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It is known that UV modulates the expression of paracrine factors that regulate melanocyte function in the skin. We have investigated the consequences of repetitive UV exposure of human skin in biopsies of 10 subjects with phototypes 2-3.5 taken 1-4 yr later. The expression of melanogenic factors (TYR, MART1, MITF), growth factors/receptors (SCF/KIT, bFGF/FGFR1, ET1/EDNRB, HGF, GM-CSF), adhesion molecules (β-catenin, E-cadherin, N-cadherin), cell cycle proteins (PCNA, cyclins D1, E2) as well as Bcl-2, DKK1 and DKK3, were analyzed by immunohistochemistry. Most of those markers showed no detectable changes at ≥1 yr after the repetitive UV irradiation. While increased expression of EDNRB protein was detected in 3 of 10 UV-irradiated subjects, there was no detectable change in the expression of ET1 protein or in EDNRB mRNA levels. In summary, only the expression of TYR, MART1 and/or EDNRB, and only in some subjects, was elevated at ≥1 yr post-UV irradiation. Thus the long-term effects of repetitive UV irradiation on human skin did not lead to significant changes in skin morphology and there is considerable subject-to-subject variation in responses. The possibility that changes in the expression and function of EDNRB triggers downstream activation of abnormal melanocyte proliferation and differentiation deserves further investigation.
The incidence of melanoma has tripled over the past 3 decades probably as a result, at least in part, from lifestyle changes that have led to an increased exposure of the fair-skinned population to ultraviolet radiation (UV) [NCI Seer Statistics, http://seer.cancer.gov/]. Epidemiological and laboratory data provide strong evidence that solar exposure is a major causative factor in melanomagenesis (Gilchrest et al., 1999). Emerging evidence suggests that there is a clear link between tanning devices and malignant melanoma (Clough-Gorr et al., 2008; International Agency for Research on Cancer, 2007; Ting et al., 2007). Pathomechanisms for the development of non-melanocytic skin cancers have already been revealed (Matsumura and Ananthaswamy, 2002; Stary et al., 1997), however, the exact mechanism(s) of UV-induced melanomagenesis in the skin in situ remains unknown. Since UV-fingerprint mutations are rare in melanomas, it has been speculated that UV causes melanoma development by indirect effects, for example by dysregulation of growth factors in the skin, as proposed in a human skin graft model for UV-induced melanomas (Berking et al., 2004). We have recently shown that UV modulates the production (by keratinocytes and by fibroblasts in vitro) of growth factors regulating melanocyte function (Brenner et al., 2005). UV is presently the only known environmental carcinogen for melanomas, however it is still controversial which wavelengths are critical. UVA has been shown to promote melanoma in a hybrid fish melanoma model (Setlow et al., 1993), while UVB promotes melanoma in several transgenic mouse models (Noonan et al., 2003).
There is an urgent need to determine the specific mechanisms that are involved in photocarcinogenesis of UV-irradiated human skin in situ. Numerous studies have examined the effects of UV on skin cells in vitro, however that experimental setting does not allow one to explore inter-individual differences such as skin phototype or minimal erythema dose (MED). The examination of UV-induced changes in UV-irradiated skin in situ, with respect to different wavelengths and doses, provides a more suitable approach to characterize UV photocarcinogenesis in the skin, particularly with respect to early events in the malignant cascade.
Our group has previously reported several studies on the acute effects of UV radiation on human skin of varying skin pigmentation phenotypes. So far, we have shown that even a single, relatively low (1 MED) UV dose (60% UVA/40% UVB) causes significant damage to DNA in epidermal cells and stimulates the production of photoprotective melanin (Tadokoro et al., 2003). Most UV-induced DNA damage is removed relatively quickly (within days), however, some UV-induced molecular changes might persist and could initiate malignant transformation in the skin. Our earlier studies examined only the short-term effects of UV on human skin in situ. To extend our understanding of the long-lasting and potentially photocarcinogenic effects of UV, we examined biopsies from sites exposed to repetitive UV irradiation several years ago. In particular, we characterized the long-lasting effects of UV on melanocytes and on keratinocytes. We examined various potential morphologic and molecular markers of malignant transformation in 2 different UV-irradiated groups. One group of 6 subjects had been repeatedly irradiated over several weeks at 3 different cumulative doses with Sunlamps emitting a UV spectrum commonly used in tanning salons (≥95% UVA/≤5% UVB) while in another group, 4 different subjects had been repeatedly irradiated over a period of 2 weeks with a solar simulator (SS, ≥90% UVA/≤10% UVB). The molecular markers examined can be divided into 6 subgroups and were selected due to their possible involvement in melanocyte transformation and/or because many previously published studies have analyzed their responses in human skin within 1 month of UV exposure:
Subjects (listed in Table 1) from 2 independent studies (Miller et al., 2008; Wolber et al., 2008) were invited to return for reexamination >1 yr after their initial UV exposures. Areas previously irradiated were identified using photos taken at the time of initial exposure, considering surface features and in some cases, pigmented areas that still remained.
Skin specimens from all subjects were stained with H&E and were carefully examined by light microscopy for morphological changes in the structure of the epidermis and/or the dermis. No morphological changes were seen in any UV-irradiated skin specimens or from the adjacent unirradiated skin specimens [Figure 1]. There were no signs that could be correlated to any clinical aspect of a localized sunburn reaction, such as a superficial inflammatory infiltrate in the dermis or the presence of sunburn cells in the epidermis. Special attention was paid to detect possible changes in the density, distribution and/or localization of melanocytes (e.g. suprabasal localization of melanocytes, formation of melanocyte cell nests). No such changes were detected, although there was a significant increase in melanocyte density in some subjects (see below).
To evaluate long-lasting changes in melanin content, the UV-irradiated skin areas and the corresponding unirradiated control tissues were examined visually and were biopsied after >1 yr post-exposure. Repetitive UV irradiation with the Sunlamp or with the solar simulator produced good early tanning reactions in all subjects. However, only 1 subject (T50) in the Sunlamp-irradiated group showed long-lasting pigmentation (LLP) in the areas exposed to the intermediate or high cumulative UV doses (Miller et al., 2008). Figure 2 shows such pigmentation at 520 d post-irradiation. None of the subjects in the SS-irradiated group had visibly increased pigmentation in the irradiated areas at the time of biopsy [Table 1].
The melanin content in each skin specimen was determined by quantitative densitometry of the Fontana-Masson stained sections [Figure 3]. Only one subject (T50) in the Sunlamp-irradiated group and one subject (B6) in the SS-irradiated group showed significantly (p<0.05) increased total amounts of melanin [Table 2].
There were no significant differences in the numbers of MITF-positive cells compared to the unirradiated controls in the UV-irradiated subjects. Although no difference could be found between the UV-irradiated and the control specimens in the number of MART1-positive cells in the Sunlamp-irradiated group, 2 subjects (B6 and B8) showed significantly higher (p<0.05) numbers of MART1-positive cells in the SS-irradiated group. In the Sunlamp-irradiated group, a significant increase in the number of TYR-positive cells compared to the unirradiated control was only found in subject T50, who was the only subject in either study group with visible pigmentation remaining in the previously UV-irradiated areas. In the SS-irradiated group, 3 out of 4 subjects (B2, B6 and B8) showed significant (p<.05) increases in the density of TYR-positive cells [Table 2, Figure 3], although no visibly increased pigmentation was noted in those previously UV-irradiated areas.
In the skin specimens examined, SCF, bFGF and ET1 were expressed in the basal epidermal layer. Between different samples, the staining intensity ranged from weak to moderate, but overall, no marked differences in expression could be detected between UV-irradiated and control specimens from either protocol. KIT expression was detected in all samples and showed a strong regular pattern of staining in the basal layers of the epidermis. FGFR1 staining was weak and was restricted to the basal epidermal layer. Expression of HGF could not be detected in the epidermis of any skin sections examined. GM-CSF expression in the skin showed irregular patterns, with some specimens showing basal expression and others showing dispersed expression throughout the whole epidermis [Figure 4]. Two of the 6 subjects in the Sunlamp-irradiated group (T35 and T47) and 1 of the 4 subjects in the SS-irradiated group (B6) showed marked differences in the expression of EDNRB in the basal epidermal layers compared to the unirradiated controls. We used a tissue array with 39 melanoma samples as a positive control for EDNRB [Figure 5].
Tissue-in situ hybridization for EDNRB mRNA in the Sunlamp- or SS- irradiated skin showed cytoplasmic staining mainly in the basal epidermal layers, but no marked difference in EDNRB mRNA expression between the UV-irradiated and control skin [Figure 5].
All skin specimens were examined for expression of various adhesion molecules (β-catenin, E- and N-cadherins). β-Catenin showed a regular strong cytoplasmic staining pattern throughout the whole epidermis with no changes in the expression between UV-irradiated and unirradiated skin. No nuclear staining pattern could be detected. In all skin specimens, E-cadherin was expressed in a regular strong cytoplasmic pattern throughout the epidermis and no marked differences between UV-irradiated and control specimens were found. N-cadherin expression could not be detected [Figure 6].
Skin specimens were analyzed for expression of the proliferative index of PCNA, cyclins D1 and E2. Neither cyclin D1 nor E2 showed a positive staining. PCNA expression showed no differences between UV-irradiated and control specimens, except for 1 subject (B6) in the SS-irradiated group. A clearly higher nuclear staining for PCNA was found in that specimen, however, double staining with TYR revealed that mainly keratinocytes, but not melanocytes, showed the increased expression of PCNA [Figure 6].
DKK1 could not be detected in any skin specimens examined, UV-irradiated or unirradiated. DKK3 expression showed a regular and strong expression pattern in the upper epidermal layers but did not exhibit any significant changes in response to UV irradiation. Bcl-2 immunoreactivity was found in melanocytes in the basal cell layer of the skin as expected, but no marked differences in the expression of Bcl-2 was noted between UV-irradiated and unirradiated specimens [Figure 6].
In the past, many in vitro and in vivo experiments have been conducted to characterize the carcinogenic effects of UV radiation on human skin cells. In vitro studies with human melanocytes (Bittner et al., 2000; Clark et al., 2000; Hipfel et al., 2000; Valery et al., 2001; Young et al., 1998b) and in vivo studies on human skin have examined the effects of short-term UV irradiation (Hachiya et al., 2004; Mass et al., 2003; Tadokoro et al., 2003; Tronnier et al., 1997; Young et al., 1998a) but so far there have been no studies about the long-lasting effects of UV. Some in vivo studies have examined molecular changes of atypical nevi (melanoma precursor lesions) (Wang et al., 1996), but it has been estimated that melanomas mainly arise in the skin de novo and in only 30% of melanocytic nevi (Wolff et al., 2005).
In our study, we tried to identify long-lasting molecular changes in human skin in situ many months after the initial repetitive UV irradiation. The analysis was mainly based on immunohistochemistry techniques and was completed by tissue in situ hybridization for the analysis of EDNRB mRNA. While this approach allowed the analysis of a considerable number of molecular factors it does not permit quantitative analysis of protein and/or RNA expression. We analyzed melanin content using Fontana-Masson staining and melanocyte density using antibodies to melanocyte-specific markers, such as MITF, MART1 and TYR. Earlier, we reported the results of 3 clinical studies measuring melanocyte density after UV irradiation that showed significant increases to levels about 3-fold higher than in unirradiated skin at up to 5 weeks after irradiation and that increase was consistent with the increased melanin content (Tadokoro et al., 2003; Tadokoro et al., 2005; Yamaguchi et al., 2006). In this study, a significant increase in MART1-positive melanocytes in 2 of 10 subjects and a significant increase in TYR-positive melanocytes in 4 of 10 subjects was found, although only 1 of those subjects still showed a visibly increased pigmentation in the UV-irradiated area. This indicates that the activation of melanocytes might persist much longer than the UV-induced pigmentation or the acute UV-induced changes in cell morphology.
As there is a wide variety of other possible genes of interest and their corresponding encoded proteins, we focused our analysis on representatives of 5 major groups of proteins where changes in expression could be involved in the transformation of melanocytes. The growth factors (and their cognate receptors) SCF/KIT, bFGF/FGFR1, ET1/EDNRB, GM-CSF/GM-CSFR and HGF/MET, are part of the paracrine network between melanocytes and keratinocytes/fibroblasts (Imokawa, 2004; Yamaguchi et al., 2007; Brenner and Hearing, 2008). SCF and ET1 are highly mitogenic for human melanocytes (Grichnik et al., 1995; 1998; Imokawa et al., 1996a). The expression of KIT, the cognate receptor for SCF, is down-regulated with progression in melanoma cell lines and tumors (Montone et al., 1997). Recently, it was shown that SCF and KIT are frequently expressed by melanomas and by dysplastic nevi suggesting an autocrine growth factor mechanism (Giehl et al., 2007). Also reported recently are studies showing that bFGF, SCF and ET3 may be involved in melanomagenesis (Berking et al., 2004). FGFR1 is the cognate receptor for bFGF and the co-expression of FGFR1 and bFGF in melanoma cells was reported to be associated with increased microvessel density (Straume and Akslen, 2002).
In contrast to KIT expression, which is gradually lost during the transformation of melanocytes to malignant melanoma, EDNRB expression is greatly enhanced and can serve as a marker of melanoma progression (Bittner et al., 2000; Demunter et al., 2001; Loftus et al., 1999). Those results and the finding that ET1 production by keratinocytes is increased following UV irradiation (Ahn et al., 1998) suggest that EDNRB as well as its ligand, ET1, contribute to melanomagenesis and progression (Demunter et al., 2001; Lahav, 2005). Increased EDNRB expression, probably coupled with epidermal hyper-secretion of ET1, could be a first step to generate local populations of melanocytes with the potential to escape from the epidermis if further changes occur (e. g. loss of E-cadherin). EDNRB has been recently reported to be up-regulated in solar lentigos (Aoki et al., 2007), which is consistent with the findings of our study, and suggests that over-expression of that receptor may result from chronic UV exposure and may be involved in the increased pigmentation of human skin following UV. One study in human skin in vivo showed an early increase in SCF and KIT mRNA expression and a subsequent increase in the expression of TYR, ET1 and EDNRB mRNA and protein 7 to 10 d after 2 MED UVB irradiation (Hachiya et al., 2004). HGF is a multifunctional cytokine, which, among other activities, acts as a growth factor for melanocytes. It has been shown that UVB irradiation leads to melanomas in neonatal HGF-transgenic mice (Noonan et al., 2001). HGF, which is expressed by fibroblasts and by melanoma cells, but not by normal melanocytes (Iyer et al., 1990; Li et al., 2001; Rosen et al., 1994) could not be detected in the epidermis of our skin specimens. GM-CSF has been shown to be secreted from keratinocytes after UVA (Imokawa et al., 1996b) or UVB irradiation (Hirobe et al., 2004) and might play an important role in regulating the proliferation and differentiation of human melanocytes after UV irradiation.
In our study, we could not detect any marked differences between the UV-irradiated skin and the unirradiated controls in long-term follow-up specimens regarding the expression of SCF, KIT, GM-CSF, bFGF, FGFR1 or ET1 in the epidermis. However, in 3 of 10 subjects, a clearly increased expression of EDNRB protein was detected in the irradiated skin; however, that was not detected at the mRNA level. Whether the increased expression of EDNRB in some of our subjects might predict an increased risk for skin cancer further in the future deserves a longer term follow-up study.
β-Catenin is a potent mediator of growth for melanoma cells and plays a dual role in cells, in cadherin-mediated cell adhesion (Steinberg and McNutt, 1999) and in the Wnt signaling pathway (Morin, 1999). E-cadherin, which is a tumor invasion suppressor, is down-regulated in most melanoma cells, and this renders them refractory to keratinocyte-mediated control and enhances their capability for invasion (Hsu et al., 2000). Staining for E-cadherin and for β-catenin resulted in strong staining patterns; however, no differences in their expression in UV-irradiated skin and in unirradiated controls were detected. Also, no expression of N-cadherin could be detected, which might indicate that changes in adhesion molecules occur in late stages of melanomagenesis and are signs of the invasive behavior of malignant skin cells.
Dysregulation of the cell cycle is a hallmark of tumor progression and increased proliferative activity of tumor cells is an important prognostic marker in many human cancers. Proliferation is regulated by the formation, activation and degradation of a series of cyclins. Widely-used immunohistochemical markers to assess cell proliferation include PCNA and Ki-67 (Linden et al., 1992). In 1 of our 10 UV-irradiated skin specimens, a strong increase in PCNA expression in keratinocytes, but not in melanocytes, was detected. We could not detect any changes in the expression of cyclin D1 or cyclin E2 in the UV-irradiated skin, which is possibly due to the fact that UV-induced changes in cell cycle proteins are early events that might already be removed at this late time-point (>1 yr).
DKK1, a secreted protein preferentially expressed by palmoplantar fibroblasts in the dermis inhibits melanocyte growth and differentiation through canonical Wnt signaling, β-catenin expression and MITF function (Yamaguchi et al., 2004). In contrast, DKK3, which is expressed at higher levels in fibroblasts in nonpalmoplantar dermis has no effect on melanocyte growth and function (Yamaguchi et al., 2005). The potential role(s) of DKK proteins in melanoma is totally unknown. An analysis of the expression profile of UVB responses in normal human melanocytes detected a >2-fold induction of DKK1 gene expression after UVB irradiation; however, in many melanoma cell lines a loss of DKK1 expression has been reported (Yang et al., 2006). A recent study found a strong reduction of DKK3 expression in human primary melanomas and metastases compared to normal skin (Kuphal et al., 2006). In our study, DKK1 could not be detected in the nonpalmoplantar skin that was UV-irradiated (confirming our earlier studies) while DKK3 expression showed a regular pattern in the upper epidermal layers and did not exhibit any significant changes in response to UV exposure.
We characterized the expression of Bcl-2 as it represents the prominent marker within the large Bcl-2 family and numerous studies have been published regarding the effects of UV irradiation on human skin with respect to Bcl-2 expression. In our study, Bcl-2 immunoreactivity was found predominantly in the basal cell layer of the skin specimens. One study that analyzed human skin in situ 6 h after a single SS-irradiation found a transient reduction of ~40% in the expression of Bcl-2 (Isoherranen et al., 1999). We could not detect any significant differences in the expression of Bcl-2 between UV-irradiated and unirradiated skin. Regarding the expression pattern of Bcl-2 after UV exposure, the literature is contradictory. One in vitro study described an induction of Bcl-2 at the mRNA level, but not at the protein level after UVB (Bivik et al., 2005). In vitro studies on human melanocytes revealed no changes in expression of Bcl-2 after UVA or UVB irradiation (Kim et al., 2000; Zhang and Rosdahl, 2003), while other groups reported that Bcl-2 levels decrease after UV irradiation (Im et al., 1998; Isoherranen et al., 1999; Kadekaro et al., 2003).
In summary, among the 20 factors examined, only MART1, TYR and EDNRB protein expression, and only in some subjects, were elevated at ≥1 yr post-UV irradiation. These findings suggest that the long-term effects of repetitive UV irradiation on human skin in these studies do not lead to significant changes in skin morphology and there is considerable subject-to-subject variation in effects on skin pigmentation. The possibility that changes in the expression of the EDNRB protein trigger downstream activation of abnormal melanocyte proliferation and, considering the key role of the melanocortin system in regulating human skin pigmentation, the long-lasting UV-induced molecular changes in the expression of factors such as proopiomelanocortin (POMC), POMC-derived peptides and melanocortin 1 receptor (MC1R), also deserves further investigation.
This study involved volunteer subjects with skin phototypes 2-3.5, as shown in Table 1, and was approved by the Research Involving Human Subjects Committees of the U.S. Food and Drug Administration and Beiersdorf AG. Written informed consent was obtained from each donor. Each subject's MED was determined prior to the start of the experiment, as detailed in (Miller et al., 2006; 2008; Wolber et al., 2008; Yamaguchi et al., 2008b). Subjects did not receive significant UV exposure between the times of the initial experimental irradiation and the long-term biopsies.
Six subjects (T11, T16, T32, T35, T47 and T50), from the study detailed in (Miller et al., 2008), were studied with long-term follow-up. For the repetitive Sunlamp-irradiation protocol, a 12-lamp tanning bed canopy (≥95%UVA, ≤5%UVB) was used and monitored as previously detailed (Miller et al., 2008). Three different repeated UV exposure regimens were used over the course of 3-4 weeks on the back of each subject. Cumulative doses were 1,900 J/m2, 2,900 J/m2 and 4,200 J/m2 for low, medium and high dose exposure regimens, respectively.
Four subjects (B1, B2, B6 and B8, from (Wolber et al., 2008), were studied with long-term follow-up. For the repetitive SS-irradiation protocol, an Oriel 1600W SS was used and doses were monitored as previously detailed (Schlenz et al., 2005; Miyamura et al., 2007; Wolber et al., 2008). Irradiations were given a total of 10 times over 2 weeks on 5 consecutive days with cumulative doses that ranged between 333 and 1030 J/m2. Irradiation doses varied between individuals depending on each subject's MED to induce comparable tanning.
Skin biopsies were taken from the control and UV-exposed sites at various times after the last UV exposure. Each biopsy was placed dermis side down on a Millipore filter and was then fixed in 4% formaldehyde, embedded in paraffin, sectioned at 3 μm-thickness, mounted on silane-coated glass slides, and then stained using immunohistochemistry, as previously described (Yamaguchi et al., 2004; 2006). Briefly, specimens were deparaffinized twice with xylene for 5 min and were then dehydrated with a graduated series of ethanol, followed by antigen retrieval via boiling in antigen unmasking solution (Vector Laboratories, Inc. Burlingame, CA, USA) for 12 min. For antigens expressed in low abundance, 1 mM EDTA-heat antigen retrieval was used. Specimens were subsequently incubated with 10% goat, 10% horse or 10% donkey serum (Vector Laboratories) for 30 min at 37°C, as appropriate, and then with primary antibodies in 5% goat serum (5% horse or 5% donkey serum respectively) at 4°C overnight. Secondary antibodies were used as appropriate for the primary antibody, Alexa Fluor 488/594 anti-mouse, anti-rabbit or anti-goat IgG (H+L) (at 1:500 dilution, Molecular Probes Inc., Eugene, OR, USA). Staining was analyzed using a Leica DMRB/DMLD fluorescence microscope, and an internal control was used each time to control for reproducible antibody staining. Negative controls omitting the primary antibody were performed each time.
Protein expression using the following antibodies was measured: SCF antibody (at 1:10 dilution; R&D Systems, Minneapolis, MN, USA), SCF R/KIT antibody (at 1:100 dilution; R&D Systems), bFGF antibody (at 1:10 dilution; R&D Systems), FGFR1 antibody (at 1:100 dilution; Abcam Inc, Cambridge, MA, USA), ET-1 antibody (at 1:200 dilution; Abcam Inc), EDNRB antibody (at 1:100 dilution; Abcam Inc), GM-CSF antibody (at 1:20 dilution; R&D Systems), HGF antibody (at 1:10 dilution; R&D Systems), PCNA antibody (at 1:200 dilution; Dako Inc, Carpinteria, CA, USA), cyclin D1 antibody (at 1:20 dilution; Zymed Laboratories, South San Francisco, CA, USA), cyclin E2 antibody (at 1:20 dilution; Cell Signaling Technology, Beverly, MA, USA), E-cadherin antibody (at 1:100 dilution; Takara Bio Inc, Shiga, Japan), N-cadherin antibody (at 1:10 dilution; Dako Inc), β-catenin antibody (at 1:100 dilution; Cell Signaling Technology), Bcl-2 antibody (at 1:20 dilution; Santa Cruz Biotechnology Inc, Santa Cruz, CA, USA), DKK-1 antibody (at 1:50 dilution; R&D Systems) and DKK-3 antibody (at 1: 100 dilution; R&D Systems).
Tissue in situ hybridization was performed as previously detailed (Passeron et al., 2007a; 2007b; Valencia et al., 2006). Oligonucleotide probes specific for human EDNRB were designed, and target sites were selected based on the analysis of sequence matches and mismatches BLAST (GenBank). Probes showed no evidence of cross-reaction with sequences of other genes including other ETR family genes. Optimal results were obtained with the following probes: sense primer 5′- CATACGATTTAGGTGACACTATAGgccatttggagctgagatgt -3′; antisense primer 5′-GCGCGTAATACGACTCACTATAGGGgacaaggaccaggcaaaaga -3′. The probes were 3′ tailed with digoxigenin-11-dUTP with a DIG RNA labeling kit (Roche, Basel, Switzerland), according to recommendations of the manufacturer. Briefly, after deparaffinization and rehydration, skin sections were immersed in antigen retrieval solution and heated in a microwave for 12 min then cooled for 20 min. Slides were then washed in glycine solution (2 mg/ml in PBS) for 10 min, washed twice in PBS, and then placed in 200 ml acetylation buffer (0.1 M triethylamine, pH 8.0, containing 0.25% acetic anhydride) for 15 min. After further washing in 4X SSC for 10 min, samples were incubated in prehybridization solution (2X SSC, 50% deionized formamide) for 1 h at 47°C. After overnight hybridization at 47°C, samples were placed in hybridization solution (Mutsuga et al., 2004) containing 10 μl purified DIG-labeled antisense riboprobe. Samples then were incubated in 10 mM Tris-HCl, 0.5 M NaCl, and 0.25 mM EDTA (TNE) buffer, treated with RNaseA for 30 min, and returned to TNE buffer for 3 min, all at 37°C. After washing in 0.1X SSC for 15 min at 47°C, samples were blocked for 30 min and incubated with anti-DIG/HRP conjugate (DAKO) for 40 min at room temperature. The tyramide signal amplification system (GenePoint kit, DAKO) was used with VIP solution (Vector Laboratories) according to the manufacturers' instructions. Samples were observed and photographed in a Leica DMRB microscope.
Melanocytes were counted following staining for tyrosinase, MART1 and MITF, and their density along the epidermal:dermal border was determined as cells/mm. Primary antibodies used were αPEP7h (at 1:750 dilution) to detect tyrosinase (Yamaguchi et al., 2004) and Ab3 (at 1:100 dilution, NeoMarkers, Fremont, CA, USA) to detect MART1. Fluorescence intensities for antibodies detecting melanocyte-specific markers were normalized against DAPI staining.
For measurements of melanin content, specimens were stained by the Fontana-Masson method (Bancroft and Stevens, 1982). Transmitted light intensity was measured by the Leica DMRB[unk]DMLD microscope and ScionImage software was used to analyze melanin quantity from integrated density in the skin sections, as previously described (Yamaguchi et al., 2006; 2008a). Five randomly selected areas of each specimen were photographed and quantitated.
Statistical analysis was performed using Microsoft Office Excel Analysis Toolpak. Statistical differences between irradiated specimens and controls were determined by Student's t-test with a two-tailed distribution (two-sample unequal variance). A p< 0.05 is defined as significant.
This research was supported by the Intramural Research Program of the National Cancer Institute at NIH, and by the Office of Science, Office of Women's Health and the Center for Devices and Radiological Health, Food and Drug Administration (FDA). The authors wish to thank Drs. Thierry Passeron and Itaru Suzuki for their advice and help on the TISH analysis.
CONFLICT OF INTEREST
The authors state no conflict of interest.