Macrophages may promote cancer growth via a GM-CSF/HB-EGF paracrine loop that is enhanced by CXCL12
- Antonella Rigo†1,
- Michele Gottardi†1,
- Alberto Zamò2,
- Pierluigi Mauri3,
- Massimiliano Bonifacio1,
- Mauro Krampera1,
- Ernesto Damiani4,
- Giovanni Pizzolo1 and
- Fabrizio Vinante1Email author
© Rigo et al; licensee BioMed Central Ltd. 2010
Received: 19 April 2010
Accepted: 14 October 2010
Published: 14 October 2010
Increased numbers of tumour-associated macrophages correlate with shortened survival in some cancers. The molecular bases of this correlation are not thoroughly understood. Events triggered by CXCL12 may play a part, as CXCL12 drives the migration of both CXCR4-positive cancer cells and macrophages and may promote a molecular crosstalk between them.
Samples of HER1-positive colon cancer metastases in liver, a tissue with high expression of CXCL12, were analysed by immunohistochemistry. In all of the patient biopsies, CD68-positive tumour-associated macrophages presented a mixed CXCL10 (M1)/CD163 (M2) pattern, expressed CXCR4, GM-CSF and HB-EGF, and some stained positive for CXCL12. Cancer cells stained positive for CXCR4, CXCL12, HER1, HER4 and GM-CSF. Regulatory interactions among these proteins were validated via experiments in vitro involving crosstalk between human mononuclear phagocytes and the cell lines DLD-1 (human colon adenocarcinoma) and HeLa (human cervical carcinoma), which express the above-mentioned ligand/receptor repertoire. CXCL12 induced mononuclear phagocytes to release HB-EGF, which activated HER1 and triggered anti-apoptotic and proliferative signals in cancer cells. The cancer cells then proliferated and released GM-CSF, which in turn activated mononuclear phagocytes and induced them to release more HB-EGF. Blockade of GM-CSF with neutralising antibodies or siRNA suppressed this loop.
CXCL12-driven stimulation of cancer cells and macrophages may elicit and reinforce a GM-CSF/HB-EGF paracrine loop, whereby macrophages contribute to cancer survival and expansion. The involvement of mixed M1/M2 GM-CSF-stimulated macrophages in a tumour-promoting loop may challenge the paradigm of tumour-favouring macrophages as polarized M2 mononuclear phagocytes.
Over the last few years, a great deal of attention has been paid to the clinical significance of macrophages that infiltrate cancer. A number of studies provide evidence that tumour-associated macrophages are a negative prognostic factor of survival [1, 2]. A recent gene-profiling study demonstrates that the overexpression of a macrophage signature and an increased number of tumour-infiltrating macrophages in diagnostic lymph-nodes are associated with poor outcome in classic Hodgkin's lymphoma patients . Other studies underline pathways leading to M2 macrophage responses that foster tumour growth [4–7]. In the end, all these studies deal with the crosstalk between tumour cells and macrophages. For instance, a regulatory loop between breast cancer cells and macrophages has been described , and the cellular expression of matrix metallopeptidase 11 seems to be relevant to disease outcome at least in classic Hodgkin's lymphoma . However, the grounds on which the above-mentioned prognostic significance rests are not so thoroughly appreciated, especially in terms of cell-to-cell molecular mechanisms.
Within the tangle of relations between macrophages and cancer cells, we tried to tease out the role that CXCL12 plays in both cancer cells and macrophages at the boundaries between cancer and inflammation. A tissue with high expression of CXCL12 (for example, liver or bone marrow) may represent a site that preferentially attracts both macrophages  and cancer cells [10, 11], which co-migrate depending on their expression of the CXCL12 receptors CXCR4 and/or CXCR7 . Ligand binding to these receptors, which are heterotrimeric guanine nucleotide-binding protein-coupled receptors (GPCR), activates matrix metallopeptidases that cleave EGF-family ligands, such as EGF or HB-EGF, from the cell membrane , leading to trans activation of HER1 on neighbouring cells . This transactivation mechanism is a general function of GPCR signalling . HER1 expressed by epithelial cancers plays a pivotal role by transducing signals that favour tumour progression [16, 17]. The macrophage-regulator GM-CSF, which is produced by some types of cancer cells [18, 19], specifically induces HB-EGF in macrophages and neutrophils .
Because mononuclear phagocytes express both CXCL12 GPCRs and HB-EGF, we argued that the recruitment of mononuclear phagocytes to a site of metastasis such as liver through CXCL12 should induce a release of HB-EGF, which is expected to activate HER1 and favour tumour progression. We found that tumour-associated macrophages and metastatic HER1-positive colon cancer in liver biopsies expressed a ligand/receptor repertoire that was consistent with our hypothesis and that in vitro CXCL12 could trigger a GM-CSF/HB-EGF paracrine loop whereby mononuclear phagocytes support cancer survival.
The blood and histological samples used in our study were in compliance with Institutional Review Board regulations.
Cells and reagents
Highly purified human mononuclear phagocytes and neutrophils were isolated from the buffy coats  of blood samples from healthy volunteers. HeLa (human cervical carcinoma), DLD-1 (human colon adenocarcinoma) and Balb/c 3T3 (Swiss mouse embryo) cell lines (purchased from ATCC, Manassas, VA) and HUVEC (human umbilical vein endothelial cells, purchased from Cambrex, Walkersville, VA) were also used. Non-adherent and adherent cells were grown in RPMI-1640 medium and DMEM or TC199 + 10% FCS (complete medium; Invitrogen, Carlsbad, CA), respectively. Cells were treated with 200 ng/mL CXCL12 (Peprotech, London, UK) or 25 ng/mL GM-CSF (Genetics Institute, Boston, MA) or 25 ng/mL HB-EGF or 100 μg/mL anti-HB-EGF or 100 μg/mL anti-GM-CSF neutralising monoclonal antibody (mAb) (R&D Systems, Minneapolis, MN) or isotypic control immunoglobulins. After growing in cultures for the appropriate times in different conditions, the cells were either lysed for total RNA extraction or used for functional assays. In some experiments, the conditioned medium was replaced with fresh medium after 24 hours of stimulation and the cells were then maintained in culture for up to 48 hours. Cell-free supernatants (SN) were stored at -80°C.
Immunochemistry on tissues and cells
Histological samples were obtained by hepatic lobectomy to excise metastatic nodules derived from colon cancer. After surgical excision, samples were put in buffered formalin, treated in an automated processor and embedded in paraffin. Four micrometre-thick slices were cut from paraffin blocks onto adhesive-coated slides. Cytological samples were obtained by allowing cells to grow on the slides. Antibodies (Ab) used included the following: CD163 (clone 10D6, 1/200; Novocastra, Newcastle-upon-Tyne, UK), CXCL10 and CXCR4 (both rabbit polyclonal, 1/500 and 1/100, respectively; Abcam, Cambridge, UK), CXCL12 (clone 7918, 1/100), GM-CSF (clone 3209, 1/100), HER1 (1/100), HER4 (1/100), and HB-EGF (clone 125923, 1/200) (all purchased from R&D Systems). Antigen retrieval was performed for all antibodies in a hot bath for 30 minutes at pH 6 (except for GM-CSF retrieval, which was performed at pH 8). For GM-CSF and HB-EGF no H2O2 blocking was performed. As controls, sequential sections or cytological slides were incubated with the Ab diluent and indifferent isotypic Ab. All procedures were performed on an automated stainer (Bond, Vision Biosystems, Melbourne, AU) using a polymer detection system (NovoLink, Novocastra).
Following stimulation for 20 minutes or 24 hours with CXCL12, 1 × 106 cells were incubated with a goat anti-human HB-EGF IgG polyclonal Ab (Oncogene, San Diego, CA) or an IgG control Ab. After washing, 5 μL of phycoerythrin-conjugated swine anti-goat IgG (Caltag Laboratories, Burlingame, CA) was added. The cells were then analysed on a FACSCalibur (Becton-Dickinson, Mountain View, CA) using the FlowJo 8.8.2 program (Tree Star, Ashland, OR).
HER1 transactivation assay
Cellular release of HB-EGF was evaluated by measuring its effect on HER1 phosphorylation at tyrosine 1068 (Y1068) using HeLa and DLD-1 as target cells. Approximately 3 × 106 effector cells (mononuclear phagocytes and neutrophils) were seeded in the upper chamber of a 0.4 μm transwell co-culture system (Costar, Cambridge, MA) and were stimulated with CXCL12 for 20 minutes. In a separate experiment, 3 × 106 mononuclear phagocytes and neutrophils were cultured in the presence or absence of CXCL12 for 24 hours and their conditioned medium was added to the target cells for 20 minutes. HeLa cells were also stimulated for 20 minutes with recombinant human HB-EGF. Subconfluent HeLa cells that had been starved for 24 hours were incubated in the presence or absence of the anti-HB-EGF neutralising Ab (R&D Systems). Target cells were harvested for protein extraction.
Cell pellets were lysed for 30 minutes in 1 mL ice-cold cell extraction buffer (Biosource, Camarillo, CA), which was supplemented with a protease inhibitor cocktail (Sigma, St. Louis, MO) and 1 mM PMSF (Sigma). After centrifugation at 13,000 rpm for 10 minutes at 4°C, aliquots of the SN were stored at -80°C.
Approximately 1 × 107 HeLa cells, which were either untreated or treated with HB-EGF for 20 minutes, were harvested for HER1 immunoprecipitation, reduction, alkylation and tryptic digestion. Ten microliters of the peptide mixture was analysed by means of an LCMS/MS system . The data handling for the identification of phosphorylated residues was performed according to Guo et al. . HB-EGF-induced HER1 phosphorylation was evaluated at Y992, Y1045, Y1068, Y1086, S1142, Y1148, Y1173, and expressed as phosphorylation ratio (phosphorylation after stimulus/basal phosphorylation).
1. HER1 pY1068 and ERK1/2 pTpY185/187. Total HER1 versus HER1 pY1068 and total ERK1/2 versus ERK1/2 pTpY-185/187 were measured in cell protein extracts using a commercially available ELISA (Biosource). The results were calculated as the ratio of phosphorylated molecules to total molecules and expressed as the percentage of phosphorylation. 2. HB-EGF and GM-CSF. The cell-free culture SN was assayed for soluble HB-EGF protein using a specific ELISA developed in our laboratory  and for GM-CSF using a commercial ELISA (R&D Systems). Only SN previously purified from HB-EGF or GM-CSF by specific crosslinking (Invitrogen) were subsequently used as agonistic SN to induce HB-EGF or GM-CSF, respectively, in cell stimulation experiments followed by ELISA tests. 3. Apoptosis. 72-hour internucleosomal DNA fragmentation as an index of apoptosis was evaluated using a cell death detection ELISA (Roche Diagnostics, Mannheim, DE) and expressed as the mean ± SD of triplicate determinations of the enrichment factor (absorbance of unstimulated cells/absorbance of stimulated cells).
Total RNA was extracted from the indicated cells. Northern blot analysis (with 10 μg RNA/lane) was performed as described . Filters were hybridised with 32P-labelled cDNA probes complementary to the HB-EGF RNA sequence, which were generated in our laboratory or with a 32P-labelled plasmid containing a cDNA probe that detected the β-actin RNA sequence.
Total cellular RNA was purified by the QIAamp RNA Blood mini kit (Qiagen, Hilden, DE) + DNase digestion (Qiagen). Templates were generated from 2 μg of RNA with the Superscript III First-Strand Synthesis System kit (Invitrogen). cDNA for GM-CSF was amplified using the following primers (Invitrogen): 5'-CTCAGAAATGTTTGACCTCCAG-3' (sense) and 5'-TGACAAGCAGAAAGTCCTTCAG-3' (antisense) for a 221 bp amplicon. The GAPDH internal control primers (SuperArray Bioscience, Frederick, MD) were used to co-amplify a specific fragment that was 436 bp long. After 30 cycles at 95°C for 15", 55°C for 30" and 72°C for 30" in a Veriti thermal cycler (Applied Biosystems, Foster City, CA) using the AmpliTaq Gold PCR master mix (Applied Biosystems), the reactions were analysed by agarose gel electrophoresis and recorded using a VersaDoc imaging system (Bio-Rad, Hercules, CA).
Cell proliferation and apoptosis
Hela, DLD-1, HUVEC and Balb/c 3T3 cells were seeded in 96-well plates in complete medium and allowed to adhere for 24 hours. They were then incubated in the absence or presence of the anti-HB-EGF neutralizing Ab (R&D Systems) and were stimulated with 25 ng/mL HB-EGF. In selected experiments, HeLa and DLD-1 were deprived of serum and cultured in the absence or presence of HB-EGF. Cell proliferation was measured by MTT incorporation  at 24, 48 and 72 hours and expressed as the proliferation index. Apoptosis was measurerd as the internucleosomal DNA fragmentation enrichment factor at 72 hours (see ELISA).
To silence the expression of GM-CSF, HeLa and DLD-1 cells were seeded on glass slides (105 cells/mL), stimulated with 200 ng/mL CXCL12 and/or 25 ng/mL HB-EGF or SN from GM-CSF-stimulated mononuclear phagocytes and transfected 48 hours using HiPerFect Transfection Reagent and siRNA (2 nM and 5 nM respectively, GM-CSF siRNA no. SI03037272 and AllStars negative control siRNA - Alexa Fluor 488; Qiagen). Transfection efficiency (> 95%) was determined by flow cytometry on trypsinized cells. Effective silencing of GM-CSF was determined by testing the induction and release of 1. GM-CSF in cancer cells (using immunohistochemistry and ELISA, after a 24-hour stimulation with HB-EGF or mononuclear phagocytes conditioned medium) and 2. HB-EGF in mononuclear phagocytes (using flow cytometry and ELISA, after a 24-hour stimulation with silenced cancer cell SN).
Student's t-test, Mann-Whitney U test and Kruskall-Wallis ANOVA by ranks were used. Differences were considered significant for p values < 0.05.
Macrophages infiltrate colon cancer metastases in liver
CXCL12 induces HB-EGF synthesis and release in mononuclear phagocytes
HB-EGF-dependent HER1 phosphorylation
CXCL12-driven release of HB-EGF from mononuclear phagocytes transactivates HER1 and supports proliferative, anti-apoptotic and angiogenic effects in bystander cells
CXCL12 and HB-EGF induce cancer cells to synthetise and release GM-CSF
Paracrine loop activated by CXCL12
As described above, CXCL12 was shown to prompt mononuclear phagocytes and cancer cells to release HB-EGF and GM-CSF, respectively. On the other hand, we have previous evidence showing that GM-CSF is a strong inducer of HB-EGF expression in mononuclear phagocytes [19, 20]. If HB-EGF released by mononuclear phagocytes can trigger the production of GM-CSF in cancer cells, a possible GM-CSF/HB-EGF paracrine loop may exist that is initially activated by CXCL12. Thus, we tested (i) HeLa and DLD-1 cancer cells for the production of GM-CSF upon HB-EGF stimulation and (ii) mononuclear phagocytes for the production of HB-EGF upon GM-CSF stimulation. This choice was based on the known differential receptor expression in mononuclear phagocytes, as opposed to cancer cells, which are usually negative for the GM-CSF receptor. Figure 7 depicts the experiments suggesting that a paracrine loop exists between Mø and HeLa or DLD-1 cancer cells. When these cancer cells were stimulated with 200 ng/mL CXCL12 and/or 25 ng/mL HB-EGF, they produced and released GM-CSF (Figures 7A, B; 8A). When mononuclear phagocytes were stimulated with CXCL12 and/or 25 ng/mL GM-CSF, they produced and released HB-EGF (Figures 2; 7B, C, D; 8B). HB-EGF mRNA transcripts and membrane protein levels were increased after 2 hours (Figures 2B; 7B) and after 24 hours of stimulation (Figures 2A, C; 7C, D; 8B). These results were reproduced by the addition of conditioned medium from mononuclear phagocytes to cancer cells and vice versa (Figures 7A, C; 8). Inhibitory anti-HB-EGF and anti-GM-CSF Abs significantly reduced the production of GM-CSF by cancer cells (Figure 8A) and HB-EGF by mononuclear phagocytes (Figure 8B), respectively. Thus, a paracrine loop may exist between mononuclear phagocytes and HeLa or DLD-1 cancer cells, as exemplified in Figure 7E. CXCL12 seems to act as an additive or synergistic agent in this positive feedback loop. The expression of these molecules as found in patient biopsy samples (Figure 1) is in line with and corroborates our findings in vitro.
Blockade of GM-CSF in cancer cells
The current study defines a novel mechanism whereby CXCL12 redirects macrophages to promote a microenvironment that is suitable for cancer survival via a GM-CSF/HB-EGF paracrine loop. To our knowledge, there are no other studies showing that human mononuclear phagocytes release and up-regulate HB-EGF, while cancer cells release and upregulate GM-CSF, when stimulated with CXCL12.
By evaluating histological samples from human colon cancer metastases in the liver, we observed that numerous HB-EGF/CXCR4-positive macrophages, which expressed both the M1 CXCL10 and the M2 CD163 markers, indicating a mixed M1/M2 microenvironment, infiltrated metastatic cancer cells. These in turn were positive for CXCR4, CXCL12, GM-CSF and HER1 (Figure 1). We then validated the mutual interactions associated with this repertoire of molecules in standard and transwell experiments performed on human mononuclear phagocytes and HeLa and DLD-1 cancer cell lines, expressing the same molecules in the same cellular distribution as macrophages and cancer in biopsy samples.
CXCL12 and GM-CSF induced mononuclear phagocytes to synthetise and release HB-EGF. Northern blotting of RNA from kinetic experiments revealed that maximal expression of HB-EGF mRNA occurred between 2 and 24 hours after CXCL12- or GM-CSF-dependent induction, leading to an increase in membrane HB-EGF molecule density (Figures 2; 7B, C). In transwell experiments, CXCL12-stimulated mononuclear phagocytes released HB-EGF that caused the phosphorylation of HER1 in HeLa and DLD-1 target cells (Figure 4B). Cell-free supernatants from CXCL12-treated mononuclear phagocytes induced HER1 phosphorylation followed by cellular proliferation in either HeLa or DLD-1 cells, an effect that was inhibited by anti-HB-EGF neutralising Abs (Figure 5).
Stimulation with CXCL12, HB-EGF or both induced GM-CSF transcripts in HeLa and DLD-1 cells. At 24 hours, immunocytochemistry revealed clear-cut staining for GM-CSF in both cell lines (Figure 7A). Their conditioned medium contained GM-CSF that induced Mø to produce HB-EGF (Figures 7C; 8B). Conversely, mononuclear phagocytes conditioned medium contained HB-EGF that induced cancer cells to produce GM-CSF (Figures 7A; 8A). These effects were largely counteracted by the addition of specific neutralising Abs (Figure 8) or by GM-CSF silencing (Figure 9). In conclusion, CXCL12 induced HB-EGF in mononuclear phagocytes and GM-CSF in HeLa and DLD-1 cancer cells, activating or enhancing a GM-CSF/HB-EGF paracrine loop.
Thus, we have evidence for a specific pathway of activation in mononuclear phagocytes (CXCL12-stimulated Mø release of HB-EGF) that may match the specific biological properties of some cancers (HeLa, DLD-1 and metastatic colon cancer). We have also documented a specific pathway of activation in cancer cells (CXCL12/HB-EGF-stimulated cancer cell release of GM-CSF) that may match the specific biological properties of mononuclear phagocytes. This interplay between mononuclear phagocytes and cancer cells may lead to an inflammatory environment that favours rather than inhibits tumour growth. Furthermore, both macrophages and cancer cells were activated upon CXCL12 stimulation in liver biopsies (Figure 1), though we could not conclusively establish whether cancer cells produced their own CXCL12 or merely internalized CXCL12, produced by stromal cells. Other studies have demonstrated that CXCL12 transactivates HER2 in breast cancer cells , enhancing the expression of CXCR4 and favouring metastases . In our work, CXCL12 has been shown to transactivate HER1 and induce GM-CSF. The latter is a specific inducer of HB-EGF, which in turn binds to HER1. HB-EGF acts as a chemotactic, pro-growth and anti-apoptotic factor in cancer cells, and plays a role as angiogenic factor by inducing endothelial cells and fibroblasts to proliferate (Figure 6). It also promotes angiogenesis by induction of VEGF . In general, HB-EGF is a powerful inducer of fibroblast activities [17, 19, 20] that are involved in orchestrating inflammation and promoting tumour growth, angiogenesis and recruitment of macrophages and cancer cells .
Therefore, the CXCL12 receptors, CXCR4 and CXCR7, should be thought of as a node that connects multiple loops [26–30], including the highly important EGF/HER loops , linking cancer (oncogenes) and inflammation . Based on our previous demonstration of the role of HER1 in the regulation of mesenchymal stem cell proliferation and differentiation , as well as on some general models [5, 31, 32], we speculate that the crosstalk between CXCL12/CXCR4 and HB-EGF/HERs may contribute to the balance between the HER1-dependent cellular responses of differentiation and self-renewal [31–34].
This study provides evidence that CXCL12 partecipates in the selective production of cytokines, leading to a GM-CSF/HB-EGF paracrine loop that may favour neoplastic growth. CXCL12 has chemotactic activity towards cancer and immune cells; in both cell types, it induces cytokines that retain pro-tumour activity and modulate the stromal component [7, 16], contributing to a tumour-permissive microenvironment. Therefore, CXCL12 signalling may provide a unifying basis for better understanding the complex relationships between cancer and inflammatory cells in terms of receptor crosstalk. For instance, the involvement of mixed M1/M2, GM-CSF-stimulated macrophages in a tumour-promoting loop challenges the view of tumour-permissive macrophages as polarized M2 mononuclear phagocytes and hints at contexts in which pro-inflammatory microenvironments may allow effective tumour-promoting activities through mediators such as GM-CSF and HB-EGF. These mediators, indeed, seem to play a role that favours both cancer and a shift towards a M1-polarized microenvironment. Eventually, such an understanding could contribute to the development of tools to interfere with recognised pathogenic signals .
This work was supported by grants from AIRC, Milan (Italy); from the Venetian Institute of Oncology (IOV), Padua (Italy); and from the Berlucchi Foundation, Brescia (Italy).
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