Involvement of MMPs in the outward remodeling of collateral mesenteric arteries
1 School of Kinesiology and Health Sciences, York University, Toronto, Ontario, Canada; and Departments of 2 Surgery and 3 Cellular and Integrative Physiology, Indiana University Medical Center, Indianapolis, Indiana Submitted 24 January 2007 ; accepted in final form 13 July 2007 Persistent elevatio...
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creator | Haas, Tara L Doyle, Jennifer L Distasi, Matthew R Norton, Laura E Sheridan, Kevin M Unthank, Joseph L |
description | 1 School of Kinesiology and Health Sciences, York University, Toronto, Ontario, Canada; and Departments of 2 Surgery and 3 Cellular and Integrative Physiology, Indiana University Medical Center, Indianapolis, Indiana
Submitted 24 January 2007
; accepted in final form 13 July 2007
Persistent elevation in shear stress within conduit or resistance arteries causes structural luminal expansion, which serves to normalize shear stress while maintaining increased flow to the downstream vasculature. Although it is known that this adaptation involves cellular proliferation and remodeling of the extracellular matrix, the specific cellular events underlying these responses are poorly understood. Matrix metalloproteinases (MMPs) contribute to extensive remodeling of the extracellular matrix in conduit vessels and vein grafts exposed to high flow. However, involvement of MMPs in remodeling of small muscular collateral arteries, which are exposed to less severe increases in shear stress, has not been tested. We utilized an established model of outward remodeling in mesenteric collateral arteries to determine whether MMPs were upregulated during the remodeling response and to test whether MMP activity was required for luminal expansion. By 4 days, MMP-2 and membrane type 1 MMP (MT1-MMP), but not MMP-9, protein levels were significantly elevated in collateral arteries, as assessed by gelatin zymography and immunostaining. MMP-2 and MT1-MMP proteins, together with their respective transcriptional activators c-Jun and Egr-1 were localized predominantly to the smooth muscle layer of the collateral arteries. The general MMP inhibitor doxycycline prevented luminal expansion of collateral arteries but did not affect the endothelial cell proliferative or medial growth responses. In conclusion, this study provides evidence that MMP-2 and MT1-MMP are upregulated in collateral arteries exposed to elevated shear stress and that MMP activity is essential for the full remodeling response that leads to outward luminal expansion.
matrix metalloproteinase; collateral artery; shear stress
Address for reprint requests and other correspondence: T. L. Haas, School of Kinesiology and Health Sciences, Rm. 341 Farquharson, York Univ., 4700 Keele St., Toronto, ON Canada M3J 1P3 (e-mail: thaas{at}yorku.ca ) |
doi_str_mv | 10.1152/ajpheart.00100.2007 |
format | Article |
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Submitted 24 January 2007
; accepted in final form 13 July 2007
Persistent elevation in shear stress within conduit or resistance arteries causes structural luminal expansion, which serves to normalize shear stress while maintaining increased flow to the downstream vasculature. Although it is known that this adaptation involves cellular proliferation and remodeling of the extracellular matrix, the specific cellular events underlying these responses are poorly understood. Matrix metalloproteinases (MMPs) contribute to extensive remodeling of the extracellular matrix in conduit vessels and vein grafts exposed to high flow. However, involvement of MMPs in remodeling of small muscular collateral arteries, which are exposed to less severe increases in shear stress, has not been tested. We utilized an established model of outward remodeling in mesenteric collateral arteries to determine whether MMPs were upregulated during the remodeling response and to test whether MMP activity was required for luminal expansion. By 4 days, MMP-2 and membrane type 1 MMP (MT1-MMP), but not MMP-9, protein levels were significantly elevated in collateral arteries, as assessed by gelatin zymography and immunostaining. MMP-2 and MT1-MMP proteins, together with their respective transcriptional activators c-Jun and Egr-1 were localized predominantly to the smooth muscle layer of the collateral arteries. The general MMP inhibitor doxycycline prevented luminal expansion of collateral arteries but did not affect the endothelial cell proliferative or medial growth responses. In conclusion, this study provides evidence that MMP-2 and MT1-MMP are upregulated in collateral arteries exposed to elevated shear stress and that MMP activity is essential for the full remodeling response that leads to outward luminal expansion.
matrix metalloproteinase; collateral artery; shear stress
Address for reprint requests and other correspondence: T. L. Haas, School of Kinesiology and Health Sciences, Rm. 341 Farquharson, York Univ., 4700 Keele St., Toronto, ON Canada M3J 1P3 (e-mail: thaas{at}yorku.ca )</description><identifier>ISSN: 0363-6135</identifier><identifier>EISSN: 1522-1539</identifier><identifier>DOI: 10.1152/ajpheart.00100.2007</identifier><identifier>PMID: 17644578</identifier><identifier>CODEN: AJPPDI</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Animals ; Arteries - surgery ; Cell Proliferation ; Collateral Circulation ; Doxycycline - pharmacology ; Early Growth Response Protein 1 - metabolism ; Enzyme Activation ; Extracellular Matrix - metabolism ; Ileum - blood supply ; Ligation ; Male ; Matrix Metalloproteinase 14 - metabolism ; Matrix Metalloproteinase 2 - metabolism ; Matrix Metalloproteinase 9 - metabolism ; Matrix Metalloproteinases - metabolism ; Mesenteric Arteries - drug effects ; Mesenteric Arteries - enzymology ; Mesenteric Arteries - metabolism ; Mesenteric Arteries - pathology ; Mesenteric Arteries - physiopathology ; Models, Animal ; Protease Inhibitors - pharmacology ; Proteases ; Proto-Oncogene Proteins c-jun - metabolism ; Rats ; Rats, Wistar ; Shear stress ; Splanchnic Circulation ; Stress, Mechanical ; Studies ; Time Factors ; Tunica Intima - drug effects ; Tunica Intima - enzymology ; Tunica Intima - metabolism ; Tunica Intima - pathology ; Tunica Intima - physiopathology ; Up-Regulation ; Veins & arteries</subject><ispartof>American journal of physiology. Heart and circulatory physiology, 2007-10, Vol.293 (4), p.H2429-H2437</ispartof><rights>Copyright American Physiological Society Oct 2007</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c422t-ec781a0ae8e794a4aa7c757950f6598708efad8c243799cc006972abcb815b543</citedby><cites>FETCH-LOGICAL-c422t-ec781a0ae8e794a4aa7c757950f6598708efad8c243799cc006972abcb815b543</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3026,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17644578$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Haas, Tara L</creatorcontrib><creatorcontrib>Doyle, Jennifer L</creatorcontrib><creatorcontrib>Distasi, Matthew R</creatorcontrib><creatorcontrib>Norton, Laura E</creatorcontrib><creatorcontrib>Sheridan, Kevin M</creatorcontrib><creatorcontrib>Unthank, Joseph L</creatorcontrib><title>Involvement of MMPs in the outward remodeling of collateral mesenteric arteries</title><title>American journal of physiology. Heart and circulatory physiology</title><addtitle>Am J Physiol Heart Circ Physiol</addtitle><description>1 School of Kinesiology and Health Sciences, York University, Toronto, Ontario, Canada; and Departments of 2 Surgery and 3 Cellular and Integrative Physiology, Indiana University Medical Center, Indianapolis, Indiana
Submitted 24 January 2007
; accepted in final form 13 July 2007
Persistent elevation in shear stress within conduit or resistance arteries causes structural luminal expansion, which serves to normalize shear stress while maintaining increased flow to the downstream vasculature. Although it is known that this adaptation involves cellular proliferation and remodeling of the extracellular matrix, the specific cellular events underlying these responses are poorly understood. Matrix metalloproteinases (MMPs) contribute to extensive remodeling of the extracellular matrix in conduit vessels and vein grafts exposed to high flow. However, involvement of MMPs in remodeling of small muscular collateral arteries, which are exposed to less severe increases in shear stress, has not been tested. We utilized an established model of outward remodeling in mesenteric collateral arteries to determine whether MMPs were upregulated during the remodeling response and to test whether MMP activity was required for luminal expansion. By 4 days, MMP-2 and membrane type 1 MMP (MT1-MMP), but not MMP-9, protein levels were significantly elevated in collateral arteries, as assessed by gelatin zymography and immunostaining. MMP-2 and MT1-MMP proteins, together with their respective transcriptional activators c-Jun and Egr-1 were localized predominantly to the smooth muscle layer of the collateral arteries. The general MMP inhibitor doxycycline prevented luminal expansion of collateral arteries but did not affect the endothelial cell proliferative or medial growth responses. In conclusion, this study provides evidence that MMP-2 and MT1-MMP are upregulated in collateral arteries exposed to elevated shear stress and that MMP activity is essential for the full remodeling response that leads to outward luminal expansion.
matrix metalloproteinase; collateral artery; shear stress
Address for reprint requests and other correspondence: T. L. Haas, School of Kinesiology and Health Sciences, Rm. 341 Farquharson, York Univ., 4700 Keele St., Toronto, ON Canada M3J 1P3 (e-mail: thaas{at}yorku.ca )</description><subject>Animals</subject><subject>Arteries - surgery</subject><subject>Cell Proliferation</subject><subject>Collateral Circulation</subject><subject>Doxycycline - pharmacology</subject><subject>Early Growth Response Protein 1 - metabolism</subject><subject>Enzyme Activation</subject><subject>Extracellular Matrix - metabolism</subject><subject>Ileum - blood supply</subject><subject>Ligation</subject><subject>Male</subject><subject>Matrix Metalloproteinase 14 - metabolism</subject><subject>Matrix Metalloproteinase 2 - metabolism</subject><subject>Matrix Metalloproteinase 9 - metabolism</subject><subject>Matrix Metalloproteinases - metabolism</subject><subject>Mesenteric Arteries - drug effects</subject><subject>Mesenteric Arteries - enzymology</subject><subject>Mesenteric Arteries - metabolism</subject><subject>Mesenteric Arteries - pathology</subject><subject>Mesenteric Arteries - physiopathology</subject><subject>Models, Animal</subject><subject>Protease Inhibitors - pharmacology</subject><subject>Proteases</subject><subject>Proto-Oncogene Proteins c-jun - metabolism</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Shear stress</subject><subject>Splanchnic Circulation</subject><subject>Stress, Mechanical</subject><subject>Studies</subject><subject>Time Factors</subject><subject>Tunica Intima - drug effects</subject><subject>Tunica Intima - enzymology</subject><subject>Tunica Intima - metabolism</subject><subject>Tunica Intima - pathology</subject><subject>Tunica Intima - physiopathology</subject><subject>Up-Regulation</subject><subject>Veins & arteries</subject><issn>0363-6135</issn><issn>1522-1539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kEtr3DAUhUVpaCZpf0GhmC6680RvWXRVQvOAhGSRroVGvh57kC1XspPOv6-mM01LIKu7uN93OByEPhK8JETQM7sZW7BxWmJMMF5SjNUbtMgfWhLB9Fu0wEyyUhImjtFJShuMsVCSvUPHREnOhaoW6O56eAz-EXoYpiI0xe3tfSq6oZhaKMI8PdlYFxH6UIPvhvWOcMF7O0G0vughZQ1i54rcI19I79FRY32CD4d7in5cfH84vypv7i6vz7_dlI5TOpXgVEUstlCB0txya5VTQmmBGyl0pXAFja0rRzlTWjuHsdSK2pVbVUSsBGen6Ms-d4zh5wxpMn2XHORqA4Q5GVkxSQilGfz8AtyEOQ65m6FUSyEZxRlie8jFkFKExoyx623cGoLNbmzzd2zzZ2yzGztbnw7R86qH-p9zWDcDX_dA263bpy6CGdtt6oIP6625mL1_gF_TczTVzHBzRTnVZqybbJ-9bj_3-c9ivwEHE6Lf</recordid><startdate>20071001</startdate><enddate>20071001</enddate><creator>Haas, Tara L</creator><creator>Doyle, Jennifer L</creator><creator>Distasi, Matthew R</creator><creator>Norton, Laura E</creator><creator>Sheridan, Kevin M</creator><creator>Unthank, Joseph L</creator><general>American Physiological Society</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>7QP</scope><scope>7QR</scope><scope>7TS</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20071001</creationdate><title>Involvement of MMPs in the outward remodeling of collateral mesenteric arteries</title><author>Haas, Tara L ; Doyle, Jennifer L ; Distasi, Matthew R ; Norton, Laura E ; Sheridan, Kevin M ; Unthank, Joseph L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c422t-ec781a0ae8e794a4aa7c757950f6598708efad8c243799cc006972abcb815b543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Arteries - surgery</topic><topic>Cell Proliferation</topic><topic>Collateral Circulation</topic><topic>Doxycycline - pharmacology</topic><topic>Early Growth Response Protein 1 - metabolism</topic><topic>Enzyme Activation</topic><topic>Extracellular Matrix - metabolism</topic><topic>Ileum - blood supply</topic><topic>Ligation</topic><topic>Male</topic><topic>Matrix Metalloproteinase 14 - metabolism</topic><topic>Matrix Metalloproteinase 2 - metabolism</topic><topic>Matrix Metalloproteinase 9 - metabolism</topic><topic>Matrix Metalloproteinases - metabolism</topic><topic>Mesenteric Arteries - drug effects</topic><topic>Mesenteric Arteries - enzymology</topic><topic>Mesenteric Arteries - metabolism</topic><topic>Mesenteric Arteries - pathology</topic><topic>Mesenteric Arteries - physiopathology</topic><topic>Models, Animal</topic><topic>Protease Inhibitors - pharmacology</topic><topic>Proteases</topic><topic>Proto-Oncogene Proteins c-jun - metabolism</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Shear stress</topic><topic>Splanchnic Circulation</topic><topic>Stress, Mechanical</topic><topic>Studies</topic><topic>Time Factors</topic><topic>Tunica Intima - drug effects</topic><topic>Tunica Intima - enzymology</topic><topic>Tunica Intima - metabolism</topic><topic>Tunica Intima - pathology</topic><topic>Tunica Intima - physiopathology</topic><topic>Up-Regulation</topic><topic>Veins & arteries</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Haas, Tara L</creatorcontrib><creatorcontrib>Doyle, Jennifer L</creatorcontrib><creatorcontrib>Distasi, Matthew R</creatorcontrib><creatorcontrib>Norton, Laura E</creatorcontrib><creatorcontrib>Sheridan, Kevin M</creatorcontrib><creatorcontrib>Unthank, Joseph L</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Haas, Tara L</au><au>Doyle, Jennifer L</au><au>Distasi, Matthew R</au><au>Norton, Laura E</au><au>Sheridan, Kevin M</au><au>Unthank, Joseph L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Involvement of MMPs in the outward remodeling of collateral mesenteric arteries</atitle><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle><addtitle>Am J Physiol Heart Circ Physiol</addtitle><date>2007-10-01</date><risdate>2007</risdate><volume>293</volume><issue>4</issue><spage>H2429</spage><epage>H2437</epage><pages>H2429-H2437</pages><issn>0363-6135</issn><eissn>1522-1539</eissn><coden>AJPPDI</coden><abstract>1 School of Kinesiology and Health Sciences, York University, Toronto, Ontario, Canada; and Departments of 2 Surgery and 3 Cellular and Integrative Physiology, Indiana University Medical Center, Indianapolis, Indiana
Submitted 24 January 2007
; accepted in final form 13 July 2007
Persistent elevation in shear stress within conduit or resistance arteries causes structural luminal expansion, which serves to normalize shear stress while maintaining increased flow to the downstream vasculature. Although it is known that this adaptation involves cellular proliferation and remodeling of the extracellular matrix, the specific cellular events underlying these responses are poorly understood. Matrix metalloproteinases (MMPs) contribute to extensive remodeling of the extracellular matrix in conduit vessels and vein grafts exposed to high flow. However, involvement of MMPs in remodeling of small muscular collateral arteries, which are exposed to less severe increases in shear stress, has not been tested. We utilized an established model of outward remodeling in mesenteric collateral arteries to determine whether MMPs were upregulated during the remodeling response and to test whether MMP activity was required for luminal expansion. By 4 days, MMP-2 and membrane type 1 MMP (MT1-MMP), but not MMP-9, protein levels were significantly elevated in collateral arteries, as assessed by gelatin zymography and immunostaining. MMP-2 and MT1-MMP proteins, together with their respective transcriptional activators c-Jun and Egr-1 were localized predominantly to the smooth muscle layer of the collateral arteries. The general MMP inhibitor doxycycline prevented luminal expansion of collateral arteries but did not affect the endothelial cell proliferative or medial growth responses. In conclusion, this study provides evidence that MMP-2 and MT1-MMP are upregulated in collateral arteries exposed to elevated shear stress and that MMP activity is essential for the full remodeling response that leads to outward luminal expansion.
matrix metalloproteinase; collateral artery; shear stress
Address for reprint requests and other correspondence: T. L. Haas, School of Kinesiology and Health Sciences, Rm. 341 Farquharson, York Univ., 4700 Keele St., Toronto, ON Canada M3J 1P3 (e-mail: thaas{at}yorku.ca )</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>17644578</pmid><doi>10.1152/ajpheart.00100.2007</doi></addata></record> |
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language | eng |
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source | MEDLINE; American Physiological Society; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
subjects | Animals Arteries - surgery Cell Proliferation Collateral Circulation Doxycycline - pharmacology Early Growth Response Protein 1 - metabolism Enzyme Activation Extracellular Matrix - metabolism Ileum - blood supply Ligation Male Matrix Metalloproteinase 14 - metabolism Matrix Metalloproteinase 2 - metabolism Matrix Metalloproteinase 9 - metabolism Matrix Metalloproteinases - metabolism Mesenteric Arteries - drug effects Mesenteric Arteries - enzymology Mesenteric Arteries - metabolism Mesenteric Arteries - pathology Mesenteric Arteries - physiopathology Models, Animal Protease Inhibitors - pharmacology Proteases Proto-Oncogene Proteins c-jun - metabolism Rats Rats, Wistar Shear stress Splanchnic Circulation Stress, Mechanical Studies Time Factors Tunica Intima - drug effects Tunica Intima - enzymology Tunica Intima - metabolism Tunica Intima - pathology Tunica Intima - physiopathology Up-Regulation Veins & arteries |
title | Involvement of MMPs in the outward remodeling of collateral mesenteric arteries |
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