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Impact of Cell Loading of Recombinant Spider Silk Based Bioinks on Gelation and Printability
Printability of bioinks encompasses considerations concerning rheology and extrudability, characterization of filament formation, shape fidelity, cell viability, and post‐printing cellular development. Recombinant spider silk based hydrogels might be a suitable material to be used in bioinks, that i...
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Published in: | Macromolecular bioscience 2022-03, Vol.22 (3), p.e2100390-n/a |
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description | Printability of bioinks encompasses considerations concerning rheology and extrudability, characterization of filament formation, shape fidelity, cell viability, and post‐printing cellular development. Recombinant spider silk based hydrogels might be a suitable material to be used in bioinks, that is, a formulation of cells and materials to be used for bioprinting. Here, the high shape fidelity of spider silk ink is shown by bioprinting the shape and size of a human aortic valve. Further the influence of the encapsulation of cells has been evaluated on spider silk hydrogel formation, hydrogel mechanics, and shape fidelity upon extrusion based bioprinting. It is shown that the presence of cells impacts the gelation of spider silk proteins differently, depending on the used silk variant. RGD‐modified spider silk hydrogels are physically crosslinked by the cells, while there is no active interaction between cells and un‐tagged spider silk proteins. Strikingly, even at cell densities up to ten million cells per milliliter, cell viability is high after extrusion‐based printing, which is a significant prerequisite for future applications. Shape fidelity of the printed constructs is demonstrated using a filament collapse test in the absence and presence of human cells.
Spider silk based bioinks show high potential for biofabrication combining high biocompatibility with gentle cell encapsulation and reliable extrusion printing. In this study, valuable insights are gained concerning gelation and rheology of spider silk bioinks dependent on cell densities. Printability is optimized by understanding temperature‐dependency of rheological behavior, used nozzle, and applied pressure. |
doi_str_mv | 10.1002/mabi.202100390 |
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Spider silk based bioinks show high potential for biofabrication combining high biocompatibility with gentle cell encapsulation and reliable extrusion printing. In this study, valuable insights are gained concerning gelation and rheology of spider silk bioinks dependent on cell densities. Printability is optimized by understanding temperature‐dependency of rheological behavior, used nozzle, and applied pressure.</description><identifier>ISSN: 1616-5187</identifier><identifier>EISSN: 1616-5195</identifier><identifier>DOI: 10.1002/mabi.202100390</identifier><identifier>PMID: 34882980</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Accuracy ; Aorta ; Aortic valve ; Bioengineering ; biofabrication ; Bioprinting ; Cell viability ; Extrudability ; Extrusion rate ; Gelation ; gelation kinetics ; Heart valves ; Hydrogels ; physical crosslinking ; Printing, Three-Dimensional ; Proteins ; Rheological properties ; Rheology ; Silk ; Spiders ; Three dimensional printing ; Tissue Engineering ; Tissue Scaffolds</subject><ispartof>Macromolecular bioscience, 2022-03, Vol.22 (3), p.e2100390-n/a</ispartof><rights>2021 The Authors. Macromolecular Bioscience published by Wiley‐VCH GmbH</rights><rights>2021 The Authors. Macromolecular Bioscience published by Wiley-VCH GmbH.</rights><rights>2021. This article is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4130-4e958b9423a1fc12833f110712c6d74bf89403e497161e983cb9030fc07cf5be3</citedby><cites>FETCH-LOGICAL-c4130-4e958b9423a1fc12833f110712c6d74bf89403e497161e983cb9030fc07cf5be3</cites><orcidid>0000-0002-0457-2423</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34882980$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lechner, Annika</creatorcontrib><creatorcontrib>Trossmann, Vanessa T.</creatorcontrib><creatorcontrib>Scheibel, Thomas</creatorcontrib><title>Impact of Cell Loading of Recombinant Spider Silk Based Bioinks on Gelation and Printability</title><title>Macromolecular bioscience</title><addtitle>Macromol Biosci</addtitle><description>Printability of bioinks encompasses considerations concerning rheology and extrudability, characterization of filament formation, shape fidelity, cell viability, and post‐printing cellular development. Recombinant spider silk based hydrogels might be a suitable material to be used in bioinks, that is, a formulation of cells and materials to be used for bioprinting. Here, the high shape fidelity of spider silk ink is shown by bioprinting the shape and size of a human aortic valve. Further the influence of the encapsulation of cells has been evaluated on spider silk hydrogel formation, hydrogel mechanics, and shape fidelity upon extrusion based bioprinting. It is shown that the presence of cells impacts the gelation of spider silk proteins differently, depending on the used silk variant. RGD‐modified spider silk hydrogels are physically crosslinked by the cells, while there is no active interaction between cells and un‐tagged spider silk proteins. Strikingly, even at cell densities up to ten million cells per milliliter, cell viability is high after extrusion‐based printing, which is a significant prerequisite for future applications. Shape fidelity of the printed constructs is demonstrated using a filament collapse test in the absence and presence of human cells.
Spider silk based bioinks show high potential for biofabrication combining high biocompatibility with gentle cell encapsulation and reliable extrusion printing. In this study, valuable insights are gained concerning gelation and rheology of spider silk bioinks dependent on cell densities. Printability is optimized by understanding temperature‐dependency of rheological behavior, used nozzle, and applied pressure.</description><subject>Accuracy</subject><subject>Aorta</subject><subject>Aortic valve</subject><subject>Bioengineering</subject><subject>biofabrication</subject><subject>Bioprinting</subject><subject>Cell viability</subject><subject>Extrudability</subject><subject>Extrusion rate</subject><subject>Gelation</subject><subject>gelation kinetics</subject><subject>Heart valves</subject><subject>Hydrogels</subject><subject>physical crosslinking</subject><subject>Printing, Three-Dimensional</subject><subject>Proteins</subject><subject>Rheological properties</subject><subject>Rheology</subject><subject>Silk</subject><subject>Spiders</subject><subject>Three dimensional printing</subject><subject>Tissue Engineering</subject><subject>Tissue Scaffolds</subject><issn>1616-5187</issn><issn>1616-5195</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNqFkM9LwzAUx4Mobk6vHiXgxUtnfrVNjtvQOZgoTm9CSdNUsrXJbFpk_70ZmxO8eHrvwed9ee8DwCVGQ4wQua1lboYEkTBQgY5AHyc4iWIs4uNDz9MeOPN-iRBOuSCnoEcZ50Rw1Afvs3otVQtdCSe6quDcycLYj-38opWrc2OlbeFibQrdwIWpVnAsvS7g2DhjVx46C6e6kq0JjbQFfG6MbcNRlWk35-CklJXXF_s6AG_3d6-Th2j-NJ1NRvNIMUxRxLSIeS4YoRKXChNOaYkxSjFRSZGyvOSCIaqZSMNDWnCqcoEoKhVKVRnnmg7AzS533bjPTvs2q41X4R1ptet8RhLEYxqkJAG9_oMuXdfYcF2gKOcxYZgHarijVOO8b3SZrRtTy2aTYZRtvWdb79nBe1i42sd2ea2LA_4jOgBiB3yZSm_-icseR-PZb_g3zueMkg</recordid><startdate>202203</startdate><enddate>202203</enddate><creator>Lechner, Annika</creator><creator>Trossmann, Vanessa T.</creator><creator>Scheibel, Thomas</creator><general>Wiley Subscription Services, Inc</general><scope>24P</scope><scope>WIN</scope><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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0457-2423</orcidid></search><sort><creationdate>202203</creationdate><title>Impact of Cell Loading of Recombinant Spider Silk Based Bioinks on Gelation and Printability</title><author>Lechner, Annika ; Trossmann, Vanessa T. ; Scheibel, Thomas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4130-4e958b9423a1fc12833f110712c6d74bf89403e497161e983cb9030fc07cf5be3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Accuracy</topic><topic>Aorta</topic><topic>Aortic valve</topic><topic>Bioengineering</topic><topic>biofabrication</topic><topic>Bioprinting</topic><topic>Cell viability</topic><topic>Extrudability</topic><topic>Extrusion rate</topic><topic>Gelation</topic><topic>gelation kinetics</topic><topic>Heart valves</topic><topic>Hydrogels</topic><topic>physical crosslinking</topic><topic>Printing, Three-Dimensional</topic><topic>Proteins</topic><topic>Rheological properties</topic><topic>Rheology</topic><topic>Silk</topic><topic>Spiders</topic><topic>Three dimensional printing</topic><topic>Tissue Engineering</topic><topic>Tissue Scaffolds</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lechner, Annika</creatorcontrib><creatorcontrib>Trossmann, Vanessa T.</creatorcontrib><creatorcontrib>Scheibel, Thomas</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Free Archive</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Macromolecular bioscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lechner, Annika</au><au>Trossmann, Vanessa T.</au><au>Scheibel, Thomas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of Cell Loading of Recombinant Spider Silk Based Bioinks on Gelation and Printability</atitle><jtitle>Macromolecular bioscience</jtitle><addtitle>Macromol Biosci</addtitle><date>2022-03</date><risdate>2022</risdate><volume>22</volume><issue>3</issue><spage>e2100390</spage><epage>n/a</epage><pages>e2100390-n/a</pages><issn>1616-5187</issn><eissn>1616-5195</eissn><abstract>Printability of bioinks encompasses considerations concerning rheology and extrudability, characterization of filament formation, shape fidelity, cell viability, and post‐printing cellular development. Recombinant spider silk based hydrogels might be a suitable material to be used in bioinks, that is, a formulation of cells and materials to be used for bioprinting. Here, the high shape fidelity of spider silk ink is shown by bioprinting the shape and size of a human aortic valve. Further the influence of the encapsulation of cells has been evaluated on spider silk hydrogel formation, hydrogel mechanics, and shape fidelity upon extrusion based bioprinting. It is shown that the presence of cells impacts the gelation of spider silk proteins differently, depending on the used silk variant. RGD‐modified spider silk hydrogels are physically crosslinked by the cells, while there is no active interaction between cells and un‐tagged spider silk proteins. Strikingly, even at cell densities up to ten million cells per milliliter, cell viability is high after extrusion‐based printing, which is a significant prerequisite for future applications. Shape fidelity of the printed constructs is demonstrated using a filament collapse test in the absence and presence of human cells.
Spider silk based bioinks show high potential for biofabrication combining high biocompatibility with gentle cell encapsulation and reliable extrusion printing. In this study, valuable insights are gained concerning gelation and rheology of spider silk bioinks dependent on cell densities. Printability is optimized by understanding temperature‐dependency of rheological behavior, used nozzle, and applied pressure.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>34882980</pmid><doi>10.1002/mabi.202100390</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-0457-2423</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Accuracy Aorta Aortic valve Bioengineering biofabrication Bioprinting Cell viability Extrudability Extrusion rate Gelation gelation kinetics Heart valves Hydrogels physical crosslinking Printing, Three-Dimensional Proteins Rheological properties Rheology Silk Spiders Three dimensional printing Tissue Engineering Tissue Scaffolds |
title | Impact of Cell Loading of Recombinant Spider Silk Based Bioinks on Gelation and Printability |
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