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Hypoxia-inducible factor 1 is a new target of microphthalmia-associated transcri

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发表于 2009-4-25 09:53 |显示全部帖子
1 INSERM U597, Biologie et physiopathologie des cellules melanocytaires, Faculty of Medicine, 06107 Nice cedex 2, France
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3 u" Q  [& |& d9 M# ?2 INSERM U634, Faculty of Medicine, 06107 Nice cedex 2, France
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( o  w- T/ u$ M8 M5 B& _  k- G5 P3 CNRS UMR 6543, Centre Antoine Lacassagne, 06189 Nice cedex 2, France: _- ^( j, i* e+ k3 Y

1 ~' G, D9 ~6 t# Z" B5 X0 z% p4 CNRS/UNSA UMR 6097, IPMC, 06560 Sophia Antipolis, France
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8 ^2 E' T6 s! J1 |( HIn melanocytes and melanoma cells -melanocyte stimulating hormone (-MSH), via the cAMP pathway, elicits a large array of biological responses that control melanocyte differentiation and influence melanoma development or susceptibility. In this work, we show that cAMP transcriptionally activates Hif1a gene in a melanocyte cell–specific manner and increases the expression of a functional hypoxia-inducible factor 1 (HIF1) protein resulting in a stimulation of Vegf expression. Interestingly, we report that the melanocyte-specific transcription factor, microphthalmia-associated transcription factor (MITF), binds to the Hif1a promoter and strongly stimulates its transcriptional activity. Further, MITF "silencing" abrogates the cAMP effect on Hif1a expression, and overexpression of MITF in human melanoma cells is sufficient to stimulate HIF1A mRNA. Our data demonstrate that Hif1a is a new MITF target gene and that MITF mediates the cAMP stimulation of Hif1a in melanocytes and melanoma cells. Importantly, we provide results demonstrating that HIF1 plays a pro-survival role in this cell system. We therefore conclude that the -MSH/cAMP pathway, using MITF as a signal transducer and HIF1 as a target, might contribute to melanoma progression.
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- Z- Q5 `& [& M% Y8 `Abbreviations used in this paper: -MSH, -melanocyte stimulating hormone; ERK2, extracellular signal-regulated kinase 2; HIF1, hypoxia-inducible factor 1; HRE, hypoxia-responsive element; MC1R, melanocortin-1 receptor; MITF, microphthalmia-associated transcription factor; NHM, normal human melanocytes; PHD2, prolyl-hydroxylase 2; siRNA, small interference RNA; VEGF, vascular endothelial growth factor.5 P2 |+ h3 y4 w2 Z

, h6 y. L2 x* k) }% _% R5 YIntroduction
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8 q) S: s- F$ B: G& [1 |In the skin physiological system, -melanocyte stimulating hormone (-MSH) constitutes an important keratinocyte secreted factor in response to the UV radiation of sunlight. Keratinocytes account for the main epidermal cell type, and melanocytes, situated at the basal layer of the epidermis, are responsible for melanin synthesis and skin color. In melanocytes, -MSH, through the binding to the melanocortin-1 receptor (MC1R) and up-regulation of the cAMP pathway, induces pigmentation by controlling several parameters of melanocyte differentiation such as melanin synthesis (melanogenesis) (Busc角 and Ballotti, 2000), dendrite outgrowth (Busc角 et al., 1998), and melanosome transport, required for melanin distribution within the skin (Passeron et al., 2004).% \/ R( r, f; q+ F
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The -MSH/MC1R/cAMP signaling pathway has also been reported to influence melanoma biology, but in contrast to the undisputed role of cAMP in promoting pigmentation, data relating cAMP to melanoma progression currently appear contradictory. -MSH has been reported to inhibit melanoma growth and adhesion (Robinson and Healy, 2002), suggesting that a compromised cAMP signaling could favor melanoma progression. In agreement with this hypothesis, variants of MC1R with altered cAMP response have been associated with high melanoma susceptibility (Valverde et al., 1995; Robinson and Healy, 2002). In contrast, -MSH and cAMP increase c-met expression in melanoma cells and could thereby favor the melanoma metastatic potential (Rusciano et al., 1999). Consistently, the CREB/ATF family of transcription factors that function downstream of the cAMP pathway have also been reported to act as survival factors and contribute to the malignant phenotype (for review see Poser and Bosserhoff, 2004).; z9 ?  ^; K  B6 w4 ]0 @7 P
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The cAMP-triggered mechanisms controlling melanocyte pigmentation have been thoroughly investigated. cAMP, through PKA and CREB activation, increases the expression of the melanocyte-specific form of microphthalmia-associated transcription factor (MITF) (Bertolotto et al., 1998a), a basic helix-loop-helix transcription factor that plays a key role not only in melanin synthesis, but also in melanocyte development and survival (Hodgkinson et al., 1993; Hughes et al., 1993).& E" J* ?. L, n/ K, {

0 o; n/ a$ t' `3 r0 pNoteworthy, in melanocytes and melanoma cells, cAMP regulates several signaling pathways that control multiple biological functions. Indeed, cAMP inhibits the phosphatidylinositol 3-kinase/AKT pathway that influences both differentiation and survival of melanocytes (Busc角 et al., 1996; Khaled et al., 2002; Larribere et al., 2004). Further, -MSH and cAMP stimulate the MAPK pathway (Englaro et al., 1995; Busc角 et al., 2000) through B-Raf activation. Indeed, B-Raf has been recently found mutated and activated in a vast majority of melanoma (Davies et al., 2002).
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To further investigate the molecular events elicited by -MSH and cAMP in melanocytes and better understand the implication of its signaling in melanoma biology, we performed a large-scale gene screening by using a DNA microarray (Moreilhon et al., 2004). We used B16 mouse melanoma cells to analyze the overall modification of gene expression after 24 h of treatment with the cAMP-elevating agent forskolin.
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Very interestingly, we found that cAMP stimulates the expression of the Hif1a gene whose protein product, hypoxia-inducible factor 1 (HIF1), constitutes the  subunit of the HIF1, a master regulator of oxygen homeostasis. After dimerization with HIF1 (also named ARNT), HIF1 binds to a consensus sequence 5'-RCGTG-3' called hypoxia-responsive element (HRE), and controls the expression of several genes involved in many aspects of cancer progression, including metabolic adaptation, apoptosis resistance, angiogenesis, invasion, and metastasis (for review see Semenza, 2002). To date, HIF1 has been shown to be tightly regulated by multiple post-translational modifications that mainly control the protein stability through the ubiquitin–proteasome pathway (Brahimi-Horn et al., 2001; Berra et al., 2003).
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In this paper, we show that cAMP transcriptionally regulates Hif1a gene expression because the cAMP-elevating agent forskolin increases Hif1a mRNA and regulates Hif1a promoter activity. cAMP increases the expression of a functional HIF1 protein that results in the induction of Vegf expression. Furthermore, the effect of cAMP on HIF1 is restricted to melanocyte cells. This cell specificity is given by MITF that binds to the Hif1a promoter and strongly stimulates its transcriptional activity. MITF silencing abrogates the effect of cAMP on HIF1 expression, and infection of human melanoma cells with an MITF-encoding adenovirus increases Hif1a mRNA expression, clearly demonstrating that Hif1a is a new MITF target gene. Because we demonstrate that HIF1 plays a pro-survival role in melanoma and we suggest that it is involved in neovascularization, we conclude that the -MSH/cAMP pathway, through a molecular cascade sequentially involving MITF and HIF1, might contribute to melanoma development.
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7 d# E3 ?6 }( }Results, Q! y& w5 ~* h% u% @* @
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Hif1a gene expression is induced by the cAMP pathway in B16 melanoma cells
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In an attempt to screen for cAMP-induced genes in melanocyte cells, we used a laboratory-designed DNA microarray (Moreilhon et al., 2004) described in the Materials and methods section. B16 mouse melanoma cells were treated (or not) with the cAMP-elevating agent forskolin for 24 h. Total mRNAs were extracted, labeled, and hybridized with microarray slides.
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- k; _- L/ m2 T" rThe induction of several already-known cAMP-regulated genes validated our array approach. The biochip analysis identified several cAMP-regulated genes which protein products have previously been clearly involved in melanogenesis (Table I) such as tyrosinase, tyrosinase-related protein 1, Mitf, or proteins involved in melanosome transport such as Myosin Va and Rab27a. These results were confirmed by real-time quantitative PCR (Table I).
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Surprisingly, cAMP clearly induced the expression of Hif1a gene (threefold stimulation; Table I). Due to the pivotal role of HIF1 transcription factor in cancer progression, we decided to thoroughly investigate the molecular mechanisms governing Hif1 gene regulation by cAMP in melanoma cells.. p9 z, o7 N1 X6 s6 L3 I( q

1 b( w& T' H0 y+ J1 ^. V$ g  [2 D( E  [+ ~9 tcAMP induces a functional HIF1 protein0 q- y& C: c1 B" Y* G

$ w+ u9 A0 d- ^- K* z2 GWestern blot experiments using a specific anti HIF1 antibody showed that HIF1 protein slightly increased at 6 h and reached its maximal levels upon 24 h of forskolin treatment. After 48 h, HIF1 protein expression remained stable (Fig. 1 A). -MSH, a physiological activator of the cAMP pathway in melanocytes, also increased HIF1 protein levels similarly to hypoxia (24 h), which was used as a positive control of HIF1 protein induction. In addition, cAMP plus hypoxia appeared to have additive effects (Fig. 1 B). The same results were obtained using normal human melanocytes (NHM). In this case we used Co2 , to mimic hypoxia (Berra et al., 2003), as a control (Fig. 1 C). Therefore, HIF1 protein increased upon cAMP up-regulation in B16 melanoma cells and NHM independently of the oxygen context.
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& J9 |7 o4 i% F6 t$ _! i5 o/ PTo evaluate whether the cAMP-induced HIF1 formed a functional transcriptional complex, we measured the activity of the 3-HRE-LUC reporter gene (Berra et al., 2003).
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The results obtained showed that the 3-HRE-LUC construct was responsive (by a five- to sixfold stimulation) to cAMP in B16 melanoma cells. Co2  stimulation was used as a positive control and again the effect of Co2  and cAMP appeared additive (Fig. 1 D).
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* O2 U7 o; p5 q8 LAmong the multiple HIF1 target genes containing an HRE core sequence in their promoter region, Vegf has been largely studied because it is required for tumor angiogenesis. We therefore analyzed the effects of cAMP in endogenous Vegf expression in B16 cells. Real-time quantitative PCR experiments showed that forskolin increased vascular endothelial growth factor (VEGF) mRNA in these melanocyte cells. As expected, Co2  highly induced Vegf and enhanced the cAMP response (Fig. 1 E). Together, these results demonstrate that cAMP induced a functional HIF1 protein.) G! ]: g9 b; B2 j6 u! |
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cAMP up-regulation if Hif1a gene transcription is cell specific. ~  C7 J8 n* [2 _8 |

; ^: z, e% H( ]+ {, @0 s% E  D% r- U8 gTo further elucidate the mechanisms by which cAMP regulates HIF1 expression, we performed Hif1a promoter activity assays. An Hif1a promoter fragment cloned upstream of the luciferase reporter gene (Wenger et al., 1998) was transfected in B16 melanoma cells. The promoter activity, monitored by the luciferase levels, increased upon cAMP treatment (Fig. 2 A). The same experiment was performed in NIH-3T3 fibroblasts, and we observed that forskolin had no impact on Hif1a promoter activity (Fig. 2 A). Furthermore, in these cells cAMP decreased Hif1a mRNA amount (Fig. 2 B). At the protein level, cAMP treatment did not affect HIF1 expression in NIH-3T3 fibroblasts (Fig. 2 C), whereas the control Co2  induced the protein expression. A comparison of the functional HIF1 protein levels between B16 melanocyte cells and NIH-3T3 nonmelanocyte cells was performed using the 3-HRE-LUC reporter system (Fig. 2 D). We observed that although forskolin significantly increased the reporter transactivation in B16 cells, this did not occur in NIH-3T3 fibroblasts. In contrast, Co2  treatment increased luciferase expression in both cell lines. These results indicate that cAMP increases Hif1 gene transcription in a melanocyte cell–specific manner.
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) _0 H9 D" N& k* ^5 s/ gMITF binds and transactivates the Hif1a promoter1 s+ Y$ A9 A1 U/ p' h' d& l

8 u# K0 V; G; }0 T5 V9 NThe cell specificity of HIF1 induction by cAMP prompted us to hypothesize the existence of specific molecular mechanisms responsible for HIF1 regulation in melanocytes and melanoma cells. Sequence analysis of the Hif1a promoter (Wenger et al., 1998) revealed 10 core E-box consensus sequences composed by the CANNTG motif (Fig. 3 A). Noteworthy, among these 10 E-boxes, 2 perfectly match with the motif of MITF binding (CACGTG) (Aksan and Goding, 1998). We therefore investigated whether MITF could account for the cell-specific cAMP regulation of HIF1 expression. To evaluate the MITF binding to the Hif1a promoter region in the endogenous chromatin context, we performed chromatin immunoprecipitation assays (Fig. 3 B). B16 cells were stimulated with the cAMP-elevating agent forskolin for 5 h to maximally increase MITF protein expression (Bertolotto et al., 1998a). Chromatin complexes were immunoprecipitated with an anti-MITF antibody and a PCR was performed using specific primers to the mouse Hif1a promoter region. As shown in Fig. 3 B, we detected a specific amplification of the Hif1a promoter region that increased after forskolin treatment. As a positive control, we used specific primers spanning the tyrosinase promoter region, which is well known to bind MITF. As expected, the tyrosinase promoter amplification also increased upon cAMP exposure. A specific band corresponding to the Hif1a or tyrosinase promoter was detected when using mouse genomic DNA. In the absence of antibody, no specific amplification was observed. Another negative control was performed by applying 40 cycles of PCR to the MITF immunoprecipitates using a primer pair to the mouse GAPDH. As expected for a sequence that does not present MITF binding sites, no GAPDH amplification was observed while a clear PCR band was detected using the genomic DNA as a template (Fig. 3 B, bottom panel). We therefore conclude that MITF binds to the Hif1a promoter in the chromatin context of B16 melanoma cells.. j' x9 k1 h$ s

6 X- l( a- T  @Next, we evaluated whether the MITF binding transactivated Hif1a promoter. Thus, we cotransfected the reporter construct encoding the Hif1a promoter fragment, together with different amounts of a plasmid encoding the MITF transcription factor. We clearly observed that MITF highly transactivated the Hif1a promoter activity in a dose-dependent manner (Fig. 3 C), whereas two other transcription factors of the same basic helix-loop-helix family, like USF and myc, did not. The functionality of the constructs encoding USF and myc was verified by their capacity to transactivate specific target promoters (unpublished data).% c2 k' l5 ^; b& `- ~* J1 c; _1 p! }

5 K+ v9 D; H6 H' \# B$ ^! u- TNext, we analyzed whether MITF could stimulate the expression of the endogenous Hif1a gene. In this aim we infected Mewo human melanoma cells either with an empty adenovirus (pCDNA3) or an adenovirus encoding MITF. 48 h after infection, total mRNAs were extracted and subjected to real-time quantitative PCR to control MITF overexpression and evaluate Hif1a expression. As shown in Fig. 3 D, MITF mRNA levels increased after MITF infection (4.6-fold) as expected, and Hif1a mRNA expression was significantly induced by MITF overexpression (3.7-fold).
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To elucidate whether MITF could also transactivate the Hif1a promoter in a nonmelanocyte cell context, we cotransfected NIH-3T3 with this promoter together with the plasmid encoding MITF. The results obtained revealed that MITF significantly increased the Hif1a promoter activity (3.5-fold) (Fig. 3 E).* S6 U/ {" j' t- a. P6 p

: X6 ^# n3 r8 R9 H/ ITogether, these results strongly indicate that MITF binds to the proximal region of the Hif1a promoter and stimulates its transactivation leading to increased expression of Hif1a mRNA in melanoma cells. Moreover, MITF seems to be sufficient to transactivate the Hif1a promoter in nonmelanocyte cells.
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MITF mediates the effect of cAMP on Hif1a promoter activity and protein expression
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  o' M- P9 y/ ^" Q$ MTo evaluate whether MITF was required for the cAMP induction of the Hif1a gene expression, B16 cells were cotransfected with the Hif1a promoter fragment together with a dominant-negative mutant of MITF (MITF DNT) lacking the NH2-terminal transactivation domain, and cells were then stimulated with forskolin. Interestingly, we observed that MITF DNT completely abolished the cAMP stimulation of the Hif1a promoter activity (Fig. 4 A). To further strengthen the MITF specificity of such response, we performed the same experiment by using specific small interference RNAs (siRNAs) targeting MITF. As a control, cells were cotransfected with the Hif1a promoter together with a nonrelevant siRNA (control siRNA). Fig. 4 B shows that MITF silencing clearly inhibited the cAMP-induced Hif1a promoter transactivation, thereby indicating that MITF mediates the cAMP effects on Hif1a gene expression.
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To study the impact of MITF on the endogenous HIF1 protein, the same siRNA approach was undertaken. The expression of MITF and HIF1 proteins was then monitored by immunofluorescence using specific antibodies to MITF (green fluorescein labeling) and HIF1 (Texas red labeling). After 24 h of stimulation with the cAMP-elevating agent forskolin we observed an increased nuclear labeling corresponding to MITF expression, as well as a significant increase in HIF1 protein (Fig. 5 A). As expected, MITF silencing led to an important inhibition of cAMP-dependent MITF induction as well as the cAMP-induced HIF1 expression. In the presence of an siRNA to silence HIF1 expression, although cAMP elevating agents expectedly increased MITF expression, HIF1 expression was inhibited in both basal and cAMP conditions. A Western blot analysis of samples treated in parallel (Fig. 5 B) confirmed the same results in a more quantitative way. We therefore demonstrate that MITF controls HIF1 transactivation and constitutes a critical step in the cAMP up-regulation of HIF1 expression.1 Y+ H" e9 `9 K+ B4 N% t( w

) B" X# d+ L: P0 K# Y9 l! H6 |1 d+ X# RMITF and HIF1 are responsible for the cAMP-dependent Vegf mRNA induction# Q: _& ]: C" w  K$ D
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Vegf being a well-known target gene of HIF1 involved in angiogenesis and tumor growth, we analyzed whether MITF and HIF1 could account for the cAMP-induced Vegf expression in B16 melanoma cells. Quantitative PCR experiments were performed on mRNAs extracted from B16 cells transfected with a control siRNA or siRNAs targeting MITF or HIF1 to deplete cells from these transcription factors, as well an siRNA to silence HIF prolyl-hydroxylase 2 (PHD2), which is specifically responsible for HIF1 protein degradation (Berra et al., 2003). We observed that MITF or HIF1 silencing inhibited the basal as well as the forskolin-induced Vegf expression, whereas PHD2 cell depletion, which increased HIF1 protein levels (unpublished data), exerted the opposite effect by significantly increasing the Vegf mRNA levels.
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These data are consistent with Vegf being a MITF-HIF1 target gene in our melanoma model, and show that the cAMP-induced Vegf expression is mediated by the MITF-HIF1 cascade.6 i& a/ C- v$ D
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HIF1 plays a pro-survival role in melanoma
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To investigate the physiological relevance of HIF1 induction in melanocyte cells, and taking into account the role attributed to HIF1 factor in cell survival, we evaluated the putative implication of HIF1 in this feature of melanoma cell physiology.
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For that we treated B16 melanoma cells with staurosporin, considered a strong cell death inducing agent, and we used an immunofluorescence analysis to detect the presence of cleaved caspase-3 as a marker of cell death. We observed that treatment with staurosporin for 6 h greatly induced caspase-3 cleavage in our cell system (Fig. 6 A). We next pretreated B16 cells for 24 h with forskolin to increase HIF1. We interestingly observed that cAMP strongly reduced the cleaved caspase-3 labeling thereby indicating that cAMP inhibits the staurosporin-induced cell death (Fig. 6 A).- I& D& `' E& Y6 o* E+ P9 t- U

, k% e+ C; c! E2 b# @( TThen we used an siRNA approach to dissect the contribution of HIF1 in this cell death protection. B16 cells were transfected with a nonrelevant siRNA or an siRNA to invalidate Hif1a expression. Cells were next treated (or not) with forskolin for 24 h, and they were finally exposed to 6 h of staurosporin. Fig. 6 B shows that in control siRNA–transfected cells, forskolin increased HIF1 protein expression and decreased caspase-3 cleavage, whereas in siRNA-Hif1–transfected cells, the forskolin-dependent decrease of caspase-3 cleavage was nearly abolished. This result indicates that HIF1 protects cells from the staurosporin-induced cell death, thereby suggesting a pro-survival role of HIF1 in the melanoma cell model., b( i. i4 Q% _
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Discussion
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In the present work, we have identified Hif1a as a new cAMP-induced gene in melanoma cells and we have characterized the molecular mechanisms underlying this regulation.1 V' K3 y. Q: N0 p9 q6 q8 n

, B1 ~) h! N$ w3 f6 ^We demonstrate for the first time that cAMP regulates Hif1a at a transcriptional level, leading to increased expression of HIF1 mRNA and protein. HIF1 forms a HIF1 complex that is functional and able to transactivate target genes such as Vegf. Very interestingly, HIF1 induction by cAMP is restricted to melanocyte cells, prompting us to propose a cell-specific regulation through the melanocyte-specific transcription factor MITF. We demonstrate that MITF binds and transactivates the Hif1a promoter, and the overexpression of MITF is sufficient to increase Hif1a mRNA levels. Furthermore, by silencing MITF or Hif1 expression, we show that cAMP-induced HIF1 expression is mediated by MITF, and that the MITF/HIF1 pathway mediates the cAMP induction of Vegf expression (a model illustrating these conclusions is shown in Fig. 7). We therefore define Hif1a as a new MITF target gene and we provide data revealing the pro-survival role of the MITF-HIF1 cascade in melanoma cells.
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HIF1 activation triggered by hypoxia is mainly governed by post-translational modifications involving hydroxylation of specific amino acid residues in the HIF1 subunit (Berra et al., 2003). Indeed, O2-dependent prolyl hydroxylation regulates proteasome-mediated destruction of HIF1, whereas asparaginyl hydroxylation blocks the interaction with the p300/CBP coactivators (for review see Lando et al., 2002). In addition to hypoxia, growth factors, vaso-active hormones, cytokines, and tumor suppressor mutations also stimulate HIF1 synthesis via activation of the phosphatidylinositol 3-kinase or MAPK pathways (Zhong et al., 2000; Zundel et al., 2000; Fukuda et al., 2002).
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8 a3 R* C) B2 ^7 Z  A' [3 J6 SAs a novelty, our study clearly demonstrates that cAMP regulates HIF1 at a transcriptional level independently of the oxygen context. To date, very few works have described a regulation of Hif1a mRNA (Jiang et al., 1997; Blouin et al., 2004; Liu et al., 2004). Nevertheless, no studies have so far dissected or identified a transcriptional mechanism accounting for HIF1 gene expression. In our work, we go further in the characterization of the molecular mechanisms that regulate Hif1a gene transcription because we identify for the first time a transcription factor (i.e., MITF) that binds and functionally transactivates the Hif1a promoter and controls this gene expression independently of the oxygen conditions.* P3 \7 G4 A* ~8 S. D$ K

- `( D4 `: {  C% W/ l- l* PWe also show that cAMP and hypoxia have additive effects on HIF1 protein levels. Both stimuli via transcriptional and post-translational mechanisms, respectively, cooperate to highly induce HIF1 protein. It is tempting to propose that, independently of the oxygen availability, MITF acts as a fine modulator of the final HIF1 protein levels to modify the biological fate of melanocytes and melanoma cells.
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In addition to regulating Hif1a transcription, we could imagine that cAMP, like hypoxia, might act on HIF1 protein stabilization by modulating its hydroxylation or enhancing its translation. This does not seem to be the case because MITF inhibition by a dominant-negative mutant or a specific siRNA completely abolishes the cAMP-induced HIF1 protein expression. However, we cannot definitively rule out the possibility that cAMP might also regulate HIF1 DNA binding or transactivation potential by controlling other HIF1 post-translational modifications such as phosphorylation. In support of that, we have previously described that cAMP specifically activates the MAPK pathway in melanocytes (Englaro et al., 1995; Busc角 et al., 2000) and the transcriptional activity of HIF1 has been reported to be stimulated upon phosphorylation by MAPK (Richard et al., 1999; Suzuki et al., 2001; Lee et al., 2002).
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HIF1 has a broad impact on gene expression (>60 direct target genes have been identified), making it a crucial element in the regulation of many cell features going from cell proliferation to motility and apoptosis. Furthermore, HIF1 has a special impact on cancer progression because of its effects on angiogenesis and glucose metabolism (Semenza, 2003). Further, HIF1 mediates tumor cell adaptive response to hypoxia by regulating genes implicated in cell survival (Semenza 2001). In nontumor cells, a recent work by Xie et al. (2005) also involves HIF1 as a survival factor that protects neurons from NGF deprivation-induced cell death. In contrast, in other contexts HIF1 has been shown to participate in hypoxia-induced cell death via interaction with p53 (Halterman and Federoff, 1999) or modulation of several pro-apoptotic targets such as NIP3 (Bruick, 2000), Noxa (Kim et al., 2004), BNIP3 and NIX (Sowter et al., 2001), RTP801 (Shoshani et al., 2002), and the recently described HGTD-P (Lee et al., 2004). In this case, MITF, by regulating HIF1 expression, would rather favor cell death. In our melanoma cell system, we find that HIF1 plays a pro-survival role, as observed by the inhibition of the staurosporin-induced caspase-3 cleavage. We can therefore imagine that the cAMP/MITF/HIF1 pathway might contribute to higher cell viability and resistance to any putative physiological or environmental stresses such as UV exposure, for example.8 z2 f9 i9 @8 D( T8 A
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The fact that cAMP increases Vegf mRNA in our melanoma cells also leads us to hypothesize an angiogenic role of the cAMP/MITF/HIF1 cascade. In agreement with this hypothesis, UV radiation has been reported to increase cutaneous angiogenesis (Bielenberg et al., 1998) and nevus growth (Menzies et al., 2004). Because -MSH production in skin is stimulated upon UV radiation, we could imagine that -MSH, by up-regulating the cAMP-MITF-HIF1 pathway could participate to the angiogenic and growth-promoting effects of UV radiation.
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5 g" X; x8 h* A4 O* C. b$ m7 g" gThus, together, these observations suggest that the stimulation of HIF1 expression by cAMP and MITF might facilitate both melanoma survival, neo-vascularization, and metabolic adaptation, thereby favoring the development of these tumors.5 O9 ?; A9 a3 U+ n
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Although the role of MITF in survival and development of melanocyte precursors has been clearly documented, the growth and survival functions of MITF in mature melanocytes and melanoma cells remain a matter of debate. Indeed, it has been demonstrated that overexpression of MITF into a melanoma cell line results in slower xenograft tumor growth (Selzer et al., 2002), and MITF was recently shown to inhibit cell growth by activating the cell cycle inhibitor INK4A (Loercher et al., 2005) as well p21CIP1 expression (Carreira et al., 2005). However, recent reports have shown that MITF is a melanoma survival factor presumably through the up-regulation of the anti-apoptotic gene BCL2 (McGill et al., 2002) and promotes melanoma cell growth by stimulating CDK2 expression (Du et al., 2004).
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All of these data suggest that MITF, as well HIF1, can elicit opposite cellular responses. The decision between pro-survival and growth inhibition might be dictated by the cellular context, the extracellular signals, the microenvironment, or the mutational status of melanoma. In our case, cAMP constitutes a signal that clearly tilts the balance toward survival and presumably angiogenesis and melanoma growth.
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In conclusion, here we show for the first time a transcriptional up-regulation of HIF1 by the melanocyte-specific transcription factor MITF, thereby establishing a possible link between MITF and melanoma survival and vascularization. Taking into account the functional plasticity of both MITF and HIF1, further studies are underway to elucidate the precise physiological relevance of the MITF-HIF1 cascade in melanoma development. Modulation of such regulatory mechanisms could provide novel therapeutic approaches to this aggressive and metastatic cancer.
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' r: s' |/ B% ^3 }) bMaterials and methods
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. J( C" Z0 F' S$ a+ cCell culture$ G( x  y# G" L9 P: A

1 H0 e8 o. j# F4 [+ T! |3 iB16/F10 (mouse melanoma cells), Mewo (human melanoma cells), and NIH 3T3 (mouse fibroblasts) were cultured in DME (GIBCO BRL) supplemented with 7% FBS (Hyclone Laboratories) and penicillin/streptomycin (100 IU/50 μg/ml; Sigma-Aldrich) in a humidified atmosphere containing 5% CO2 in air at 37°C. Primary human melanocytes (NHM) were obtained from neonatal foreskins of Caucasian individuals, and grown in MCDB medium (GIBCO BRL) according to a modification of the method of Eisinger and Marko (1982) and Aberdam et al. (1993). Before cAMP treatment, NHM were depleted in forskolin for at least 24 h.& b7 d" w5 L) a% ^- A% t- S' u0 a

+ Q2 \, [7 I0 }$ B3 Z, a0 f9 ]When indicated, cells were treated with forskolin (20 μM), -MSH (1 μM), or cobalt (200 μM) to mimic hypoxia. To induce caspase-3 cleavage, cells were treated with 1 μM staurosporin (Calbiochem) for 6 h. Hypoxic conditions were produced by incubation of cells in a sealed "Bug-Box" anaerobic workstation (Ruskin Technologies). The oxygen in this workstation was maintained at 1–2%, with the residual gas mixture being 93–94% nitrogen and 5% CO2.
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Plasmids, adenovirus, siRNAs, and PCR oligonucleotide sequences
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" J: R; O8 Z- F* m: B- A7 {The plasmid encoding the mouse Hif1a promoter fragment upstream of the luciferase reporter gene was provided by Dr. R. Wenger (University of Zürich, Zürich, Switzerland). The 3-HRE-LUC reporter vector contains three copies of the HRE from the erythropoietin promoter cloned upstream of a minimal thymidine kinase promoter and the luciferase reporter gene (Berra et al., 2003). The plasmids encoding the mouse MITF and MITFDNT are described in Bertolotto et al. (1998a). The adenovirus encoding MITF is reported in Gaggioli et al. (2003).8 Y/ b1 P* b& l* l5 P
0 u1 ~4 [  x$ e
The DNA sequence corresponding to the siRNA-targeting Mitf is: 5'-GGTGAATCGGATCATCAAG-3'; Hif1a: 5'-CCTATATCCCAATGGATGATG-3'. As nonrelevant siRNAs (control siRNAs) we used the siLUC: 5'-CGTACGCGGAATACTTCGA-3' and the Drosophila melanogaster Hif1a (SIMA): 5'-CCTCATCCCGATCGATGATG-3' described in Berra et al. (2003). The mouse siRNA sequence targeting PHD2 was: 5'-GAACTCAAGCCCAATTCAGTT-3'.' o" L5 W' c8 l$ d3 [

7 P& V( H6 T( y# [The oligonucleotides to amplify the Hif1a and tyrosinase promoter regions were: 5'-CACGGGCACGAAGTGTTCCTTTG-3' (forward) and 5'-GCTCAGCCGCACCCGTCACT-3' (reverse) for Hif1a and 5'-GATCTCTAAATACAACAGGCT-3' (forward) and 5'-TCATACAAAATCTGCACCAA-3' (reverse) for tyrosinase, and to amplify GAPDH we used: 5'-TGGTATGACAACGAATTTG-3' (forward) and 5'-TCTACATGGCAACTGT-GAGG-3' (reverse).
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+ M  L# p  z! x$ L" LThe oligonucleotide sequences corresponding to mouse Hif1a, Mitf, tyrosinase, tyrosinase-related protein 1, MyoVa and Rab27a, and human MITF and HIF1A used for real-time quantitative PCR are available upon request.* Y) W9 |4 g! p7 L: \

0 j$ g* x" k" ^6 n; uAntibodies
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9 T3 I4 Y( J, v4 U# F. w1 f! JThe mAb to MITF (C5) was obtained from Dr. D. Fisher (Dana Farber Cancer Institute, Boston, MA; Weilbaecher et al., 1998). The polyclonal anti-MITF antibody used for the chromatin immunoprecipitation assays is described in Bertolotto et al. (1996). The rabbit anti-HIF1 (antiserum 2087) is described in Richard et al. (1999) and the monoclonal anti-HIF1 antibody used for the HIF1/caspase-3 double labeling was from Abcam. The pAb to cleaved caspase-3 was from Cell Signaling. The pAb anti-extracellular signal-regulated kinase 2 (ERK2) is from Santa Cruz Biotechnologies, Inc. The anti–mouse and anti–rabbit peroxidase-conjugated secondary antibodies as well as the FITC and Texas red–conjugated anti–mouse and anti–rabbit antibodies were from Dakopatts.1 y+ U" Q! S; @; u5 p5 T$ j

7 K4 z) A1 l% c4 hBiochips screening. `( d! n- q+ f6 W# L) g
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The laboratory-designed microarray containing 4,200 genes was previously described (Moreilhon et al., 2004). The list of probes spotted on the microarray is available at http://medlab.ipmc.cnrs.fr/gene_List.html. Total RNAs (10 μg) were reverse transcribed using the CyScribe First-Strand cDNA labeling kit (RPN 6200; Amersham Biosciences). Microarrays were hybridized with the Cy3/Cy5 mixed sample overnight at 42°C, and were washed at RT in 1x SSC/0.03% SDS for 5 min, in 0.2x SSC for 5 min, and in 0.05x SSC for 5 min. Slides were scanned using a confocal scanner (Scan Array 5000; GSI Lumonics). Images were analyzed by the Quant Array software.
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Quantitative real-time one-step RT-PCR and Western blot
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/ Y0 U0 g/ @3 u6 W9 Q8 b4 ?1 |# ?RNAs were extracted using TRIzol reagent (Invitrogen) and Rneasy protect mini kit (QIAGEN). mRNA expression levels were quantified by real-time one-step RT-PCR using SYBR-Green PCR Master Mix (Applied Biosystems). The results are the average of three separate experiments.
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For the Western blot analysis, subconfluent cells were lysed in Laemmli buffer. The protein concentration was determined using the Lowry assay and 50 μg total cell extracts was resolved by SDS-PAGE (7.5% for HIF1 detection) and electrophoretically transferred onto a PVDF membrane (Millipore). Immunoreactive bands were visualized using the ECL system (Amersham Biosciences).! a) W$ X9 `* N( @6 w

6 @7 D7 u' R% v# W3 {- ]Chromatin immunoprecipitation assay/ _6 V4 Z& S+ h: G% V- f3 v

$ y, U2 Z. i) J% [4 ZB16 cells were stimulated (or not) with forskolin for 5 h and were then treated with 1% formaldehyde for 5 min at 37°C and for 30 min at 4°C. Next, cells were harvested and suspended in the lysis buffer (10 mM Hepes, 1.5 mM MgCl2, 10 mM KCl, 0.5 mM DTT, 0.1% NP-40, and protease inhibitors). After 10 min incubation on ice, cells were centrifuged (5,000 rpm, 5 min at 4°C) to pellet the nuclei. Nuclei were then suspended in the nuclei lysis buffer (50 mM Tris-Cl, pH 8.1, 10 mM EDTA, 1% SDS, and protease inhibitors) and incubated on ice for 10 min. The sheared chromatin was then immunoprecipitated using (or not) a specific polyclonal anti-MITF antibody (Bertolotto et al., 1998b). After immunoprecipitation, the cross-link was reverted by heat treatment (67°C overnight and proteinase K digestion). The genomic captured fragments were then recovered by phenol-chloroform extraction. Identification of the captured Hif1a or tyrosinase promoter fragments was performed by PCR analysis using the promoter primers. 30 cycles of PCR were performed and the amplified products were analyzed on a 2% agarose gel.
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, W" \; P; h$ F" u+ r+ a* n; O0 I# WTransfections and luciferase assays* y- H* S* j: m, ^

- J, u, \# U; i8 A1 y1 F  dB16 melanoma cells and NIH-3T3 fibroblasts were seeded in 24-well dishes, and transient transfections were performed the following day using 2 μl Lipofectamine (GIBCO BRL) and 0.5 μg total plasmid DNA or 20 nM annealed siRNAs, in a 200-μl final volume. pCMVGal was cotransfected with the test plasmids to control the variability of transfection efficiency in the reporter assays. 24 h after transfection, soluble extracts were harvested in 50 μl of lysis buffer and assayed for luciferase and -galactosidase activities. All transfections were repeated several times using different plasmid preparations.- v- B% r: O! G- p3 x1 ]+ e  t- l0 z

3 F7 W3 p3 L, x+ _/ n# rImmunofluorescence microscopy. l/ x0 y* A3 S( X- S  l* h" {" P

% o. m4 w. ~& s$ _2 @/ _5 JsiRNA-transfected B16 melanoma cells cultured on glass coverslips were washed three times in PBS, fixed for 20 min in 3% PFA, washed again, and incubated for 10 min in 50 mM NH4Cl. After three more washes, cells were incubated with the primary antibody diluted in PBS containing 0.5% BSA and 0.02% saponin for 1 h, washed abundantly in PBS, and incubated for another hour with the appropriate conjugated secondary antibody. After washing, the coverslips were incubated with bisbenzidine (0.5 μg/ml) to stain the nuclei, they were mounted on glass slides, and viewed with an Axiophot fluorescent microscope (Carl Zeiss MicroImaging, Inc.), using a 40x/0.75 Plan Neofluar objective lens. To acquire the images, a COHU (High performance CCD camera) and the Q-Fish (Leica) informatic software was used.
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Acknowledgments
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We are grateful to the facilities of the Nice-Sophia Antipolis Transcriptome Platform of the Marseille-Nice Genopole in which the microarray experiments were carried out. We thank Dr. R. Wenger for providing the Hif1a promoter construct and Dr. D. Fisher for the C5 anti-MITF antibody. We also thank Dr. P. Pognonec for the plasmids encoding USF and myc. We are very grateful to Dr. P. Lenormand for all his help and unconditional support in this work.( ~/ W* ^/ S# R7 r! j. \( p$ H

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Weilbaecher, K.N., C.L. Hershey, C.M. Takemoto, M.A. Horstmann, T.J. Hemesath, A.H. Tashjian, and D.E. Fisher. 1998. Age-resolving osteopetrosis: a rat model implicating microphthalmia and the related transcription factor TFE3. J. Exp. Med. 187:775–785.) E( Y: k. i0 U2 I, s

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( D5 w7 B/ ^: c" `+ y5 AZhong, H., K. Chiles, D. Feldser, E. Laughner, C. Hanrahan, M.M. Georgescu, J.W. Simons, and G.L. Semenza. 2000. Modulation of hypoxia-inducible factor 1 expression by the epidermal growth factor/phosphatidylinositol 3-kinase/PTEN/AKT/FRAP pathway in human prostate cancer cells: implications for tumor angiogenesis and therapeutics. Cancer Res. 60:1541–1545.
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Zundel, W., C. Schindler, D. Haas-Kogan, A. Koong, F. Kaper, E. Chen, A.R. Gottschalk, H.E. Ryan, R.S. Johnson, A.B. Jefferson, et al. 2000. Loss of PTEN facilitates HIF-1-mediated gene expression. Genes Dev. 14:391–396.(Roser Busc角, Edurne Berra)

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发表于 2015-5-21 19:15 |显示全部帖子
回复一下  

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发表于 2015-6-1 11:08 |显示全部帖子
勤奋真能造就财富吗?  

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发表于 2015-6-30 19:14 |显示全部帖子
干细胞之家微信公众号
回答了那么多,没有加分了,郁闷。。  

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发表于 2015-7-3 13:08 |显示全部帖子
不错 不错  比我强多了  

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发表于 2015-7-10 09:18 |显示全部帖子
哈哈,有意思~顶顶 ,继续顶顶。继续顶哦  

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发表于 2015-7-24 08:18 |显示全部帖子
我又回复了  

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发表于 2015-8-8 08:35 |显示全部帖子
来几句吧  

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发表于 2015-8-9 19:07 |显示全部帖子
应该加分  

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发表于 2015-9-3 12:08 |显示全部帖子
嘿嘿......哈哈......呵呵.....哟~呼  
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