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The transcription factor p63 is required for proper epidermal barrier formation and maintenance. Herein, we used chromatin immunoprecipitation coupled with DNA sequencing to identify novel p63 target genes involved in normal human epidermal keratinocyte (NHEKs) growth and differentiation. We identified over 2000 genomic sites bound by p63, of which 82 were also transcriptionally regulated by p63 in NHEKs. Through the discovery of interleukin-1-α as a p63 target gene, we identified that p63 is a regulator of epithelial–mesenchymal crosstalk. Further, three-dimensional organotypic co-cultures revealed TCF7L1, another novel p63 target gene, as a regulator of epidermal proliferation and differentiation, providing a mechanism by which p63 maintains the proliferative potential of basal epidermal cells. The discovery of new target genes links p63 to diverse signaling pathways required for epidermal development, including regulation of paracrine signaling to proliferative potential. Further mechanistic insight into p63 regulation of epidermal cell growth and differentiation is provided by the identification of a number of novel p63 target genes in this study.
p63, a homolog of p53, is required for proper epidermal development.1, 2 Owing to multiple transcriptional promoters in the 5′ end of the gene, p63 is expressed either containing (TA) or lacking (ΔN) an N-terminal acidic transactivation domain. Further, alternative C-terminal processing results in one of three splice variants (α, β or γ). Although a number of isoforms are possible, ΔNp63α is the predominantly expressed isoform in human epithelial cells.3, 4, 5 ΔNp63 was originally characterized as having dominant-negative properties toward TAp63 isoforms and p53;6 however, ΔNp63 can also positively regulate transcription owing to an additional N-terminal transactivation domain.7, 8
p63−/− mice display severe developmental defects, the most notable being a complete lack of complex epithelia.1, 2 Further, these phenotypes are recapitulated in humans bearing heterozygous germline p63 mutations.9, 10 p63 expression is localized to the basal layer of complex epithelia and it has been speculated that p63 is required to maintain the proliferative potential of epidermal stem cells.1, 11 Additional studies have suggested that p63 is crucial for commitment of stem cells to an epidermal cell fate.2 Ectopic p63 expression is sufficient to induce stratification of a single-layered epithelium,12 suggesting that it is a critical regulator of epidermal differentiation.
Several approaches have been used to identify downstream effectors of p63, including microarray analysis,4, 5, 13, 14 chromatin immunoprecipitation (ChIP)-based methods,15, 16 and ChIP-on-ChIP.17, 18 Results from these studies provide valuable insight into the mechanisms by which p63 controls molecular signaling. However, the vast majority of studies aimed at identifying p63-regulated signaling pathways have used established, immortalized and tumor-derived cell lines, all of which may not be ideally suited for understanding p63 function in normal, non-tumorigenic basal epithelium. The aim of this study was to identify p63-regulated signaling pathways that function in normal human epithelial cells.
Herein, we used a ChIP-based approach coupled with gene expression analysis of primary human epidermal keratinocytes (NHEKs) to identify transcriptional targets of p63. We identified over 2000 p63-bound genes and 338 p63-regulated genes, of which 82 genes were direct p63 target genes. By analyzing the role(s) of select target genes in epidermis development, we provide mechanistic insight into signaling pathways and functions regulated by p63 during expansion and maintenance of stratified epithelia.
To identify p63-bound genomic loci in rapidly proliferating normal human basal epithelial cells, we used a ChIP-based discovery method and primary cultures of NHEKs, as they express robust levels of ΔNp63α (Figure 1a) and are able to recapitulate epidermal differentiation in a two- and three-dimensional culture system.3, 19 NHEKs express low levels of a faster migrating protein that crossreacts with the p63-specific antibody; however, it does not migrate at the same position as any p63 isoforms by SDS-PAGE and is likely a breakdown product (ref.3 and Figure 1a). ChIP was performed to purify chromatin-bound p63 using the H129 polyclonal antibody that specifically recognizes p63α isoforms. Initial analysis revealed an enrichment of known p63 binding sites located near the p21, MDM2, and Jagged-1 genes (Figure 1b) and validated our immunoprecipitation conditions.
Having validated our pool of chromatin fragments, we used GenPathway FactorPath Discovery technology to identify novel sites bound by p63. FactorPath Discovery has previously been used to identify genomic fragments bound by a number of DNA-interacting proteins.20, 21 Over 5000 p63-bound chromatin fragments were isolated, sequenced, and mapped to the human genome, with sequences mapping within 10kb of known genes considered for further analysis. Using these criteria resulted in 2879 p63-bound genes (see Materials and Methods). Numerous previously identified p63 target genes were present in this dataset, including p21, MDM2, stratifin, IGFBP-3, PTPN14, RUNX1, P-cadherin, S100A2, and claudin-1, among others. Moreover, comparison of our dataset with a previously published p63 ChIP-on-ChIP17 identified 874 genes (P<0.0001) common between both datasets (Figure 1c), further validating the ability of our assay to identify novel p63 genomic binding sites.
As transcription factor binding to a gene does not necessitate transcriptional regulation, we performed microarray analysis to determine which of the identified p63 binding sites were associated with transcriptional regulation of nearby genes. NHEKs were transduced with a retrovirus expressing an shRNA targeting the DNA-binding domain of p63 (p63DBD) or GFP as a control,4 puromycin selected, and harvested for protein and RNA. Significant p63 knockdown was observed at the protein level (Figure 1d). As a threshold, we analyzed all genes displaying a minimum of two-fold change in transcript levels after p63 depletion. Using these criteria, we identified 338 genes displaying a p63-dependent expression pattern (Supplementary Table S1). Of these, 82 were present in the ChIP dataset (Figure 1e) and we focused subsequent analyses on the 82 genes (Supplementary Table S2).
Functional annotation of the 82 target genes provided additional validation and insight into the role of p63 in biological processes (Supplementary Table S3). ‘Cellular movement', one of the most significantly enriched categories represented by the p63 target genes, is supported by recent data identifying p63 as a regulator of migration and the epithelial-to-mesenchymal transition.4, 22, 23 In addition, a number of functional annotations are supported by the phenotype of p63−/− animals, such as ‘cellular development', ‘tissue development', and ‘hair and skin development and function'.1, 2 Overall, associating the 82 candidate genes with enriched functional processes and pathways added further confidence that our approach identified valid p63 target genes.
As a secondary screen, we performed semiquantitative ChIP using a unique p63 antibody (4A4) than used to generate the initial ChIP dataset (H129). For this validation, we focused on a subset of 14 genes exhibiting a minimum of two-fold regulation by p63, and that we could link to epidermal biology through previous publications. The known p63 binding site located in the p21 promoter and an exon sequence located in the GAPDH gene were used as positive and negative controls, respectively. Statistically significant p63 binding to promoter or intronic sequences was observed for 11 of the 14 genes analyzed (Figure 2).
In secondary analyses to confirm p63-dependent transcriptional regulation of select target genes, NHEKs were transduced with siRNA-expressing adenovirus targeting the p63DBD, or shuttle adenovirus as a control.5 This knockdown strategy is unique from the retrovirus used to generate initial microarray datasets. After successful p63 depletion at the protein level (Figure 3a), qPCR analyses revealed that all target genes analyzed displayed p63-regulated transcript changes that were consistent with those observed in our initial microarray observations (Figure 3b), validating these genes as bona fide p63-regulated genes.
Despite its low, often undetectable protein levels, recent evidence suggests that endogenous TAp63 isoforms can regulate target gene expression and differentiation of primary epithelial cells.19, 24 As our siRNAs target all p63 isoforms, we designed independent siRNAs that specifically target TAp63 and tested the efficacy of each against exogenous TAp63γ in H1299 cells, which lack detectable expression of any p53 family members. We observed a robust knockdown of TAp63γ at the protein level (Figure 3c). Further, we confirmed that these siRNAs do not target TAp73β (Figure 3d), or endogenous p53 and ΔNp63 isoforms (Figure 3e). To test the dependency of target gene expression on TAp63, we transfected non-silencing (NS) or TAp63-specific siRNAs into NHEKs to deplete endogenous TAp63 levels. Specific knockdown of endogenous TAp63, but not ΔNp63, isoforms was confirmed by qPCR (Figure 3f). At 48λh after transfection, target gene expression was determined and compared with those changes observed after depleting all p63 isoforms (compare 3G to 3B). Although all analyzed genes were dependent on ΔNp63 isoforms for expression, consistent with ΔNp63α being the predominant isoform expressed in epithelial cells, few, if any, genes showed a significant dependence on TAp63 for expression. Taken collectively, these data suggest that, of the target genes analyzed, ΔNp63 isoforms function as the primary regulator of transcriptional regulation.
Consistent with the role of p63 in maintaining proliferative potential in normal basal epithelium,1 amplification of its genomic locus is observed in squamous cell carcinomas,25 particularly those derived from tissues of the head and neck (HNSCC). To analyze the expression of our novel p63 target genes versus p63 in an in vivo setting, we used two publicly available HNSCC gene expression datasets.26, 27 We used the gene expression profiles of tumors exhibiting high versus low p63 expression (Supplementary Figure S1A) and compared the expression of our target genes between each subset. Of the 82 novel p63 targets, 25 genes exhibited differential expression patterns in HNSCC, when clustered for p63 expression (Supplementary Figure S1B). Of note, many p63 target genes were not differentially expressed in these datasets. We speculate that the latter is owing to differential expression of p53, p73, or other co-factors between normal and tumor cells, or the relative contribution of TAp63 versus ΔNp63 expression, which was not possible to assess from the tumor microarray expression data. Nevertheless, the correlation between 25 target genes and p63 status in an in vivo setting further supports our findings that these target genes contribute to p63-mediated biological processes in both normal and tumorigenic settings. Given this observation, we chose to functionally analyze two of these genes and determine the mechanism by which they contribute to p63-regulated biological processes.
Interleukin-1-α (IL1A) is a secreted factor important for maintaining epidermal homeostasis by regulating fibroblast-derived cytokines.28 Expressed in basal keratinocytes, IL1A is secreted to dermal fibroblasts where it induces the expression of fibroblast-derived growth factors, such as KGF, GM-CSF, and FGF10.29 These factors, in return, induce both the proliferation and differentiation of epidermal keratinocytes, thus completing an essential paracrine loop (Figure 4a).30, 31
The identification of IL1A as a p63 target gene in keratinocytes led us to hypothesize that p63 regulation of secreted cytokines is important for paracrine control of fibroblast-derived cytokines that are essential for proper development and maintenance of the epidermis. Consistent with this hypothesis, siRNA-mediated depletion of p63 in NHEKs (Figure 4b) resulted in significantly lower levels of secreted IL1A, as measured by ELISA (Figure 4c). To determine whether NHEKs could induce fibroblast-derived cytokine expression in a paracrine manner, we cultured dermal fibroblasts (NHDFs) in media conditioned by NHEKs. After NHDF growth in NHEK-conditioned medium for 48h, we observed a significant induction of the fibroblast-derived growth factors, KGF, FGF10, and GM-CSF, relative to unconditioned keratinocyte media (Figures 4d and e). To test our hypothesis that p63 regulates, in a paracrine manner, the expression of fibroblast-specific cytokines, we transfected NHEKs with control, p63, or IL1A-specific siRNA, and collected conditioned media from the cultures. IL1A depletion was verified by qPCR analysis in NHEKs (Figure 4f). NHDFs cultured in the medium conditioned by NHEKs depleted of p63 had significantly reduced the production of KGF, FGF10, and GM-CSF, relative to control cells (Figures 4g–i), suggesting that p63 signaling in keratinocytes is important for promoting epidermis–dermis paracrine signaling. Of note, these data were not a result of overall decrease in NHEK cell number following p63 knockdown, as we observed minimal cell death and detachment following transfection (data not shown). Interestingly, we observed a similar, slightly less robust, inhibition of cytokine production using the conditioned medium from NHEKs expressing reduced levels of IL1A (Figures 4g–i). We were not able to further inhibit cytokine production by depleting p63 and IL1A concomitantly, suggesting that the majority of paracrine signaling controlled by p63 is owing to its regulation of IL1A expression.
Of these fibroblast-derived cytokines, KGF binds to its cognate keratinocyte receptor, KGFR, on basal epidermal cell, and it acts as a potent mitogen to induce proliferation of epidermal progenitor cells. We hypothesized that p63 may also regulate the expression of KGFR in basal epidermal cells. Indeed, the expression of KGFR was significantly reduced after p63 knockdown (Figure 4j), suggesting that p63 acts to regulate KGFR expression in basal keratinocytes. Collectively, through the identification of IL1A as a p63 target gene, we discovered a role for p63 in regulating paracrine signaling pathways between epidermal keratinocytes and dermal fibroblasts.
TCF7L1 is a downstream component of the Wnt signaling pathway. It acts as an effector to control the transcriptional state of Wnt-regulated target genes. Recent data suggest that TCF7L1 can control cell fate lineage commitment in multipotent skin stem cells.32 In addition, induction of TCF7L1 in mouse epidermal progenitor cells is sufficient to abrogate terminal differentiation and maintain an undifferentiated cell fate.33
We analyzed TCF7L1 expression during calcium-induced NHEK differentiation in monolayer. Consistent with p63 expression, TCF7L1 levels correlated with the undifferentiated state of keratinocytes and significantly decreased as cells underwent terminal differentiation (Figures 5a and c, control lanes). From these data, we hypothesized that TCF7L1 is important for maintaining the undifferentiated state of p63-expressing, rapidly growing NHEKs. To test this hypothesis, we used control or TCF7L1-overexpressing NHEKs and induced terminal differentiation in culture. Ectopic TCF7L1 expression decreased mRNA levels of filaggrin, loricrin, and involucrin (Figure 5b), substantially reduced the protein levels of loricrin and crosslinked involucrin (Figure 5c), and thus attenuated differentiation. In both settings, calcium-induced differentiation decreased ΔNp63α levels by 6 days, providing additional evidence that TCF7L1 functions downstream of p63 (Figure 5c). These data further supported our hypothesis that TCF7L1 is crucial for maintaining a rapidly growing, undifferentiated state of p63-expressing keratinocytes.
To determine the function of endogenous TCF7L1 in NHEKs, we used a three-dimensional organotypic co-culture (OTC) model system to analyze differentiation in control NHEKs as compared with TCF7L1-deficient NHEKs. Like cultured NHEKs grown in the monolayer, the predominant isoform of p63 expressed in epidermal portion of OTCs is ΔNp63α (Supplementary Figure S2). To modulate endogenous TCF7L1 levels, we transfected NHEKs with TCF7L1-specific siRNAs, as well as with NS siRNAs to serve as a control. Although significant TCF7L1 depletion was achieved, endogenous p63 protein levels were not altered (Figure 6a). At 24h after transfection, NHEKs were plated onto gels composed of rat-tail collagen embedded with normal human dermal fibroblasts and lifted to the air–liquid interface. After 10 days, cultures were harvested and in situ expression of various proteins analyzed by immunofluorescence. In control cultures, involucrin expression was detected in the upper spinous layers, whereas filaggrin, loricrin, and keratin 2 were largely restricted to the stratum granulosum (Figure 6b). In TCF7L1-depleted cultures, we observed an earlier onset of all observed differentiation markers, with involucrin being present throughout all suprabasal layers. Furthermore, filaggrin, loricrin, and keratin 2, typically restricted to the stratum granulosum, were already detectable in spinous layers of the epidermis (Figure 6b). We did not observe measurable differences in the cell–cell contact protein E-cadherin, suggesting that the effects of TCF7L1 depletion is limited to proteins involved in terminal differentiation. These data suggest that keratinocytes, when depleted of TCF7L1 expression, prematurely initiate a program of terminal differentiation in OTC.
We hypothesized that following TCF7L1 depletion, increased differentiation would be accompanied by decreased proliferation. As seen in Figures 6b and c, there was a significant decrease in the number of 5-bromodeoxyuridine (BrdU)-positive cells in siTCF7L1 cultures compared with control cultures. Coupled with our ectopic TCF7L1 data, our studies suggest that TCF7L1-depleted keratinocytes are unable to maintain an undifferentiated state. Moreover, we identified a number of Wnt target genes that displayed significant expression changes following p63 depletion in NHEKs (Supplementary Figure S3), consistent with the transcriptional regulatory function of TCF7L1. Our combined use of a genomic approach to identify new target genes, and an organotypic assay to screen for functions downstream of p63, allowed us to mechanistically link p63 signaling to a critical proliferation/differentiation switch (TCF7L1) in stratified epithelia.
A recent study by Truong et al.19 reported that 231 genes were regulated in a p63-dependent manner in NHEKs grown in an organotypic culture. However, the experimental design did not reveal which of these genes were direct targets of p63 regulation. By overlaying our ChIP dataset with the microarray dataset from this previous study, we identified 32 additional genes as directly regulated by p63 in primary keratinocytes (Table 1). Thus, we were able to extend the use of our ChIP dataset outside this study to further identify novel p63 target genes using publicly available expression datasets.
In this study, we used a ChIP-based methodology, coupled with expression microarray, to identify p63 binding sites in NHEKs. Although previous studies have used ChIP-based approaches to identify p63-bound genomic regions in numerous epithelial models,16 ours is the first study in primary human keratinocytes. We discovered 874 genes (P<0.0001) in common between our ChIP dataset and a previously published ChIP-on-ChIP dataset.17 Despite significant overlap, the large number of genes unique to p63 regulation in NHEKs, versus the transformed ME180 cell line, suggests that there are significant differences between p63 signaling in normal keratinocytes as compared with immortalized and/or tumorigenic settings.
Coupling ChIP-based data with microarray analyses allowed for rapid identification of 82 p63 target genes in NHEKs, and secondary validation of our datasets were crucial in ruling out false-positive genes. This validation included the use of a second p63 antibody to confirm the ChIP results, along with the use of a unique p63-specific siRNA to corroborate the microarray expression dataset. Furthermore, we identified in vivo correlations between the expression of p63 and direct target genes in HNSCC, suggesting that these genes are important for mediating the function of p63 in a tumorigenic environment. We are currently working to identify the role(s) of these genes in a tumorigenic setting, and these studies will provide insight into how p63 functions in both normal and tumor-derived epithelia.
Expressed in basal, proliferating, keratinocytes, IL1A is required for the induction of fibroblast-specific cytokines involved in paracrine signaling between the epidermis and the dermis.28 We discovered that keratinocyte-specific p63 expression is important for the induction of fibroblast-derived cytokines. Further, p63 regulates the keratinocyte-specific KGFR, a trans-membrane receptor that binds fibroblast-derived KGF. Our data are consistent with a previous report linking p63 and KGFR in thymic epithelial cells.34 Most importantly, our data show that p63 is important for regulating target gene expression in the epidermis, and the expression of fibroblast-specific growth factors that promote epidermis development in a paracrine manner. Although our data suggest that p63 regulates paracrine signaling primarily through IL1A production, we cannot rule out the possibility that p63 also regulates the expression of additional secreted factors that function in epithelial–mesenchymal paracrine pathways.
Psoriasis, an epidermal disorder characterized by hyperproliferation, hypodifferentiation, and increased p63 expression,35 further links p63 to paracrine pathways mediated by IL1A. Consistent with our discovery of IL1A being induced by p63, previous studies identified increased expression of KGF and FGF10 in the stroma adjacent to psoriatic lesions.36 On the basis of our data, we would hypothesize that the increased stromal levels of KGF and FGF10 are a direct result of IL1A induction by p63, which is upregulated during psoriatic remodeling.35
We showed that TCF7L1 functions to maintain the undifferentiated state of basal keratinocytes. Ectopically expressed TCF7L1 was sufficient to abrogate calcium-induced NHEK differentiation. In OTC, TCF7L1 depletion was sufficient to prematurely induce differentiation, suggesting that it acts to repress differentiation pathways in human keratinocytes and thus have an important role in tissue homeostasis. These data are consistent with previous studies showing that ectopic TCF3, the mouse TCF7L1 homolog, was sufficient to induce an undifferentiated, proliferative state in mouse keratinocytes.33 There is additional evidence from Xenopus studies that link p63 to TCF7L1. In Xenopus, xTcf3−/− embryos display severely expanded mesodermally derived structures, suggesting that it may act to repress transcriptional programs responsible for mesoderm differentiation.37 We recently identified a role for ΔNp63 as a repressor of mesoderm development during Xenopus embryogenesis.38 Further research is necessary to determine whether ΔNp63 transcriptionally regulates xTcf3 during Xenopus development. Given that previous reports describe p63 as a regulator of proliferation and differentiation in basal epithelial cells,1 our linkage of p63 to TCF7L1 expression in basal epithelial cells provides mechanistic insight into how p63 regulates the maintenance of epithelial progenitor cells.
Lastly, our ChIP dataset proved useful to further identify p63 target genes in a previously published study.19 Overlaying our ChIP dataset with microarray data from their study identified 32 additional p63 target genes not present in this study, such as claudin-1, Jagged-1, and RUNX1, all known p63 target genes, as well as keratinocyte differentiation genes, such as SERPINE1 and PKP1. Ultimately, our ChIP dataset, used in conjunction with microarray analyses, will provide a tiered panel to identify direct versus indirect regulation of target genes by p63 in gene expression analyses.
In conclusion, we show that p63 acts to regulate both cell autonomous and non-autonomous pathways involved in keratinocyte growth and differentiation. Our study provides numerous novel p63 target genes that will be of value to future investigation of transcriptional networks involved in complex epithelia development and differentiated function.
Primary NHEKs were obtained and cultured as described previously.3 Primary human dermal fibroblasts were obtained from the Vanderbilt Skin Disease Research core and cultured in Dulbecco's minimal Eagle's medium (DMEM) supplemented with 10% fetal bovine serum and 1% penicillin–streptomycin. The retrovirus-packaging cell line, Phoenix, was cultured in DMEM supplemented with 10% fetal bovine serum and 1% penicillin–streptomycin. All cells were cultured at 37°C with 5% CO2. Terminal differentiation of NHEKs was performed as described previously.3
Protein lysates were prepared from NHEKs as described previously.3 Western analysis was performed as described previously3 with the following primary antibodies: anti-p63 monoclonal antibody 4A4 (Santa Cruz, Santa Cruz, CA, USA), anti-p73 A300 (Bethyl, Montgomery, TX, USA), anti-p53 clone DO-1 (Santa Cruz), anti-TCF7L1 (Santa Cruz), loricrin (Covance, Princeton, NJ, USA), involucrin, and β-actin polyclonal antibody I-19 (Santa Cruz).
Formaldehyde crosslinking and chromatin preparation and ChIP were carried out as described previously.15 For ChIP data generation and semiquantitative ChIP PCR experiments, rapidly growing NHEKs were crosslinked and submitted to GenPathway Inc. (San Diego, CA, USA) according to their FactorPath protocol. The complete p63 ChIP dataset is accessible through Gene Expression Omnibus (GEO, http://www.ncbi.nlm.nih.gov/geo/).
siRNA-mediated disruption of p63 for microarray data generation was performed using the pRetroSuper system as described in ref.4 RNA was harvested and Affymetrix microarray analysis was performed in duplicate as described previously.4 All gene expression data from microarray experiments and genomic location information from the p63 ChIP experiment have been deposited in the National Center for Biotechnology Information GEO (http://www.ncbi.nlm.nih.gov/geo/). The GeneSpring GX software (Agilent, Santa Clara, CA, USA) was used for statistical analyses and transcript annotations. For tumor analysis, publicly available expression data from GSE3524 and GSE2280 were pooled and used to identify tumors with high and low p63 mRNA expression, as measured by mRNA levels. The 82-gene p63 signature was analyzed in these two tumor subgroups to identify genes differentially regulated in tumors relative to p63 expression.
For validation studies, p63 was depleted using adenoviruses expressing siRNAs targeting the p63DBD or a shuttle control virus as described previously.5 For TA-specific knockdown experiments, TAp63 was depleted using the following siRNA oligonucleotides: siTAp63-1, 5′-CAGAAGATGGTGCGACAAA-3′ siTAP63-2, 5′-GCACACAGACAAATGAATT-3′ and siTAp63-3, 5′-ACTTGAACTTTGTGGATGA-3′. For TCF7L1 knockdown studies, siRNA (Dharmacon Inc., Lafayette, CO, USA) was electroporated into primary NHEKs as per the manufacturer's instructions (Amaxa Biosystems, Walkersville, MD, USA). For immunofluorescence, sections were processed as described previously.39 After primary incubation, sections were incubated with the appropriate secondary antibody (AlexaFluor 488 or 546) (Molecular Probes and Invitrogen, Carlsbad, CA, USA). Nuclei were stained using TOPRO-3 (Invitrogen). Sections were analyzed on a Zeiss Inverted LSM510 confocal microscope (Vanderbilt-Ingram Cancer Center Cell Imaging Shared Resource, Nashville, TN, USA). Primary antibodies used were as follows: loricrin (Covance, Princeton, NJ, USA), involucrin, and filaggrin (Santa Cruz), and E-cadherin (BD Biosciences, Franklin Lake, NJ, USA). For proliferation analyses, the OTCs were incubated with a mixture of BrdU and 5-bromodeoxycytidine (Sigma, St Louis, MO, USA; both 63.5μM, added to the culture medium) for 18h before being terminated. DNA incorporation of these nucleotide analogs in replicating cells was detected on cryosections with a monoclonal antibody anti-BrdU antibody (BD Biosciences) after sequential methanol and acetone fixation as described above and 10min incubation with 1.5M HCl at room temperature followed by thorough rinsing in PBS. To determine the proliferative indices, BrdU-labeled and all basal cell nuclei were counted in at least three vision fields of three to five sections of each culture specimen.
OTCs were prepared as described previously.40 Type I collagen was purchased from BD Biosciences. The gels, containing primary fibroblasts and representing the dermal equivalents, were incubated in DMEM supplemented with 10% fetal bovine serum and 50μg ascorbic acid per ml. Culture medium was changed every 2 days and cultures were harvested for analysis 10 days after lift.
This work was supported by NIH Grants CA70856 and CA105436 (JAP), ES00267 and CA68485 (core services), and NIH Training Grant T32CA078136-08 (CEB). We thank Dr Christopher Barbieri for generating the shp63DBD retrovirus and Dr Leif Ellisen for providing the siRNA adenoviruses. The Krt2 antibody was kindly provided by Dr Lutz Langbein (DKFZ). We would like to thank members of the Pietenpol laboratory for critical reading of the manuscript and helpful discussions.
The authors declare no conflict of interest.
Supplementary Information accompanies the paper on Cell Death and Disease website (http://www.nature.com/cddis)