Role of MMP-9 in the breakdown of barrier integrity of the corneal endothelium in response to TNF-α

TNF-α induces loss of barrier integrity of the corneal endothelium through mechanisms involving the activation of p38 MAP kinase. This study has investigated the role of matrix metalloproteinase-9 (MMP-9), known to be activated by mechanisms downstream of p38 MAP kinase, on the breakdown of the barr...

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Veröffentlicht in:Experimental eye research 2014-05, Vol.122, p.77-85
Hauptverfasser: Rajashekhar, Gangaraju, Shivanna, Mahesh, Kompella, Uday B., Wang, Yueren, Srinivas, Sangly P.
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container_title Experimental eye research
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creator Rajashekhar, Gangaraju
Shivanna, Mahesh
Kompella, Uday B.
Wang, Yueren
Srinivas, Sangly P.
description TNF-α induces loss of barrier integrity of the corneal endothelium through mechanisms involving the activation of p38 MAP kinase. This study has investigated the role of matrix metalloproteinase-9 (MMP-9), known to be activated by mechanisms downstream of p38 MAP kinase, on the breakdown of the barrier integrity. Experiments were performed with primary cultures of bovine corneal endothelium. Changes in the trans-endothelial electrical resistance (TER), a measure of barrier integrity, were measured by electric cell-substrate impedance sensing. The integrity of the apical junctional assembly was imaged by immunolocalization of ZO-1. MMP-9 activity in the conditioned medium of cells treated with TNF-α was visualized by gelatin zymography. Transcriptional activation of MMP-9 was assessed by real-time RT-PCR. Exposure to TNF-α led to significant disruption of ZO-1 and also caused a continuous decline in TER for more than 20 h. These effects were opposed by cycloheximide (protein synthesis inhibitor), GM-6001 (broad spectrum inhibitor of MMPs), minocycline (MMP-2 and MMP-9 inhibitor), and MMP-9 inhibitor I (selective MMP-9 inhibitor). Cycloheximide, GM-6001, and MMP-9 inhibitor I also attenuated the increase in permeability to FITC-dextran (10 kDa). In addition, TNF-α led to an increased MMP-9 activity in the conditioned medium as well as a nearly 20-fold increase in mRNA for MMP-9 but not for MMP-2. The functional activity and increase in mRNA levels of MMP-9 were blocked by SB-203580 (selective p38 MAP kinase inhibitor) and cycloheximide. In conclusion, transcriptional and translational activation of MMP-9, downstream of p38 MAP kinase signaling, is involved in the (TNF-α)-induced loss of corneal endothelial barrier integrity. •Barrier integrity of corneal endothelium is critical for maintenance of corneal transparency.•TNF-alpha is a major cytokine in the anterior chamber during allograft rejection and uveitis.•TNF-alpha breaks down the barrier integrity of the endothelium through the activation of p38 MAP kinase.•This research shows that MMP-9 is a downstream target of p38 MAP kinase.
doi_str_mv 10.1016/j.exer.2014.03.004
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This study has investigated the role of matrix metalloproteinase-9 (MMP-9), known to be activated by mechanisms downstream of p38 MAP kinase, on the breakdown of the barrier integrity. Experiments were performed with primary cultures of bovine corneal endothelium. Changes in the trans-endothelial electrical resistance (TER), a measure of barrier integrity, were measured by electric cell-substrate impedance sensing. The integrity of the apical junctional assembly was imaged by immunolocalization of ZO-1. MMP-9 activity in the conditioned medium of cells treated with TNF-α was visualized by gelatin zymography. Transcriptional activation of MMP-9 was assessed by real-time RT-PCR. Exposure to TNF-α led to significant disruption of ZO-1 and also caused a continuous decline in TER for more than 20 h. These effects were opposed by cycloheximide (protein synthesis inhibitor), GM-6001 (broad spectrum inhibitor of MMPs), minocycline (MMP-2 and MMP-9 inhibitor), and MMP-9 inhibitor I (selective MMP-9 inhibitor). Cycloheximide, GM-6001, and MMP-9 inhibitor I also attenuated the increase in permeability to FITC-dextran (10 kDa). In addition, TNF-α led to an increased MMP-9 activity in the conditioned medium as well as a nearly 20-fold increase in mRNA for MMP-9 but not for MMP-2. The functional activity and increase in mRNA levels of MMP-9 were blocked by SB-203580 (selective p38 MAP kinase inhibitor) and cycloheximide. 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This study has investigated the role of matrix metalloproteinase-9 (MMP-9), known to be activated by mechanisms downstream of p38 MAP kinase, on the breakdown of the barrier integrity. Experiments were performed with primary cultures of bovine corneal endothelium. Changes in the trans-endothelial electrical resistance (TER), a measure of barrier integrity, were measured by electric cell-substrate impedance sensing. The integrity of the apical junctional assembly was imaged by immunolocalization of ZO-1. MMP-9 activity in the conditioned medium of cells treated with TNF-α was visualized by gelatin zymography. Transcriptional activation of MMP-9 was assessed by real-time RT-PCR. Exposure to TNF-α led to significant disruption of ZO-1 and also caused a continuous decline in TER for more than 20 h. These effects were opposed by cycloheximide (protein synthesis inhibitor), GM-6001 (broad spectrum inhibitor of MMPs), minocycline (MMP-2 and MMP-9 inhibitor), and MMP-9 inhibitor I (selective MMP-9 inhibitor). Cycloheximide, GM-6001, and MMP-9 inhibitor I also attenuated the increase in permeability to FITC-dextran (10 kDa). In addition, TNF-α led to an increased MMP-9 activity in the conditioned medium as well as a nearly 20-fold increase in mRNA for MMP-9 but not for MMP-2. The functional activity and increase in mRNA levels of MMP-9 were blocked by SB-203580 (selective p38 MAP kinase inhibitor) and cycloheximide. In conclusion, transcriptional and translational activation of MMP-9, downstream of p38 MAP kinase signaling, is involved in the (TNF-α)-induced loss of corneal endothelial barrier integrity. •Barrier integrity of corneal endothelium is critical for maintenance of corneal transparency.•TNF-alpha is a major cytokine in the anterior chamber during allograft rejection and uveitis.•TNF-alpha breaks down the barrier integrity of the endothelium through the activation of p38 MAP kinase.•This research shows that MMP-9 is a downstream target of p38 MAP kinase.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>24667088</pmid><doi>10.1016/j.exer.2014.03.004</doi><tpages>9</tpages></addata></record>
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source MEDLINE; Access via ScienceDirect (Elsevier)
subjects Animals
Cattle
Cells, Cultured
corneal endothelium
Cycloheximide - pharmacology
Dextrans - metabolism
Electric Impedance
Endothelium, Corneal - drug effects
Endothelium, Corneal - enzymology
Fluorescein-5-isothiocyanate - analogs & derivatives
Fluorescein-5-isothiocyanate - metabolism
Gene Expression Regulation - physiology
Matrix Metalloproteinase 9 - physiology
Matrix Metalloproteinase Inhibitors - pharmacology
matrix metalloproteinases
p38 MAP kinase
Protein Synthesis Inhibitors - pharmacology
Real-Time Polymerase Chain Reaction
tight junctions
Tight Junctions - drug effects
Tight Junctions - enzymology
TNF-α
Tumor Necrosis Factor-alpha - pharmacology
Zonula Occludens-1 Protein - metabolism
title Role of MMP-9 in the breakdown of barrier integrity of the corneal endothelium in response to TNF-α
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