where 1 standard erythema dose is equivalent to an erythemal radial exposure of 100 J/m2) on each of 10 consecutive days, followed 24 hours later by a single dose of 3-MED UV-B on a small body area (left buttock, 10 × 10 cm); group C contained 29 individuals who were irradiated with a single dose of 3-MED UV-B on a small body area (left buttock, 10 × 10 cm); and group D contained 10 individuals who were irradiated with a single dose of 4-MED UV-B on a small body area (left buttock, 10 × 10 cm). The whole-body UV-B was generated by 100-W B12 lamps (Philips), giving an even field of irradiance (285-340 nm) of approximately 3.85 mW/cm2 on the skin surface at 20 cm from the source. The SSR was generated by 100-W Cleo Natural lamps (Philips) in 2 half-cabinets, giving an even field of irradiance (4% UV-B and 96% UV-A) of approximately 4.95 mW/cm2 on the skin surface 20 cm from the source. The spectrum emitted by the Cleo Natural lamp is shown in Figure 1. Measurement of the intensity of the lamps was performed using a Solar Light 3-D UV meter (Solar Light Co, Philadelphia, Pennsylvania). The Waldmann phototesting device was used to irradiate the 10 × 10-cm area of the buttock with 3- or 4-MED UV-B.
Heparinized blood samples were taken from the volunteers in all 4 groups before irradiation. In groups A and B, they were also collected 24 hours after the final daily exposure and again 24 hours after the single UV-B exposure, and in groups C and D, they were also collected 24 hours after the single UV-B exposure. The PBMCs were isolated by centrifugation in Histopaque-1077 (Sigma Diagnostic, St Louis, Missouri) density gradients. The interphase region containing PBMCs was collected, the cells were washed twice and then fixed in 1% methanol-free formaldehyde (Polysciences Europe, Eppelheim, Germany) for 15 minutes at 0°C, before being permeabilized in 70% ethanol (30 minutes at 0°C).
For practical reasons, apoptosis was assessed at a single time, 24 hours after the final UV exposure. This point was thought most appropriate as demonstrated in studies of apoptosis in PBMCs irradiated in vitro with a range of UV-A and UV-B wave bands.22
A modification of the TUNEL assay was used to assess DNA fragmentation (APO-BRDU kit; Phoenix Flow Systems, San Diego, California).23 In this method, the 3′-OH termini of the DNA strand breaks serve as primers and become labeled with bromodeoxyuridine (BrdU) when incubated with BrdU triphosphate in a reaction catalyzed by exogenous terminal deoxynucleotidyl transferase. The incorporated BrdU is immunocytochemically detected by BrdU antibody conjugated to fluorescence isothiocyanate (FITC). After the fixed and permeabilized cells were incubated with the APO-BRDU reagents (60 minutes at room temperature and in the dark), cellular DNA was counterstained for 30 minutes (at room temperature and in the dark) with a mixture of 5-mg/mL propidium iodide and 100-mg/mL RNase A (DNase-free) (Sigma Aldrich, Brodby, Denmark). Then, cell green (FITC) vs red (propidium iodide) fluorescence was measured by dual-color flow cytometry. The percentage of TUNEL-positive cells was expressed as an apoptotic index.
Detection of the PARP cleavage product, p89, is a hallmark of effector caspase activation during apoptosis.24 The fixed permeabilized PBMCs were incubated with the PARP primary rabbit antibody (Santa Cruz Biotechnology Inc, Santa Cruz, California), used at a dilution of 1:1000 (overnight at 4°C) before being incubated for 2 hours at room temperature with secondary anti–rabbit IgG alkaline phosphatase–conjugated antibody (Sigma Chemical Co, St Louis, Missouri). Cell fluorescence was measured subsequently by flow cytometry.
The PBMCs were fixed as described in the “Blood Samples and Isolation of PBMCs” subsection before being permeabilized with 0.1% polysorbate 20 (Tween 20) in phosphate-buffered saline (Amersham Biosciences, Freiburg, Germany) immediately prior to the protein expression measurements. The Bcl-2 family members (Bax, Bak, Bcl-2, and Mcl-1) and the p53 family members (p53 and p73) were assessed. The primary antibodies used, their dilutions, and time of incubation were the following: mouse anti-p53 FITC-conjugated monoclonal antibody (clone DO-7; DAKO, Glostrup, Denmark), 1:30 dilution and 30-minute incubation time; mouse anti-Bcl-2, FITC-conjugated monoclonal antibody (DAKO), 1:15 dilution and 30-minute incubation time; mouse anti-p73 FITC-conjugated monoclonal antibody (NeoMarkers Inc, Fremont, California), 1:10 dilution and 30-minute incubation time; rabbit anti-Bax antibody (DAKO), 1:400 dilution and 60-minute incubation time; and rabbit anti–Mcl-1 antibody (Calbiochem-Novabiochem Corporation, San Diego, California), 1:500 dilution and 60-minute incubation time. Secondary swine anti-rabbit or goat anti-mouse antibodies were used at dilutions ranging from 1:20 to 1:50, as appropriate, with a 30-minute incubation time. All incubations were performed at room temperature, and, in the case of the fluorochrome-labeled antibodies, in the dark. Protein expression was measured by flow cytometry and was assessed as mean fluorescence intensity.
All fluorescence measurements were performed by flow cytometry (FACScan; Becton-Dickinson Biosciences, San Jose, California), using standard emission filters and the CellQuest software (Becton Dickinson Biosciences) was used to process the data. Ten thousand cells per sample were processed routinely in all experiments.
For the statistical analysis of data obtained, the range of the measured variable and the median (SD) values were calculated, using statistical software (STATISTICA, version 5.0; StatSoft Inc, Tulsa, Oklahoma). The data are presented as the medians (SDs) of the multiple experiments. The nonparametric Wilcoxon pair test was used to compare the results before and after irradiation. The correlation between features was evaluated using the Spearman R test. Comparisons and correlations were considered significant when P < .05.
Repeated low-dose exposures to UV-B or SSR did not result in reddening of the skin or edema, but a slight increase in pigmentation was observed. The single high-dose UV-B exposure induced well-defined erythema, in some cases with blistering if given on its own or following the repeated exposures.
The PBMCs were examined for apoptosis 24 hours after the final irradiation by the TUNEL and PARP cleavage methods. Because the apoptotic index assessed by the TUNEL assay correlated significantly with the percentage of cells displaying PARP cleavage (R = −0.87; P < .001), only the TUNEL results are shown in full (Table 2). A significantly higher apoptotic index was found following the 10 repeated suberythemal UV-B or SSR exposures, while irradiation with the single erythemal UV-B dose on a small body area on its own or following the repeated UV-B or SSR doses did not cause any significant alteration in the apoptotic index. Statistical analysis also revealed that in the heparinized blood samples collected 24 hours after the final daily exposure there was a significantly higher apoptotic index of PBMCs in group B (following 10 repeated SSR exposures) compared with group A (following 10 repeated UV-B exposures)(P < .001).
Possible mechanisms leading to the activation of apoptosis were examined by measuring the expression of several apoptosis-regulating proteins from the Bcl-2 and p53 families in volunteers who responded to irradiation by increased apoptosis of PBMCs (Figure 2). The baseline protein expression in the PBMCs (before irradiation) was found to differ to some extent between subjects. Therefore, to reveal changes as a result of UV exposure, statistical comparison was performed by the paired samples analysis (Wilcoxon pair test). In group A, repeated UV-B exposures induced a significant decrease in expression of 2 antiapoptotic proteins, Mcl-1 and Bcl-2 (P < .001 and P = .01, respectively), with subsequent increase in the Bax to Bcl-2 ratio (before UV-B, 0.8 [0.6], and after UV-B, 2.0 [0.3]; P = .04) in the PBMCs. In group B, repeated SSR exposures induced a significant increase in the expression of the proapoptotic proteins Bax and p73 (P = .002 and .01, respectively). As a consequence of Bax protein overexpression, the Bax to Bcl-2 ratio increased approximately 3-fold (P = .007). There was no significant change in expression of any of these proteins in the PBMCs after the subsequent irradiation with 3-MED UV-B in groups A and B. Similarly there was no change from the preirradiation level of expression following the single 3- or 4-MED UV-B exposure in groups C and D (results not shown).
There are scarce data regarding the possible effects of in vivo UVR on circulating PBMCs, although UV-induced apoptosis occurs in the skin and some studies have evaluated apoptosis following in vitro irradiation of PBMCs or of lymphocytes.25,26 Kern et al27 demonstrated that UV-B irradiation led to the apoptosis of PBMCs with the shedding of L-selectin, the adhesion molecule that is required for lymphocyte trafficking into lymph nodes, blood vessels, and inflamed tissues. Breuckmann et al28 showed that UV-B irradiation of human T lymphocytes in vitro led to DNA damage followed by apoptosis, while UV-A1 irradiation caused structural and functional changes leading to the immediate initiation of apoptosis with early membrane rupture. In the most recent of these reports, Tuchinda et al22 have compared different sources of UVR for their relative ability in vitro to activate apoptotic pathways in human PBMCs. They found that UV-A and UV-B could induce both the intrinsic and extrinsic pathways of apoptosis but that UV-B showed a higher potency to initiate apoptosis compared with UV-A. Furthermore, a higher level of energy was required to induce apoptosis if the source was narrowband (UV-A1 or TL-01) rather than broadband (UV-B or UV-A).
The aim of the present study was to assess whether repeated suberythemal whole-body UV-B or SSR had any effect on apoptosis in circulating PBMCs of healthy subjects. We chose the exposures to try to reflect natural solar UVR, when many people go outside for limited periods on a daily basis in the summer months. We estimate that the doses of UV-B and SSR given daily were equivalent to being in the sun for about 35 and 15 minutes, respectively, around midday on a clear sky summer day in mid-Europe. There was increased apoptosis of the PBMCs as a result of either regimen, with the SSR being significantly more effective than the UV-B radiation. This effect could be due to the different proportions of UV-A and UV-B in the 2 sources used in the study—the UV-B lamps emit approximately 54% UV-B and 46% UV-A, while the SSR lamps emit 4% UV-B and 96% UV-A. UV-A wavelengths penetrate more effectively into the dermis than the UV-B wavelengths, and hence, the SSR could have had a more marked apoptotic effect on the PBMCs as the blood circulated through the small vessels in this skin compartment. Alternatively, different immune mediators might have been produced in the epidermis in response to the UV-B or SSR exposures, which then circulated systemically with varied effects on apoptosis in the PBMCs.
Having revealed that these small repeated UV doses increased apoptosis significantly in the circulating PBMCs, we then investigated possible mechanisms by monitoring the expression of several proteins involved in the regulation of apoptosis. The results showed distinct differences between the UV-B and the SSR response. Following the UV-B exposures, there was a decrease in the expression of the antiapoptotic proteins Bcl-2 and Mcl-2 and an enhancement of the Bax to Bcl-2 ratio, while following the SSR exposures, there was an increase in the expression of the proapoptotic proteins p73 and Bax in addition to an enhancement of the Bax to Bcl-2 ratio. Although keratinocytes are well known to be sensitive to UV-B–induced apoptosis,15- 18 lymphocytes are actually quite resistant. However, Wikonkal et al29 showed that for ionizing radiation the lymphocytes are more sensitive. At present, UV-A is well known to generate reactive oxygen species via photosensitization, producing some of the same free radicals as ionizing radiation.30 Thus, based on our study, we may suppose that UV-A, but not UV-B, induces apoptosis of lymphocytes via photosensitized oxygen radicals.
Although the repeated whole-body suberythemal UV-B or SSR exposures enhanced apoptosis in the PBMCs, administering the 3- or 4-MED UV-B doses on a small body area did not. Thus, an erythematous UV dose applied locally, even following the repeated suberythemal UV exposures, was not sufficient to cause a measurable alteration in apoptosis in the PBMCs, although there is evidence that this type of irradiation can initiate significant changes in immune responses both locally and systemically.31
In conclusion, our results have shown that repeated low-dose UV exposures of healthy subjects can lead to an increase in apoptosis of circulating PMBCs. Whether this change contributes significantly to the immunosuppression that follows UVR is not known at this stage, and further studies are required. In addition, this study adds to others12,13,19,20,31,32 on the potentially harmful effects of even small doses of UVR on the human immune system.
Correspondence: Piotr Smolewski, MD, PhD, Department of Hematology, Medical University of Lodz, Copernicus Memorial Hospital, 2 Ciolkowskiego St, 93-510 Lodz, Poland (email@example.com).
Accepted for Publication: April 19, 2008.
Author Contributions: Drs Narbutt and Smolewski had full access to all the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. Study concept and design: Narbutt and Smolewski. Acquisition of data: Cebula and Lesiak. Analysis and interpretation of data: Narbutt, Cebula, Lesiak, Sysa-Jedrzejowska, Norval, Robak, and Smolewski. Drafting of the manuscript: Narbutt, Lesiak, Norval, and Smolewski. Critical revision of the manuscript for important intellectual content: Sysa-Jedrzejowska, Robak, and Smolewski. Statistical analysis: Smolewski. Obtained funding: Narbutt, Norval, Robak, and Smolewski. Administrative, technical, and material support: Cebula, Sysa-Jedrzejowska, and Lesiak. Study supervision: Smolewski.
Financial Disclosure: None reported.
Funding/Support: This study was funded by the Medical University of Lodz projects 503-1019-1 and 502-11-352.