Differential involvement of MMP-2 and VEGF during muscle stretch- versus shear stress-induced angiogenesis
1 Department of Kinesiology and Health Sciences, York University, Toronto, Ontario, Canada M3J 1P3; 2 Department of Physiology, University of Birmingham, Birmingham, United Kingdom B15 2TT; and 3 Department of Biological Sciences, Oakland University, Rochester, Michigan 48309-4401 Capillary growt...
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Veröffentlicht in: | American journal of physiology. Heart and circulatory physiology 2002-10, Vol.283 (4), p.H1430-H1438 |
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container_title | American journal of physiology. Heart and circulatory physiology |
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creator | Rivilis, Irina Milkiewicz, Malgorzata Boyd, Pamela Goldstein, Jason Brown, Margaret D Egginton, Stuart Hansen, Fay M Hudlicka, Olga Haas, Tara L |
description | 1 Department of Kinesiology and Health Sciences,
York University, Toronto, Ontario, Canada M3J 1P3;
2 Department of Physiology, University of
Birmingham, Birmingham, United Kingdom B15 2TT; and
3 Department of Biological Sciences, Oakland
University, Rochester, Michigan 48309-4401
Capillary growth in skeletal
muscle occurs via the dissimilar processes of abluminal sprouting or
longitudinal splitting, which can be initiated by muscle stretch and
elevated shear stress, respectively. The distinct morphological
hallmarks of these types of capillary growth suggest that discrete sets
of angiogenic mediators play a role in each situation. Because
proteolysis and proliferation are two key steps associated with
capillary growth, we tested whether differences in the regulation of
matrix metalloproteinases (MMPs) or VEGF may be associated with the two
types of capillary growth. We found significant increases in MMP-2
total protein and percent activation, and membrane type-1 MMP mRNA
levels, compared with controls after muscle stretch but not after shear
stress stimulation. In contrast, VEGF protein and endothelial
cell proliferation increased after either angiogenic stimulus. We
observed that MMP-2 regulation occurs independent of VEGF signaling,
because VEGF did not induce MMP-2 production or activation in isolated
endothelial cells. Our data suggest that the involvement of MMPs in
capillary growth is dependent on the nature of the angiogenic stimulus.
matrix metalloproteinase |
doi_str_mv | 10.1152/ajpheart.00082.2002 |
format | Article |
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York University, Toronto, Ontario, Canada M3J 1P3;
2 Department of Physiology, University of
Birmingham, Birmingham, United Kingdom B15 2TT; and
3 Department of Biological Sciences, Oakland
University, Rochester, Michigan 48309-4401
Capillary growth in skeletal
muscle occurs via the dissimilar processes of abluminal sprouting or
longitudinal splitting, which can be initiated by muscle stretch and
elevated shear stress, respectively. The distinct morphological
hallmarks of these types of capillary growth suggest that discrete sets
of angiogenic mediators play a role in each situation. Because
proteolysis and proliferation are two key steps associated with
capillary growth, we tested whether differences in the regulation of
matrix metalloproteinases (MMPs) or VEGF may be associated with the two
types of capillary growth. We found significant increases in MMP-2
total protein and percent activation, and membrane type-1 MMP mRNA
levels, compared with controls after muscle stretch but not after shear
stress stimulation. In contrast, VEGF protein and endothelial
cell proliferation increased after either angiogenic stimulus. We
observed that MMP-2 regulation occurs independent of VEGF signaling,
because VEGF did not induce MMP-2 production or activation in isolated
endothelial cells. Our data suggest that the involvement of MMPs in
capillary growth is dependent on the nature of the angiogenic stimulus.
matrix metalloproteinase</description><identifier>ISSN: 0363-6135</identifier><identifier>EISSN: 1522-1539</identifier><identifier>DOI: 10.1152/ajpheart.00082.2002</identifier><identifier>PMID: 12234794</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Antihypertensive Agents - pharmacology ; Capillaries - drug effects ; Capillaries - physiology ; Cells, Cultured ; Endothelial Growth Factors - metabolism ; Lymphokines - metabolism ; Male ; Matrix Metalloproteinase 2 - metabolism ; Matrix Metalloproteinases, Membrane-Associated ; Metalloendopeptidases - genetics ; Muscle Contraction - physiology ; Muscle Fibers, Skeletal - cytology ; Muscle Fibers, Skeletal - enzymology ; Muscle, Skeletal - blood supply ; Muscle, Skeletal - physiology ; Neovascularization, Physiologic - physiology ; Prazosin - pharmacology ; Rats ; Rats, Sprague-Dawley ; RNA, Messenger - analysis ; Stress, Mechanical ; Vascular Endothelial Growth Factor A ; Vascular Endothelial Growth Factors</subject><ispartof>American journal of physiology. Heart and circulatory physiology, 2002-10, Vol.283 (4), p.H1430-H1438</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c459t-8b0880adba2deb3dac97985fc3036286849b462cf8d64a88aad56a82517d4a3a3</citedby><cites>FETCH-LOGICAL-c459t-8b0880adba2deb3dac97985fc3036286849b462cf8d64a88aad56a82517d4a3a3</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/12234794$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rivilis, Irina</creatorcontrib><creatorcontrib>Milkiewicz, Malgorzata</creatorcontrib><creatorcontrib>Boyd, Pamela</creatorcontrib><creatorcontrib>Goldstein, Jason</creatorcontrib><creatorcontrib>Brown, Margaret D</creatorcontrib><creatorcontrib>Egginton, Stuart</creatorcontrib><creatorcontrib>Hansen, Fay M</creatorcontrib><creatorcontrib>Hudlicka, Olga</creatorcontrib><creatorcontrib>Haas, Tara L</creatorcontrib><title>Differential involvement of MMP-2 and VEGF during muscle stretch- versus shear stress-induced angiogenesis</title><title>American journal of physiology. Heart and circulatory physiology</title><addtitle>Am J Physiol Heart Circ Physiol</addtitle><description>1 Department of Kinesiology and Health Sciences,
York University, Toronto, Ontario, Canada M3J 1P3;
2 Department of Physiology, University of
Birmingham, Birmingham, United Kingdom B15 2TT; and
3 Department of Biological Sciences, Oakland
University, Rochester, Michigan 48309-4401
Capillary growth in skeletal
muscle occurs via the dissimilar processes of abluminal sprouting or
longitudinal splitting, which can be initiated by muscle stretch and
elevated shear stress, respectively. The distinct morphological
hallmarks of these types of capillary growth suggest that discrete sets
of angiogenic mediators play a role in each situation. Because
proteolysis and proliferation are two key steps associated with
capillary growth, we tested whether differences in the regulation of
matrix metalloproteinases (MMPs) or VEGF may be associated with the two
types of capillary growth. We found significant increases in MMP-2
total protein and percent activation, and membrane type-1 MMP mRNA
levels, compared with controls after muscle stretch but not after shear
stress stimulation. In contrast, VEGF protein and endothelial
cell proliferation increased after either angiogenic stimulus. We
observed that MMP-2 regulation occurs independent of VEGF signaling,
because VEGF did not induce MMP-2 production or activation in isolated
endothelial cells. Our data suggest that the involvement of MMPs in
capillary growth is dependent on the nature of the angiogenic stimulus.
matrix metalloproteinase</description><subject>Animals</subject><subject>Antihypertensive Agents - pharmacology</subject><subject>Capillaries - drug effects</subject><subject>Capillaries - physiology</subject><subject>Cells, Cultured</subject><subject>Endothelial Growth Factors - metabolism</subject><subject>Lymphokines - metabolism</subject><subject>Male</subject><subject>Matrix Metalloproteinase 2 - metabolism</subject><subject>Matrix Metalloproteinases, Membrane-Associated</subject><subject>Metalloendopeptidases - genetics</subject><subject>Muscle Contraction - physiology</subject><subject>Muscle Fibers, Skeletal - cytology</subject><subject>Muscle Fibers, Skeletal - enzymology</subject><subject>Muscle, Skeletal - blood supply</subject><subject>Muscle, Skeletal - physiology</subject><subject>Neovascularization, Physiologic - physiology</subject><subject>Prazosin - pharmacology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>RNA, Messenger - analysis</subject><subject>Stress, Mechanical</subject><subject>Vascular Endothelial Growth Factor A</subject><subject>Vascular Endothelial Growth Factors</subject><issn>0363-6135</issn><issn>1522-1539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM1u1DAUhS0EosPAEyAhr9hl6t_EEStUOi1SK1gUtpYT3yQeOT_YycC8PZ7OQNmwsmyf7-jeD6G3lGwolezS7KYOTJg3hBDFNowQ9gyt0g_LqOTlc7QiPOdZTrm8QK9i3KWcLHL-El1QxrgoSrFCu0-uaSDAMDvjsRv2o99Dn654bPD9_deMYTNY_P36ZovtEtzQ4n6JtQcc5wBz3WV4DyEuEcfjMI-vMWZusEsNNrGtG1sYILr4Gr1ojI_w5nyu0bft9cPVbXb35ebz1ce7rBaynDNVEaWIsZVhFipuTV0WpZJNzdM6TOVKlJXIWd0omwujlDFW5kYxSQsrDDd8jd6feqcw_lggzrp3sQbvzQDjEnXBSCkkKVOQn4J1GGMM0OgpuN6Eg6ZEHxXrP4r1o2J9VJyod-f6perBPjFnpylweQp0ru1-ugB66g7RjX5sD0-NTHEt9C0Vaa01-vB_Yrt4_wC_5r_oP6SebMN_A7deoQs</recordid><startdate>20021001</startdate><enddate>20021001</enddate><creator>Rivilis, Irina</creator><creator>Milkiewicz, Malgorzata</creator><creator>Boyd, Pamela</creator><creator>Goldstein, Jason</creator><creator>Brown, Margaret D</creator><creator>Egginton, Stuart</creator><creator>Hansen, Fay M</creator><creator>Hudlicka, Olga</creator><creator>Haas, Tara L</creator><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>20021001</creationdate><title>Differential involvement of MMP-2 and VEGF during muscle stretch- versus shear stress-induced angiogenesis</title><author>Rivilis, Irina ; Milkiewicz, Malgorzata ; Boyd, Pamela ; Goldstein, Jason ; Brown, Margaret D ; Egginton, Stuart ; Hansen, Fay M ; Hudlicka, Olga ; Haas, Tara L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c459t-8b0880adba2deb3dac97985fc3036286849b462cf8d64a88aad56a82517d4a3a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Animals</topic><topic>Antihypertensive Agents - pharmacology</topic><topic>Capillaries - drug effects</topic><topic>Capillaries - physiology</topic><topic>Cells, Cultured</topic><topic>Endothelial Growth Factors - metabolism</topic><topic>Lymphokines - metabolism</topic><topic>Male</topic><topic>Matrix Metalloproteinase 2 - metabolism</topic><topic>Matrix Metalloproteinases, Membrane-Associated</topic><topic>Metalloendopeptidases - genetics</topic><topic>Muscle Contraction - physiology</topic><topic>Muscle Fibers, Skeletal - cytology</topic><topic>Muscle Fibers, Skeletal - enzymology</topic><topic>Muscle, Skeletal - blood supply</topic><topic>Muscle, Skeletal - physiology</topic><topic>Neovascularization, Physiologic - physiology</topic><topic>Prazosin - pharmacology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>RNA, Messenger - analysis</topic><topic>Stress, Mechanical</topic><topic>Vascular Endothelial Growth Factor A</topic><topic>Vascular Endothelial Growth Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rivilis, Irina</creatorcontrib><creatorcontrib>Milkiewicz, Malgorzata</creatorcontrib><creatorcontrib>Boyd, Pamela</creatorcontrib><creatorcontrib>Goldstein, Jason</creatorcontrib><creatorcontrib>Brown, Margaret D</creatorcontrib><creatorcontrib>Egginton, Stuart</creatorcontrib><creatorcontrib>Hansen, Fay M</creatorcontrib><creatorcontrib>Hudlicka, Olga</creatorcontrib><creatorcontrib>Haas, Tara 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>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>Rivilis, Irina</au><au>Milkiewicz, Malgorzata</au><au>Boyd, Pamela</au><au>Goldstein, Jason</au><au>Brown, Margaret D</au><au>Egginton, Stuart</au><au>Hansen, Fay M</au><au>Hudlicka, Olga</au><au>Haas, Tara L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential involvement of MMP-2 and VEGF during muscle stretch- versus shear stress-induced angiogenesis</atitle><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle><addtitle>Am J Physiol Heart Circ Physiol</addtitle><date>2002-10-01</date><risdate>2002</risdate><volume>283</volume><issue>4</issue><spage>H1430</spage><epage>H1438</epage><pages>H1430-H1438</pages><issn>0363-6135</issn><eissn>1522-1539</eissn><abstract>1 Department of Kinesiology and Health Sciences,
York University, Toronto, Ontario, Canada M3J 1P3;
2 Department of Physiology, University of
Birmingham, Birmingham, United Kingdom B15 2TT; and
3 Department of Biological Sciences, Oakland
University, Rochester, Michigan 48309-4401
Capillary growth in skeletal
muscle occurs via the dissimilar processes of abluminal sprouting or
longitudinal splitting, which can be initiated by muscle stretch and
elevated shear stress, respectively. The distinct morphological
hallmarks of these types of capillary growth suggest that discrete sets
of angiogenic mediators play a role in each situation. Because
proteolysis and proliferation are two key steps associated with
capillary growth, we tested whether differences in the regulation of
matrix metalloproteinases (MMPs) or VEGF may be associated with the two
types of capillary growth. We found significant increases in MMP-2
total protein and percent activation, and membrane type-1 MMP mRNA
levels, compared with controls after muscle stretch but not after shear
stress stimulation. In contrast, VEGF protein and endothelial
cell proliferation increased after either angiogenic stimulus. We
observed that MMP-2 regulation occurs independent of VEGF signaling,
because VEGF did not induce MMP-2 production or activation in isolated
endothelial cells. Our data suggest that the involvement of MMPs in
capillary growth is dependent on the nature of the angiogenic stimulus.
matrix metalloproteinase</abstract><cop>United States</cop><pmid>12234794</pmid><doi>10.1152/ajpheart.00082.2002</doi></addata></record> |
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identifier | ISSN: 0363-6135 |
ispartof | American journal of physiology. Heart and circulatory physiology, 2002-10, Vol.283 (4), p.H1430-H1438 |
issn | 0363-6135 1522-1539 |
language | eng |
recordid | cdi_pubmed_primary_12234794 |
source | MEDLINE; American Physiological Society; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | Animals Antihypertensive Agents - pharmacology Capillaries - drug effects Capillaries - physiology Cells, Cultured Endothelial Growth Factors - metabolism Lymphokines - metabolism Male Matrix Metalloproteinase 2 - metabolism Matrix Metalloproteinases, Membrane-Associated Metalloendopeptidases - genetics Muscle Contraction - physiology Muscle Fibers, Skeletal - cytology Muscle Fibers, Skeletal - enzymology Muscle, Skeletal - blood supply Muscle, Skeletal - physiology Neovascularization, Physiologic - physiology Prazosin - pharmacology Rats Rats, Sprague-Dawley RNA, Messenger - analysis Stress, Mechanical Vascular Endothelial Growth Factor A Vascular Endothelial Growth Factors |
title | Differential involvement of MMP-2 and VEGF during muscle stretch- versus shear stress-induced angiogenesis |
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