Endothelial cell activation by hemodynamic shear stress derived from arteriovenous fistula for hemodialysis access
Intimal hyperplasia (IH) is the first cause of failure of an arteriovenous fistula (AVF). The aim of the present study was to investigate the effects on endothelial cells (ECs) of shear stress waveforms derived from AVF areas prone to develop IH. We used a cone-and-plate device to obtain real-time c...
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Veröffentlicht in: | American journal of physiology. Heart and circulatory physiology 2016-01, Vol.310 (1), p.H49-H59 |
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description | Intimal hyperplasia (IH) is the first cause of failure of an arteriovenous fistula (AVF). The aim of the present study was to investigate the effects on endothelial cells (ECs) of shear stress waveforms derived from AVF areas prone to develop IH. We used a cone-and-plate device to obtain real-time control of shear stress acting on EC cultures. We exposed human umbilical vein ECs for 48 h to different shear stimulations calculated in a side-to-end AVF model. Pulsatile unidirectional flow, representative of low-risk stenosis areas, induced alignment of ECs and actin fiber orientation with flow. Shear stress patterns of reciprocating flow, derived from high-risk stenosis areas, did not affect EC shape or cytoskeleton organization, which remained similar to static cultures. We also evaluated flow-induced EC expression of genes known to be involved in cytoskeletal remodeling and expression of cell adhesion molecules. Unidirectional flow induced a significant increase in Kruppel-like factor 2 mRNA expression, whereas it significantly reduced phospholipase D1, α4-integrin, and Ras p21 protein activator 1 mRNA expression. Reciprocating flow did not increase Kruppel-like factor 2 mRNA expression compared with static controls but significantly increased mRNA expression of phospholipase D1, α4-integrin, and Ras p21 protein activator 1. Reciprocating flow selectively increased monocyte chemoattractant protein-1 and IL-8 production. Furthermore, culture medium conditioned by ECs exposed to reciprocating flows selectively increased smooth muscle cell proliferation compared with unidirectional flow. Our results indicate that protective vascular effects induced in ECs by unidirectional pulsatile flow are not induced by reciprocating shear forces, suggesting a mechanism by which oscillating flow conditions may induce the development of IH in AVF and vascular access dysfunction. |
doi_str_mv | 10.1152/ajpheart.00098.2015 |
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The aim of the present study was to investigate the effects on endothelial cells (ECs) of shear stress waveforms derived from AVF areas prone to develop IH. We used a cone-and-plate device to obtain real-time control of shear stress acting on EC cultures. We exposed human umbilical vein ECs for 48 h to different shear stimulations calculated in a side-to-end AVF model. Pulsatile unidirectional flow, representative of low-risk stenosis areas, induced alignment of ECs and actin fiber orientation with flow. Shear stress patterns of reciprocating flow, derived from high-risk stenosis areas, did not affect EC shape or cytoskeleton organization, which remained similar to static cultures. We also evaluated flow-induced EC expression of genes known to be involved in cytoskeletal remodeling and expression of cell adhesion molecules. Unidirectional flow induced a significant increase in Kruppel-like factor 2 mRNA expression, whereas it significantly reduced phospholipase D1, α4-integrin, and Ras p21 protein activator 1 mRNA expression. Reciprocating flow did not increase Kruppel-like factor 2 mRNA expression compared with static controls but significantly increased mRNA expression of phospholipase D1, α4-integrin, and Ras p21 protein activator 1. Reciprocating flow selectively increased monocyte chemoattractant protein-1 and IL-8 production. Furthermore, culture medium conditioned by ECs exposed to reciprocating flows selectively increased smooth muscle cell proliferation compared with unidirectional flow. Our results indicate that protective vascular effects induced in ECs by unidirectional pulsatile flow are not induced by reciprocating shear forces, suggesting a mechanism by which oscillating flow conditions may induce the development of IH in AVF and vascular access dysfunction.</description><identifier>ISSN: 0363-6135</identifier><identifier>EISSN: 1522-1539</identifier><identifier>DOI: 10.1152/ajpheart.00098.2015</identifier><identifier>PMID: 26497959</identifier><identifier>CODEN: AJPPDI</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Actin Cytoskeleton - metabolism ; Arteriovenous Shunt, Surgical - adverse effects ; Cell adhesion & migration ; Cell Proliferation ; Cell Shape ; Cells, Cultured ; Culture Media, Conditioned - metabolism ; Cytokines - genetics ; Cytokines - metabolism ; Endothelium ; Gene expression ; Gene Expression Regulation ; Heart failure ; Hemodialysis ; Hemodynamics ; Human Umbilical Vein Endothelial Cells - metabolism ; Human Umbilical Vein Endothelial Cells - pathology ; Humans ; Hyperplasia ; Mechanotransduction, Cellular ; Molecules ; Myocytes, Smooth Muscle - metabolism ; Myocytes, Smooth Muscle - pathology ; Paracrine Communication ; Pulsatile Flow ; Renal Dialysis ; RNA, Messenger - metabolism ; Shear stress ; Signal Transduction ; Stress, Mechanical ; Time Factors</subject><ispartof>American journal of physiology. Heart and circulatory physiology, 2016-01, Vol.310 (1), p.H49-H59</ispartof><rights>Copyright © 2016 the American Physiological Society.</rights><rights>Copyright American Physiological Society Jan 1, 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c399t-1b94928870881b5ea80cbbcf1594f11b452cdfa72b648d04865150cbad0d625f3</citedby><cites>FETCH-LOGICAL-c399t-1b94928870881b5ea80cbbcf1594f11b452cdfa72b648d04865150cbad0d625f3</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/26497959$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Franzoni, Marco</creatorcontrib><creatorcontrib>Cattaneo, Irene</creatorcontrib><creatorcontrib>Longaretti, Lorena</creatorcontrib><creatorcontrib>Figliuzzi, Marina</creatorcontrib><creatorcontrib>Ene-Iordache, Bogdan</creatorcontrib><creatorcontrib>Remuzzi, Andrea</creatorcontrib><title>Endothelial cell activation by hemodynamic shear stress derived from arteriovenous fistula for hemodialysis access</title><title>American journal of physiology. Heart and circulatory physiology</title><addtitle>Am J Physiol Heart Circ Physiol</addtitle><description>Intimal hyperplasia (IH) is the first cause of failure of an arteriovenous fistula (AVF). The aim of the present study was to investigate the effects on endothelial cells (ECs) of shear stress waveforms derived from AVF areas prone to develop IH. We used a cone-and-plate device to obtain real-time control of shear stress acting on EC cultures. We exposed human umbilical vein ECs for 48 h to different shear stimulations calculated in a side-to-end AVF model. Pulsatile unidirectional flow, representative of low-risk stenosis areas, induced alignment of ECs and actin fiber orientation with flow. Shear stress patterns of reciprocating flow, derived from high-risk stenosis areas, did not affect EC shape or cytoskeleton organization, which remained similar to static cultures. We also evaluated flow-induced EC expression of genes known to be involved in cytoskeletal remodeling and expression of cell adhesion molecules. Unidirectional flow induced a significant increase in Kruppel-like factor 2 mRNA expression, whereas it significantly reduced phospholipase D1, α4-integrin, and Ras p21 protein activator 1 mRNA expression. Reciprocating flow did not increase Kruppel-like factor 2 mRNA expression compared with static controls but significantly increased mRNA expression of phospholipase D1, α4-integrin, and Ras p21 protein activator 1. Reciprocating flow selectively increased monocyte chemoattractant protein-1 and IL-8 production. Furthermore, culture medium conditioned by ECs exposed to reciprocating flows selectively increased smooth muscle cell proliferation compared with unidirectional flow. Our results indicate that protective vascular effects induced in ECs by unidirectional pulsatile flow are not induced by reciprocating shear forces, suggesting a mechanism by which oscillating flow conditions may induce the development of IH in AVF and vascular access dysfunction.</description><subject>Actin Cytoskeleton - metabolism</subject><subject>Arteriovenous Shunt, Surgical - adverse effects</subject><subject>Cell adhesion & migration</subject><subject>Cell Proliferation</subject><subject>Cell Shape</subject><subject>Cells, Cultured</subject><subject>Culture Media, Conditioned - metabolism</subject><subject>Cytokines - genetics</subject><subject>Cytokines - metabolism</subject><subject>Endothelium</subject><subject>Gene expression</subject><subject>Gene Expression Regulation</subject><subject>Heart failure</subject><subject>Hemodialysis</subject><subject>Hemodynamics</subject><subject>Human Umbilical Vein Endothelial Cells - metabolism</subject><subject>Human Umbilical Vein Endothelial Cells - pathology</subject><subject>Humans</subject><subject>Hyperplasia</subject><subject>Mechanotransduction, Cellular</subject><subject>Molecules</subject><subject>Myocytes, Smooth Muscle - metabolism</subject><subject>Myocytes, Smooth Muscle - pathology</subject><subject>Paracrine Communication</subject><subject>Pulsatile Flow</subject><subject>Renal Dialysis</subject><subject>RNA, Messenger - metabolism</subject><subject>Shear stress</subject><subject>Signal Transduction</subject><subject>Stress, Mechanical</subject><subject>Time Factors</subject><issn>0363-6135</issn><issn>1522-1539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkV1LwzAYhYMobk5_gSABb7zpzEeTNpcy5gcMvNHrkuaDZbTNTNpB_72pc154FUKec97z5gBwi9ESY0Ye5W6_NTL0S4SQKJcEYXYG5umFZJhRcQ7miHKacUzZDFzFuEscKzi9BDPCc1EIJuYgrDvt-61pnGygMk0DperdQfbOd7Ae4da0Xo-dbJ2CcRoHYx9MjFCb4A5GQxt8C1OKdPUH0_khQutiPzQSWh-O-uQ9RheTtUrSa3BhZRPNze-5AJ_P64_Va7Z5f3lbPW0yRYXoM1yLXJCyLFBZ4poZWSJV18piJnKLcZ0zorSVBal5XmqUl5xhlhCpkeaEWboAD0ffffBfg4l91bo4rSg7k2JWuGAU4TRBJPT-H7rzQ-hSuonijOTpxxJFj5QKPsZgbLUPrpVhrDCqpkqqUyXVTyXVVElS3f16D3Vr9J_m1AH9BuNui2w</recordid><startdate>20160101</startdate><enddate>20160101</enddate><creator>Franzoni, Marco</creator><creator>Cattaneo, Irene</creator><creator>Longaretti, Lorena</creator><creator>Figliuzzi, Marina</creator><creator>Ene-Iordache, Bogdan</creator><creator>Remuzzi, Andrea</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>20160101</creationdate><title>Endothelial cell activation by hemodynamic shear stress derived from arteriovenous fistula for hemodialysis access</title><author>Franzoni, Marco ; Cattaneo, Irene ; Longaretti, Lorena ; Figliuzzi, Marina ; Ene-Iordache, Bogdan ; Remuzzi, Andrea</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c399t-1b94928870881b5ea80cbbcf1594f11b452cdfa72b648d04865150cbad0d625f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Actin Cytoskeleton - metabolism</topic><topic>Arteriovenous Shunt, Surgical - adverse effects</topic><topic>Cell adhesion & migration</topic><topic>Cell Proliferation</topic><topic>Cell Shape</topic><topic>Cells, Cultured</topic><topic>Culture Media, Conditioned - metabolism</topic><topic>Cytokines - genetics</topic><topic>Cytokines - metabolism</topic><topic>Endothelium</topic><topic>Gene expression</topic><topic>Gene Expression Regulation</topic><topic>Heart failure</topic><topic>Hemodialysis</topic><topic>Hemodynamics</topic><topic>Human Umbilical Vein Endothelial Cells - metabolism</topic><topic>Human Umbilical Vein Endothelial Cells - pathology</topic><topic>Humans</topic><topic>Hyperplasia</topic><topic>Mechanotransduction, Cellular</topic><topic>Molecules</topic><topic>Myocytes, Smooth Muscle - metabolism</topic><topic>Myocytes, Smooth Muscle - pathology</topic><topic>Paracrine Communication</topic><topic>Pulsatile Flow</topic><topic>Renal Dialysis</topic><topic>RNA, Messenger - metabolism</topic><topic>Shear stress</topic><topic>Signal Transduction</topic><topic>Stress, Mechanical</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Franzoni, Marco</creatorcontrib><creatorcontrib>Cattaneo, Irene</creatorcontrib><creatorcontrib>Longaretti, Lorena</creatorcontrib><creatorcontrib>Figliuzzi, Marina</creatorcontrib><creatorcontrib>Ene-Iordache, Bogdan</creatorcontrib><creatorcontrib>Remuzzi, Andrea</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>Franzoni, Marco</au><au>Cattaneo, Irene</au><au>Longaretti, Lorena</au><au>Figliuzzi, Marina</au><au>Ene-Iordache, Bogdan</au><au>Remuzzi, Andrea</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Endothelial cell activation by hemodynamic shear stress derived from arteriovenous fistula for hemodialysis access</atitle><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle><addtitle>Am J Physiol Heart Circ Physiol</addtitle><date>2016-01-01</date><risdate>2016</risdate><volume>310</volume><issue>1</issue><spage>H49</spage><epage>H59</epage><pages>H49-H59</pages><issn>0363-6135</issn><eissn>1522-1539</eissn><coden>AJPPDI</coden><abstract>Intimal hyperplasia (IH) is the first cause of failure of an arteriovenous fistula (AVF). The aim of the present study was to investigate the effects on endothelial cells (ECs) of shear stress waveforms derived from AVF areas prone to develop IH. We used a cone-and-plate device to obtain real-time control of shear stress acting on EC cultures. We exposed human umbilical vein ECs for 48 h to different shear stimulations calculated in a side-to-end AVF model. Pulsatile unidirectional flow, representative of low-risk stenosis areas, induced alignment of ECs and actin fiber orientation with flow. Shear stress patterns of reciprocating flow, derived from high-risk stenosis areas, did not affect EC shape or cytoskeleton organization, which remained similar to static cultures. We also evaluated flow-induced EC expression of genes known to be involved in cytoskeletal remodeling and expression of cell adhesion molecules. Unidirectional flow induced a significant increase in Kruppel-like factor 2 mRNA expression, whereas it significantly reduced phospholipase D1, α4-integrin, and Ras p21 protein activator 1 mRNA expression. Reciprocating flow did not increase Kruppel-like factor 2 mRNA expression compared with static controls but significantly increased mRNA expression of phospholipase D1, α4-integrin, and Ras p21 protein activator 1. Reciprocating flow selectively increased monocyte chemoattractant protein-1 and IL-8 production. Furthermore, culture medium conditioned by ECs exposed to reciprocating flows selectively increased smooth muscle cell proliferation compared with unidirectional flow. Our results indicate that protective vascular effects induced in ECs by unidirectional pulsatile flow are not induced by reciprocating shear forces, suggesting a mechanism by which oscillating flow conditions may induce the development of IH in AVF and vascular access dysfunction.</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>26497959</pmid><doi>10.1152/ajpheart.00098.2015</doi></addata></record> |
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subjects | Actin Cytoskeleton - metabolism Arteriovenous Shunt, Surgical - adverse effects Cell adhesion & migration Cell Proliferation Cell Shape Cells, Cultured Culture Media, Conditioned - metabolism Cytokines - genetics Cytokines - metabolism Endothelium Gene expression Gene Expression Regulation Heart failure Hemodialysis Hemodynamics Human Umbilical Vein Endothelial Cells - metabolism Human Umbilical Vein Endothelial Cells - pathology Humans Hyperplasia Mechanotransduction, Cellular Molecules Myocytes, Smooth Muscle - metabolism Myocytes, Smooth Muscle - pathology Paracrine Communication Pulsatile Flow Renal Dialysis RNA, Messenger - metabolism Shear stress Signal Transduction Stress, Mechanical Time Factors |
title | Endothelial cell activation by hemodynamic shear stress derived from arteriovenous fistula for hemodialysis access |
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