Three-dimensional culture of mouse pancreatic islet on a liver-derived perfusion-decellularized bioscaffold for potential clinical application
The cutting-edge technology of three-dimensional liver decellularized bioscaffold has a potential to provide a microenvironment that is suitable for the resident cells and even develop a new functional organ. Liver decellularized bioscaffold preserved the native extracellular matrix and three-dimens...
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Veröffentlicht in: | Journal of biomaterials applications 2015-10, Vol.30 (4), p.379-387 |
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creator | Xu, Tianxin Zhu, Mingyan Guo, Yibing Wu, Di Huang, Yan Fan, Xiangjun Zhu, Shajun Lin, Changchun Li, Xiaohong Lu, Jingjing Zhu, Hui Zhou, Pengcheng Lu, Yuhua Wang, Zhiwei |
description | The cutting-edge technology of three-dimensional liver decellularized bioscaffold has a potential to provide a microenvironment that is suitable for the resident cells and even develop a new functional organ. Liver decellularized bioscaffold preserved the native extracellular matrix and three-dimensional architecture in support of the cell culture. The goal of this study was to discover if three-dimensional extracellular matrix derived from mouse liver could facilitate the growth and maintenance of physiological functions of mouse isolated islets. We generated a whole organ liver decellularized bioscaffold which could successfully preserve extracellular matrix proteins and the native vascular channels using 1% Triton X-100/0.1% ammonium protocol. To evaluate the potential of decellularized liver as a scaffold for islets transplantation, the liver decellularized bioscaffold was infused with mouse primary pancreatic islets which were obtained through Collagenase P digestion protocol. Its yield, morphology, and quality were estimated by microscopic analysis, dithizone staining, insulin immunofluorescence and glucose stimulation experiments. Comparing the three-dimensional culture in liver decellularized bioscaffold with the orthodoxy two-dimensional plate culture, hematoxylin-eosin staining, immunohistochemistry, and insulin gene expression were tested. Our results demonstrated that the liver decellularized bioscaffold could support cellular culture and maintenance of cell functions. In contrast with the conventional two-dimensional culture, three-dimensional culture system could give rise to an up-regulated insulin gene expression. These findings demonstrated that the liver bioscaffold by a perfusion-decellularized technique could serve as a platform to support the survival and function of the pancreatic islets in vitro. Meanwhile three-dimensional culture system had a superior role in contrast with the two-dimensional culture. This study advanced the field of regenerative medicine towards the development of a liver decellularized bioscaffold capable of forming a neo-organ and could be used as potential clinical application. |
doi_str_mv | 10.1177/0885328215587610 |
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Liver decellularized bioscaffold preserved the native extracellular matrix and three-dimensional architecture in support of the cell culture. The goal of this study was to discover if three-dimensional extracellular matrix derived from mouse liver could facilitate the growth and maintenance of physiological functions of mouse isolated islets. We generated a whole organ liver decellularized bioscaffold which could successfully preserve extracellular matrix proteins and the native vascular channels using 1% Triton X-100/0.1% ammonium protocol. To evaluate the potential of decellularized liver as a scaffold for islets transplantation, the liver decellularized bioscaffold was infused with mouse primary pancreatic islets which were obtained through Collagenase P digestion protocol. Its yield, morphology, and quality were estimated by microscopic analysis, dithizone staining, insulin immunofluorescence and glucose stimulation experiments. Comparing the three-dimensional culture in liver decellularized bioscaffold with the orthodoxy two-dimensional plate culture, hematoxylin-eosin staining, immunohistochemistry, and insulin gene expression were tested. Our results demonstrated that the liver decellularized bioscaffold could support cellular culture and maintenance of cell functions. In contrast with the conventional two-dimensional culture, three-dimensional culture system could give rise to an up-regulated insulin gene expression. These findings demonstrated that the liver bioscaffold by a perfusion-decellularized technique could serve as a platform to support the survival and function of the pancreatic islets in vitro. Meanwhile three-dimensional culture system had a superior role in contrast with the two-dimensional culture. This study advanced the field of regenerative medicine towards the development of a liver decellularized bioscaffold capable of forming a neo-organ and could be used as potential clinical application.</description><identifier>ISSN: 0885-3282</identifier><identifier>EISSN: 1530-8022</identifier><identifier>DOI: 10.1177/0885328215587610</identifier><identifier>PMID: 26006767</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Animals ; Cells, Cultured ; Culture ; Extracellular Matrix - chemistry ; Gene expression ; Insulin ; Islets of Langerhans - cytology ; Islets of Langerhans Transplantation ; Liver ; Liver - chemistry ; Maintenance ; Male ; Mice ; Mice, Inbred C57BL ; Primary Cell Culture - methods ; Staining ; Three dimensional ; Tissue Engineering - methods ; Tissue Scaffolds - chemistry ; Two dimensional</subject><ispartof>Journal of biomaterials applications, 2015-10, Vol.30 (4), p.379-387</ispartof><rights>The Author(s) 2015</rights><rights>The Author(s) 2015.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c506t-2597e4d1d2c9c195347a61e0b3d063ac26849a322349e8ad15646755113ec2573</citedby><cites>FETCH-LOGICAL-c506t-2597e4d1d2c9c195347a61e0b3d063ac26849a322349e8ad15646755113ec2573</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/0885328215587610$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/0885328215587610$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,780,784,21819,27924,27925,43621,43622</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26006767$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xu, Tianxin</creatorcontrib><creatorcontrib>Zhu, Mingyan</creatorcontrib><creatorcontrib>Guo, Yibing</creatorcontrib><creatorcontrib>Wu, Di</creatorcontrib><creatorcontrib>Huang, Yan</creatorcontrib><creatorcontrib>Fan, Xiangjun</creatorcontrib><creatorcontrib>Zhu, Shajun</creatorcontrib><creatorcontrib>Lin, Changchun</creatorcontrib><creatorcontrib>Li, Xiaohong</creatorcontrib><creatorcontrib>Lu, Jingjing</creatorcontrib><creatorcontrib>Zhu, Hui</creatorcontrib><creatorcontrib>Zhou, Pengcheng</creatorcontrib><creatorcontrib>Lu, Yuhua</creatorcontrib><creatorcontrib>Wang, Zhiwei</creatorcontrib><title>Three-dimensional culture of mouse pancreatic islet on a liver-derived perfusion-decellularized bioscaffold for potential clinical application</title><title>Journal of biomaterials applications</title><addtitle>J Biomater Appl</addtitle><description>The cutting-edge technology of three-dimensional liver decellularized bioscaffold has a potential to provide a microenvironment that is suitable for the resident cells and even develop a new functional organ. Liver decellularized bioscaffold preserved the native extracellular matrix and three-dimensional architecture in support of the cell culture. The goal of this study was to discover if three-dimensional extracellular matrix derived from mouse liver could facilitate the growth and maintenance of physiological functions of mouse isolated islets. We generated a whole organ liver decellularized bioscaffold which could successfully preserve extracellular matrix proteins and the native vascular channels using 1% Triton X-100/0.1% ammonium protocol. To evaluate the potential of decellularized liver as a scaffold for islets transplantation, the liver decellularized bioscaffold was infused with mouse primary pancreatic islets which were obtained through Collagenase P digestion protocol. Its yield, morphology, and quality were estimated by microscopic analysis, dithizone staining, insulin immunofluorescence and glucose stimulation experiments. Comparing the three-dimensional culture in liver decellularized bioscaffold with the orthodoxy two-dimensional plate culture, hematoxylin-eosin staining, immunohistochemistry, and insulin gene expression were tested. Our results demonstrated that the liver decellularized bioscaffold could support cellular culture and maintenance of cell functions. In contrast with the conventional two-dimensional culture, three-dimensional culture system could give rise to an up-regulated insulin gene expression. These findings demonstrated that the liver bioscaffold by a perfusion-decellularized technique could serve as a platform to support the survival and function of the pancreatic islets in vitro. Meanwhile three-dimensional culture system had a superior role in contrast with the two-dimensional culture. This study advanced the field of regenerative medicine towards the development of a liver decellularized bioscaffold capable of forming a neo-organ and could be used as potential clinical application.</description><subject>Animals</subject><subject>Cells, Cultured</subject><subject>Culture</subject><subject>Extracellular Matrix - chemistry</subject><subject>Gene expression</subject><subject>Insulin</subject><subject>Islets of Langerhans - cytology</subject><subject>Islets of Langerhans Transplantation</subject><subject>Liver</subject><subject>Liver - chemistry</subject><subject>Maintenance</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Primary Cell Culture - methods</subject><subject>Staining</subject><subject>Three dimensional</subject><subject>Tissue Engineering - methods</subject><subject>Tissue Scaffolds - chemistry</subject><subject>Two dimensional</subject><issn>0885-3282</issn><issn>1530-8022</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU9P3DAQxa0KVLaUe0_IRy5p_d_OsUJAKyH1Qs-R155Qr5w42AkSfAg-cx3tlgNSJU4z8vvNG9sPoS-UfKVU62_EGMmZYVRKoxUlH9CGSk4aQxg7QptVblb9BH0qZUcIka1QH9EJU4QorfQGvdz9yQCNDwOMJaTRRuyWOC8ZcOrxkJYCeLKjy2Dn4HAoEWacRmxxDI-QGw-5Vo8nyP2yGtQTBzEu0ebwXIVtSMXZvk_R4z5lPKUZxjmse2IYg6uNnaZYm7lOf0bHvY0Fzg71FP2-vrq7_NHc_rr5efn9tnGSqLlhstUgPPXMtY62kgttFQWy5Z4obh1TRrSWM8ZFC8Z6KpVQWkpKOTgmNT9FF3vfKaeHBcrcDaGs97Yj1Dd39XN12ypG3oNKypjRXLwDFUKtEZiKkj3qciolQ99NOQw2P3WUdGu23dts68j5wX3ZDuBfB_6FWYFmDxR7D90uLbnGWf5v-BfJUazl</recordid><startdate>20151001</startdate><enddate>20151001</enddate><creator>Xu, Tianxin</creator><creator>Zhu, Mingyan</creator><creator>Guo, Yibing</creator><creator>Wu, Di</creator><creator>Huang, Yan</creator><creator>Fan, Xiangjun</creator><creator>Zhu, Shajun</creator><creator>Lin, Changchun</creator><creator>Li, Xiaohong</creator><creator>Lu, Jingjing</creator><creator>Zhu, Hui</creator><creator>Zhou, Pengcheng</creator><creator>Lu, Yuhua</creator><creator>Wang, Zhiwei</creator><general>SAGE Publications</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>7X8</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7SR</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>F28</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20151001</creationdate><title>Three-dimensional culture of mouse pancreatic islet on a liver-derived perfusion-decellularized bioscaffold for potential clinical application</title><author>Xu, Tianxin ; Zhu, Mingyan ; Guo, Yibing ; Wu, Di ; Huang, Yan ; Fan, Xiangjun ; Zhu, Shajun ; Lin, Changchun ; Li, Xiaohong ; Lu, Jingjing ; Zhu, Hui ; Zhou, Pengcheng ; Lu, Yuhua ; Wang, Zhiwei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c506t-2597e4d1d2c9c195347a61e0b3d063ac26849a322349e8ad15646755113ec2573</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Cells, Cultured</topic><topic>Culture</topic><topic>Extracellular Matrix - chemistry</topic><topic>Gene expression</topic><topic>Insulin</topic><topic>Islets of Langerhans - cytology</topic><topic>Islets of Langerhans Transplantation</topic><topic>Liver</topic><topic>Liver - chemistry</topic><topic>Maintenance</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Primary Cell Culture - methods</topic><topic>Staining</topic><topic>Three dimensional</topic><topic>Tissue Engineering - methods</topic><topic>Tissue Scaffolds - chemistry</topic><topic>Two dimensional</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xu, Tianxin</creatorcontrib><creatorcontrib>Zhu, Mingyan</creatorcontrib><creatorcontrib>Guo, Yibing</creatorcontrib><creatorcontrib>Wu, Di</creatorcontrib><creatorcontrib>Huang, Yan</creatorcontrib><creatorcontrib>Fan, Xiangjun</creatorcontrib><creatorcontrib>Zhu, Shajun</creatorcontrib><creatorcontrib>Lin, Changchun</creatorcontrib><creatorcontrib>Li, Xiaohong</creatorcontrib><creatorcontrib>Lu, Jingjing</creatorcontrib><creatorcontrib>Zhu, Hui</creatorcontrib><creatorcontrib>Zhou, Pengcheng</creatorcontrib><creatorcontrib>Lu, Yuhua</creatorcontrib><creatorcontrib>Wang, Zhiwei</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</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><collection>Engineered Materials Abstracts</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of biomaterials applications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xu, Tianxin</au><au>Zhu, Mingyan</au><au>Guo, Yibing</au><au>Wu, Di</au><au>Huang, Yan</au><au>Fan, Xiangjun</au><au>Zhu, Shajun</au><au>Lin, Changchun</au><au>Li, Xiaohong</au><au>Lu, Jingjing</au><au>Zhu, Hui</au><au>Zhou, Pengcheng</au><au>Lu, Yuhua</au><au>Wang, Zhiwei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Three-dimensional culture of mouse pancreatic islet on a liver-derived perfusion-decellularized bioscaffold for potential clinical application</atitle><jtitle>Journal of biomaterials applications</jtitle><addtitle>J Biomater Appl</addtitle><date>2015-10-01</date><risdate>2015</risdate><volume>30</volume><issue>4</issue><spage>379</spage><epage>387</epage><pages>379-387</pages><issn>0885-3282</issn><eissn>1530-8022</eissn><abstract>The cutting-edge technology of three-dimensional liver decellularized bioscaffold has a potential to provide a microenvironment that is suitable for the resident cells and even develop a new functional organ. Liver decellularized bioscaffold preserved the native extracellular matrix and three-dimensional architecture in support of the cell culture. The goal of this study was to discover if three-dimensional extracellular matrix derived from mouse liver could facilitate the growth and maintenance of physiological functions of mouse isolated islets. We generated a whole organ liver decellularized bioscaffold which could successfully preserve extracellular matrix proteins and the native vascular channels using 1% Triton X-100/0.1% ammonium protocol. To evaluate the potential of decellularized liver as a scaffold for islets transplantation, the liver decellularized bioscaffold was infused with mouse primary pancreatic islets which were obtained through Collagenase P digestion protocol. Its yield, morphology, and quality were estimated by microscopic analysis, dithizone staining, insulin immunofluorescence and glucose stimulation experiments. Comparing the three-dimensional culture in liver decellularized bioscaffold with the orthodoxy two-dimensional plate culture, hematoxylin-eosin staining, immunohistochemistry, and insulin gene expression were tested. Our results demonstrated that the liver decellularized bioscaffold could support cellular culture and maintenance of cell functions. In contrast with the conventional two-dimensional culture, three-dimensional culture system could give rise to an up-regulated insulin gene expression. These findings demonstrated that the liver bioscaffold by a perfusion-decellularized technique could serve as a platform to support the survival and function of the pancreatic islets in vitro. Meanwhile three-dimensional culture system had a superior role in contrast with the two-dimensional culture. This study advanced the field of regenerative medicine towards the development of a liver decellularized bioscaffold capable of forming a neo-organ and could be used as potential clinical application.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>26006767</pmid><doi>10.1177/0885328215587610</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Cells, Cultured Culture Extracellular Matrix - chemistry Gene expression Insulin Islets of Langerhans - cytology Islets of Langerhans Transplantation Liver Liver - chemistry Maintenance Male Mice Mice, Inbred C57BL Primary Cell Culture - methods Staining Three dimensional Tissue Engineering - methods Tissue Scaffolds - chemistry Two dimensional |
title | Three-dimensional culture of mouse pancreatic islet on a liver-derived perfusion-decellularized bioscaffold for potential clinical application |
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