水动力流灌注生物反应器体外培养转基因小鼠肝组织

Che-Wei Wu, S. Sivashankar, S. Puttaswamy, Hui-Ling Lin, Kuo-Wei Chang, C. Yeh, Cheng-Hsien Liu
{"title":"水动力流灌注生物反应器体外培养转基因小鼠肝组织","authors":"Che-Wei Wu, S. Sivashankar, S. Puttaswamy, Hui-Ling Lin, Kuo-Wei Chang, C. Yeh, Cheng-Hsien Liu","doi":"10.1109/NEMS.2012.6196740","DOIUrl":null,"url":null,"abstract":"We report a Poly methyl methacrylate (PMMA) bioreactor in which hepatitis B virus (HBV) infected transgenic mice liver tissue has been cultured for long term with the continuous flow of culture medium, surrounded by mesothelial cells to provide 3-dimensional culturing conditions with adequate nutrient exchange. PDMS membrane was fabricated and a layer of mesothelial cells were cultured on it. Further this membrane was deformed and positioned on the microchannel by suction through the holes at the bottom of the channel. Liver tissue of transgenic mice was introduced on PDMS membrane. The experimental results proved that the proposed bioreactor portrays the in-vivo conditions better, with substantial improvement of liver-specific functions such as sufficient antigen expression, better structural integrity when compared to conventional static culture method. The in-vitro culture period of sliced liver tissue in our bioreactor was extended for 9 days to facilitate drug screening applications.","PeriodicalId":156839,"journal":{"name":"2012 7th IEEE International Conference on Nano/Micro Engineered and Molecular Systems (NEMS)","volume":"47 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2012-03-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"In-vitro transgenic mice liver tissue culture via hydrodynamic flow perfusion bioreactor\",\"authors\":\"Che-Wei Wu, S. Sivashankar, S. Puttaswamy, Hui-Ling Lin, Kuo-Wei Chang, C. Yeh, Cheng-Hsien Liu\",\"doi\":\"10.1109/NEMS.2012.6196740\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"We report a Poly methyl methacrylate (PMMA) bioreactor in which hepatitis B virus (HBV) infected transgenic mice liver tissue has been cultured for long term with the continuous flow of culture medium, surrounded by mesothelial cells to provide 3-dimensional culturing conditions with adequate nutrient exchange. PDMS membrane was fabricated and a layer of mesothelial cells were cultured on it. Further this membrane was deformed and positioned on the microchannel by suction through the holes at the bottom of the channel. Liver tissue of transgenic mice was introduced on PDMS membrane. The experimental results proved that the proposed bioreactor portrays the in-vivo conditions better, with substantial improvement of liver-specific functions such as sufficient antigen expression, better structural integrity when compared to conventional static culture method. The in-vitro culture period of sliced liver tissue in our bioreactor was extended for 9 days to facilitate drug screening applications.\",\"PeriodicalId\":156839,\"journal\":{\"name\":\"2012 7th IEEE International Conference on Nano/Micro Engineered and Molecular Systems (NEMS)\",\"volume\":\"47 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2012-03-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"2012 7th IEEE International Conference on Nano/Micro Engineered and Molecular Systems (NEMS)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/NEMS.2012.6196740\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"2012 7th IEEE International Conference on Nano/Micro Engineered and Molecular Systems (NEMS)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/NEMS.2012.6196740","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

摘要

我们报道了一种聚甲基丙烯酸甲酯(PMMA)生物反应器,用连续流动的培养基长期培养乙型肝炎病毒(HBV)感染的转基因小鼠肝组织,并将其包围在间皮细胞中,以提供三维培养条件和充分的营养交换。制备PDMS膜,在其上培养一层间皮细胞。此外,通过通道底部的孔吸力,该膜被变形并定位在微通道上。将转基因小鼠肝组织置于PDMS膜上。实验结果证明,与传统的静态培养方法相比,该生物反应器能更好地描述体内条件,具有明显改善肝脏特异性功能,如抗原表达充足,结构完整性更好。我们将切片肝组织在生物反应器中的体外培养时间延长了9天,以方便药物筛选应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In-vitro transgenic mice liver tissue culture via hydrodynamic flow perfusion bioreactor
We report a Poly methyl methacrylate (PMMA) bioreactor in which hepatitis B virus (HBV) infected transgenic mice liver tissue has been cultured for long term with the continuous flow of culture medium, surrounded by mesothelial cells to provide 3-dimensional culturing conditions with adequate nutrient exchange. PDMS membrane was fabricated and a layer of mesothelial cells were cultured on it. Further this membrane was deformed and positioned on the microchannel by suction through the holes at the bottom of the channel. Liver tissue of transgenic mice was introduced on PDMS membrane. The experimental results proved that the proposed bioreactor portrays the in-vivo conditions better, with substantial improvement of liver-specific functions such as sufficient antigen expression, better structural integrity when compared to conventional static culture method. The in-vitro culture period of sliced liver tissue in our bioreactor was extended for 9 days to facilitate drug screening applications.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信