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Thrombin-Induced VEGF Expression in Human Retinal Pigment Epithelial Cells

From the Department of Ophthalmology, University of Michigan, Ann Arbor, Michigan.

PURPOSE. The purpose of the present study was to investigate the effects of thrombin and thrombin in combination with other proangiogenic factors on VEGF expression in hRPE cells.

METHODS. hRPE cells were stimulated with thrombin TNF-, monocytes, and TGF-ß2. After stimulation, conditioned medium and lysed cells were subjected to ELISA, Western blot analysis, immunocytochemistry, and RT-PCR analyses. Inhibitors specific for various signal transduction pathways were used to determine the signaling pathways involved.

RESULTS. Treatment of RPE cells with thrombin resulted in dose- and time-dependent increases in VEGF mRNA levels and protein production. hRPE VEGF expression is predominantly protease-activated receptor (PAR)-1 dependent. Approximately 80% of thrombin-induced VEGF secretion was abrogated by inhibitors of MAPK/ERK kinase (MEK), p38, c-Jun NH2-terminal kinase (JNK), protein tyrosine kinase (PTK), phosphatidylinositol 3-kinase (PI3K), protein kinase C (PKC), nuclear factor-B (NF-B), and reactive oxygen species (ROS). Analyses of VEGF protein production and mRNA synthesis revealed that VEGF induction by thrombin plus TNF- or coculture with monocytes was additive, whereas that by co-incubation with TGF-ß2 was synergistic. The costimulated VEGF production by TGF-ß2 plus thrombin was an average of three times higher than the sum of that induced by each agent alone. Furthermore, BAPTA [bis-(o-aminophenoxy)ethane-N,N',N'-tetraacetic acid], a calcium chelator, blocked the VEGF secretion induced by thrombin and thrombin plus TGF-ß2 by 65% and 20%, respectively, but had no effect on that induced by TGF-ß2 alone.

CONCLUSIONS. Thrombin alone and in combination with TNF-, monocytes, and TGF-ß2 potently stimulated VEGF expression in hRPE cells via multiple signaling pathways. The thrombin-induced calcium mobilization may play an important permissive role in maximizing TGF-ß2–induced VEGF expression in RPE cells.

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