Layer-by-Layer Tissue Microfabrication Supports Cell Proliferation In Vitro and In Vivo
Layer-by-layer biofabrication represents a novel strategy to create three-dimensional living structures with a controlled internal architecture, using cell micromanipulation technologies. Laser assisted bioprinting (LAB) is an effective printing method for patterning cells, biomolecules, and biomate...
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Veröffentlicht in: | Tissue engineering. Part C, Methods Methods, 2012-01, Vol.18 (1), p.62-70 |
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creator | Catros, Sylvain Guillemot, Fabien Nandakumar, Anandkumar Ziane, Sophia Moroni, Lorenzo Habibovic, Pamela van Blitterswijk, Clemens Rousseau, Benoit Chassande, Olivier Amédée, Joëlle Fricain, Jean-Christophe |
description | Layer-by-layer biofabrication represents a novel strategy to create three-dimensional living structures with a controlled internal architecture, using cell micromanipulation technologies. Laser assisted bioprinting (LAB) is an effective printing method for patterning cells, biomolecules, and biomaterials in two dimensions. “Biopapers,” made of thin polymer scaffolds, may be appropriate to achieve three-dimensional constructs and to reinforce mechanical properties of printed materials. The aim of this work was to evaluate the effect of the tridimensional organization of cells and biomaterials on cell proliferation
in vitro
and
in vivo
. The experimental LAB setup was comprised of an infrared laser, focused onto a glass ribbon coated with an absorbing layer of gold. The cell bioink was made of MG63 cells (50 millions cells/mL in culture medium and 1% alginate), transduced with Luciferase gene for tracking and quantification. The printing substrate was a 100-μm-thick polycaprolacton (PCL) electrospun scaffold. The building sequence comprised sequential layers of cells and PCL scaffolds stacked using two different tridimensional arrangements, which were compared in this study (layer-by-layer vs. seeding on a single locus of the scaffolds). Then the cell-seeded materials were cultured
in vitro
or implanted
in vivo
in NOD-SCID mice. The qualitative follow-up involved scanning electron microscopy (SEM) observations, live-dead assays, and histology. The cell amount was quantified by photon imager during 21 days
in vitro
and 2 months
in vivo
. Live- dead assay and SEM revealed that the cells survived after printing and spread onto PCL membranes. Circle-shaped patterns were maintained
in vitro
during the first week but they were no longer observable after 2 weeks, due to cell proliferation. Luciferase tracking displayed that the cell amount was increased
in vitro
and
in vivo
when the materials and the cells where stacked layer by layer. Histological sections of the
in vivo
samples revealed a thicker fibrous tissue in the layer-by-layer samples. We have demonstrated in this study that PCL electrospun biopapers can act as a shock-absorbing mattress for cell printing and could further support cell proliferation. The layer-by-layer printing provided an appropriate 3D environment for cell survival and enhanced cell proliferation
in vitro
and
in vivo
. |
doi_str_mv | 10.1089/ten.tec.2011.0382 |
format | Article |
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in vitro
and
in vivo
. The experimental LAB setup was comprised of an infrared laser, focused onto a glass ribbon coated with an absorbing layer of gold. The cell bioink was made of MG63 cells (50 millions cells/mL in culture medium and 1% alginate), transduced with Luciferase gene for tracking and quantification. The printing substrate was a 100-μm-thick polycaprolacton (PCL) electrospun scaffold. The building sequence comprised sequential layers of cells and PCL scaffolds stacked using two different tridimensional arrangements, which were compared in this study (layer-by-layer vs. seeding on a single locus of the scaffolds). Then the cell-seeded materials were cultured
in vitro
or implanted
in vivo
in NOD-SCID mice. The qualitative follow-up involved scanning electron microscopy (SEM) observations, live-dead assays, and histology. The cell amount was quantified by photon imager during 21 days
in vitro
and 2 months
in vivo
. Live- dead assay and SEM revealed that the cells survived after printing and spread onto PCL membranes. Circle-shaped patterns were maintained
in vitro
during the first week but they were no longer observable after 2 weeks, due to cell proliferation. Luciferase tracking displayed that the cell amount was increased
in vitro
and
in vivo
when the materials and the cells where stacked layer by layer. Histological sections of the
in vivo
samples revealed a thicker fibrous tissue in the layer-by-layer samples. We have demonstrated in this study that PCL electrospun biopapers can act as a shock-absorbing mattress for cell printing and could further support cell proliferation. The layer-by-layer printing provided an appropriate 3D environment for cell survival and enhanced cell proliferation
in vitro
and
in vivo
.</description><identifier>ISSN: 1937-3384</identifier><identifier>EISSN: 1937-3392</identifier><identifier>DOI: 10.1089/ten.tec.2011.0382</identifier><identifier>PMID: 21895563</identifier><language>eng</language><publisher>United States: Mary Ann Liebert, Inc</publisher><subject>Animals ; Biocompatible Materials - chemistry ; Cell Culture Techniques ; Cell Line, Tumor ; Cell Proliferation ; Cell Survival ; Cellular biology ; Histology ; Humans ; Materials Testing ; Mice ; Mice, SCID ; Microscopy, Electron, Scanning - methods ; Microtechnology ; Regeneration ; Tissue engineering ; Tissue Engineering - methods ; Tissue Scaffolds</subject><ispartof>Tissue engineering. Part C, Methods, 2012-01, Vol.18 (1), p.62-70</ispartof><rights>2012, Mary Ann Liebert, Inc.</rights><rights>(©) Copyright 2012, Mary Ann Liebert, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c455t-a73d54e22810cf7974128e2589a7ad1b8977ff1679a67fbef4475075fedcbb123</citedby><cites>FETCH-LOGICAL-c455t-a73d54e22810cf7974128e2589a7ad1b8977ff1679a67fbef4475075fedcbb123</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21895563$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Catros, Sylvain</creatorcontrib><creatorcontrib>Guillemot, Fabien</creatorcontrib><creatorcontrib>Nandakumar, Anandkumar</creatorcontrib><creatorcontrib>Ziane, Sophia</creatorcontrib><creatorcontrib>Moroni, Lorenzo</creatorcontrib><creatorcontrib>Habibovic, Pamela</creatorcontrib><creatorcontrib>van Blitterswijk, Clemens</creatorcontrib><creatorcontrib>Rousseau, Benoit</creatorcontrib><creatorcontrib>Chassande, Olivier</creatorcontrib><creatorcontrib>Amédée, Joëlle</creatorcontrib><creatorcontrib>Fricain, Jean-Christophe</creatorcontrib><title>Layer-by-Layer Tissue Microfabrication Supports Cell Proliferation In Vitro and In Vivo</title><title>Tissue engineering. Part C, Methods</title><addtitle>Tissue Eng Part C Methods</addtitle><description>Layer-by-layer biofabrication represents a novel strategy to create three-dimensional living structures with a controlled internal architecture, using cell micromanipulation technologies. Laser assisted bioprinting (LAB) is an effective printing method for patterning cells, biomolecules, and biomaterials in two dimensions. “Biopapers,” made of thin polymer scaffolds, may be appropriate to achieve three-dimensional constructs and to reinforce mechanical properties of printed materials. The aim of this work was to evaluate the effect of the tridimensional organization of cells and biomaterials on cell proliferation
in vitro
and
in vivo
. The experimental LAB setup was comprised of an infrared laser, focused onto a glass ribbon coated with an absorbing layer of gold. The cell bioink was made of MG63 cells (50 millions cells/mL in culture medium and 1% alginate), transduced with Luciferase gene for tracking and quantification. The printing substrate was a 100-μm-thick polycaprolacton (PCL) electrospun scaffold. The building sequence comprised sequential layers of cells and PCL scaffolds stacked using two different tridimensional arrangements, which were compared in this study (layer-by-layer vs. seeding on a single locus of the scaffolds). Then the cell-seeded materials were cultured
in vitro
or implanted
in vivo
in NOD-SCID mice. The qualitative follow-up involved scanning electron microscopy (SEM) observations, live-dead assays, and histology. The cell amount was quantified by photon imager during 21 days
in vitro
and 2 months
in vivo
. Live- dead assay and SEM revealed that the cells survived after printing and spread onto PCL membranes. Circle-shaped patterns were maintained
in vitro
during the first week but they were no longer observable after 2 weeks, due to cell proliferation. Luciferase tracking displayed that the cell amount was increased
in vitro
and
in vivo
when the materials and the cells where stacked layer by layer. Histological sections of the
in vivo
samples revealed a thicker fibrous tissue in the layer-by-layer samples. We have demonstrated in this study that PCL electrospun biopapers can act as a shock-absorbing mattress for cell printing and could further support cell proliferation. The layer-by-layer printing provided an appropriate 3D environment for cell survival and enhanced cell proliferation
in vitro
and
in vivo
.</description><subject>Animals</subject><subject>Biocompatible Materials - chemistry</subject><subject>Cell Culture Techniques</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation</subject><subject>Cell Survival</subject><subject>Cellular biology</subject><subject>Histology</subject><subject>Humans</subject><subject>Materials Testing</subject><subject>Mice</subject><subject>Mice, SCID</subject><subject>Microscopy, Electron, Scanning - methods</subject><subject>Microtechnology</subject><subject>Regeneration</subject><subject>Tissue engineering</subject><subject>Tissue Engineering - methods</subject><subject>Tissue Scaffolds</subject><issn>1937-3384</issn><issn>1937-3392</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkU1LxDAQhoMofv8AL1K8eOqaSZsmOcriF6wo-HUsaTuBSLdZk1bYf29q1YMXPYTMTJ55mclLyBHQGVCpznrsZj3WM0YBZjSTbIPsgspEmmWKbf7EMt8heyG8UlrQQqhtssNAKs6LbJe8LPQafVqt088gebQhDJjc2to7oytva91b1yUPw2rlfB-SObZtcu9daw366e2mS55t712iu2ZK3t0B2TK6DXj4de-Tp8uLx_l1uri7upmfL9I657xPtcganiNjEmhthBI5MImMS6WFbqCSSghjIE6tC2EqNHkuOBXcYFNXFbBsn5xOuivv3gYMfbm0oY4z6g7dEErFCikVCPibhLwoeCbySJ78Il_d4Lu4RoREwRmDEYIJih8VgkdTrrxdar8ugZajO2V0J566HN0pR3diz_GX8FAtsfnp-LYjAmICxrLuutZihb7_h_QHC0eeKw</recordid><startdate>20120101</startdate><enddate>20120101</enddate><creator>Catros, Sylvain</creator><creator>Guillemot, Fabien</creator><creator>Nandakumar, Anandkumar</creator><creator>Ziane, Sophia</creator><creator>Moroni, Lorenzo</creator><creator>Habibovic, Pamela</creator><creator>van Blitterswijk, Clemens</creator><creator>Rousseau, Benoit</creator><creator>Chassande, Olivier</creator><creator>Amédée, Joëlle</creator><creator>Fricain, Jean-Christophe</creator><general>Mary Ann Liebert, Inc</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>7QP</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>7QO</scope></search><sort><creationdate>20120101</creationdate><title>Layer-by-Layer Tissue Microfabrication Supports Cell Proliferation In Vitro and In Vivo</title><author>Catros, Sylvain ; 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Part C, Methods</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Catros, Sylvain</au><au>Guillemot, Fabien</au><au>Nandakumar, Anandkumar</au><au>Ziane, Sophia</au><au>Moroni, Lorenzo</au><au>Habibovic, Pamela</au><au>van Blitterswijk, Clemens</au><au>Rousseau, Benoit</au><au>Chassande, Olivier</au><au>Amédée, Joëlle</au><au>Fricain, Jean-Christophe</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Layer-by-Layer Tissue Microfabrication Supports Cell Proliferation In Vitro and In Vivo</atitle><jtitle>Tissue engineering. Part C, Methods</jtitle><addtitle>Tissue Eng Part C Methods</addtitle><date>2012-01-01</date><risdate>2012</risdate><volume>18</volume><issue>1</issue><spage>62</spage><epage>70</epage><pages>62-70</pages><issn>1937-3384</issn><eissn>1937-3392</eissn><abstract>Layer-by-layer biofabrication represents a novel strategy to create three-dimensional living structures with a controlled internal architecture, using cell micromanipulation technologies. Laser assisted bioprinting (LAB) is an effective printing method for patterning cells, biomolecules, and biomaterials in two dimensions. “Biopapers,” made of thin polymer scaffolds, may be appropriate to achieve three-dimensional constructs and to reinforce mechanical properties of printed materials. The aim of this work was to evaluate the effect of the tridimensional organization of cells and biomaterials on cell proliferation
in vitro
and
in vivo
. The experimental LAB setup was comprised of an infrared laser, focused onto a glass ribbon coated with an absorbing layer of gold. The cell bioink was made of MG63 cells (50 millions cells/mL in culture medium and 1% alginate), transduced with Luciferase gene for tracking and quantification. The printing substrate was a 100-μm-thick polycaprolacton (PCL) electrospun scaffold. The building sequence comprised sequential layers of cells and PCL scaffolds stacked using two different tridimensional arrangements, which were compared in this study (layer-by-layer vs. seeding on a single locus of the scaffolds). Then the cell-seeded materials were cultured
in vitro
or implanted
in vivo
in NOD-SCID mice. The qualitative follow-up involved scanning electron microscopy (SEM) observations, live-dead assays, and histology. The cell amount was quantified by photon imager during 21 days
in vitro
and 2 months
in vivo
. Live- dead assay and SEM revealed that the cells survived after printing and spread onto PCL membranes. Circle-shaped patterns were maintained
in vitro
during the first week but they were no longer observable after 2 weeks, due to cell proliferation. Luciferase tracking displayed that the cell amount was increased
in vitro
and
in vivo
when the materials and the cells where stacked layer by layer. Histological sections of the
in vivo
samples revealed a thicker fibrous tissue in the layer-by-layer samples. We have demonstrated in this study that PCL electrospun biopapers can act as a shock-absorbing mattress for cell printing and could further support cell proliferation. The layer-by-layer printing provided an appropriate 3D environment for cell survival and enhanced cell proliferation
in vitro
and
in vivo
.</abstract><cop>United States</cop><pub>Mary Ann Liebert, Inc</pub><pmid>21895563</pmid><doi>10.1089/ten.tec.2011.0382</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Biocompatible Materials - chemistry Cell Culture Techniques Cell Line, Tumor Cell Proliferation Cell Survival Cellular biology Histology Humans Materials Testing Mice Mice, SCID Microscopy, Electron, Scanning - methods Microtechnology Regeneration Tissue engineering Tissue Engineering - methods Tissue Scaffolds |
title | Layer-by-Layer Tissue Microfabrication Supports Cell Proliferation In Vitro and In Vivo |
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