VEGF-independent angiogenic pathways induced by PDGF-C

PDGF-C is angiogenic in different models

PDGF-C is abundantly expressed in most of the highly angiogenic tissues, such as the placenta, ovary and embryo tissues [1, 3, 20]. Indeed, the angiogenic activity of PDGF-C occurs in many different organs and tissues. Infusion of PDGF-C protein alone increased the revascularization of ischemic mouse hearts, and induced angiogenesis in mouse ischemic hind limb [6]. In addition, the angiogenic activity of PDGF-C is comparable to that of VEGF in different model systems, such as in the aortic ring assay, chorioallantoic membrane assay and cornea pocket assay [3, 5]. The potent angiogenic activity of PDGF-C is linked to its effects on endothelial progenitor cells, bone marrow cells and mature vascular cells by promoting their recruitment, proliferation, differentiation and migration respectively [6, 7]. In the eye, PDGF-C also plays critical roles in choroidal, retinal and cornea neovascularization via its effects on multiple cellular targets, such as the vascular mural and endothelial cells, macrophages, choroidal fibroblasts, and retinal pigment epithelial (RPE) cells [5, 19].

The critical role of PDGF-C in tumor angiogenesis has been documented in different types of tumors [13, 16, 17]. It is particularly important to note that in tumors expressing a high level of PDGF-C, tumor blood vessels developed efficiently even when VEGF was inhibited [16]. This demonstrated that PDGF-C does not require VEGF activity to fulfill its angiogenic function. A combination therapy using both anti-PDGF-C and anti- VEGF antibodies was more effective in inhibiting tumor angiogenesis than using anti-VEGF treatment alone [16]. Furthermore, it is noteworthy that in the PDGF- C-overexpressing tumors, the permeability of the tumor blood vessels was decreased [17], in contrast to the VEGF-induced blood vessels, which are often leaky. The fact that PDGF-C-induced blood vessels are functionally different from the ones induced by VEGF supports that PDGF-C uses different mechanisms than VEGF to build blood vessels.

Broad range of cellular targets of PDGF-C

One important functional characteristic of PDGF-C is that it has a considerably broad range of cellular targets (Table 1). We have shown that PDGF-C promotes the proliferation, survival and migration of vascular pericytes, endothelial cells and fibroblasts [19]. Several groups have shown that PDGF-C has direct effects on macrophages. PDGF-C regulates gene expression in macrophages [19], and promotes their migration [21] and proliferation [22]. Moreover, PDGF-C induces proliferation and migration of retinal pigment epithelial cells [23]. PDGF-C also promotes the proliferation, survival and migration of vascular endothelial cells, smooth muscle cells (SMC) and their progenitors [6, 16]. In tumors, PDGF-C plays a critical role in recruiting fibroblasts associated with tumor drug resistance [15, 16, 24]. Vascular cells are the most important cellular components in pathological angiogenesis. In addition, other cell types, such as fibroblasts, macrophages and retinal pigment epithelial cells also play critical roles in different types of pathological neovascularization [25, 26]. It is noteworthy that pericytes, smooth muscle cells, fibroblasts, macrophages, retinal pigment epithelial cells, mesangial cells [27] and hepatic stellate cells [28] are not typical cellular targets of VEGF, which mainly affects vascular endothelial cells. Thus, at cellular level, the angiogenic pathways induced by PDGF-C are unique and different from those induced by VEGF.

VEGF-independent angiogenic pathways induced by PDGF-C

Much insight into the VEGF-independent angiogenic pathways induced by PDGF-C has derived from studies on tumor angiogenesis. For example, in tumors overexpressing PDGF-C, treatment with an anti- VEGFR-2 antibody, which blocks the VEGF pathway, had no effect on tumor angiogenesis, while it decreased blood vessel density in the control tumors without PDGF-C overexpression, demonstrating that the PDGF- C-induced angiogenesis was not mediated by the VEGF pathway [17]. Indeed, this notion was further supported by the findings that in VEGF-deficient fibrosarcomas, tumor angiogenesis still developed without VEGF, and the PDGFR-α-mediated recruitment of stromal fibroblasts was believed to be responsible for the persistent tumor angiogenesis [29], further affirming a VEGF-independent tumor angiogenesis induced by PDGF-C. Moreover, these observations were corroborated by the findings from yet another study showing that in certain types of tumors that are resistant to anti-VEGF therapy, PDGF-C was responsible for mediating the VEGF-independent tumor angiogenesis by modulating the angiogenic properties of tumor-associated fibroblasts [16]. In addition, it is recently reported that in the kidney, PDGF-C induced proliferation of glomerular endothelial cells in a VEGF- independent manner [22], indicating that the VEGF- independent effect of PDGF-C is likely a general event. Indeed, more evidence of the VEGF-independent angiogenic pathways induced by PDGF-C comes from studies on pathological ocular angiogenesis, such as choroidal and retinal neovascularization [19]. In both a laser-induced choroidal neovascularization (CNV) model and an ischemia-induced retinal angiogenesis model, the expression level of PDGF-C increased markedly. In these models, PDGF-C inhibition affected not only vascular mural and endothelial cells, but also macrophages, choroidal fibroblasts and retinal pigment epithelial cells, which are not prototypical cellular targets of VEGF. At gene regulation level, PDGF-C significantly upregulated the expression of PDGF-B and PDGF receptors in macrophages and retinal pigment epithelial cells, and PDGF-C inhibition downregulated their expression [19]. PDGF-B is known to be one of the most potent stimuli of pathological angiogenesis [30-34]. These findings indicate that PDGF-C may be functionally related to the PDGF-B-induced angiogenic pathways.

Taken together, accumulating data have shown that PDGF-C can induce VEGF-independent angiogenesis via at least three interrelated pathways:

(1) The vascular cell pathway: PDGF-C has direct effects on all three types of vascular cells, endothelial cells, pericytes and smooth muscle cells, by promoting their proliferation, survival and migration. Vascular pericytes and smooth muscle cells are classic cellular targets of the PDGFs [35]. In addition, certain types of vascular endothelial cells express the PDGF receptors [6, 36, 37] and respond to PDGF-C stimulation directly. PDGF-C thus can induce new blood vessel formation by increasing the number and availability of all three types of vascular cells (Fig. 1).

(2) The tissue stroma pathway: Tissue stroma consists of blood vessels, extracellular matrix (ECM), mesenchymal cells, inflammatory cells, nerves, lymphatic vessels, etc. These components form a scaffold to support and promote new blood vessels to grow. Fibroblasts are the major component of mesenchymal cells and are one of the major sources of angiogenic growth factors, extracellular matrix, and ECM-degrading proteases such as the matrix metalloproteinases (MMPs). Fibroblasts can also regulate inflammation and epithelial differentiation. There are a minimal number of fibroblasts in normal stroma in most organs. However, under pathological conditions, the number of fibroblasts increases due to the upregulated expression of chemotactant and mitogenic factors. Because of their critical contributions to pathological angiogenesis, fibroblasts may represent an important cellular target in antiangiogenic therapy [38]. PDGF-C has been shown to be one of the most potent stimuli for fibroblast proliferation, migration and recruitment [1, 3, 39]. A significant part of the angiogenic activity of PDGF-C is therefore exerted via its effect on fibroblasts (Fig. 2).

Figure 1:

Effect of PDGF-c on three types of vascular cells.

PDGF-C promotes the proliferation, survival and migration of all three types of vascular cells: endothelial cells (EC), pericytes and smooth muscle cells (SMC). Vascular pericytes and smooth muscle cells are known to be classic cellular targets of the PDGFs. In addition, certain types of vascular endothelial cells express the PDGF receptors and respond to PDGF-C directly. PDGF-C thus can induce angiogenesis by increasing the number and availability of all the three types of vascular cells.

Figure 2:

Effect of PDGF-C on fibroblasts.

Fibroblasts are the principal component of mesenchymal cells and are a major source of host-derived angiogenic growth factors (GF), extracellular matrix (ECM), and ECM-degrading proteases, such as the matrix metalloproteinases (MMP). Under pathological conditions, the number of fibroblasts is increased due to the upregulated expression of chemotactant and mitogenic factors. PDGF-C is one of the most potent stimuli of fibroblast proliferation, migration and recruitment. Part of the angiogenic activity of PDGF-C is therefore exerted via its effect on fibroblasts.

(3) The inflammatory cell pathway: It is known that different types of inflammatory cells, such as macrophages, monocytes and neutrophils, play critical roles in the VEGF-independent pathological angiogenesis by producing a broad array of angiogenic growth factors and cytokines, generating conduits for new blood vessels through proteolytic mechanisms, and promoting the remodeling of arterioles into arteries [40, 41]. Particularly, macrophages are known to play a key role in promoting pathological angiogenesis in the retina and choroid in the eye [42]. Macrophages are required for the angiogenic switch of quiescent blood vessels in pathological conditions, and accumulation of macrophages accelerates this process [43]. Several groups have reported that PDGF-C is a potent regulator of macrophage migration, proliferation and gene expression [19, 21, 22, 44]. PDGF-C therefore can promote angiogenesis via its direct effect on macrophages (Fig. 3).

Figure 3:

Effect of PDGF-c on macrophages.

Macrophages play critical roles in VEGF-independent pathological angiogenesis by producing a broad array of angiogenic growth factors (GF), cytokines and proteolytic proteinases, such as the matrix metalloproteinases (MMP). Macrophages are required for the angiogenic switch of blood vessels in pathological conditions, and accumulation of macrophages accelerates pathological angiogenesis. Several groups have reported that PDGF-C regulates macrophage migration, proliferation and gene expression. PDGF-C therefore can promote angiogenesis via its effect on macrophages.

After being intensively studied for about two decades, VEGF has been commonly viewed as a master angiogenic factor in both developmental and pathological angiogenesis [45, 46]. The importance of PDGF-C in neovessel formation, however, is only at the beginning of being realized. The function of PDGF-C in developmental angiogenesis still needs to be explored [8]. The role of PDGF-C in pathological angiogenesis, by contrast, has been better investigated [5, 6, 16, 18, 19]. In many models, the angiogenic effect of PDGF-C was as potent as that of VEGF, such as in the cornea [5], ischemic heart and limb [6]. Moreover, in pathological ocular angiogenesis, PDGF-C inhibition suppressed neovascularization to a similar degree as VEGF inhibition [19]. Thus, at least under certain pathological conditions, PDGF-C is as potent as VEGF in inducing angiogenesis, and is therefore as critical as VEGF to be inhibited when the growth of new blood vessels is harmful.