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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Veröffentlicht in:American journal of physiology. Heart and circulatory physiology 2007-10, Vol.293 (4), p.H2429-H2437
Hauptverfasser: Haas, Tara L, Doyle, Jennifer L, Distasi, Matthew R, Norton, Laura E, Sheridan, Kevin M, Unthank, Joseph L
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container_issue 4
container_start_page H2429
container_title American journal of physiology. Heart and circulatory physiology
container_volume 293
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
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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. 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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. 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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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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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