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Production of an Optimized Tissue-Engineered Pig Connective Tissue for the Reconstruction of the Urinary Tract
Nonurological autologous tissues are used for urethral reconstruction to correct urinary tract disorders but are still leading to complications. Other substitutes have been studied on small animal models without great success. For preclinical tests, we selected the porcine model for its similarity t...
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Published in: | Tissue engineering. Part A 2011-06, Vol.17 (11-12), p.1625-1633 |
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container_end_page | 1633 |
container_issue | 11-12 |
container_start_page | 1625 |
container_title | Tissue engineering. Part A |
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creator | Ouellet, Gabrielle Dubé, Jean Gauvin, Robert Laterreur, Véronique Bouhout, Sara Bolduc, Stéphane |
description | Nonurological autologous tissues are used for urethral reconstruction to correct urinary tract disorders but are still leading to complications. Other substitutes have been studied on small animal models without great success. For preclinical tests, we selected the porcine model for its similarity to the human urinary tract. Up to now, porcine skin fibroblasts were not able to synthesize enough extracellular matrix under standard conditions to sustain the formation of an adequate tissue for transplantation purposes. Therefore, our goal was to optimize the harvesting site and culture conditions to obtain a thick and easy to handle porcine fibroblast tissue. The oral mucosa was found to be the ideal harvesting site, and a culture temperature of 39°C enabled the formation of a good porcine fibroblast sheet. We successfully superimpose three fibroblast sheets that merged into a thick and resistant tissue where physiological extracellular matrix was produced. Mechanical resistance evaluation by uniaxial traction on the three-layer fibroblast constructs also demonstrated its suitable properties. The production of this porcine connective tissue offers an interesting option in the field of urological tissue engineering. Autologous experiments on a larger animal model are now possible and accessible, allowing the performance of long-term
in vivo
studies. |
doi_str_mv | 10.1089/ten.tea.2010.0324 |
format | article |
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in vivo
studies.</description><identifier>ISSN: 1937-3341</identifier><identifier>EISSN: 1937-335X</identifier><identifier>DOI: 10.1089/ten.tea.2010.0324</identifier><identifier>PMID: 21288158</identifier><language>eng</language><publisher>United States: Mary Ann Liebert, Inc</publisher><subject>Animals ; Biomechanical Phenomena ; Care and treatment ; Cell Proliferation ; Cells, Cultured ; Connective Tissue - physiology ; Connective tissues ; Diagnosis ; Elastic Modulus ; Extracellular Matrix - metabolism ; Fibroblasts - cytology ; Fluorescent Antibody Technique ; Hogs ; Humans ; Mouth Mucosa - cytology ; Optimization techniques ; Original Articles ; Physiological aspects ; Regenerative Medicine - methods ; Skin - cytology ; Sus scrofa ; Temperature ; Tensile Strength ; Tissue engineering ; Tissue Engineering - methods ; Tissues ; Urinary Tract - pathology ; Urinary tract diseases ; Urologic diseases</subject><ispartof>Tissue engineering. Part A, 2011-06, Vol.17 (11-12), p.1625-1633</ispartof><rights>2011, Mary Ann Liebert, Inc.</rights><rights>COPYRIGHT 2011 Mary Ann Liebert, Inc.</rights><rights>(©) Copyright 2011, Mary Ann Liebert, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-57fd28d8614870ac3342a5b1788bf3650f5ce5655606d321b767fe637e5290fb3</citedby><cites>FETCH-LOGICAL-c474t-57fd28d8614870ac3342a5b1788bf3650f5ce5655606d321b767fe637e5290fb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.liebertpub.com/doi/epdf/10.1089/ten.tea.2010.0324$$EPDF$$P50$$Gmaryannliebert$$H</linktopdf><linktohtml>$$Uhttps://www.liebertpub.com/doi/full/10.1089/ten.tea.2010.0324$$EHTML$$P50$$Gmaryannliebert$$H</linktohtml><link.rule.ids>314,780,784,3042,21723,27924,27925,55291,55303</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21288158$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ouellet, Gabrielle</creatorcontrib><creatorcontrib>Dubé, Jean</creatorcontrib><creatorcontrib>Gauvin, Robert</creatorcontrib><creatorcontrib>Laterreur, Véronique</creatorcontrib><creatorcontrib>Bouhout, Sara</creatorcontrib><creatorcontrib>Bolduc, Stéphane</creatorcontrib><title>Production of an Optimized Tissue-Engineered Pig Connective Tissue for the Reconstruction of the Urinary Tract</title><title>Tissue engineering. Part A</title><addtitle>Tissue Eng Part A</addtitle><description>Nonurological autologous tissues are used for urethral reconstruction to correct urinary tract disorders but are still leading to complications. Other substitutes have been studied on small animal models without great success. For preclinical tests, we selected the porcine model for its similarity to the human urinary tract. Up to now, porcine skin fibroblasts were not able to synthesize enough extracellular matrix under standard conditions to sustain the formation of an adequate tissue for transplantation purposes. Therefore, our goal was to optimize the harvesting site and culture conditions to obtain a thick and easy to handle porcine fibroblast tissue. The oral mucosa was found to be the ideal harvesting site, and a culture temperature of 39°C enabled the formation of a good porcine fibroblast sheet. We successfully superimpose three fibroblast sheets that merged into a thick and resistant tissue where physiological extracellular matrix was produced. Mechanical resistance evaluation by uniaxial traction on the three-layer fibroblast constructs also demonstrated its suitable properties. The production of this porcine connective tissue offers an interesting option in the field of urological tissue engineering. Autologous experiments on a larger animal model are now possible and accessible, allowing the performance of long-term
in vivo
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Dubé, Jean ; Gauvin, Robert ; Laterreur, Véronique ; Bouhout, Sara ; Bolduc, Stéphane</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-57fd28d8614870ac3342a5b1788bf3650f5ce5655606d321b767fe637e5290fb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Biomechanical Phenomena</topic><topic>Care and treatment</topic><topic>Cell Proliferation</topic><topic>Cells, Cultured</topic><topic>Connective Tissue - physiology</topic><topic>Connective tissues</topic><topic>Diagnosis</topic><topic>Elastic Modulus</topic><topic>Extracellular Matrix - metabolism</topic><topic>Fibroblasts - cytology</topic><topic>Fluorescent Antibody Technique</topic><topic>Hogs</topic><topic>Humans</topic><topic>Mouth Mucosa - cytology</topic><topic>Optimization techniques</topic><topic>Original Articles</topic><topic>Physiological aspects</topic><topic>Regenerative Medicine - methods</topic><topic>Skin - cytology</topic><topic>Sus scrofa</topic><topic>Temperature</topic><topic>Tensile Strength</topic><topic>Tissue engineering</topic><topic>Tissue Engineering - methods</topic><topic>Tissues</topic><topic>Urinary Tract - pathology</topic><topic>Urinary tract diseases</topic><topic>Urologic diseases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ouellet, Gabrielle</creatorcontrib><creatorcontrib>Dubé, Jean</creatorcontrib><creatorcontrib>Gauvin, Robert</creatorcontrib><creatorcontrib>Laterreur, Véronique</creatorcontrib><creatorcontrib>Bouhout, Sara</creatorcontrib><creatorcontrib>Bolduc, Stéphane</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>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science 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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Science Journals</collection><collection>ProQuest Biological Science Journals</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>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Tissue engineering. Part A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ouellet, Gabrielle</au><au>Dubé, Jean</au><au>Gauvin, Robert</au><au>Laterreur, Véronique</au><au>Bouhout, Sara</au><au>Bolduc, Stéphane</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Production of an Optimized Tissue-Engineered Pig Connective Tissue for the Reconstruction of the Urinary Tract</atitle><jtitle>Tissue engineering. Part A</jtitle><addtitle>Tissue Eng Part A</addtitle><date>2011-06-01</date><risdate>2011</risdate><volume>17</volume><issue>11-12</issue><spage>1625</spage><epage>1633</epage><pages>1625-1633</pages><issn>1937-3341</issn><eissn>1937-335X</eissn><abstract>Nonurological autologous tissues are used for urethral reconstruction to correct urinary tract disorders but are still leading to complications. Other substitutes have been studied on small animal models without great success. For preclinical tests, we selected the porcine model for its similarity to the human urinary tract. Up to now, porcine skin fibroblasts were not able to synthesize enough extracellular matrix under standard conditions to sustain the formation of an adequate tissue for transplantation purposes. Therefore, our goal was to optimize the harvesting site and culture conditions to obtain a thick and easy to handle porcine fibroblast tissue. The oral mucosa was found to be the ideal harvesting site, and a culture temperature of 39°C enabled the formation of a good porcine fibroblast sheet. We successfully superimpose three fibroblast sheets that merged into a thick and resistant tissue where physiological extracellular matrix was produced. Mechanical resistance evaluation by uniaxial traction on the three-layer fibroblast constructs also demonstrated its suitable properties. The production of this porcine connective tissue offers an interesting option in the field of urological tissue engineering. Autologous experiments on a larger animal model are now possible and accessible, allowing the performance of long-term
in vivo
studies.</abstract><cop>United States</cop><pub>Mary Ann Liebert, Inc</pub><pmid>21288158</pmid><doi>10.1089/ten.tea.2010.0324</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Biomechanical Phenomena Care and treatment Cell Proliferation Cells, Cultured Connective Tissue - physiology Connective tissues Diagnosis Elastic Modulus Extracellular Matrix - metabolism Fibroblasts - cytology Fluorescent Antibody Technique Hogs Humans Mouth Mucosa - cytology Optimization techniques Original Articles Physiological aspects Regenerative Medicine - methods Skin - cytology Sus scrofa Temperature Tensile Strength Tissue engineering Tissue Engineering - methods Tissues Urinary Tract - pathology Urinary tract diseases Urologic diseases |
title | Production of an Optimized Tissue-Engineered Pig Connective Tissue for the Reconstruction of the Urinary Tract |
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