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Colonization by human fibroblasts of polypropylene prosthesis in a composite form for hernia repair
Purpose Abdominal wall hernia is one of the commonest surgical disorders worldwide, and there is no single gold-standard operative technique to repair it. In an effort to improve techniques and technologies to reinforce hernia repair, synthetic meshes are employed. In this study, a new prosthesis (n...
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Published in: | Hernia : the journal of hernias and abdominal wall surgery 2013-04, Vol.17 (2), p.241-248 |
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container_end_page | 248 |
container_issue | 2 |
container_start_page | 241 |
container_title | Hernia : the journal of hernias and abdominal wall surgery |
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creator | Canuto, R. A. Saracino, S. Oraldi, M. Festa, V. Festa, F. Muzio, G. Chiaravalloti, A. |
description | Purpose
Abdominal wall hernia is one of the commonest surgical disorders worldwide, and there is no single gold-standard operative technique to repair it. In an effort to improve techniques and technologies to reinforce hernia repair, synthetic meshes are employed. In this study, a new prosthesis (named composite) formed of two polypropylene layers, one macroporous (named mesh) and one transparent (named film), was examined to evaluate its capability to enable cell proliferation without inducing cell death. Inflammatory processes were also examined.
Methods
Human fibroblasts BJ were seeded on multiwells, on which composite or film had been placed. After 7, 14, and 21 days, cell growth and viability, deposition of collagen, and release of IL-6, IL-1β, and TNF-α were evaluated.
Results
The “in vitro” protocol showed the composite to be colonized by human fibroblasts on the polypropylene macroporous mesh side; no cell growth occurred on the film. The slowdown of cell growth observed between 14 and 21 days was accompanied by an increase in type I collagen deposition and marked fibroblast activity. Inflammatory cytokines initially increased, followed by their reduction beginning at 14 days.
Conclusions
The new prosthesis comprising two polypropylene layers of differing morphologies can be colonized by fibroblasts on the side facing the abdominal wall, whereas no cell growth occurs on the side facing the viscera. The transient inflammation, observed at early experimental times, is probably important for the healing process. |
doi_str_mv | 10.1007/s10029-012-0996-0 |
format | article |
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Abdominal wall hernia is one of the commonest surgical disorders worldwide, and there is no single gold-standard operative technique to repair it. In an effort to improve techniques and technologies to reinforce hernia repair, synthetic meshes are employed. In this study, a new prosthesis (named composite) formed of two polypropylene layers, one macroporous (named mesh) and one transparent (named film), was examined to evaluate its capability to enable cell proliferation without inducing cell death. Inflammatory processes were also examined.
Methods
Human fibroblasts BJ were seeded on multiwells, on which composite or film had been placed. After 7, 14, and 21 days, cell growth and viability, deposition of collagen, and release of IL-6, IL-1β, and TNF-α were evaluated.
Results
The “in vitro” protocol showed the composite to be colonized by human fibroblasts on the polypropylene macroporous mesh side; no cell growth occurred on the film. The slowdown of cell growth observed between 14 and 21 days was accompanied by an increase in type I collagen deposition and marked fibroblast activity. Inflammatory cytokines initially increased, followed by their reduction beginning at 14 days.
Conclusions
The new prosthesis comprising two polypropylene layers of differing morphologies can be colonized by fibroblasts on the side facing the abdominal wall, whereas no cell growth occurs on the side facing the viscera. The transient inflammation, observed at early experimental times, is probably important for the healing process.</description><identifier>ISSN: 1265-4906</identifier><identifier>EISSN: 1248-9204</identifier><identifier>DOI: 10.1007/s10029-012-0996-0</identifier><identifier>PMID: 22996952</identifier><language>eng</language><publisher>Paris: Springer-Verlag</publisher><subject>Abdominal Surgery ; Cell Proliferation ; Cells, Cultured ; Collagen Type I - metabolism ; Cytokines - metabolism ; Hernia, Abdominal - surgery ; Humans ; Immunohistochemistry ; Medicine ; Medicine & Public Health ; Original Article ; Polypropylenes ; Prostheses and Implants ; Prosthesis Design ; Surgical Mesh ; Wound Healing - physiology</subject><ispartof>Hernia : the journal of hernias and abdominal wall surgery, 2013-04, Vol.17 (2), p.241-248</ispartof><rights>Springer-Verlag 2012</rights><rights>Springer-Verlag France 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c415t-76ed4d0f3c6a98fe7a9d9423cd93bd341989002881e9635f3fa9680ed20ab4093</citedby><cites>FETCH-LOGICAL-c415t-76ed4d0f3c6a98fe7a9d9423cd93bd341989002881e9635f3fa9680ed20ab4093</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22996952$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Canuto, R. A.</creatorcontrib><creatorcontrib>Saracino, S.</creatorcontrib><creatorcontrib>Oraldi, M.</creatorcontrib><creatorcontrib>Festa, V.</creatorcontrib><creatorcontrib>Festa, F.</creatorcontrib><creatorcontrib>Muzio, G.</creatorcontrib><creatorcontrib>Chiaravalloti, A.</creatorcontrib><title>Colonization by human fibroblasts of polypropylene prosthesis in a composite form for hernia repair</title><title>Hernia : the journal of hernias and abdominal wall surgery</title><addtitle>Hernia</addtitle><addtitle>Hernia</addtitle><description>Purpose
Abdominal wall hernia is one of the commonest surgical disorders worldwide, and there is no single gold-standard operative technique to repair it. In an effort to improve techniques and technologies to reinforce hernia repair, synthetic meshes are employed. In this study, a new prosthesis (named composite) formed of two polypropylene layers, one macroporous (named mesh) and one transparent (named film), was examined to evaluate its capability to enable cell proliferation without inducing cell death. Inflammatory processes were also examined.
Methods
Human fibroblasts BJ were seeded on multiwells, on which composite or film had been placed. After 7, 14, and 21 days, cell growth and viability, deposition of collagen, and release of IL-6, IL-1β, and TNF-α were evaluated.
Results
The “in vitro” protocol showed the composite to be colonized by human fibroblasts on the polypropylene macroporous mesh side; no cell growth occurred on the film. The slowdown of cell growth observed between 14 and 21 days was accompanied by an increase in type I collagen deposition and marked fibroblast activity. Inflammatory cytokines initially increased, followed by their reduction beginning at 14 days.
Conclusions
The new prosthesis comprising two polypropylene layers of differing morphologies can be colonized by fibroblasts on the side facing the abdominal wall, whereas no cell growth occurs on the side facing the viscera. The transient inflammation, observed at early experimental times, is probably important for the healing process.</description><subject>Abdominal Surgery</subject><subject>Cell Proliferation</subject><subject>Cells, Cultured</subject><subject>Collagen Type I - metabolism</subject><subject>Cytokines - metabolism</subject><subject>Hernia, Abdominal - surgery</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Original Article</subject><subject>Polypropylenes</subject><subject>Prostheses and Implants</subject><subject>Prosthesis Design</subject><subject>Surgical Mesh</subject><subject>Wound Healing - physiology</subject><issn>1265-4906</issn><issn>1248-9204</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNp1kU1r3DAQhkVpaNK0P6CXIuilFyf6Wq3mGJY0DQR6ac5CtkddBVtyJPuw-fWR2TSEQi-jgXnmnRm9hHzh7IIztr0sNQpoGBcNA9ANe0fOuFCmAcHU-zXXm0YB06fkYykPjDGjtPlAToWoOGzEGel2aUgxPLk5pEjbA90vo4vUhzandnBlLjR5OqXhMOU0HQaMSGtW5j2WUGiI1NEujVMqYUbqUx7XQPeYY3A04-RC_kROvBsKfn55z8n9j-vfu5_N3a-b293VXdMpvpmbrcZe9czLTjswHrcOelBCdj3ItpeKg4F6rzEcQcuNl96BNgx7wVyrGMhz8v2oWxd8XLDMdgylw2FwEdNSLJccNDdKqop--wd9SEuOdbuVMnWsBlEpfqS6enHJ6O2Uw-jywXJmVwfs0QFbHbCrA5bVnq8vyks7Yv_a8ffLKyCOQKml-Afzm9H_VX0GX4KRZQ</recordid><startdate>20130401</startdate><enddate>20130401</enddate><creator>Canuto, R. A.</creator><creator>Saracino, S.</creator><creator>Oraldi, M.</creator><creator>Festa, V.</creator><creator>Festa, F.</creator><creator>Muzio, G.</creator><creator>Chiaravalloti, A.</creator><general>Springer-Verlag</general><general>Springer Nature B.V</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>3V.</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20130401</creationdate><title>Colonization by human fibroblasts of polypropylene prosthesis in a composite form for hernia repair</title><author>Canuto, R. A. ; Saracino, S. ; Oraldi, M. ; Festa, V. ; Festa, F. ; Muzio, G. ; Chiaravalloti, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-76ed4d0f3c6a98fe7a9d9423cd93bd341989002881e9635f3fa9680ed20ab4093</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Abdominal Surgery</topic><topic>Cell Proliferation</topic><topic>Cells, Cultured</topic><topic>Collagen Type I - metabolism</topic><topic>Cytokines - metabolism</topic><topic>Hernia, Abdominal - surgery</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Original Article</topic><topic>Polypropylenes</topic><topic>Prostheses and Implants</topic><topic>Prosthesis Design</topic><topic>Surgical Mesh</topic><topic>Wound Healing - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Canuto, R. A.</creatorcontrib><creatorcontrib>Saracino, S.</creatorcontrib><creatorcontrib>Oraldi, M.</creatorcontrib><creatorcontrib>Festa, V.</creatorcontrib><creatorcontrib>Festa, F.</creatorcontrib><creatorcontrib>Muzio, G.</creatorcontrib><creatorcontrib>Chiaravalloti, A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Hernia : the journal of hernias and abdominal wall surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Canuto, R. A.</au><au>Saracino, S.</au><au>Oraldi, M.</au><au>Festa, V.</au><au>Festa, F.</au><au>Muzio, G.</au><au>Chiaravalloti, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Colonization by human fibroblasts of polypropylene prosthesis in a composite form for hernia repair</atitle><jtitle>Hernia : the journal of hernias and abdominal wall surgery</jtitle><stitle>Hernia</stitle><addtitle>Hernia</addtitle><date>2013-04-01</date><risdate>2013</risdate><volume>17</volume><issue>2</issue><spage>241</spage><epage>248</epage><pages>241-248</pages><issn>1265-4906</issn><eissn>1248-9204</eissn><abstract>Purpose
Abdominal wall hernia is one of the commonest surgical disorders worldwide, and there is no single gold-standard operative technique to repair it. In an effort to improve techniques and technologies to reinforce hernia repair, synthetic meshes are employed. In this study, a new prosthesis (named composite) formed of two polypropylene layers, one macroporous (named mesh) and one transparent (named film), was examined to evaluate its capability to enable cell proliferation without inducing cell death. Inflammatory processes were also examined.
Methods
Human fibroblasts BJ were seeded on multiwells, on which composite or film had been placed. After 7, 14, and 21 days, cell growth and viability, deposition of collagen, and release of IL-6, IL-1β, and TNF-α were evaluated.
Results
The “in vitro” protocol showed the composite to be colonized by human fibroblasts on the polypropylene macroporous mesh side; no cell growth occurred on the film. The slowdown of cell growth observed between 14 and 21 days was accompanied by an increase in type I collagen deposition and marked fibroblast activity. Inflammatory cytokines initially increased, followed by their reduction beginning at 14 days.
Conclusions
The new prosthesis comprising two polypropylene layers of differing morphologies can be colonized by fibroblasts on the side facing the abdominal wall, whereas no cell growth occurs on the side facing the viscera. The transient inflammation, observed at early experimental times, is probably important for the healing process.</abstract><cop>Paris</cop><pub>Springer-Verlag</pub><pmid>22996952</pmid><doi>10.1007/s10029-012-0996-0</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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source | Springer Nature:Jisc Collections:Springer Nature Read and Publish 2023-2025: Springer Reading List |
subjects | Abdominal Surgery Cell Proliferation Cells, Cultured Collagen Type I - metabolism Cytokines - metabolism Hernia, Abdominal - surgery Humans Immunohistochemistry Medicine Medicine & Public Health Original Article Polypropylenes Prostheses and Implants Prosthesis Design Surgical Mesh Wound Healing - physiology |
title | Colonization by human fibroblasts of polypropylene prosthesis in a composite form for hernia repair |
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