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Originally published In Press as doi:10.1074/jbc.M700440200 on July 12, 2007

J. Biol. Chem., Vol. 282, Issue 37, 26767-26774, September 14, 2007
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CXCL12 Activates a Robust Transcriptional Response in Human Prostate Epithelial Cells*

Lesa A. Begley, James W. MacDonald, Mark L. Day, and Jill A. Macoska1

From the Department of Urology and the Comprehensive Cancer Center, University of Michigan, Ann Arbor, Michigan 48109

Received for publication, January 16, 2007 , and in revised form, July 12, 2007.


   ABSTRACT
TOP
 ABSTRACT
INTRODUCTION
 EXPERIMENTAL PROCEDURES
 RESULTS
 DISCUSSION
 REFERENCES
 
CXCL12 is a CXC-type chemokine that plays important roles in hematopoiesis, development, and organization of the immune system and supports the survival or growth of a variety of normal or malignant cell types. Our laboratory recently showed that CXCL12 is secreted by aging stromal fibroblast cells and is a major paracrine factor that specifically stimulates the proliferation of prostate epithelial cells. The current study shows that this CXCL12-mediated proliferative response may be either ERK-dependent or ERK-independent. Moreover, CXCL12 initiates a previously undefined and complex global transcriptional response in prostate epithelial cells. This CXCL12-mediated transcriptional response directly stimulates the expression of genes encoding proteins that are involved in the promotion of cellular proliferation and progression through the cell cycle, tumor metastasis, and cellular motility, and directly represses the transcription of genes encoding proteins involved in cell-cell adhesion and resistance to apoptosis. Thus, CXCL12 may play a major role in the etiology of benign proliferative disease in the context of an aging tissue microenvironment.


   INTRODUCTION
TOP
 ABSTRACT
 INTRODUCTION
EXPERIMENTAL PROCEDURES
 RESULTS
 DISCUSSION
 REFERENCES
 
Many studies have shown that paracrine interactions help regulate the proliferation of both stromal and epithelial cells in the prostate and other endocrine organs (1–5). However, previous studies have not been designed to examine how aging as a risk factor contributes to potential changes in stromal/epithelial paracrine interactions permissive for cellular proliferation. This is an important concern, because the coincident development of benign proliferative disease in the prostate with increasing patient age suggests that paracrine interactions may become dysfunctional and promote cellular proliferation as a consequence of the aging process. Moreover, the gradual increase in prostate volume with patient age that is characteristic of benign prostatic enlargement and benign prostatic hyperplasia suggests that mechanisms fostering low level, but cumulative, cellular proliferation are involved in the etiology of this disease.

Recent studies from our laboratory utilizing an in vitro model system to examine the effects of the aging microenvironment on the development of benign proliferative disease in the human prostate demonstrated that paracrine interactions between human prostate epithelial cells and stromal fibroblasts are disrupted in aging prostate tissues. Specifically, these studies showed that the CXC-type chemokine, CXCL12, is secreted by aging human prostate stromal fibroblasts at sub-nanomolar quantities that stimulate the proliferation of prostate epithelial cells (6). CXC-type chemokines have two conserved cysteines separated by one unconserved amino acid. There are several members of the CXC-type chemokine family with both conserved and diverse functions, although all CXC-type chemokines signal though membrane-bound G-protein-coupled receptors (7). Many studies to date have focused on the role of CXCL12 in the acquisition and expression of an invasive, metastatic phenotype in human solid tumors, most notably, breast and prostate cancer (8–16, 18). Taken together, these studies suggested that CXCL12 may play a role in acquisition of the proliferative phenotype in benign, and perhaps malignant, proliferative diseases of the prostate.

CXCL12-mediated signaling activates molecules known to stimulate gene transcription and cellular proliferation, including ERK2 and NF{kappa}B (6, 19). However, the definition and extent of the CXCL12-mediated transcriptional response, and the potential impact of this transcriptional response on expression of the proliferative phenotype, have not been elucidated. To address this issue, we have now evaluated the molecular signatures of prostate epithelial cells stimulated with sub-nanomolar levels of CXCL12 similar to those secreted by aging prostate stroma and known to stimulate cellular proliferation. These studies reveal that CXCL12-mediated signaling induces a robust transcriptional response in prostate epithelial cells that includes the up-regulation of genes encoding proteins that promote cellular proliferation and resistance to apoptosis, as well as the down-regulation of genes encoding proteins that normally act to promote apoptosis, cell-cell adhesion, and cell cycle arrest. This is the first report to show that CXCL12-mediated signaling induces a robust transcriptional response that may facilitate the acquisition of a proliferative and invasive phenotype by prostate epithelial cells.


   EXPERIMENTAL PROCEDURES
TOP
 ABSTRACT
 INTRODUCTION
 EXPERIMENTAL PROCEDURES
RESULTS
 DISCUSSION
 REFERENCES
 
Cell Cultures—N15C6 cells, developed as described previously, were used at passages 35–45 and were maintained in 5% HIE media (Ham's F-12 (Mediatech Inc., Herndon, VA) with 5% fetal bovine serum (Invitrogen), 5 µg/ml insulin, 10 ng/ml EGF, 1 µg/ml hydrocortisone (Sigma) or in defined serum-free HIE media supplemented to 5 mM ethanolamine (Sigma-Aldrich), 10 mM HEPES (Sigma-Aldrich), 5 µg/µl transferrin (Sigma-Aldrich), 10 µM 3,3',5-triiodo-L-thyronine (Sigma-Aldrich), 50 µM sodium selenite (Sigma-Aldrich), 0.1% bovine serum albumin (JRH Biosciences, Lenexa, KS), 0.05 mg/ml gentamycin (Invitrogen), and 0.5 µg/ml fungizone (Cambrex Bioscience, Walkersville, MD). N15C6 cells are non-transformed prostate epithelial cells and grow continuously in culture but do not form colonies in soft agar or tumors in immunocompromised mice (20, 21). LNCaP cells, a widely used transformed prostate epithelial cell line originating from a prostate cancer lymph node metastasis, were acquired from the American Type Culture Collection (ATCC# CRL-1740), were maintained in 10% RPMI media and 0.5 µg/ml fungizone, and were used at passages 25–35 (22).

Proliferation Assays—Cellular proliferation was assessed after plating cells at 50,000 cell/well in triplicate in 6-well plates and counting cells after 24 and 96 h of incubation as described previously (20). To assess the effects of exogenous CXCL12 on cellular proliferation, recombinant human SDF1 {alpha}/CXCL12 (R&D Systems, 350-NS) was added at the desired concentration in 1 ml of SF HIE (or 1 ml of SF HIE alone for control) to each well. The cells were re-fed at 48 and 72 h growth and counted at 24 and 96 h growth. Cell counts were normalized to 50,000 cells at 24 h to account for any plating discrepancies. Averages and standard deviations of cell number were calculated for each time point under each media condition. Experiments utilizing U0126 were performed as above, except that cells were pre-treated for 2 h with either 0.05% Me2SO (vehicle) or 0.05% Me2SO plus 5 µM U0126 before the addition of CXCL12. Cells were maintained in media containing U0126 and/or Me2SO for the duration of the experiment. For the antibody blockade experiments, 10,000 cells per well were plated in triplicate in 24-well dishes and preincubated with mouse anti-human CXCR4 (BD Pharmingen 555971) and rabbit anti-human CXCR7/RDC1 (Abcam ab12870-50) or mouse anti-human CXCR2 (BIOSOURCE AHR1532X) at 1 µg/ml for 1 h prior to CXCL12 addition. Cells were maintained in media containing appropriate antibodies for the entirety of the experiment, and cells were counted at 24 and 96 h as above.

Affymetrix Human Genome U133 plus 2.0 Array Data Acquisition—RNA was purified from trypsinized cultured cells by homogenization in TRIzol (Invitrogen) and additional processing using the RNeasy (Qiagen) cleanup procedure. 10 µgof RNA was used to obtain labeled cRNA following the Affymetrix Standard protocol. Expression intensity values for each gene were estimated using a method called Robust Multiarray Average using tools available through Bioconductor. GeneChip gene expression values were normalized using a quantile normalization procedure.

Quantitative Real-time PCR—All quantitative real-time assays were conducted as previously described with an Applied Biosystems 7900HT instrument and reagents (21). Cells were grown to 70% confluence in 60 mM dishes prior to RNA purification using the TRIzol reagent (Invitrogen). Experiments utilizing U0126 were performed as above, except that cells were treated with Me2SO (vehicle) or Me2SO plus 5 µM U0126 for 2 h, then grown in the presence or absence of CXCL12. For all experiments, 1 µg of RNA was reverse transcribed by use of Superscript III reverse transcriptase (Invitrogen). The resulting cDNA was diluted 1:100. Real-time PCR was performed by use of Assays on Demand (Applied Biosystems, Foster City, CA) according to the manufacturer's instructions. Reactions were performed in triplicate, including notemplate controls and an endogenous control probe, RPLPO (ribosomal protein, large, PO), to assess template concentration. Cycle numbers to threshold were calculated by subtracting averaged control from averaged experimental values, and fold gene expression was calculated by raising these values to the log 2. 6-Carboxy-fluorescine-conjugated, gene-specific assays were Hs00152928_m1 for EGR1, Hs00193306_m1 for EGFR, Hs00170433_m1 for ERBB2, and Hs99999902_m1 for the control, RPLPO.

Western Blot and Protein Analysis—Cells were lysed, proteins were resolved by electrophoresis, and electroblotting was carried out as described previously (6, 23). Proteins were detected using antibodies against phospho-ERK1/2 (Cell Signaling #9101), total ERK1/2 (Cell Signaling, #9102), CXCR4 (Abcam #ab2074), CXCR7 (also known as RDC1, Abcam #ab12870), ELK-1 (Cell Signaling #9182), phospho ELK-1 (Cell Signaling #9181), and beta-actin (#sc-1615, Santa Cruz Biotechnology, Santa Cruz, CA), in conjunction with an ECL detection system. Secondary antibodies included goat anti-rabbit (Cell Signaling, #7074) and goat anti-mouse (Santa Cruz Biotechnology, #SC-2005), and both were used at a 1:5000 concentration. Immunoblots shown are representative of triplicate experiments. Densitometric quantitation of immunoblot films was accomplished by scanning the original films and converting the tiff files to grayscale images. Images were inverted, and mean band intensities were measured using ImageJ (National Institutes of Health). The mean intensity of adjacent background was also measured for each band and subtracted from band intensity.

Statistical Analysis—Densitometric data from three experiments was averaged, and standard deviations were calculated for graphical depiction and statistical analysis. Normalized array-acquired transcript expression values were analyzed using a t-statistic test and by calculation of -fold change between data sets. Genes that exhibited both a large t-statistic (>10.0) and a large -fold change (>2.0) were considered to be differentially expressed. All other data were assessed by t test or analysis of variance with p < 0.05 considered statistically significant.


   RESULTS
TOP
 ABSTRACT
 INTRODUCTION
 EXPERIMENTAL PROCEDURES
 RESULTS
DISCUSSION
 REFERENCES
 
ERK Dependence of CXCL12-mediated Cellular Proliferation—Previous studies have shown that both transformed PC3 and LNCaP, as well as non-transformed N15C6 and BPH-1 prostate epithelial cells, express CXCR4, one of the receptors for CXCL12 (6, 19, 24). We now show that these cells also robustly express CXCR7, a recently identified second receptor that recognizes CXCL12 (Fig. 1A) (25). Our laboratory has previously shown that the stimulation of non-transformed N15C6 and transformed LNCaP cells with CXCL12 at sub-nanomolar levels similar to those secreted by aging prostate stromal fibroblasts induces these cells to proliferate (6). As seen in Fig. 1B, N15C6 cells stimulated with 1 pM or 10 pM CXCL12 proliferate to levels significantly higher than those achieved by unstimulated cells (p < 0.001). This proliferation is maintained even after the cells are pre-treated with an antibody against an unrelated chemokine receptor, CXCR2 (Fig. 1B). However, pretreatment with antibodies against the CXCL12-specific receptor, CXCR4, or against both CXCR4 and CXCR7, significantly (p < 0.001) and equivalently ablated the ability of CXCL12 to stimulate proliferation. Thus, CXCL12-stimulated cellular proliferation is mediated through interactions with receptors that specifically recognize this chemokine.


Figure 1
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  		FIGURE 1.
Receptor specificity and ERK dependence of CXCL12-mediated cellular proliferation. A, immunoblot demonstrating that PC3 (lane 1), LNCaP (lane 2), N15C6 (lane 3), and BPH-1 (lane 4) prostate epithelial cells abundantly express CXCR7 (also known as RDC1), a receptor that binds CXCL12. The primary antibody concentrations used were 1:1000 for CXCR7 and 1:5000 for actin (as loading control). B, N15C6 prostate epithelial cells grown for 96 h in serum-free HIE media supplemented with 1 pM CXCL12 (white bars) or 10 pM CXCL12 (gray bars) proliferated to significantly higher levels than cells grown in serum-free HIE media alone (*, p < 0.001). Cellular growth following preincubation with an antibody against an unrelated chemokine receptor, CXCR2, followed by supplementation with CXCL12 and maintenance of growth in CXCL12 plus anti-CXCR2-containing media was similar to that observed for non-pre-treated cells grown in CXCL12-supplemented media and was significantly higher than that in serum-free HIE media alone (*, p < 0.001). Preincubation of cells for 1 h with 1 µg/ml antibody against CXCR4, a receptor for CXCL12, followed by supplementation with CXCL12 and maintenance of growth in CXCL12 plus anti-CXCR4-containing media significantly ablated the proliferative response (#, p < 0.001). Preincubation of cells for 1 h with 1 µg/ml antibodies against both known receptors for CXCL12, CXCR4 and CXCR7, followed by supplementation with CXCL12 and maintenance of growth in CXCL12 plus anti-CXCR4/CXCR7-containing media also significantly ablated the proliferative response (#, p < 0.001), although not significantly more so than that obtained upon pre-treatment with anti-CXCR4 alone. All data are shown normalized to growth in un-supplemented SF HIE media, which was set at 1-fold. C, LNCaP cells demonstrate minimal ERK phosphorylation (pERK) upon treatment with 100 ng/ml EGF or 50 pM CXCL12. Primary antibody concentrations used were 1:500 for phosphoERK and 1:2000 for total ERK. Phosphorylation of ERK relative to total ERK quantitated from the immunoblot is shown in the densitometry plot as pERK/tERK. D, N15C6 cells grown in SF HIE media, pre-treated for 2 h with the solvent control 0.05% Me2SO, then supplemented with 1, 10, or 1000 pM CXCL12 demonstrate rapid and transient ERK phosphorylation (pERK) at 5 and 10 min post-stimulation compared with cells at the initiation of the experiment (time 0). Pre-treatment of the cells the MEK1 inhibitor, U0126 (dissolved in 0.05% Me2SO), either reduces (1 µM) or ablates (5 µM) ERK phosphorylation. Primary antibody concentrations used were as described in B. E, densitometry plot of the immunoblots shown in C demonstrates phosphorylation of ERK relative to total ERK (pERK/tERK). All values are normalized to those obtained for the 0 time point, which was considered 1-fold for comparative purposes. Cells pre-treated with 0.05% Me2SO then treated with 1, 10, or 1000 pM CXCL12 for 5 or 10 min demonstrated significantly higher levels of ERK phosphorylation than those at time 0 (*, p < 0.001). Cells pretreated with 1 µM or 5 µM U0126 in 0.05% Me2SO then treated with 1, 10, or 1000 pM CXCL12 for 5 or 10 min demonstrated levels of ERK phosphorylation at or below those obtained at time 0 (#, p < 0.001). F, N15C6 cells (black triangles) grown in SF HIE with 0.05% Me2SO plus 10 pM CXCL12 (+) proliferated significantly better than those grown in SF HIE with 0.05% Me2SO (–) (*, p < 0.001). Proliferation was significantly reduced in N15C6 cells (white triangles) grown under the same conditions but with the addition of 5 µM U0126 (#, p < 0.001). LNCaP cells treated in a similar manner but supplemented with 50 pM CXCL12 did not demonstrate significant differences in growth between cells treated with the solvent control (black squares) or inhibitor (white squares).

 


Figure 2
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  		FIGURE 2.
CXCL12 mediates the activation of ELK-1. A, immunoblot analysis shows that N15C6 cells demonstrate rapid and transient phosphorylation of the ELK-1 transcription factor (pELK-1) after exposure to 10 or 1000 pM CXCL12. Primary antibody concentrations used were 1:1000 for pELK-1 and 1:1000 for total ELK-1. B, densitometry plot of the immunoblots shown in A demonstrate phosphorylation of ELK-1 relative to total ELK-1 (p/ELK-1/tELK-1). All values are normalized to those obtained for the 0 time point, which was set at 1-fold for comparative purposes. Phosphorylation levels significantly higher than those observed at time 0 are indicated by the asterisk (p < 0.05). C, immunoblot analysis shows that LNCaP cells demonstrate rapid and transient phosphorylation of the ELK-1 transcription factor (pELK-1) after exposure to 5 pM, 50 pM, or 500 pM CXCL12. Primary antibody concentrations used were as in A. D, densitometry plot of the immunoblots shown in C demonstrates phosphorylation of ELK-1 relative to total ELK-1 (p/ELK-1/tELK-1). All values are normalized to those obtained for the 0 time point, which was set at 1-fold for comparative purposes. Phosphorylation levels significantly higher than that those observed at time 0 are indicated by the asterisk (p < 0.05).

 
The Ras-mediated mitogen-activated kinase pathway is known to stimulate cellular proliferation. In this pathway, mitogen-activated protein kinase/extracellular signal-regulated kinase kinase 1 (MEK1) phosphorylates ERK, which in turn phosphorylates and activates other molecules, including transcription factors, involved in cellular proliferation. Treatment of prostate epithelial cells with nanomolar levels of CXCL12 has been shown to activate the MEK/ERK pathway and promote cytokine secretion, angiogenesis, and transendothelial cellular migration (19, 26). Our laboratory has also shown that both sub-nanomolar and nanomolar levels of CXCL12 stimulate MEK/ERK pathway activation in prostate epithelial cells (Fig. 1, C–E, and Ref. 6). However, LNCaP cells treated with CXCL12 at the sub-nanomolar levels that stimulate a proliferative response, e.g. 50 pM, demonstrate only a modest activation of ERK (Fig. 1C). In contrast, N15C6 cells treated with CXCL12 at the sub-nanomolar levels that stimulate a proliferative response, e.g. 1 pM or 10 pM, demonstrated rapid, transient ERK phosphorylation and activation (Fig. 1, D and E) (6). The observed differential extent of ERK activation in N15C6 and LNCaP cells treated with levels of CXCL12 known to stimulate proliferation in each cell line suggested that ERK activation might not be equivalently required for CXCL12-mediated proliferation in both cell lines. To test this, the MEK1 inhibitor, U0126, was utilized to inhibit the ability of MEK1 to phosphorylate ERK, thus preventing ERK activation. As seen in Fig. 1D, treatment of N15C6 cells with 1 pM, 10 pM, or 1000 pM CXCL12 resulted in rapid and transient MEK1-mediated ERK phosphorylation. However, cotreatment of the cells with CXCL12 and 1.0 µM or 5.0 µM U0126 greatly diminished ERK phosphorylation. Densitometric analysis of the immunoblot confirmed these observations and showed that cells pre-treated with either concentration of inhibitor failed to phosphorylate ERK in response to treatment with CXCL12 (Fig. 1E). Moreover, the proliferative response of N15C6 cells to CXCL12 was nearly ablated when the cells were co-treated with CXCL12 and 5.0 µM U0126 in 0.05% Me2SO compared with co-treatment with CXCL12 without inhibitor in 0.05% Me2SO (Fig. 1F). In contrast, the proliferative response of LNCaP cells to CXCL12 was not affected by co-treatment with U0126 (Fig. 1F).

CXCL12-mediated Signaling Activates ELK1 and Promotes EGR1 Gene Transcription—Both N15C6 and LNCaP cells were next examined for CXCL12-mediated activation of ELK-1, an Ets domain-type transcription factor that is itself activated through phosphorylation by both MAPK-dependent and -independent mechanisms (27, 28). N15C6 and LNCaP prostate epithelial cells stimulated with CXCL12 demonstrated rapid and transient phosphorylation of ELK-1 as visualized by immunoblotting and quantitated by densitometry (Fig. 2). ELK-1 is a transcriptional activator of the early growth response 1 (EGR1) gene, which encodes a C2H2-type zinc-finger protein that is induced by mitogenic stimulation and has been shown to stimulate tumor cell growth, play a role in tumor progression, and stimulate angiogenesis and improved survival of tumor cells (29). Quantitative reverse transcription-PCR assays showed that both N15C6 and LNCaP cells, stimulated with low, picomolar levels of CXCL12 similar to those observed to promote N15C6 and LNCaP cellular proliferation, rapidly and robustly accumulate EGR1 gene transcript (Fig. 3A).


Figure 3
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  		FIGURE 3.
CXCL12 mediates a robust transcriptional response. A, quantitative real-time PCR of RNA purified from N15C6 cells pre-treated with 0.05% Me2SO then treated with 10 pM CXCL12 (black triangles) or LNCaP cells pre-treated with 0.05%Me2SO then treated with 50 pM CXCL12(blacksquares)demonstratesrapid and robust transcription of the EGR1 gene (*, p < 0.001). This response is significantly dampened when the cells are first pretreated for 2 h with 5 µM U0126 in 0.05% Me2SO (white triangles, N15C6 cells; white squares, LNCaP cells) (#, p < 0.001). B, quantitative real-time PCR of RNA purified from N15C6 cells treated for 30 min with 10 pM CXCL12 or LNCaP cells treated with 50 pM CXCL12 (black bars) demonstrates a robust and significant accumulation of transcript from the EGFR gene (*, p < 0.001) and a significant decrease in transcription of the ERBB2 gene (#, p < 0.05) compared with treated cells at 0 min (gray bars), parallel to RNA profiling results obtained using Affymetrix GeneChips. C, principal components analysis of the CXCL12-stimulated transcriptional response is shown for N15C6 and LNCaP cells in SF HIE media after a 2-h pre-treatment with 0.05% Me2SO (white dots and dotted ovals), the same but pre-treated with 0.05% Me2SO and stimulated with 10 pM (N15C6) or 50 pM (LNCaP) CXCL12 (black dots and black ovals), or pre-treated with 0.05% Me2SO plus 5µM U0126 and stimulated with 10 pM (N15C6) or 50 pM (LNCaP) CXCL12 (gray dots and gray ovals). Each experiment was performed twice, and both sets of data are shown. The significant separation along both components (PC1 and PC2) between the transcriptional responses resulting from Me2SO and Me2SO plus CXCL12 treatments demonstrates that CXCL12 induces a robust transcriptional response in both cell lines. The separation between the transcriptional responses resulting from Me2SO plus CXCL12 and Me2SO plus CXCL12 plus U0126 treatments is greater for N15C6 than for LNCaP cells, suggesting that the CXCL12-mediated transcriptional response is more ERK-dependent for N15C6 than LNCaP cells.

 
ERK Dependence of CXCL12-mediated EGR1 Gene Transcription—The specificity of the EGR1 gene transcriptional response to CXCL12-mediated ERK signaling was next examined using the MEK1 inhibitor, U0126. For these experiments, cells plated in triplicate at 50,000 cells/well were pre-treated with 0.05% Me2SO or 0.05% Me2SO and 5 µM U0126 (Cell Signaling) for 2 h, then stimulated with CXCL12 at concentrations shown previously to induce EGR1 gene transcription, e.g. 10 pM CXCL12 for N15C6 cells and 50 pM CXCL12 for LNCaP cells. As seen in Fig. 3A, pre-treatment with the MEK1 inhibitor inhibited the EGR1 gene transcriptional response in both cell lines but more profoundly in N15C6 than LNCaP cells. These results suggest that CXCL12-mediated EGR1 gene transcription is more ERK-dependent in N15C6 than LNCaP cells.

CXCL12 Stimulates a Global Transcriptional Response in Prostate Epithelial Cells That Is Partially ERK-dependent—We had previously reported that both non-transformed N15C6 and transformed LNCaP prostate epithelial cells respond proliferatively to low, picomolar levels of CXCL12, similar to those secreted by aging human prostate stromal fibroblasts (6). The observation that these same levels of CXCL12 stimulated ELK1 activation and EGR1 gene transcription raised the possibility that other genes may also be transcribed in response to CXCL12 stimulation. To explore this possibility, N15C6 and LNCaP cells were treated in replicate with CXCL12 and the MEK1 inhibitor, U0126, in 0.05% Me2SO; CXCL12 and 0.05% Me2SO; or 0.05% Me2SO alone, for 30 min. The cells were immediately lysed, and the purified RNA was subjected to gene expression profiling using Affymetrix Human Genome U133 Plus 2.0 Arrays. The results of these experiments showed that N15C6 cells demonstrated up-regulation of 370 genes and down-regulation of 162 genes at significance levels of p < 0.05 and -fold levels >1.5 consequent to stimulation with 10 pM CXCL12. LNCaP cells demonstrated up-regulation of 185 genes and down-regulation of 413 genes consequent to stimulation with 50 pM CXCL12 (Table 1). Thus, the transcriptional response of N15C6 cells to CXCL12 stimulation was largely positive and resulted in the up-regulation of the majority (370/532, or 70%) of genes differentially transcribed. In contrast, the transcriptional response of LNCaP cells to CXCL12 stimulation was largely negative and resulted in the transcriptional repression of the majority (413/598, or 69%) of genes differentially transcribed.


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  		TABLE 1
Summary of CXCL12-regulated transcriptional response in N15C6 and LNCaP cells

 
Although the gene transcription profiles induced by CXCL12 were largely different between N15C6 and LNCaP cells, 85 genes were transcribed in common (Table 2). The use of both the Gene Ontology and Information Hyperlinked over Proteins data bases permitted a limited functional assessment of proteins encoded by genes commonly transcriptionally down- or up-regulated consequent to CXCL12 stimulation (30). This assessment showed that the predicted functional consequences of loss of expression for many of the proteins encoded by the 52 commonly down-regulated genes and 33 up-regulated genes was consistent with promoting cellular proliferation or tumor progression. Quantitative real-time PCR of RNA purified from N15C6 or LNCaP cells treated for 30 min with CXCL12 demonstrates a robust and significant accumulation of transcript from the EGFR gene and a significant decrease in transcription of the ERBB2 gene compared with treated cells at 0 min, parallel to RNA profiling results obtained using Affymetrix GeneChips (Fig. 3B and Table 2).


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  		TABLE 2
Genes commonly transcriptionally regulated by CXCL12 in N15C6 and LNCaP cells

 
Differential ERK Dependence of the CXCL12-stimulated Transcriptional Response—Co-treatment of N15C6 or LNCaP cells with CXCL12 and 5 µM U0126 reduced the number of differentially expressed genes in both cell lines compared with treatment with CXCL12 alone. The proportion of differentially expressed genes that were down-regulated consequent to treatment with CXCL12 plus U0126 was 91% (296/325 genes) for N15C6 cells and 45% (13/39) for LNCaP cells (Table 3). 7 of the 39 genes affected transcriptionally by the treatment of LNCaP cells with both CXCL12 and U0126 were similarly affected in N15C6 cells, including ITGB4 (up-regulated) and CD44, EGR1, IL8, MAFF, TXNIP, and ARRDC4 (down-regulated). Reports in the literature suggest that the majority of these genes are transcriptionally regulated by ERK 1/2 (ITGB4, CD44, EGR1, and IL8) or inflammatory cytokines (MAFF) (30).


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  		TABLE 3
Common N15C6 and LNCaP transcriptional response to CXCL12 plus U0126

 
A principal components analysis of the gene expression profiling data shows that N15C6 or LNCaP cells treated with 0.05% Me2SO or CXCL12 and 0.05% Me2SO are widely separated along the first two principal components, consistent with the observed robust CXCL12-stimulated transcriptional response exhibited by both cell lines (Fig. 3C). Although the gene expression profiles of CXCL12 plus Me2SO-treated compared with CXCL12 plus U0126 plus Me2SO-treated N15C6 cells are also distinctly separated in the principal components analysis plot, those of similarly treated LNCaP cells demonstrate considerable overlap along the first principal component (PC1) and some overlap along the second principal component (PC2) (Fig. 3C). This analysis is consistent with the observation that CXCL12-stimulated transcriptional responses in N15C6 cells is more ERK-dependent than that observed for LNCaP cells.


   DISCUSSION
TOP
 ABSTRACT
 INTRODUCTION
 EXPERIMENTAL PROCEDURES
 RESULTS
 DISCUSSION
REFERENCES
 
CXCL12 is a CXC-type chemokine that activates downstream signaling through binding the G-protein-coupled receptors, CXCR4 or CXCR7. CXCL12 has been shown to play important roles in hematopoiesis, development, and organization of the immune system (31). Recent studies demonstrated that CXCL12 also supports the survival or growth of a variety of normal or malignant cell types. For example, Orimo et al. (32) recently showed that carcinoma-associated fibroblasts extracted from human breast tumors promote the growth of breast carcinoma cells significantly more than those of normal fibroblasts and that this effect was at least partially mediated by stromally-derived CXCL12. We have previously reported that CXCL12 is secreted at sub-nanomolar levels by aging human prostate stromal fibroblasts and that these levels of CXCL12 stimulate prostate epithelial cell proliferation (6). The current study shows that sub-nanomolar levels of CXCL12 similar to those secreted by aging fibroblasts stimulate a proliferative and robust transcriptional response in both pre-malignant and malignant prostate epithelial cells.

Consistent with data shown here, the MEK/ERK pathway can be activated in prostate epithelial cells by nanomolar levels of CXCL12. Activation of the MEK/ERK pathway at these levels of CXCL12 has been shown to promote cytokine secretion and transendothelial cellular migration by prostate epithelial cells (19, 26). Experiments reported here also show that prostate epithelial cells stimulated with sub-nanomolar levels of CXCL12, comparable to those secreted by aging prostate stroma, demonstrated differential ERK activation. Non-transformed N15C6 cells transiently but robustly activate ERK, whereas transformed LNCaP cells minimally activate ERK, in response to sub-nanomolar levels of CXCL12. Moreover, experiments utilizing the MEK1 inhibitor, U0126, showed that ERK activation was required for CXCL12-mediated cellular proliferation in non-transformed N15C6 but not transformed LNCaP, prostate epithelial cells.

In addition to stimulating cellular proliferation, activated ERK can translocate from the cytoplasm to the nucleus and, in turn, phosphorylate and activate several downstream effectors, including the transcription factor, ELK-1 (33). ELK-1, in turn, can activate the promoters of multiple genes containing serum response elements (e.g. EGR1) or ternary complex factor binding sites (34, 35). Although ERK phosphorylation in response to CXCL12 was clearly more robust in N15C6 compared with LNCaP cells, both cell lines demonstrated ELK-1 phosphorylation consequent to CXCL12 stimulation. Several studies have shown that ELK-1 can be phosphorylated and activated by multiple MAPKs, including ERK, JNK, and p38 (27, 28). Taken together, these results suggest that the common CXCL12-mediated proliferative and transcriptional responses observed for prostate epithelial cells may, in fact, be governed by multiple signaling pathways.

In addition to stimulating EGR1 gene transcription, the studies reported here show, for the first time, that CXCL12 stimulates a robust, global transcriptional response in both non-transformed N15C6 and transformed LNCaP prostate epithelial cells. Although these responses were largely contrary, that is, CXCL12-stimulated differential gene transcriptional was up-regulatory in N15C6 but repressive in LNCaP cells, they also resulted in the transcriptional regulation of a common set of genes that encoded proteins consistent with the promotion of cellular proliferation. In particular, the transcriptional down-regulation of several genes encoding proteins that normally promote cell cycle arrest, including TP53, MAFK, CUGBP1, CDK2, and CDK9 or resistance to apoptosis, e.g. HIPK3, MAPK8IP2, and CANX, by CXCL12 might functionally promote cellular proliferation. Similarly, the observed transcriptional down-regulation of genes encoding proteins involved in cell-cell adhesion, including CDH1, CTNNB1, CPSF1, EXOSC6, ITGB4, LOXL2, and SORBS3, or of genes involved in cytoskeleton organization, including MAPRE3, DOCK9, ARPC4, and MARCKS, could facilitate cellular motility, a trait associated with tumor progression and metastasis. Conversely, several genes that encode proteins that are overexpressed in many tumor types, some of which are functionally involved in cellular proliferation and tumor metastasis, including EGFR, CD44, ANKRD12, JMJD1C, and STRAP, were up-regulated consequent to CXCL12 stimulation. Moreover, two of these genes, CD44 and EGFR, are known to be transcriptionally induced by EGR1, which is itself encoded by a gene transcriptionally up-regulated by CXCL12. Thus, CXCL12 stimulates a complex transcriptional response, which includes the common regulation of a set of genes encoding proteins involved in cellular proliferation.

The studies reported here were initiated to further understand how observed changes in stromal/epithelial paracrine interactions consequent to aging are permissive for cellular proliferation in the human prostate and may promote the development of benign prostatic enlargement and benign prostatic hyperplasia. Previous studies have shown that benign prostatic enlargement comprises a gradual increase in prostatic volume that occurs over decades of life. Benign prostatic enlargement is characterized by low level, but cumulative, cellular proliferation that increases post-pubertal prostatic volume by ~0.8–1.6%, equivalent to only 0.2–0.4 ml, per year (36, 17). Our previous studies, as well as those shown here, demonstrate that CXCL12 secreted at sub-nanomolar levels by aging prostate stromal fibroblasts stimulates a significant, low level proliferative response in prostate epithelial cells (6). Taken together, these findings suggest that the modest rate of cellular proliferation stimulated by CXCL12 in vitro essentially mimics the gradual rate of cellular proliferation characteristic of prostatic enlargement in vivo.

In summary, these studies show that, in addition to the activation of signaling pathways that trigger phenotypic responses typically associated with malignant transformation, e.g. cellular proliferation and motility/invasion, CXCL12 initiates a robust and complex transcriptional response in prostate epithelial cells. The potential net result of this transcriptional response is the promotion of these same phenotypic responses, including cellular proliferation and progression through the cell cycle, tumor metastasis, and cellular motility; impaired cell-cell adhesion, and resistance to apoptosis. Importantly, these effects are stimulated at low, sub-nanomolar levels of CXCL12 similar to those secreted by aging prostate stromal fibroblasts. Together, these results suggest that CXCL12 may be an important paracrine factor that plays a central role in the promotion of proliferative disease in the aging prostate. Future studies should elucidate how the proteins encoded by genes that are transcriptionally activated or repressed consequent to CXCL12-mediated activities contribute to the development of such disease.


   FOOTNOTES
 
* This work was supported by NIDDK/National Institutes of Health Award 1 P50 DK065313 from the George M. O'Brien Center for Urologic Research at the University of Michigan (to J. A. M.), UMCCC Support Grant 5 P30 CA46592, and funds awarded by Domino's Pizza, L.L.C. The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact. Back

1 To whom correspondence should be addressed: Dept. of Urology, The University of Michigan, 6217 Cancer Center and Geriatrics Center, 1500 East Medical Center Dr., Ann Arbor, MI 48109-0944. Tel.: 734-647-8121; Fax: 734-647-9271; E-mail: jcoska{at}umich.edu.

2 The abbreviations used are: ERK, extracellular signal-regulated kinase; EGF, epidermal growth factor; MEK1, MAPK/ERK kinase; MAPK, mitogen-activated protein kinase; EGR1, early growth response 1. Back



   REFERENCES
TOP
 ABSTRACT
 INTRODUCTION
 EXPERIMENTAL PROCEDURES
 RESULTS
 DISCUSSION
 REFERENCES
 

  1. Allinen, M., Beroukhim, R., Cai, L., Brennan, C., Jaana Lahti-Domenici, J., Huang, H., Porter, D., Hu, M., Chin, L., Richardson, A., Schnitt, S., Sellers, W. R., and Polyak, K. (2004) Cancer Cell 6, 17–32[CrossRef][Medline] [Order article via Infotrieve]
  2. Cunha, G. R., Hayward, S. W., Dahiya, R., and Foster, B. A. (1996) Acta Anat. 155, 63–72[Medline] [Order article via Infotrieve]
  3. Hayward, S. W., Haughney, P. C., Rosen, M. A., Greulich, K. M., Weier, H. U., Dahiya, R., and Cunha, G. R. (1998) Differentiation 63, 131–140[CrossRef][Medline] [Order article via Infotrieve]
  4. Olumi, A. F., Grossfeld, G. D., Hayward, S. W., Carroll, P. R., Tlsty, T. D., and Cunha, G. R. (1996) Cancer Res. 59, 5002–5011
  5. Olumi, A. F., Dazin, P., and Tlsty, T. D. (1998) Cancer Res. 58, 4525–4530[Abstract/Free Full Text]
  6. Begley, L., Monteleon, C., Shah, R. B., Macdonald, J. W., and Macoska, J. A. (2005) Aging Cell 4, 291–298[CrossRef][Medline] [Order article via Infotrieve]
  7. Koch, A. E. (2005) Arthritis Rheum. 52, 710–721[CrossRef][Medline] [Order article via Infotrieve]
  8. Cabioglu, N., Summy, J., Miller, C., Parikh, N. U., Sahin, A. A., Tuzlali, S., Pumiglia, K., Gallick, G. E., and Price, J. E. (2005) Cancer Res. 65, 6493–6497[Abstract/Free Full Text]
  9. Chen, Y., Stamatoyannopoulos, G., and Song, C. Z. (2003) Cancer Res. 63, 4801–4804[Abstract/Free Full Text]
  10. Fernandis, A. Z., Prasad, A., Band, H., Klosel, R., and Ganju, R. K. (2004) Oncogene 23, 157–167[CrossRef][Medline] [Order article via Infotrieve]
  11. Lapteva, N., Yang, A. G., Sanders, D. E., Strube, R. W., and Chen, S. Y. (2005) Cancer Gene Ther. 12, 84–89[CrossRef][Medline] [Order article via Infotrieve]
  12. Mochizuki, H., Matsubara, A., Teishima, J., Mutaguchi, K., Yasumoto, H., Dahiya, R., Usui, T., and Kamiya, K. (2004) Biochem. Biophys. Res. Commun. 320, 656–663[CrossRef][Medline] [Order article via Infotrieve]
  13. Porcile, C., Bajetto, A., Barbieri, F., Barbero, S., Bonavia, R., Biglieri, M., Pirani, P., Florio, T., and Schettini, G. (2005) Exp. Cell Res. 308, 241–253[CrossRef][Medline] [Order article via Infotrieve]
  14. Signoret, N., Oldridge, J., Pelchen-Matthews, A., Klasse, P. J., Tran, T., Brass, L. F., Rosenkilde, M. M., Schwartz, T. W., Holmes, W., Dallas, W., Luther, M. A., Wells, T. N., Hoxie, J. A., and Marsh, M. (1997) J. Cell Biol. 139, 651–664[Abstract/Free Full Text]
  15. Spano, J. P., Andre, F., Morat, L., Sabatier, L., Besse, B., Combadiere, C., Deterre, P., Martin, A., Azorin, J., Valeyre, D., Khayat, D., Le Chevalier, T., and Soria, J. C. (2004) Ann. Oncol. 15, 613–617[Abstract/Free Full Text]
  16. Taichman, R. S., Cooper, C., Keller, E. T., Pienta, K. J., Taichman, N. S., and McCauley, L. K. (2002) Cancer Res. 62, 1832–1837[Abstract/Free Full Text]
  17. Jakobsen, H., Torp-Pedersen, S., and Juul, N. (1988) Scand. J. Urol Nephrol. Suppl. 107, 26–31
  18. Muller, A., Homey, B., Soto, H., Ge, N., Catron, D., Buchanan, M. E., McClanahan, T., Murphy, E., Yuan, W., Wagner, S. N., Barrera, J. L., Mohar, A., Verastegui, E., and Zlotnik, A. (2001) Nature 410, 50–56[CrossRef][Medline] [Order article via Infotrieve]
  19. Wang, J., Sun, Y., Song, W., Norb, J. E., Wang, C. Y., and Taichman, R. S. (2005) Cell. Signalling 17, 1578–1592[CrossRef][Medline] [Order article via Infotrieve]
  20. Macoska, J. A., Paris, P., Collins, C., Andaya, A., Beheshti, B., Chaib, H., Kant, R., Begley, L., MacDonald, J. W., and Squire, J. A. (2004) Cytogenetics 154, 36–43
  21. Begley, L., Keeney, D., Beheshti, B., Squire, J. A., Kant, R., Chaib, H., Macdonald, J. W., Rhim, J., and Macoska, J. A. (2006) Genes Chromosomes Cancer 45, 136–146[CrossRef][Medline] [Order article via Infotrieve]
  22. Horoszewicz, J. S., Leong, S. S., Kawinski, E., Karr, J. P., Rosenthal, H., Chu, T. M., Mirand, E. A., and Murphy, G. P. (1983) Cancer Res. 43, 1809–1818[Abstract/Free Full Text]
  23. Chaib, H., Rubin, M. A., Mucci, N. R., Li, L., Taylor, J. M. G., Day, M., Rhim, J. S., and Macoska, J. A. (2001) Cancer Res. 61, 2390–2394[Abstract/Free Full Text]
  24. Ao, M., Franco, O. E., Park, D., Raman, D., Williams, K., and Hayward, S. W. (2007) Cancer Res. 67, 4244–4253[Abstract/Free Full Text]
  25. Burns, J. M., Summers, B. C., Wang, Y., Melikian, A., Berahovich, R., Miao, Z., Penfold, M. E., Sunshine, M. J., Littman, D. R., Kuo, C. J., Wei, K., McMaster, B. E., Wright, K., Howard, M. C., and Schall, T. J. (2006) J. Exp. Med. 203, 2201–2213[Abstract/Free Full Text]
  26. Kukreja, P., Abdel-Mageed, A. B., Mondal, D., Liu, K., and Agrawal, K. C. (2005) Cancer Res. 65, 9891–9898[Abstract/Free Full Text]
  27. Chung, K. C., Gomes, I., Wang, D., Lau, L. F., and Rosner, M. R. (1998) Mol. Cell Biol. 18, 2272–2281[Abstract/Free Full Text]
  28. Mohney, R. P., Das, M., Bivona, T. G., Hanes, R., Adams, A. G., Philips, M. R., and O'Bryan, J. P. (2003) J. Biol. Chem. 278, 47038–47045[Abstract/Free Full Text]
  29. Adamson, E. D., and Mercola, D. (2002) Tumour Biol. 23, 93–102[CrossRef][Medline] [Order article via Infotrieve]
  30. Hoffmann, R., and Valencia, A. (2004) Nat. Genet. 36, 664[CrossRef][Medline] [Order article via Infotrieve]
  31. Burger, J. A., and Kipps, T. J. (2006) Blood 107, 1761–1767[Abstract/Free Full Text]
  32. Orimo, A., Gupta, P. B., Sgroi, D. C., Arenzana-Seisdedos, F., Delaunay, T., Naeem, R., Carey, V. J., Richardson, A. L., and Weinberg, R. A. (2005) Cell 121, 335–348[CrossRef][Medline] [Order article via Infotrieve]
  33. Torii, S., Yamamoto, T., Tsuchiya, Y., and Nishida, E. (2006) Cancer Sci. 97, 697–702[CrossRef][Medline] [Order article via Infotrieve]
  34. Buchwalter, G., Gross, C., and Wasylyk, B. (2004) Gene (Amst.) 324, 1–14[CrossRef][Medline] [Order article via Infotrieve]
  35. Sun, Q., Chen, G., Streb, J. W., Long, X., Yang, Y., Stoeckert, C. J., and Miano, J. M. (2006) Genome Res. 16, 197–207[Abstract/Free Full Text]
  36. Jacobsen, S. J., Girman, C. J., and Lieber, M. M. (2001) Urology 58, 5–16; discussion 16[Medline] [Order article via Infotrieve]

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