Three-dimensional culture of human proximal tubular epithelial cells for an in vitro evaluation of drug-induced kidney injury

运输机 有机阴离子转运蛋白1 肾 药品 体外 药理学 毒性 急性肾损伤 有机阳离子转运蛋白 细胞内 化学 ATP结合盒运输机 医学 生物 生物化学 内科学 基因
作者
Hiroshi Arakawa,Daichi Higuchi,Etsushi Takahashi,Kohei Matsushita,Shiho Nedachi,Hanwei Peng,Moeno Kadoguchi,Kaoru Morimura,Ayano Araki,Masayuki Kondo,Naoki Ishiguro,Yoichi Jimbo,Ikumi Tamai
出处
期刊:Journal of Pharmaceutical Sciences [Elsevier BV]
卷期号:113 (11): 3255-3264 被引量:1
标识
DOI:10.1016/j.xphs.2024.08.009
摘要

Highlights•Renal proximal tubular epithelial cells (RPTECs) are the main targets of drug-induced kidney injury; however, no useful evaluation system is currently available.•We evaluated kidney injuries induced by 32 nephrotoxic drugs for up to 28 days using three-dimensional cultured RPTECs (3D-RPTECs) with enhanced expression of drug transporters.•The predictive performance of 3D-RPTECs for drug-induced kidney injury was better than conventional 2D-cultured RPTECs and HK-2 cells.•3D-RPTECs are useful for in vitro evaluation of RPTEC injury by measuring intracellular ATP levels.AbstractDrug-induced kidney injury (DIKI) is the major cause of acute kidney injury (AKI). Renal proximal tubular epithelial cells (RPTECs) are the primary target sites of DIKI and express transporters involved in renal drug disposition. In the present study, we focused on three-dimensionally cultured human RPTECs (3D-RPTECs) with elevated expression of drug transporters to investigate their utility in DIKI evaluation. Intracellular ATP levels in 3D-RPTECs are reduced by tenofovir and cisplatin that are substrates of an organic anion transporter 1 and an organic cation transporter 2, respectively. In addition, 3D-RPTECs were exposed to 17 and 15 drugs that are positive and negative to RPTEC toxicity, respectively, for up to 28 d. The 20 % decreasing concentration of drugs for ATP amount (EC20) was obtained, and the ratio of EC20 values and clinical maximum concentration (Cmax) ≤100 were used as cut-off value to evaluate potential of DIKI. The sensitivities of 3D-RPTECs were 82.4 % and 88.2 % after 7 d and 28 d of drug exposure, respectively, and the specificities were 100 % and 93.3 %, respectively. The predictive performance of 3D-RPTECs was higher than that of two-dimensional cultured RPTECs and the kidney cell line HK-2. In conclusion, 3D-RPTECs are useful for in vitro evaluation of RPTEC injury by measuring intracellular ATP levels.
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