近端小管球体的产生用于肾毒性评估

D. Kim, J. Lim, Cho-Rok Jung, H. Kang
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引用次数: 0

摘要

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。
Generation of proximal tubule spheroids for nephrotoxicity assessment
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 Approximately 20% of new drugs that were safe in preclinical studies were withdrawn from clinical trials due to nephrotoxicity, which means the current renal cell lines used in preclinical trials have limitations for the accurate detection of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.
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