PDGF-CC blockade inhibits pathological angiogenesis by acting on multiple cellular and molecular targets
2010 (English)In: Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, E-ISSN 1091-6490, Vol. 107, no 27, 12216-12221 p.Article in journal (Refereed) Published
The importance of identifying VEGF-independent pathways in pathological angiogenesis is increasingly recognized as a result of the emerging drug resistance to anti-VEGF therapies. PDGF-CC is the third member of the PDGF family discovered after more than two decades of studies on PDGF-AA and PDGF-BB. The biological function of PDGF-CC and the underlying cellular and molecular mechanisms remain largely unexplored. Here, using different animal models, we report that PDGF-CC inhibition by neutralizing antibody, shRNA, or genetic deletion suppressed both choroidal and retinal neovascularization. Importantly, we revealed that PDGF-CC targeting acted not only on multiple cell types important for pathological angiogenesis, such as vascular mural and endothelial cells, macrophages, choroidal fibroblasts and retinal pigment epithelial cells, but also on the expression of other important angiogenic genes, such as PDGF-BB and PDGF receptors. At a molecular level, we found that PDGF-CC regulated glycogen synthase kinase (GSK)-3beta phosphorylation and expression both in vitro and in vivo. Activation of GSK3beta impaired PDGF-CC-induced angiogenesis, and inhibition of GSK3beta abolished the antiangiogenic effect of PDGF-CC blockade. Thus, we identified PDGF-CC as an important candidate target gene for antiangiogenic therapy, and PDGF-CC inhibition may be of therapeutic value in treating neovascular diseases.
Place, publisher, year, edition, pages
2010. Vol. 107, no 27, 12216-12221 p.
choroidal neovascularization, glycogen synthase kinase-3 beta, vascular biology, retinal neovascularization, ocular disease
Medical and Health Sciences
IdentifiersURN: urn:nbn:se:uu:diva-130834DOI: 10.1073/pnas.1004143107ISI: 000279572100033PubMedID: 20566880OAI: oai:DiVA.org:uu-130834DiVA: diva2:351451