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...
Gespeichert in:
Veröffentlicht in: | Experimental eye research 2014-05, Vol.122, p.77-85 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 85 |
---|---|
container_issue | |
container_start_page | 77 |
container_title | Experimental eye research |
container_volume | 122 |
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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1523406559</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0014483514000724</els_id><sourcerecordid>1523406559</sourcerecordid><originalsourceid>FETCH-LOGICAL-c356t-734df099e7d49262a997395450e3d914abce18e423f83dc8bd8b49ea95890b933</originalsourceid><addsrcrecordid>eNp9kElOxDAQRS0Egma4AAuUJZuEcuwMltggxCQxCcHacuwKuEnHjZ1mOBYX4Uw4amDJynL9V1-qR8guhYwCLQ-mGb6jz3KgPAOWAfAVMqEgyhQAqlUygZikvGbFBtkMYRqnjFd8nWzkvCwrqOsJMXeuw8S1ydXVbSoS2yfDEyaNR_Vs3Fs_Jo3y3qKP2YCP3g4f43CktPM9qi7B3rj47-xiNhZ4DHPXB0wGl9xfn6Zfn9tkrVVdwJ2fd4s8nJ7cH5-nlzdnF8dHl6lmRTmkFeOmBSGwMlzkZa6EqJgoeAHIjKBcNRppjTxnbc2MrhtTN1ygEkUtoBGMbZH9Ze_cu5cFhkHObNDYdapHtwiSFjnjUBaFiGi-RLV3IXhs5dzbmfIfkoIc7cqpHO3K0a4EJqPduLT3079oZmj-Vn51RuBwCWC88jVKk0Fb7DUa61EP0jj7X_83I4KK6w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1523406559</pqid></control><display><type>article</type><title>Role of MMP-9 in the breakdown of barrier integrity of the corneal endothelium in response to TNF-α</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Rajashekhar, Gangaraju ; Shivanna, Mahesh ; Kompella, Uday B. ; Wang, Yueren ; Srinivas, Sangly P.</creator><creatorcontrib>Rajashekhar, Gangaraju ; Shivanna, Mahesh ; Kompella, Uday B. ; Wang, Yueren ; Srinivas, Sangly P.</creatorcontrib><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.</description><identifier>ISSN: 0014-4835</identifier><identifier>EISSN: 1096-0007</identifier><identifier>DOI: 10.1016/j.exer.2014.03.004</identifier><identifier>PMID: 24667088</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>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</subject><ispartof>Experimental eye research, 2014-05, Vol.122, p.77-85</ispartof><rights>2014 Elsevier Ltd</rights><rights>Copyright © 2014 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-734df099e7d49262a997395450e3d914abce18e423f83dc8bd8b49ea95890b933</citedby><cites>FETCH-LOGICAL-c356t-734df099e7d49262a997395450e3d914abce18e423f83dc8bd8b49ea95890b933</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.exer.2014.03.004$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24667088$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rajashekhar, Gangaraju</creatorcontrib><creatorcontrib>Shivanna, Mahesh</creatorcontrib><creatorcontrib>Kompella, Uday B.</creatorcontrib><creatorcontrib>Wang, Yueren</creatorcontrib><creatorcontrib>Srinivas, Sangly P.</creatorcontrib><title>Role of MMP-9 in the breakdown of barrier integrity of the corneal endothelium in response to TNF-α</title><title>Experimental eye research</title><addtitle>Exp Eye Res</addtitle><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.</description><subject>Animals</subject><subject>Cattle</subject><subject>Cells, Cultured</subject><subject>corneal endothelium</subject><subject>Cycloheximide - pharmacology</subject><subject>Dextrans - metabolism</subject><subject>Electric Impedance</subject><subject>Endothelium, Corneal - drug effects</subject><subject>Endothelium, Corneal - enzymology</subject><subject>Fluorescein-5-isothiocyanate - analogs & derivatives</subject><subject>Fluorescein-5-isothiocyanate - metabolism</subject><subject>Gene Expression Regulation - physiology</subject><subject>Matrix Metalloproteinase 9 - physiology</subject><subject>Matrix Metalloproteinase Inhibitors - pharmacology</subject><subject>matrix metalloproteinases</subject><subject>p38 MAP kinase</subject><subject>Protein Synthesis Inhibitors - pharmacology</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>tight junctions</subject><subject>Tight Junctions - drug effects</subject><subject>Tight Junctions - enzymology</subject><subject>TNF-α</subject><subject>Tumor Necrosis Factor-alpha - pharmacology</subject><subject>Zonula Occludens-1 Protein - metabolism</subject><issn>0014-4835</issn><issn>1096-0007</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kElOxDAQRS0Egma4AAuUJZuEcuwMltggxCQxCcHacuwKuEnHjZ1mOBYX4Uw4amDJynL9V1-qR8guhYwCLQ-mGb6jz3KgPAOWAfAVMqEgyhQAqlUygZikvGbFBtkMYRqnjFd8nWzkvCwrqOsJMXeuw8S1ydXVbSoS2yfDEyaNR_Vs3Fs_Jo3y3qKP2YCP3g4f43CktPM9qi7B3rj47-xiNhZ4DHPXB0wGl9xfn6Zfn9tkrVVdwJ2fd4s8nJ7cH5-nlzdnF8dHl6lmRTmkFeOmBSGwMlzkZa6EqJgoeAHIjKBcNRppjTxnbc2MrhtTN1ygEkUtoBGMbZH9Ze_cu5cFhkHObNDYdapHtwiSFjnjUBaFiGi-RLV3IXhs5dzbmfIfkoIc7cqpHO3K0a4EJqPduLT3079oZmj-Vn51RuBwCWC88jVKk0Fb7DUa61EP0jj7X_83I4KK6w</recordid><startdate>20140501</startdate><enddate>20140501</enddate><creator>Rajashekhar, Gangaraju</creator><creator>Shivanna, Mahesh</creator><creator>Kompella, Uday B.</creator><creator>Wang, Yueren</creator><creator>Srinivas, Sangly P.</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20140501</creationdate><title>Role of MMP-9 in the breakdown of barrier integrity of the corneal endothelium in response to TNF-α</title><author>Rajashekhar, Gangaraju ; Shivanna, Mahesh ; Kompella, Uday B. ; Wang, Yueren ; Srinivas, Sangly P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-734df099e7d49262a997395450e3d914abce18e423f83dc8bd8b49ea95890b933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Cattle</topic><topic>Cells, Cultured</topic><topic>corneal endothelium</topic><topic>Cycloheximide - pharmacology</topic><topic>Dextrans - metabolism</topic><topic>Electric Impedance</topic><topic>Endothelium, Corneal - drug effects</topic><topic>Endothelium, Corneal - enzymology</topic><topic>Fluorescein-5-isothiocyanate - analogs & derivatives</topic><topic>Fluorescein-5-isothiocyanate - metabolism</topic><topic>Gene Expression Regulation - physiology</topic><topic>Matrix Metalloproteinase 9 - physiology</topic><topic>Matrix Metalloproteinase Inhibitors - pharmacology</topic><topic>matrix metalloproteinases</topic><topic>p38 MAP kinase</topic><topic>Protein Synthesis Inhibitors - pharmacology</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>tight junctions</topic><topic>Tight Junctions - drug effects</topic><topic>Tight Junctions - enzymology</topic><topic>TNF-α</topic><topic>Tumor Necrosis Factor-alpha - pharmacology</topic><topic>Zonula Occludens-1 Protein - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rajashekhar, Gangaraju</creatorcontrib><creatorcontrib>Shivanna, Mahesh</creatorcontrib><creatorcontrib>Kompella, Uday B.</creatorcontrib><creatorcontrib>Wang, Yueren</creatorcontrib><creatorcontrib>Srinivas, Sangly P.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Experimental eye research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rajashekhar, Gangaraju</au><au>Shivanna, Mahesh</au><au>Kompella, Uday B.</au><au>Wang, Yueren</au><au>Srinivas, Sangly P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Role of MMP-9 in the breakdown of barrier integrity of the corneal endothelium in response to TNF-α</atitle><jtitle>Experimental eye research</jtitle><addtitle>Exp Eye Res</addtitle><date>2014-05-01</date><risdate>2014</risdate><volume>122</volume><spage>77</spage><epage>85</epage><pages>77-85</pages><issn>0014-4835</issn><eissn>1096-0007</eissn><abstract>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.</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> |
fulltext | fulltext |
identifier | ISSN: 0014-4835 |
ispartof | Experimental eye research, 2014-05, Vol.122, p.77-85 |
issn | 0014-4835 1096-0007 |
language | eng |
recordid | cdi_proquest_miscellaneous_1523406559 |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T18%3A41%3A25IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Role%20of%20MMP-9%20in%20the%20breakdown%20of%20barrier%20integrity%20of%20the%20corneal%20endothelium%20in%20response%20to%20TNF-%CE%B1&rft.jtitle=Experimental%20eye%20research&rft.au=Rajashekhar,%20Gangaraju&rft.date=2014-05-01&rft.volume=122&rft.spage=77&rft.epage=85&rft.pages=77-85&rft.issn=0014-4835&rft.eissn=1096-0007&rft_id=info:doi/10.1016/j.exer.2014.03.004&rft_dat=%3Cproquest_cross%3E1523406559%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1523406559&rft_id=info:pmid/24667088&rft_els_id=S0014483514000724&rfr_iscdi=true |