High Doses Of UV-B Research Articles

Effects of UV-B radiation on anatomical characteristics, phenolic compounds and gene expression of the phenylpropanoid pathway in highbush blueberry leaves

The effects of increased doses of UV-B radiation on anatomical, biochemical and molecular features of leaves of two highbush blueberry (Vaccinium corymbosum L. cv. Brigitta and Bluegold) genotypes were investigated. Plants were grown in a solid substrate and exposed to 0, 0.07, 0.12 and 0.19 Wm−2 of biologically effective UV-B radiation for up to 72 h. Leaf thickness and the adaxial epidermis thickness fell more than 3-fold in both genotypes at the highest UV-B dose. Moreover, in Bluegold an evident disorganization in the different cell layers was observed at the highest UV-B radiation. A significant decrease in chlorophyll a/b after 6 h in Brigitta under the greater UV-B doses was observed. Anthocyanin and total phenolics were increased, especially at 0.19 Wm−2, when compared to the control in both genotypes. Chlorogenic acid was the most abundant hydroxycinnamic acid in Brigitta, and was significantly higher (P ≤ 0.05) than in Bluegold leaves. Regarding the expression of phenylpropanoid genes, only the transcription factor VcMYBPA1 showed a significant and sustained induction at higher doses of UV-B radiation in both genotypes compared to the controls. Thus, the reduction of leaf thickness concomitant with a lower lipid peroxidation and rapid enhancement of secondary metabolites, accompanied by a stable induction of the VcMYBPA1 transcription factor suggest a better performance against UV-B radiation of the Brigitta genotype.

Topical pimecrolimus inhibits high-dose UVB irradiation-induced epidermal Langerhans cell migration, via regulation of TNF-α and E-cadherin.

BackgroundTopical pimecrolimus has been shown to reverse epidermal CD1a+ Langerhans cell reduction induced by high-dose ultraviolet (UV)B irradiation, but the mechanism is still unclear. This study aimed to investigate the possible mechanism of the effect of pimecrolimus on high-dose UVB-irradiated epidermal Langerhans cells.MethodsForty human foreskin tissues were divided into four groups: control; pimecrolimus-only; UVB-only; and UVB + pimecrolimus. All tissues were cultured, and each tissue was cut into four pieces, corresponding to four time points (0 hours, 18 hours, 24 hours, and 48 hours). We collected the tissues and culture medium at each time point. The percentage of CD1a+ cells in medium was detected by flow cytometry. The tissues were detected for messenger (m)RNA and protein expression of tumor necrosis factor (TNF)-α, interleukin (IL)-1β, and E-cadherin, by reverse-transcription polymerase chain reaction (PCR) and Western blot.ResultsAt 18 hours, 24 hours, and 48 hours, the CD1a+ cells in the culture medium of the UVB-only group and the UVB + pimecrolimus group were significantly more than in the control group, while the CD1a+ cells of the UVB + pimecrolimus group was less than of the UVB-only group. For both the UVB-only group and UVB + pimecrolimus group, TNF-α expression (by both reverse-transcription PCR and Western blot) of the tissues was clearly higher and E-cadherin expression was significantly lower compared with the control group, at 18 hours, 24 hours, and 48 hours. For the UVB + pimecrolimus group, TNF-α was clearly lower and E-cadherin was significantly higher compared with the UVB-only group.ConclusionTopical pimecrolimus inhibited epidermal Langerhans cell migration induced by high-dose UVB irradiation, via regulation of TNF-α and E-cadherin.

Low and high doses of UV-B differentially modulate chlorpyrifos-induced alterations in nitrogen metabolism of cyanobacteria

The present study assessed the comparative responses on the specific growth rate, nitrogen metabolism and enzymes associated with nitrogen metabolism in two nitrogen fixing cyanobacteria—Nostoc muscorum and Phormidium foveolarum exposed to two UV-B doses (low; UV-BL: 0.5472kJm−2 and high; UV-BH: 5.472kJm−2) and two doses of the insecticide chlorpyrifos (O,O-diethyl O-3,5,6-trichloro-2-pyridyl phosphorothioate; low i.e. CPL, 1µgml−1 and high i.e. CPH, 2µgml−1) singly and in combination. The specific growth rate, NO3− and NO2− uptake, nitrate assimilating enzymes – nitrate reductase and nitrite reductase and ammonium assimilating enzymes – glutamine synthetase and glutamate synthase were severely affected when treated either with CPH or/and UV-BH while glutamate dehydrogenase exhibited a stimulatory response. CPL also reduced all the measured parameters (except GDH activity) after 24h, however, a stimulatory effect was observed after 72h due to an increase in nitrogen metabolism (and other antioxidant) enzymes during this period. UV-BL did not cause significant alteration in the studied parameters while in combination with CP doses, it either alleviated the inhibitory effects or further enhanced the CPL induced activities of these enzymes (except GDH). Overall results indicate the resistant nature of P. foveolarum against the inhibitory doses of UV-B and chlorpyrifos in comparison to N. muscorum.

Re-interpreting plant morphological responses to UV-B radiation.

There is a need to reappraise the effects of UV-B radiation on plant morphology in light of improved mechanistic understanding of UV-B effects, particularly elucidation of the UV RESISTANCE LOCUS 8 (UVR8) photoreceptor. We review responses at cell and organismal levels, and explore their underlying regulatory mechanisms, function in UV protection and consequences for plant fitness. UV-induced morphological changes include thicker leaves, shorter petioles, shorter stems, increased axillary branching and altered root:shoot ratios. At the cellular level, UV-B morphogenesis comprises changes in cell division, elongation and/or differentiation. However, notwithstanding substantial new knowledge of molecular, cellular and organismal UV-B responses, there remains a clear gap in our understanding of the interactions between these organizational levels, and how they control plant architecture. Furthermore, despite a broad consensus that UV-B induces relatively compact architecture, we note substantial diversity in reported phenotypes. This may relate to UV-induced morphological changes being underpinned by different mechanisms at high and low UV-B doses. It remains unproven whether UV-induced morphological changes have a protective function involving shading and decreased leaf penetration of UV-B, counterbalancing trade-offs such as decreased photosynthetic light capture and plant-competitive abilities. Future research will need to disentangle seemingly contradictory interactions occurring at the threshold UV dose where regulation and stress-induced morphogenesis overlap.

Cortisol release in response to UVB exposure in Xiphophorus fish

Xiphophorus fishes are comprised of 26 known species. Interspecies hybridization between select species has been utilized to produce experimental models to study melanoma development. Xiphophorus melanoma induction protocols utilize ultraviolet light (UVB) to induce DNA damage and associated downstream tumorigenesis. However, the impact of induced stress caused by the UVB treatment of the experimental animals undergoing tumor induction protocols has not been assessed. Stress is an adaptive physiological response to excessive or unpredictable environmental stimuli. The stress response in fishes may be measured by an assay of cortisol released into the water. Here, we present results from investigations of stress response during an experimental treatment and UVB exposure in Xiphophorus maculatus Jp 163 B, Xiphophorus couchianus, and F1 interspecies hybrids produced from the mating X. maculatus Jp 163 B×X. couchianus. Overall, cortisol release rates for males and females after UVB exposure showed no statistical differences. At lower UVB doses (8 and 16kJ/m2), X. couchianus exhibited 2 fold higher levels of DNA damage then either X. maculatus or the F1 hybrid. However, based on the cortisol release rates, none of the fish types tested induced a primary stress response at the UVB lower doses (8 and 16kJ/m2). In contrast, at a very high UVB dose (32kJ/m2) both X. maculatus and the F1 hybrid showed a 5 fold increase in the cortisol release rate. To determine the effect of pigmentation on UVB induced stress, wild type and albino Xiphophorus hellerii were exposed to UVB (32kJ/m2). Albino X. hellerii exhibited 3.7 fold increase in the cortisol release while wild type X. hellerii did not exhibit a significant cortisol response to UVB. Overall, the data suggest the rather low UVB doses often employed in tumor induction protocols do not induce a primary stress response in Xiphophorus fishes.

Vulnerability of Patagonian planktonic copepods to fluctuations in temperature and UV radiation

The aim of this investigation is to address the impact of fluctuations in temperature and ultraviolet radiation (UVR) on three species of South American copepods, Boeckella antiqua, B. gracilis and B. brevicaudata. These copepods are cold stenotherm and occur in high latitude lakes of South America and in mountain lakes in the Andes. The forecast scenarios for climate change in southern South America anticipate raising temperature and UVR levels. These changes may have the potential to impact high altitude and latitude ecosystems, including lakes and their cold adapted biota, such as those in Patagonia. Laboratory experiments, consisting of 10 day and 2 day incubations, were set up to analyse copepod mortality in relation with: (i) temperature, and (ii) the combined effect of temperature (5, 8, 12, 16, 20°C) and UV-B dose (61, 194 and 324 J m−2). The results obtained showed up that temperature is a limiting factor for B. brevicaudata that did not survive above 12°C. B. antiqua and B. gracilis withstood the temperature range although their mortality was higher at 12-16°C. The survivorship of these copepod species to radiation was found to depend on the UV-B dose, resulting in higher mortality at the highest UV-B dose. Overall, at least one Boeckella species showed an acute sensitivity to increasing temperature, and the three species studied proved tolerant to the UV-B experimental exposure. The survivorship patterns observed in Boeckella species reflect clearly their adaptation to high solar radiation exposure and to temperate to cold environmental conditions.

Induction of alloantigen-specific CD4+ T regulatory Type 1 cells by alloantigen immunization and ultraviolet-B irradiation: a pilot study in murine transplantation models with skin and cardiac allografts.

The use of ultraviolet (UV)-B irradiation after alloantigen immunization is unknown because previous studies focused on UV-B irradiation before immunization. Here, we investigated immunosuppressive effects induced by UV-B irradiation after immunization, and examined the phenotype of induced regulatory T cells and the possible mechanism of induction. B6 mice (H-2(b)) were intravenously immunized by splenocytes from CBF1 mice (H-2(b/d)). One week after alloantigen immunization, B6 mice received high-dose UV-B irradiation (40 kJ/m(2)). Four weeks after UV-B irradiation, proliferation assays (n=4, in each), transplantations with skin or cardiac allografts (n=5, in each), cytokines in mixed lymphocyte culture (n=6, in each), and adoptive transfer of CD4(+) T cells to naïve B6 mice (n=5, in each) were performed. Mice were divided into 4 groups: untreated control, immunized control, UV-irradiated control, and an immunized and UV-irradiated group. B6C3F1 mice (H-2(b/k)) were used as irrelevant alloantigen with immunization controls. Anti-IL-10 monoclonal antibody was used to block IL-10 before and after UV-B irradiation. Immune responses against the immunizing antigen were markedly suppressed in immunized and UV-irradiated mice in an alloantigen-specific manner. Surprisingly, CD4(+) T cells from immunized and UV-irradiated mice produced significantly larger amounts of IL-10, in an alloantigen-specific manner. Moreover, alloantigen-specific immunosuppression via CD4(+) regulatory T cells was transferable to naïve B6 mice. IL-10 blocking clearly abrogated alloantigen-specific immunosuppression, indicating that UV-B irradiation evoked T regulatory type 1 cells. This study demonstrates for the first time that immunization and UV irradiation induces alloantigen-specific CD4(+) T regulatory type 1 cells, and that IL-10 plays an important role for this induction.

EFFECT OF OXIDASE STRESSES ON GLUCOSINOLATES PROFILE IN BROCCOLI FLORETS DURING POSTHARVEST STORAGE

Stresses cause production of reactive oxygen species in plant bodies and high levels of stress can be harmful to plant tissues. When sub-acute doses of stresses are applied to postharvest crops, beneficial effects can occur through activation of protection mechanisms. In broccoli (Brassica oleracea), such mechanisms can be induction of glucosinolates and phenolic compounds, which are also beneficial to human health. The objective of this work was to examine sub-acute or hormetic doses as well as extreme doses of UV-B, ozone and hydrogen peroxide on the content of glucosinolates during postharvest storage. Broccoli florets were exposed to hormetic and high doses of UV-B (0, 1.5 and 7.5 kJ m(-2)); O(3) (5 ppm for 0, 60 and 720 min) and H(2)O(2) (0, 1.25 and 5 mM for 3 h). The profile of glucosinolates and hydroxy-cinnamic acids was determined for up to 14 days in broccoli florets stored at 4°C by LC-MS. The expression of glucosinolate pathway genes (p450 of the CYP79 family-A2, B3 and F1) and phenylpropanoids pathway genes (PAL, CS and F3H1) were also monitored. Titer of neoglucobrassin in UV-B treated broccoli florets at 1.5 kJ m(-2) was the highest at the end of the 14 days of storage. However, up regulated expression of genes CYP79B3 and CoL were observed with the high UV-B dose of 7.5 kJ m-(2) throughout and at the beginning of the storage, respectively. Both O(3) and H(2)O(2) increased the titers of 4-methoxy-glucobrassicin and 4-hydroxy-glucobrassicin; and the florets treated with high ozone dose (5 ppm for 720 min) exhibited an over expression of genes CYP79F1 and CYP79B3, at the beginning of the storage. Results showed a good correlation between gene expression of CYP79B3, and the titers of indole glucosinolates in treated broccoli florets, suggesting that the target of the applied stresses is likely to be the branch pathway of indole glucosinolates.

The Effects of Enhanced Ultraviolet-B Radiation on the Biology of Green and Brown Morphs ofSitobion avenae(Hemiptera: Aphididae)

The effects of enhanced UV-B radiation on the biology of green and brown morphs of Sitobion avenae (F.) (Hemiptera: Aphididae) were tested under laboratory conditions. The two S. avenae morphs were exposed directly to different doses (0, 216, 432, and 864 kJ/m(2)) of artificial UV-B. Under low doses of UV-B (216 kJ/m(2)), the nymphal development period was significantly shorter, whereas mean relative growth, total fecundity, and gross reproductive rate were significantly higher for both aphid morphs compared with those morphs under control treatments (0 kJ/m(2)). Under high doses of UV-B (432 kJ/m(2) and/or 864 kJ/m(2)), the nymphal development period was significantly longer, whereas the reproductive period, postreproductive period, difference in weight, mean relative growth, and life table parameters were significantly reduced for both aphid morphs. Moreover, the nymphal development period was significantly shorter and the differences in weight, mean relative growth, total fecundity, and life table parameters were significantly higher for the brown morph under high doses of UV-B compared with the green morph. The results showed that enhanced UV-B affects the performance of the green and brown S. avenae morphs from positively to negatively. The brown morph exhibited stronger adaptability than the green morph at high doses of UV-B.

Growth conditions influence UVB sensitivity and oxidative damage in an estuarine bacterial isolate

The dose-dependent variation of oxidative cellular damage imposed by UVB exposure in a representative estuarine bacterial strain, Pseudomonas sp. NT5I1.2B, was studied at different growth phases (mid-exponential, late-exponential, and stationary), growth temperatures (15 °C and 25 °C) and growth media (nutrient-rich Tryptic Soy Broth [TSB] and nutrient-poor M9). Survival and markers of oxidative damage (lipid peroxidation, protein carbonylation, DNA strand breakage, and DNA-protein cross-links) were monitored during exposure to increasing UVB doses (0-60 kJ m(-2)). Oxidative damage did not follow a clear linear dose-dependent pattern, particularly at high UVB doses (>10 kJ m(-2)), suggesting a dynamic interaction between damage induction and repair during irradiation and/or saturation of oxidative damage. Survival of stationary phase cells generally exceeded that of exponential phase cells by up to 33.5 times; the latter displayed enhanced levels of DNA-protein cross-links (up to 15.6-fold) and protein carbonylation (up to 6.0-fold). Survival of mid-exponential phase cells was generally higher at 15 °C than at 25 °C (up to 6.6-fold), which was accompanied by lower levels of DNA strand breaks (up to 4000-fold), suggesting a temperature effect on reactive oxygen species (ROS) generation and/or ROS interaction with cellular targets. Survival under medium-high UVB doses (>10 kJ m(-2)) was generally higher (up to 5.4-fold) in cells grown in TSB than in M9. These results highlight the influence of growth conditions preceding irradiation on the extent of oxidative damage induced by UVB exposure in bacteria.

Comparing intraspecific responses of 12 winter wheat cultivars to different doses of ultraviolet-B radiation

In this study, intraspecific responses of 12 winter wheat cultivars to different doses of ultraviolet-B radiation (UV-B) were analyzed and compared. The results showed that the low UV-B dose of 3.24kJm−2d−1 generally inhibited the plant height, but promoted the dry weight and photochemical reflectance index (PRI). The high UV-B dose of 5.40kJm−2d−1 inhibited most of the indexes, especially plant height and fresh weight. Under the treatments of two UV-B doses, the response indexes (RIs) of plant height, dry weight, fresh weight, carotenoid, and anthocyanin were all significantly correlated with the cumulative stress response index (CSRI). The RIs of carotenoid and anthocyanin exhibited higher correlations with dry weight and fresh weight, indicating that these indexes were vital to UV-B tolerance. By comparing the correlations of the seven indexes between two doses of UV-B radiation, the responses of 12 cultivars’ plant height and dry weight to different doses of UV-B were very significant (P<0.01). Thus, when comparing the UV-B tolerance of different winter wheat seedlings, no matter using high dose or low dose UV-B, the index of plant height should be concerned first and dry weight could be used secondarily. Among 12 winter wheat cultivars, Nongda 6081 exhibited significant resistance to two doses of UV-B radiation while others were variable. Differences in the accumulation of UV-absorbing compounds induced by UV-B in leaves may be the main and direct reason for the intraspecific differences between resistant and sensitive cultivars.

The Reversibility of UV‐B Induced Alterations in Optical Properties of the Rabbit Cornea Depends on Dose of UV Irradiation

Solar UVB radiation evokes photokeratitis, accompanied by increased corneal hydration and changes in corneal transparency, resulting in increased light absorption. Corneal optical properties are disturbed and visual acuity decreased. The aim of this study was to investigate the reversibility of these UVB-induced changes. Rabbit corneas were irradiated with UVB doses of 0.5Jcm(-2) or 1.01Jcm(-2) during 4days. Some rabbits were sacrificed after the last irradiation and some 2months later. Corneas were investigated spectrophotometrically for light absorption, and corneal hydration was evaluated by central corneal thickness with an ultrasonic pachymeter. Corneal impression cytologies were examined immunohistochemically for proinflammatory cytokines and malondialdehyde. The increased corneal light absorption, hydration and the staining of immunohistochemical markers found in corneas after irradiation returned to normal values during 2months in corneas irradiated with the lower UVB dose. In contrast, in corneas irradiated with the higher UVB dose, a moderate but statistically significant increase in corneal light absorption, hydration and positive immunohistochemical stainings remained as residual changes. This was in contrast to normal corneas, where the staining of proinflammatory cytokines as well as malondialdehyde was negative. In conclusion, the reversibility of UVB-induced disturbances was dependent on UVB dose.

Abstract B43: Dose-response on the chemopreventive effects of sarcophine-diol on UVB-induced skin tumor development in SKH-1 hairless mice.

Abstract Sarcophine-diol (SD) is a lactone ring-opened analogue of sarcophine. It has shown chemopreventive effects on chemically-induced skin tumor development in female CD-1 mice, as well as in a UVB-induced skin tumor development model in hairless SKH-1 mice at a dose of 30 μg SD applied topically and 180 mJ/cm2 UVB. The objective of this study was to determine the dose-response on the chemopreventive effects of SD on SKH-1 hairless mice when exposed to a UVB radiation dose of 30 mJ/cm2. This UVB dose better represents chronic human skin exposure to sunlight leading to skin cancer than previous studies applying much higher UVB doses. Carcinogenesis was initiated and promoted by UVB radiation. Female hairless SKH-1 mice were divided into 5 groups. The control group was topically treated with 200 μL of acetone (vehicle), and the SD treatment groups were topically treated with SD (30 μg, 45 μg, and 60 μg dissolved in 200 μL of acetone) 1 hour before UVB radiation (30 mJ/cm2). The last group of animals received 60 μg SD/200 μl acetone without UVB exposure. These treatments were continued for 27 weeks. Tumor multiplicity and tumor volumes were recorded on a weekly basis for 27 weeks. Weight gain and any signs of toxicity were closely monitored as well. Histological characteristics and the proliferating cell nuclear antigen (PCNA) were evaluated in the mice skin collected at the end of the experiment. The dose-response study proved a modest increase in chemopreventive effects with the increase in SD dose, reflected in reduced tumor multiplicities and tumor volumes. SD also reduced the number of cells positively stained with PCNA proliferation marker in mice skin. The study also showed that SD applications without UVB exposure had no effect on the structure of mice skin. The results from this study suggest that broader range doses of SD are necessary to improve the chemopreventive effects. Citation Format: Ruth F. Guillermo, Xiaoying Zhang, Radhey S. Kaushik, David Zeman, Safwat A. Ahmed, Sherief Khalifa, Hesham Fahmy, Chandradhar Dwivedi. Dose-response on the chemo-preventive effects of sarcophine-diol on UVB-induced skin tumor development in SKH-1 hairless mice. [abstract]. In: Proceedings of the Eleventh Annual AACR International Conference on Frontiers in Cancer Prevention Research; 2012 Oct 16-19; Anaheim, CA. Philadelphia (PA): AACR; Cancer Prev Res 2012;5(11 Suppl):Abstract nr B43.

UV-B radiation: “When does the stressor cause stress?”

Exposure to UV-B radiation can cause stress in plants Solar UV-B radiation (280 315 nm) has long been recognized as being potentially damaging to living organisms. Indeed, the literature on plant UV-B radiation effects has for decades been dominated by reports on UV-B mediated stress, including growth retardation, macroscopic injuries and oxidative damage (Caldwell et al., 1994; Searles et al., 2001). These negative effects comprise damaging effects on genetic material (formation pre-mutagenic cyclobutane pyrimidine dimers [CPD] and pyrimidine [6-4] pyrimidinone dimers), photosynthetic performance (in-tandem degradation of D1-D2 core proteins of photosystem II, inactivation RUBISCO, altered stomatal function) and a range of other cellular targets (see Jansen et al., 1998; Searles et al., 2001; Jordan 2002; Rozema et al., 2005; Jenkins, 2009). In this issue Lidon et al. (2012a) review our current understanding of the deleterious effects of UV-B on photosynthesis. UV-B damage is paralleled by the formation of lipid peroxidation products such as malondialdehyde (MDA) (Hideg et al., 2003; Lidon and Ramalho, 2011) and increased oxidation of antioxidants such as glutathione (Kalbin et al., 1997), both of which reflect the oxidative character of the UV-caused stress conditions. Consistently, UV-induced ROS have been measured using EPR spin trap reporters in both leaves (Hideg and Vass, 1996) and in isolated thylakoids (Lidon et al., 2012b) exposed to high doses of UV-B.

Dose-Response on the Chemopreventive Effects of Sarcophine-Diol on UVB-Induced Skin Tumor Development in SKH-1 Hairless Mice

Sarcophine-diol (SD) is a lactone ring-opened analogue of sarcophine. It has shown chemopreventive effects on chemically-induced skin tumor development in female CD-1 mice, as well as in a UVB-induced skin tumor development model in hairless SKH-1 mice at a dose of 30 μg SD applied topically and 180 mJ/cm2 UVB. The objective of this study was to determine the dose-response on the chemopreventive effects of SD on SKH-1 hairless mice when exposed to a UVB radiation dose of 30 mJ/cm2. This UVB dose better represents chronic human skin exposure to sunlight leading to skin cancer than previous studies applying much higher UVB doses. Carcinogenesis was initiated and promoted by UVB radiation. Female hairless SKH-1 mice were divided into five groups. The control group was topically treated with 200 μL of acetone (vehicle), and the SD treatment groups were topically treated with SD (30 μg, 45 μg, and 60 μg dissolved in 200 μL of acetone) 1 h before UVB radiation (30 mJ/cm2). The last group of animals received 60 μg SD/200 μL acetone without UVB exposure. These treatments were continued for 27 weeks. Tumor multiplicity and tumor volumes were recorded on a weekly basis for 27 weeks. Weight gain and any signs of toxicity were also closely monitored. Histological characteristics and the proliferating cell nuclear antigen (PCNA) were evaluated in the mice skin collected at the end of the experiment. The dose-response study proved a modest increase in chemopreventive effects with the increase in SD dose. SD reduced the number of cells positively stained with PCNA proliferation marker in mice skin. The study also showed that SD application without UVB exposure has no effect on the structure of skin. The results from this study suggest that broader range doses of SD are necessary to improve the chemopreventive effects.

UV-B resistance as a criterion for the selection of desert microalgae to be utilized for inoculating desert soils

The adaption capability of microalgae species to intense UV-B radiation is an important feature for their survival under the harsh growth conditions they have to face when used for inoculating unconsolidated sand soils in desert areas. In this study, the responses of photosynthetic activity, reactive oxygen species (ROS) generation, and DNA strand breaks to UV-B radiation in four microalgae isolated from artificially induced biological soil crusts were investigated. It was found that low UV-B doses easily inhibited the photosynthetic activity and induced serious DNA damage in Chlorella vulgaris. Microcoleus vaginatus showed the capability to withstand only moderate doses of UV-B, while Nostoc was capable of facing high doses of UV-B due to its lower generation of ROS and higher capability to repair photosystem II (PSII) and DNA damages. On the other hand, Scytonema javanicum showed additional strategies to survive UV-B irradiance, namely the closure of PSII when ROS generation increased rapidly, in addition to a high repair ability of PSII and DNA damage. The results obtained point out different resistance and defense mechanisms of the four microalgae in response to UV-B irradiance and suggest that the strain of Nostoc sp. tested is the most suitable for surviving under the high UV irradiation levels typical of desertified areas.

Nickel and ultraviolet-B stresses induce differential growth and photosynthetic responses in Pisum sativum L. seedlings.

Enhanced level of UV-B radiation and heavy metals in irrigated soils due to anthropogenic activities are deteriorating the environmental conditions necessary for growth and development of plants. The present study was undertaken to study the individual and interactive effects of heavy metal nickel (NiCl(2)·6H(2)O; 0.01, 0.1, 1.0 mM) and UV-B exposure (0.4 W m(-2); 45 min corresponds to 1.08 KJ m(-2)) on growth performance and photosynthetic activity of pea (Pisum sativum L.) seedlings. Ni treatment at high doses (0.1 and 1.0 mM Ni) and UV-B alone reduced chlorophyll content and photosynthetic activity (oxygen yield, carbon fixation, photorespiration, and PSI, PSII, and whole chain electron transport activities), and declining trends continued with combined doses. In contrast to this, Ni at 0.01 mM appeared to be stimulatory for photosynthetic pigments and photosynthetic activity, thereby enhanced biomass was observed at this concentration. However, combined dose (UV-B + 0.01 mM Ni) caused inhibitory effects. Carotenoids showed different responses to each stress. Nickel at high doses strongly inhibited PSII activity and the inhibition was further intensified when chloroplasts were simultaneously exposed to UV-B radiation. PSI activity appeared to be more resistant to each stress. High doses of Ni (0.1 and 1.0 mM) and UV-B alone interrupted electron flow at the oxygen evolving complex. Similar damaging effects were caused by 0.01 and 0.1 mM Ni together with UV-B, but the damage extended to PSII reaction center in case of 1.0 mM Ni in combination with UV-B. In conclusion, the results demonstrate that low dose of Ni stimulated the growth performance of pea seedlings in contrast to its inhibitory role at high doses. However, UV-B alone and together with low as well as high doses of Ni proved to be toxic for P. sativum L.

Abstract 268: Regulation of the UDP-glucuronosyltransferases (UGTs) by UV exposure in human melanocytes

Abstract The UDP-glucuronosyltransferase (UGT) family of enzymes catalyzes the glucuronidation of a variety of endogenous compounds such as bilirubin and steroid hormones, as well as xenobiotics including chemotherapeutic agents and environmental carcinogens. Glucuronidation of these substrates inactivates them by making them more hydrophilic and easily excreted. UGTs are expressed primarily in the liver, but are also expressed in several extra-hepatic tissues including prostate, breast, colon, lung, brain, kidney, bladder and ovary. We have demonstrated that three UGT family members (UGT2B7, UGT2B10 and UGT2B15) are normally expressed in human melanocytes isolated form neonatal foreskin. Further, we screened several primary and metastatic melanoma cells lines for UGT expression. Interestingly, of all the melanoma cell lines screened only WM115, a primary melanoma, had UGT expression. Again, only UGT2B7, UGT2B10 and UGT2B15 were detected. UGT expression was not detected in another primary melanoma cell line, WM3211, or in any of the four metastatic melanoma cell line assayed suggesting that loss of UGT expression occurs during melanoma progression. To elucidate if ultraviolet (UV) light could be the underlying cause to the disappearance of UGTs in melanoma progression, human melanocytes were subjected to UV-B radiation at low and high (sunburn) doses. Melanocytes were collected at 1, 5 and 24 Hrs post UV-B treatment and UGT expression was analyzed by quantitative real-time PCR. Expression of UGT2B7, UGT2B10 and UGT2B15 all was significantly reduced in response to both low and high dose UV-B. In general, loss of UGT expression was observed even at 1 hour after exposure, reached maximal low levels at 5 hours and started to return to normal levels at 24 hours post exposure. We hypothesize that reduction of UGT expression in melanocytes following a sunburn would increase an individuals risk for melanoma since the UGTs detoxify environmental carcinogens. This hypothesis is consistent with a causative role for UV in melanoma in which ‘classical’ UV-induced DNA damage is not observed; a problem that has long puzzled investigators. Citation Format: {Authors}. {Abstract title} [abstract]. In: Proceedings of the 103rd Annual Meeting of the American Association for Cancer Research; 2012 Mar 31-Apr 4; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2012;72(8 Suppl):Abstract nr 268. doi:1538-7445.AM2012-268

Imiquimod attenuates the growth of UVB‐Induced SCC in mice through Th1/Th17 cells

Imiquimod (IMQ), a Toll-like receptor (TLR) 7/8 agonist, has been used to treat various skin neoplasms, including genital warts, actinic keratoses, and superficial basal cell carcinomas. Although IMQ has been recognized to activate both innate and adaptive immunity, the underlying mechanism(s) by which IMQ exerts its anti-tumor activity in vivo remains largely unknown. In this study, we took advantage of skin cancer-prone mice to characterize the effects of IMQ on ultraviolet irradiation (UV)-induced de novo carcinogenesis. Transgenic mice with keratinocytes expressing constitutively activated Stat3 (K5.Stat3C mice) developed squamous cell carcinomas (SCC in situ) as early as after 14 wk of UVB irradiation, while wild-type mice required much higher doses of UVB with more than 25 wk of UVB irradiation to produce SCC. Topical treatment of K5.Stat3C mice with IMQ attenuated UVB-induced epidermal dysplasia (SCC in situ). In addition, SCC growth due to increased total irradiation doses was significantly attenuated by IMQ treatment. Topical IMQ treatment induced T cell and plasmacytoid dendritic cell infiltrates at the tumor sites, where levels of IL-12/23p40, IL-12p35, IL-23p19, IL-17A, and IFN-γ mRNAs were up-regulated. Immunohistochemistry revealed T cell infiltrates consisting of T1, Th17, and CD8(+) T cells. We speculate that topical IMQ treatment attenuates the de novo growth of UVB-induced SCC through activation of Th17/Th1 cells and cytotoxic T lymphocytes.

Ostracod valves as efficient UV protection

One of the major consequences of climate change is the increase of ultraviolet radiation, especially UVB (280-315 nm). This has important consequences for organisms and ecosystems. In surface freshwater ecosystems with transparent water, UV can easily penetrate deeply. Here, we used three different experimental approaches to examine the response of non-marine ostracods and cladocerans to UVB radiation: estimating lethal doses, determining how much UVB is blocked by the valves, and analysing valve chemical compositions. For most investigated crustaceans, we found a strong correlation between the amount of UVB that is blocked by the valves and the lethal UVB doses. Most ostracod valves blocked between 60% and 80% of UVB radiation, thus providing effective shielding. Pigmented species from temporary habitats were best protected. These species also showed high lethal UVB doses of 110 kJ m 2 to 214 kJ m 2. In the waterflea Daphnia magna, valves only stopped ca 35% of UVB radiation, and the lethal dose was half that of the doses estimated for ostracods. Since there were no significant differences in chemical composition of the valves between the investigated species, other factors must be responsible for the observed differences, which remain to be identified.