TGF-beta- and CTGF-mediated fibroblast recruitment influences early outward vein graft remodeling
1 University of Florida College of Medicine and the Malcom Randall Veterans Affairs Medical Center, and 2 Department of Obstetrics and Gynecology University of Florida College of Medicine, Gainesville, Florida Submitted 15 December 2006 ; accepted in final form 16 March 2007 Luminal shearing forces...
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Veröffentlicht in: | American journal of physiology. Heart and circulatory physiology 2007-07, Vol.293 (1), p.H482-H488 |
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container_title | American journal of physiology. Heart and circulatory physiology |
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creator | Jiang, Zhihua Yu, Peng Tao, Ming Fernandez, Chessy Ifantides, Cristos Moloye, Olajompo Schultz, Gregory S Ozaki, C. Keith Berceli, Scott A |
description | 1 University of Florida College of Medicine and the Malcom Randall Veterans Affairs Medical Center, and 2 Department of Obstetrics and Gynecology University of Florida College of Medicine, Gainesville, Florida
Submitted 15 December 2006
; accepted in final form 16 March 2007
Luminal shearing forces have been shown to impact both geometric remodeling and the development of intimal hyperplasia. Less well studied is the influence of intramural wall stresses on vessel growth and adaptation. Using a vein graft-fistula configuration to isolate the impact of circumferential wall stress, we identify the reorganization of adventitial myofibroblasts as the dominant histological event that limits early outward remodeling of vein grafts in response to elevated wall stress. We hypothesize that increased production of transforming growth factor- (TGF- ) and connective tissue growth factor (CTGF) induces recruitment of myofibroblasts, promotes adventitial reorganization, and limits early outward remodeling in response to increased intramural wall stress. Vein grafts with a distal arteriovenous fistula in the neck of rabbits were constructed, resulting in a fourfold differential in circumferential wall stress. Using this model, we demonstrate 1 ) elevated wall stress augments the production of TGF- and CTGF, 2 ) increased TGF- expression and CTGF expression are correlated with the enhanced differentiation from fibroblasts to myofibroblasts, as evidenced by the significant increase in the -actin-positive cells in adventitia, and 3 ) the levels of TGF- , CTGF, and -actin are inversely correlated with the magnitude of outward remodeling of the graft wall. Increased wall stress after vein graft implantation appears to induce a TGF- - and CTGF-mediated recruitment of adventitial fibroblasts and a conversion to a myofibroblast phenotype. Although important in the maintenance of wall stability in the face of an increased mechanical load, this adventitial adaptation limits early outward remodeling of the vein conduit and may prove deleterious in maintaining long-term vein graft patency.
connective tissue growth factor; transforming growth factor- ; vascular remodeling; hemodynamics; wall stress
Address for reprint requests and other correspondence: S. A. Berceli, PO Box 100286, Gainesville, FL 32610-0286 (e-mail: bercesa{at}surgery.ufl.edu ) |
doi_str_mv | 10.1152/ajpheart.01372.2006 |
format | Article |
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Submitted 15 December 2006
; accepted in final form 16 March 2007
Luminal shearing forces have been shown to impact both geometric remodeling and the development of intimal hyperplasia. Less well studied is the influence of intramural wall stresses on vessel growth and adaptation. Using a vein graft-fistula configuration to isolate the impact of circumferential wall stress, we identify the reorganization of adventitial myofibroblasts as the dominant histological event that limits early outward remodeling of vein grafts in response to elevated wall stress. We hypothesize that increased production of transforming growth factor- (TGF- ) and connective tissue growth factor (CTGF) induces recruitment of myofibroblasts, promotes adventitial reorganization, and limits early outward remodeling in response to increased intramural wall stress. Vein grafts with a distal arteriovenous fistula in the neck of rabbits were constructed, resulting in a fourfold differential in circumferential wall stress. Using this model, we demonstrate 1 ) elevated wall stress augments the production of TGF- and CTGF, 2 ) increased TGF- expression and CTGF expression are correlated with the enhanced differentiation from fibroblasts to myofibroblasts, as evidenced by the significant increase in the -actin-positive cells in adventitia, and 3 ) the levels of TGF- , CTGF, and -actin are inversely correlated with the magnitude of outward remodeling of the graft wall. Increased wall stress after vein graft implantation appears to induce a TGF- - and CTGF-mediated recruitment of adventitial fibroblasts and a conversion to a myofibroblast phenotype. Although important in the maintenance of wall stability in the face of an increased mechanical load, this adventitial adaptation limits early outward remodeling of the vein conduit and may prove deleterious in maintaining long-term vein graft patency.
connective tissue growth factor; transforming growth factor- ; vascular remodeling; hemodynamics; wall stress
Address for reprint requests and other correspondence: S. A. Berceli, PO Box 100286, Gainesville, FL 32610-0286 (e-mail: bercesa{at}surgery.ufl.edu )</description><identifier>ISSN: 0363-6135</identifier><identifier>EISSN: 1522-1539</identifier><identifier>DOI: 10.1152/ajpheart.01372.2006</identifier><identifier>PMID: 17369455</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Cell Movement ; Connective Tissue Growth Factor ; Fibroblasts - cytology ; Fibroblasts - metabolism ; Graft Survival - physiology ; Immediate-Early Proteins - metabolism ; Intercellular Signaling Peptides and Proteins - metabolism ; Jugular Veins - cytology ; Jugular Veins - metabolism ; Jugular Veins - transplantation ; Male ; Rabbits ; Transforming Growth Factor beta - metabolism</subject><ispartof>American journal of physiology. Heart and circulatory physiology, 2007-07, Vol.293 (1), p.H482-H488</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c393t-8c05f0a6c56dc5a4b9f0b710f3e3191ad652fca0f6367a41472ff730aef723a83</citedby><cites>FETCH-LOGICAL-c393t-8c05f0a6c56dc5a4b9f0b710f3e3191ad652fca0f6367a41472ff730aef723a83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3039,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17369455$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jiang, Zhihua</creatorcontrib><creatorcontrib>Yu, Peng</creatorcontrib><creatorcontrib>Tao, Ming</creatorcontrib><creatorcontrib>Fernandez, Chessy</creatorcontrib><creatorcontrib>Ifantides, Cristos</creatorcontrib><creatorcontrib>Moloye, Olajompo</creatorcontrib><creatorcontrib>Schultz, Gregory S</creatorcontrib><creatorcontrib>Ozaki, C. Keith</creatorcontrib><creatorcontrib>Berceli, Scott A</creatorcontrib><title>TGF-beta- and CTGF-mediated fibroblast recruitment influences early outward vein graft remodeling</title><title>American journal of physiology. Heart and circulatory physiology</title><addtitle>Am J Physiol Heart Circ Physiol</addtitle><description>1 University of Florida College of Medicine and the Malcom Randall Veterans Affairs Medical Center, and 2 Department of Obstetrics and Gynecology University of Florida College of Medicine, Gainesville, Florida
Submitted 15 December 2006
; accepted in final form 16 March 2007
Luminal shearing forces have been shown to impact both geometric remodeling and the development of intimal hyperplasia. Less well studied is the influence of intramural wall stresses on vessel growth and adaptation. Using a vein graft-fistula configuration to isolate the impact of circumferential wall stress, we identify the reorganization of adventitial myofibroblasts as the dominant histological event that limits early outward remodeling of vein grafts in response to elevated wall stress. We hypothesize that increased production of transforming growth factor- (TGF- ) and connective tissue growth factor (CTGF) induces recruitment of myofibroblasts, promotes adventitial reorganization, and limits early outward remodeling in response to increased intramural wall stress. Vein grafts with a distal arteriovenous fistula in the neck of rabbits were constructed, resulting in a fourfold differential in circumferential wall stress. Using this model, we demonstrate 1 ) elevated wall stress augments the production of TGF- and CTGF, 2 ) increased TGF- expression and CTGF expression are correlated with the enhanced differentiation from fibroblasts to myofibroblasts, as evidenced by the significant increase in the -actin-positive cells in adventitia, and 3 ) the levels of TGF- , CTGF, and -actin are inversely correlated with the magnitude of outward remodeling of the graft wall. Increased wall stress after vein graft implantation appears to induce a TGF- - and CTGF-mediated recruitment of adventitial fibroblasts and a conversion to a myofibroblast phenotype. Although important in the maintenance of wall stability in the face of an increased mechanical load, this adventitial adaptation limits early outward remodeling of the vein conduit and may prove deleterious in maintaining long-term vein graft patency.
connective tissue growth factor; transforming growth factor- ; vascular remodeling; hemodynamics; wall stress
Address for reprint requests and other correspondence: S. A. Berceli, PO Box 100286, Gainesville, FL 32610-0286 (e-mail: bercesa{at}surgery.ufl.edu )</description><subject>Animals</subject><subject>Cell Movement</subject><subject>Connective Tissue Growth Factor</subject><subject>Fibroblasts - cytology</subject><subject>Fibroblasts - metabolism</subject><subject>Graft Survival - physiology</subject><subject>Immediate-Early Proteins - metabolism</subject><subject>Intercellular Signaling Peptides and Proteins - metabolism</subject><subject>Jugular Veins - cytology</subject><subject>Jugular Veins - metabolism</subject><subject>Jugular Veins - transplantation</subject><subject>Male</subject><subject>Rabbits</subject><subject>Transforming Growth Factor beta - metabolism</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>eNp1kMtu2zAQRYmiQeOm_YIChVbdySE1Iml1Vxh1UiBANu6aGElDmwH1KEk19d9Hjt1klRUx4Ll3BoexL4IvhZDFNT6Me8KQllyALpYF5-odW8w_RS4kVO_ZgoOCXAmQl-xjjA-cc6kVfGCXQoOqSikXDLc3m7ymhHmGfZutj2NHrcNEbWZdHYbaY0xZoCZMLnXUp8z11k_UNxSzeb8_ZMOUHjG02V9yfbYLaI98N7TkXb_7xC4s-kifz-8V-735uV3f5nf3N7_WP-7yBipI-arh0nJUjVRtI7GsK8trLbgFAlEJbJUsbIPcKlAaS1HqwloNHMnqAnAFV-zbqXcMw5-JYjKdiw15jz0NUzSaa77iCmYQTmAThhgDWTMG12E4GMHN0az5b9Y8mzVHs3Pq67l-qmdBr5mzyhn4fgL2brd_dIHMuD9EN_hhdzCbyfst_Usv1UUFRpjbclWYsbVzePl2-OWc1xA8AWBwnXU</recordid><startdate>20070701</startdate><enddate>20070701</enddate><creator>Jiang, Zhihua</creator><creator>Yu, Peng</creator><creator>Tao, Ming</creator><creator>Fernandez, Chessy</creator><creator>Ifantides, Cristos</creator><creator>Moloye, Olajompo</creator><creator>Schultz, Gregory S</creator><creator>Ozaki, C. 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Keith ; Berceli, Scott A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c393t-8c05f0a6c56dc5a4b9f0b710f3e3191ad652fca0f6367a41472ff730aef723a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Cell Movement</topic><topic>Connective Tissue Growth Factor</topic><topic>Fibroblasts - cytology</topic><topic>Fibroblasts - metabolism</topic><topic>Graft Survival - physiology</topic><topic>Immediate-Early Proteins - metabolism</topic><topic>Intercellular Signaling Peptides and Proteins - metabolism</topic><topic>Jugular Veins - cytology</topic><topic>Jugular Veins - metabolism</topic><topic>Jugular Veins - transplantation</topic><topic>Male</topic><topic>Rabbits</topic><topic>Transforming Growth Factor beta - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jiang, Zhihua</creatorcontrib><creatorcontrib>Yu, Peng</creatorcontrib><creatorcontrib>Tao, Ming</creatorcontrib><creatorcontrib>Fernandez, Chessy</creatorcontrib><creatorcontrib>Ifantides, Cristos</creatorcontrib><creatorcontrib>Moloye, Olajompo</creatorcontrib><creatorcontrib>Schultz, Gregory S</creatorcontrib><creatorcontrib>Ozaki, C. 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Heart and circulatory physiology</jtitle><addtitle>Am J Physiol Heart Circ Physiol</addtitle><date>2007-07-01</date><risdate>2007</risdate><volume>293</volume><issue>1</issue><spage>H482</spage><epage>H488</epage><pages>H482-H488</pages><issn>0363-6135</issn><eissn>1522-1539</eissn><abstract>1 University of Florida College of Medicine and the Malcom Randall Veterans Affairs Medical Center, and 2 Department of Obstetrics and Gynecology University of Florida College of Medicine, Gainesville, Florida
Submitted 15 December 2006
; accepted in final form 16 March 2007
Luminal shearing forces have been shown to impact both geometric remodeling and the development of intimal hyperplasia. Less well studied is the influence of intramural wall stresses on vessel growth and adaptation. Using a vein graft-fistula configuration to isolate the impact of circumferential wall stress, we identify the reorganization of adventitial myofibroblasts as the dominant histological event that limits early outward remodeling of vein grafts in response to elevated wall stress. We hypothesize that increased production of transforming growth factor- (TGF- ) and connective tissue growth factor (CTGF) induces recruitment of myofibroblasts, promotes adventitial reorganization, and limits early outward remodeling in response to increased intramural wall stress. Vein grafts with a distal arteriovenous fistula in the neck of rabbits were constructed, resulting in a fourfold differential in circumferential wall stress. Using this model, we demonstrate 1 ) elevated wall stress augments the production of TGF- and CTGF, 2 ) increased TGF- expression and CTGF expression are correlated with the enhanced differentiation from fibroblasts to myofibroblasts, as evidenced by the significant increase in the -actin-positive cells in adventitia, and 3 ) the levels of TGF- , CTGF, and -actin are inversely correlated with the magnitude of outward remodeling of the graft wall. Increased wall stress after vein graft implantation appears to induce a TGF- - and CTGF-mediated recruitment of adventitial fibroblasts and a conversion to a myofibroblast phenotype. Although important in the maintenance of wall stability in the face of an increased mechanical load, this adventitial adaptation limits early outward remodeling of the vein conduit and may prove deleterious in maintaining long-term vein graft patency.
connective tissue growth factor; transforming growth factor- ; vascular remodeling; hemodynamics; wall stress
Address for reprint requests and other correspondence: S. A. Berceli, PO Box 100286, Gainesville, FL 32610-0286 (e-mail: bercesa{at}surgery.ufl.edu )</abstract><cop>United States</cop><pmid>17369455</pmid><doi>10.1152/ajpheart.01372.2006</doi></addata></record> |
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source | MEDLINE; American Physiological Society Paid; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Animals Cell Movement Connective Tissue Growth Factor Fibroblasts - cytology Fibroblasts - metabolism Graft Survival - physiology Immediate-Early Proteins - metabolism Intercellular Signaling Peptides and Proteins - metabolism Jugular Veins - cytology Jugular Veins - metabolism Jugular Veins - transplantation Male Rabbits Transforming Growth Factor beta - metabolism |
title | TGF-beta- and CTGF-mediated fibroblast recruitment influences early outward vein graft remodeling |
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