Generation of proximal tubule spheroids for nephrotoxicity assessment

D. Kim, J. Lim, Cho-Rok Jung, H. Kang
{"title":"Generation of proximal tubule spheroids for nephrotoxicity assessment","authors":"D. Kim, J. Lim, Cho-Rok Jung, H. Kang","doi":"10.51335/organoid.2022.2.e30","DOIUrl":null,"url":null,"abstract":"To date, nephrotoxicity in new drug development has been evaluated through two-dimensional culture of representative cell lines, such as HK-2 and human proximal tubule epithelial cells (hPTECs). Approximately 20% of new drugs that were safe in preclinical studies were withdrawn from clinical trials due to nephrotoxicity, which means the current renal cell lines used in preclinical trials have limitations for the accurate detection of nephrotoxicity. Here, we established proximal tubule cell lines from immortalized mixed primary renal cells and generated functional proximal tubule cell spheroids, which expressed all apical basolateral transporters and showed epithelial polarity. Moreover, they showed a more sensitive drug response than hPTECs, which have been commonly used as in vitro kidney models. Taken together, the proximal tubule cells described in this study provide a more stable, reproducible, and accurate in vitro kidney model for predicting nephrotoxicity, which could help early compound development.","PeriodicalId":100198,"journal":{"name":"Brain Organoid and Systems Neuroscience Journal","volume":"25 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-10-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brain Organoid and Systems Neuroscience Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.51335/organoid.2022.2.e30","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

To date, nephrotoxicity in new drug development has been evaluated through two-dimensional culture of representative cell lines, such as HK-2 and human proximal tubule epithelial cells (hPTECs). Approximately 20% of new drugs that were safe in preclinical studies were withdrawn from clinical trials due to nephrotoxicity, which means the current renal cell lines used in preclinical trials have limitations for the accurate detection of nephrotoxicity. Here, we established proximal tubule cell lines from immortalized mixed primary renal cells and generated functional proximal tubule cell spheroids, which expressed all apical basolateral transporters and showed epithelial polarity. Moreover, they showed a more sensitive drug response than hPTECs, which have been commonly used as in vitro kidney models. Taken together, the proximal tubule cells described in this study provide a more stable, reproducible, and accurate in vitro kidney model for predicting nephrotoxicity, which could help early compound development.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
近端小管球体的产生用于肾毒性评估
迄今为止,通过代表性细胞系(如HK-2和人近端小管上皮细胞(hptec))的二维培养,已经评估了新药开发中的肾毒性。在临床前研究中安全的新药中,约有20%因肾毒性退出临床试验,这意味着目前用于临床前试验的肾细胞系在准确检测肾毒性方面存在局限性。在这里,我们从永生化混合原代肾细胞中建立近端小管细胞系,并产生功能性近端小管细胞球体,表达所有根尖基底外侧转运蛋白并显示上皮极性。此外,它们比通常用于体外肾脏模型的hptec表现出更敏感的药物反应。综上所述,本研究中描述的近端小管细胞为预测肾毒性提供了一个更稳定、可重复和准确的体外肾脏模型,这可能有助于早期化合物的开发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Ageing and brain research networks in Norway StressMatic: Bridging innovation and reliability in animal models of stress Harmony in the brain: A narrative review on the shared neural substrates of emotion regulation and creativity Unravelling neuroinflammation-mediated mitochondrial dysfunction in mild cognitive impairment: Insights from targeted metabolomics Modeling Alzheimer's disease using cerebral organoids: Current challenges and prospects
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1