Pigment epithelium-derived factor acts as an opponent of growth-stimulatory factors in retinal glial-endothelial cell interactions

• Published in: Glia Vol. 55; no. 6; pp. 642 - 651
• Main Authors: Yafai, Yousef, Lange, Johannes, Wiedemann, Peter, Reichenbach, Andreas, Eichler, Wolfram
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 15.04.2007
• Subjects: angiogenesis; Animals; Cattle; Cell Communication - physiology; Cell Proliferation - drug effects; Cells, Cultured; Coculture Techniques; cytokine; Endothelial Cells - cytology; Endothelial Cells - metabolism; Enzyme Activation - drug effects; Enzyme Activation - physiology; Extracellular Signal-Regulated MAP Kinases - drug effects; Extracellular Signal-Regulated MAP Kinases - metabolism; Eye Proteins - metabolism; Eye Proteins - pharmacology; Growth Inhibitors - metabolism; Growth Inhibitors - pharmacology; Guinea Pigs; Intercellular Signaling Peptides and Proteins - metabolism; Intercellular Signaling Peptides and Proteins - secretion; MAP Kinase Signaling System - drug effects; MAP Kinase Signaling System - physiology; Müller cell; Neovascularization, Pathologic - metabolism; Neovascularization, Pathologic - physiopathology; Nerve Growth Factors - metabolism; Nerve Growth Factors - pharmacology; Neuroglia - cytology; Neuroglia - metabolism; Oxygen Consumption - drug effects; Oxygen Consumption - physiology; PEDF; Pigment Epithelium of Eye - cytology; Pigment Epithelium of Eye - metabolism; Pigment Epithelium of Eye - secretion; proliferation; retina; Retina - cytology; Retina - metabolism; Retinal Artery - cytology; Retinal Artery - drug effects; Retinal Artery - metabolism; Serpins - metabolism; Serpins - pharmacology; Vascular Endothelial Growth Factor A - antagonists & inhibitors; Vascular Endothelial Growth Factor A - metabolism; Vascular Endothelial Growth Factor A - secretion
• ISSN: 0894-1491; 1098-1136
• DOI: 10.1002/glia.20495

Pigment epithelium‐derived factor (PEDF), a glycoprotein with pleiotropic functions, is naturally occuring in the eye and considered as crucial to prevent pathological angiogenesis. Since retinal glial (Müller) cells produce PEDF, the authors have studied its impact on glial–endothelial cellular interactions. Bovine retinal endothelial cells were cultured in the presence of culture media originating from primary Müller cells, and endothelial proliferation as well as phosphorylation of the mitogen‐activated protein kinases extracellular signal‐regulated kinases (ERK)‐1/‐2 were investigated. The concerted activity of Müller‐cell derived soluble mediators attenuated endothelial proliferation and ERK‐1/‐2 activation, regardless of whether the Müller cells were preincubated under normoxia or hypoxia, and even though the endothelial cells were stimulated by vascular endothelial growth factor‐A (VEGF). This inhibitory activity was no longer demonstrable if high levels of basic fibroblast growth factor or VEGF were supplied, suggesting that in cases of pathological neovascularization, overproduction of proangiogenic mediators overrides the “antiangiogenic background” provided by Müller cells. However, neutralizing the activity of PEDF partially restored endothelial cell proliferation and resulted in increased ERK‐1/‐2 activation, which is in concordance with findings demonstrating that exogenously applied PEDF is able to suppress VEGF‐induced ERK‐1/‐2 phosphorylation. PEDF production by Müller cells is not only regulated by retinal oxygen but also by the activity of soluble factors released from retinal endothelial cells. For instance, PEDF levels were significantly elevated in glial (Müller)–endothelial cell cocultures as compared with bovine retinal endothelial cell‐free Müller cell cultures. These results have implications for the pathogenesis of retinal neovascularization since the Müller cell may be regarded as a central control element which modulates retinal PEDF levels and, thus, is of critical importance for adjusting the balance between proangiogenic and antiangiogenic mediators. © 2007 Wiley‐Liss, Inc.