Effect of Nitric Oxide on the Expression of Matrix Metalloproteinase and Its Association with Migration of Cultured Trabecular Meshwork Cells.
- Author:
Jae Woo KIM
1
Author Information
- Publication Type:Original Article
- Keywords: Matrix metalloproteinase; Migration; Nitric oxide; Trabecular meshwork cells
- MeSH: Cell Movement/*drug effects; Cell Survival/drug effects; Cells, Cultured; DNA Primers/chemistry; Gene Expression Regulation, Enzymologic/*physiology; Humans; Matrix Metalloproteinases/*genetics; Nitric Oxide Donors/*pharmacology; RNA, Messenger/genetics; Real-Time Polymerase Chain Reaction; S-Nitroso-N-Acetylpenicillamine/*pharmacology; Tissue Inhibitor of Metalloproteinase-2/*genetics; Trabecular Meshwork/cytology/*drug effects/enzymology
- From:Korean Journal of Ophthalmology 2016;30(1):66-75
- CountryRepublic of Korea
- Language:English
- Abstract: PURPOSE: To determine the effect of exogenous nitric oxide (NO) on the migration of trabecular meshwork (TM) cells and its association with expression of matrix metalloproteinases (MMPs). METHODS: Primary human TM cells treated with 1 or 10 microM S-nitroso-N-acetyl-penicillamine (SNAP) and examined for changes in adherence. TM cells were seeded onto transwell culture inserts, and changes in their migratory activity were quantified. Reverse transcription polymerase chain reaction was performed to determine the relative changes in mRNA expression of MMPs and tissue inhibitor of metalloproteinases (TIMPs). RESULTS: Treatment with SNAP did not significantly suppress TM cell adhesion or migration (p > 0.05). Treatment of TM cells with 10 microM SNAP decreased expression of MMP-2 and increased expression of membrane type MMP-1 and TIMP-2. Treatment with interleukin-1alpha triggered MMP-3 expression but did not exert significant effects on MMP-3 activation in response to SNAP. CONCLUSIONS: These data suggest that NO revealed no significant effect on the migration of TM cells because NO decreased MMP-2 and increased TIMP-2 expression. Although expression of certain MMPs and TIMPs change in response to NO donors, NO may modulate trabecular outflow by changing the cellular production of extracellular matrix without having a significant effect on the migration of TM cells.
