Platelet-derived growth factor alpha and beta receptors have overlapping functional activities towards fibroblasts
© Donovan et al.; licensee BioMed Central Ltd. 2013
Received: 9 January 2013
Accepted: 5 April 2013
Published: 10 May 2013
Platelet-derived growth factor (PDGF) signalling is essential for many key cellular processes in mesenchymal cells. As there is redundancy in signalling between the five PDGF ligand isoforms and three PDGF receptor isoforms, and deletion of either of the receptors in vivo produces an embryonic lethal phenotype, it is not know which ligand and receptor combinations mediate specific cellular functions. Fibroblasts are key mediators in wound healing and tissues repair. Recent clinical trials using broad spectrum tyrosine kinase inhibitors in fibrotic diseases have highlighted the need to further examine the specific cellular roles each of the tyrosine kinases plays in fibrotic processes. In this study, we used PDGFR-specific neutralising antibodies to dissect out receptor-specific signalling events in fibroblasts in vitro, to further understand key cellular processes involved in wound healing and tissue repair.
Neutralising antibodies against PDGFRs were shown to block signalling through PDGFRα and PDGFRβ receptors, reduce human PDGF-AA and PDGF-BB-induced collagen gel remodelling in dermal fibroblasts, and reduce migration stimulated by all PDGF ligands in human dermal and lung fibroblasts.
PDGFRα and PDGFRβ neutralising antibodies can be a useful tool in studying PDGFR isoform-specific cellular events.
While PDGF ligands have considerable overlap in their cellular signalling, individual ligands have also been found to control, or are dominant in, specific cellular events. PDGF-AA is a potent mitogen for cardiac fibroblasts and has been shown to be critical in lung alveolar myofibroblast development and alveogenesis[13, 14]. PDGF-BB is required in the ontogeny of kidney mesangial cells and has been shown to be essential for development of the vasculature and vascular integrity. PDGF-CC has been implicated in all phases of wound healing while blockade of PDGF-CC signalling inhibits pathological angiogenesis by acting on multiple cellular and molecular targets. PDGF-DD is thought to stimulate angiogenesis and deposition of ECM and to be involved in hepatic and renal fibrosis. It is also thought to be involved in VSMC phenotypic modulation and is upregulated in endothelial cells exposed to atherosclerosis-prone flow patterns.
In vitro, PDGFR isoforms have been shown to be potent activators of fibroblast proliferation, migration and survival. Although stimulation of PDGFRα and PDGFRβ evokes similar signal transduction cascades, in vitro studies suggest distinct requirements for specific pathways to initiate particular receptor-mediated functions. For example, while activation of both receptors evoke mitogenic signals, stimulation of PDGFRα inhibits chemotaxis of fibroblasts and smooth muscle cells; in contrast, PDGFRβ activation potently stimulates fibroblast chemotaxis[9, 19].
Recent studies have attempted to dissect PDGFR-specific events using genetically defined mouse embryonic fibroblasts (MEFS) expressing PDGFRα, PDGFRβ, both or neither. These cells were generated by transducing PDGFRβ−/− cells with retroviral expression vectors for PDGFRα, PDGFRβ or both. Microarray gene expression array analysis provided some interesting insights. No genes were differentially expressed in the double null cells, suggesting minimal receptor-independent signalling. Whilst there is considerable overlap between PDGFRα and PDGFRβ signalling, this study identified transcripts that were differentially expressed between the cell lines. Thirty-three gene sets (functional groups of genes) were activated by PDGFRα only and 15 genes sets by PDGFRβ only. Interestingly, 25 genes sets were specifically activated by the heterodimeric receptors, for example, PDGFRα/β-activated components of the NFkB and interleukin (IL)-6 pathways, PDGFRα-activated C21-steroid hormone biosynthesis, and PDGFRβ activated the angiogenesis and epidermal growth factor receptor (EGFR) signalling pathways. The PDGFRα null cell line but not the PDGFRβ null or wild type (WT) showed differential expression of guanosine diphosphate (GDP) signalling genes. Conversely, the differentially expressed gene sets particular to the PDGFRβ null and WT cell lines characterise ketosteroid metabolism. Whilst these types of studies provide a reasonable genetic characterisation, they supply very little functional information, especially given that MEFs do not necessarily reflect the behaviour of adult fibroblasts.
Inhibition of both PDGFRs by broad-spectrum tyrosine kinase inhibitors such as Gleevec (which also inhibits c-Abl, c-kit and VEGFR) is used in the treatment of gastrointestinal stromal tumours and chronic mylogenous leukaemia[21–23]. They have been shown to reduce proliferation of normal mesangial cells via reduction in STAT3 phosphorylation and of fibroblasts via reduction in PDGFRβ phosphorylation. Gleevec treatment has also been shown to reduce the synthesis of ECM proteins in a model of dermal fibrosis. These data suggest that PDGFR is regarded as a key molecular target in the development of anti-fibrotic therapies.
Taken together, these in vitro studies implicate PDGFR signalling in fibroblast function during tissue repair and scarring, however, questions still remain regarding the underlying mechanism(s) and specificity of PDGF ligand-receptor function. In this report, we used PDGFR-specific neutralising antibodies to block signalling through either PDGFRα or PDGFRβ to dissect out receptor-specific signalling events in vitro. We also analyse the role of the receptors on fibroblast migration and collagen gel contraction.
Phosphorylation of PDGFR by PDGFAA, BB, CC and DD
Effect of blocking antibody on phosphorylation and signal transduction
Effects of PDGFR neutralising antibodies on collagen gel contraction
Effect of PDGFR neutralising antibodies on fibroblast migration
Fibroblasts play a critical role in wound healing and tissue repair. Signalling through the PDGF/PDGFR axis is a key feature of enhanced migration and ECM synthesis and are required for correct wound healing. However, dysregulated activity and function of PDGFs are also believed to be important determinants of human diseases including excessive dermal scarring, many forms of organ-based tissue fibrosis as well as vascular diseases such as atherosclerosis and pulmonary hypertension. It remains to be established whether a particular combination of PDGF/PDGFR is implicated in promoting certain disease pathologies.
The phosphorylation pattern of PDGFRα and PDGFRβ in response to PDGF-ligand stimulation observed in this study is similar to that previously reported[28–31]. Whilst it is firmly established that PDGF-AA is most specific for PDGFRα in vitro, reports vary as to whether phosphorylation of PDGFRs in response to PDGF-DD stimulation is PDGFRβ-specific or also stimulates PDGFRα[11, 32]. Our studies indicated that in primary human dermal fibroblasts PDGF-DD stimulates PDGFRα and PDGFRβ to a similar extent, consistent with the findings of LaRochelle et al.. However, a similar pattern of PDGFRα phosphorylation is not observed in lung fibroblasts. Phosphorylation of PDGFRα does not appear to have the same ligand specificity as dermal fibroblasts and was shown to be stimulated by all PDGF ligands. This tissue-specific difference in PDGFR stimulation is a previously unreported finding and a subject of further investigation.
As deletion of either PDGFR in vivo produces an embryonic lethal phenotype, it is difficult to assess the roles of the individual PDGF receptors[33–35]. Much of the previous in vivo work is therefore focused on the contribution of PDGFR in embryonic development. However, some conditional models also exist and work on these models is becoming increasingly prevalent.
Similarly, in vitro it has been difficult to dissect out receptor-specific signalling pathways as PDGFRs are reported to have redundancy and display compensatory effects. Previous work by Wu et al. used specific PDGFR knockout cell lines created by generating MEFS from double knockout mice, then transducing retroviral PDGFRα or PDGFRβ vectors into the cells to express one or other of the proteins. However, these analyses must be interpreted with caution as MEFS do not reflect adult fibroblast function and behaviour. Studies that examine the effect of specific point mutations of the PDGFRs in downstream signing pathways have been useful in dissecting receptor-specific cellular events[37–39]. However, they offer only limited insights in to the overall function of the receptor. Conversely, small-molecular inhibitors such as Gleevec are too broad in their range of target molecules to define PDGFR-specific cellular effects.
Ingram et al. have used PDGF-AA neutralising antibodies to great effect in the study of cytokine involvement in lung fibrosis. In this report we investigate the use of PDGFR-specific neutralising antibodies in dissecting out PDGFRα- and PDGFRβ-specific events in functional assays migration and collagen gel remodelling.
We show that neutralising antibodies against PDGFRα and PDGFRβ block signalling through PDGFRα and PDGFRβ receptors as expected. The phosphorylation of each PDGFR receptor was reduced when cells were treated with specific anti-PDGFRα or anti-PDGFRβ neutralising antibodies. Similarly we have shown that the neutralising antibodies abrogate the signal from PDGFRα in specific downstream signalling cascades. This is best illustrated in the reduction of pERK in response to anti-PDGFRα neutralising antibodies in dermal fibroblasts (Figure 4). In order to determine the efficacy of both the neutralising antibodies, we previously analysed the phosphorylation of their PDGFR-α or PDGFR-β receptors using different antibodies raised against a number of different phosphorylation sites (PDGFR-α Y751 and Y1021, PDGFR-β Y1018 and Y754) (data not shown). In each case we found that both PDGFR-α and PDGFR-β were not activated and were henceforth satisfied that the neutralising antibodies had abrogated normal signal transduction through the receptors. However, stimulation of pERK was observed when treated with anti-PDGFRβ alone and in the presence of PDGF-AA and PDGF-BB ligands. Whilst Anti-PDGFRβ has been previously reported to bind the receptor at a site other than that of the ligand, and hence not stimulate the receptor in the conventional manner, it may however be acting as an auto-antibody. As phosphorylation of PDGFRβ was not observed in our measurements, it may be that the signal transduction pathway that mediates the phosphorylation of ERK may be acting through a different phosphorylation site on the PDGFRβ receptor. We have similarly observed a reduction in pAkt in the presence of anti-PDGFR neutralising antibodies compared to stimulation with PDGF-AA and PDGF-BB ligand in both skin and lung fibroblasts (data not shown). We do not observe significant activation of the receptor above the levels of the ligand alone in lung fibroblasts. The presence of auto-antibodies that stimulate PDGFRs has previously been reported by Baroni et al.. We suggest that the neutralisation effect might be limited to actions mediated by specific phosphorylation sites on the PDGFRβ.
We also show that PDGFR-neutralising antibodies reduce PDGF-induced collagen gel remodelling and PDGF-mediated migration in a manner that reflects known, well-established receptor/ligand specificities (Figure 1). The role of PDGF in cell migration has long been established[4, 11]. However, much of the current research has used the universal PDGF ligand (PDGF-BB) when examining the role of PDGF signalling in migration. The extent of dermal fibroblast migration under the various conditions investigated here is in accordance with the known receptor/ligand specificities. This supports the findings of Gao et al. who also showed that depletion of PDGFRβ in dermal fibroblasts results in decreased migration and therefore validates the use of neutralising antibodies as a method of dissecting PDGFR-specific events.
The anti-PDGFRα and anti-PDGFRβ antibodies bind at a different site on the receptors to that of the ligands and henceforth do not act in a competitive manner. As a consequence of this, it appears as though the neutralising antibodies do not block signalling through the PDGFRα/PDGFRβ heterodimer as phosphorylation of the PDGFRα receptor was still observed when cells were treated with anti-PDGFRα and stimulated with the universal PDGF ligand, PDGF-BB. This is difficult to prove for the PDGFRβ in the context of this study as there is no PDGFRβ-specific ligand. This would obviously have to be taken into consideration in any future studies as a potential caveat. However, this does enable specific investigation of signalling via PDGFR homodimers only.
Similarly to other deletion strategies, the use of neutralisation antibodies has caveats associated with the extent and length of effect. However, this study has shown that PDGFRα and PDGFRβ neutralising antibodies can be a useful tool in studying PDGFR isoform-specific cellular events.
Human dermal and lung fibroblasts were isolated and cultured as previously described. Cells were maintained in Dulbecco’s-modified Eagle’s medium (DMEM; Life Technologies Ltd., UK) supplemented with 10% foetal bovine serum (Life Technologies), 100 U/ml penicillin and 100 mg/ml streptomycin (Life Technologies) and cultured in a humidified atmosphere of 5% CO2. At confluence, cells were passaged 1:4 using trypsin-EDTA (Life Technologies).
Treatment with neutralising antibodies
Cells were cultured in to 90% confluence in DMEM 10% FBS and serum starved (DMEM 0% FBS) overnight. Neutralising antibodies to either PDGFRα or PDGFRβ (R&D Systems, UK) were added (10 μg/ml - ND50 1–6 μg/ml based on the manufacturer’s guidelines) to the cells in fresh serum-free media and incubated for 1 h at room temperature. Cells were then stimulated with vehicle, PDGF-AA, PDGF-DD, PDGF-CC (R&D Systems) or PDGF-BB (Abcam UK), at various concentrations (0–200 ng/ml) for either 15 min for Western blot analysis or 24 h for migration assays.
Western blot analysis
Cell layers were washed in ice-cold PBS and lysed in RIPA buffer containing protease and phosphate inhibitors (Sigma UK). Equal amounts of protein (20 μg) were subjected to SDS/PAGE using 4–12% Bis Tris gels (Life Technologies). Proteins were blotted onto nitrocellulose as previously described, and proteins were detected using anti-PDGFRα, anti-PDGFRβ, anti-GAPDH (Abcam, UK), anti-phospho PDGFRα, anti-phospho PDGFRβ, (R&D Systems), anti-ERK and anti-phospho ERK antibodies followed by an appropriate HRP-conjugated secondary antibody (Cell Signalling, UK). Antibody binding was visualised Proteins were detected using an enhanced chemiluminescence kit (Amersham/GE Healthcare, UK).
Cells were plated in 96-well plates and cultured in DMEM 10% FBS to 100% confluency, then serum-starved overnight. The cell layers were scratched using a 96 pin floating array (V and P Scientific, USA) and washed 2× in PBS. All media subsequently used were supplemented with mitomycin C (5 ng/ml; Sigma) to block cell proliferation. Cells were then treated with PDGFR neutralising antibodies as described above, then stimulated with PDGF-AA, PDGFR-BB, PDGF-CC, PDGF-DD (20 ng/ml) or vehicle for 24 h and imaged using an Olympus CK2 microscope (Olympus, UK) and Ziess axiocam MR camera (Carl Zeiss Ltd., UK). Mean density of cells that had migrated into the scratched area was calculated using Axio Vision software (Carl Zeiss Ltd.).
Remodelling of collagen matrices
Twenty-four-well plates were coated with 2% bovine serum albumin (BSA) in PBS (2 ml/well) and incubated at 37°C overnight. The plates were then washed 3× with PBS. A collagen gel solution, consisting of one part 0.2 M N-2-hydroxyethylpiperazine-N’-2ethanesulphonic acid (HEPES), pH 8.0, four parts collagen [3 mg/ml, First Link (UK) Ltd., UK] and five parts DMEM was prepared. Cells were treated with neutralising antibodies against either PDGFRα or PDGFRβ (10 μg/ml) at room temperature for 1 h. A cell/collagen suspension was made, with a final concentration of 80,000 cells/ml and 1.2 mg/ml collagen. The cell/collagen suspension (1 ml per well) was added to the plates and incubated at 37°C to allow the collagen to polymerise. After 1 h, 1 ml of DMEM containing PDGF-AA, PDGFR-BB (20 ng/ml) or no serum control was gently added to each well resulting in detachment of the collagen gels from the tissue culture plastic. After 24 h, gels were measured and weighed as a measure of gel contraction.
Bovine serum albumin
Epidermal growth factor receptor
Extracellular signal-regulated kinase
Nuclear factor kappa-light-chain-enhancer of activated B cells
Platelet- derived growth factor
Platelet-derived growth factor receptor
Phospho extracellular signal-regulated kinase
Vascular epidermal growth factor receptor
Vascular smooth muscle cell
The work was supported by Arthritis Research UK Grant 18420 and The Rosetrees Trust.
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