Sasaki Hayato, Sugiyama Makoto, Sasaki Nobuya
Laboratory of Laboratory Animal Science and Medicine, School of Veterinary Medicine, Kitasato University, 35-1, Higashi-23, Towada, Aomori, 034-8628, Japan.
Laboratory of Veterinary Anatomy, School of Veterinary Medicine, Kitasato University, Towada, 034-8628, Japan.
Cytotechnology. 2019 Feb;71(1):45-56. doi: 10.1007/s10616-018-0261-1. Epub 2019 Jan 2.
The human cell line HK-2 is most commonly used as a model of renal proximal tubular epithelial cells (PTECs) for various studies despite the absence or low expression of transporters characteristic of parental PTECs. In an effort to develop reliable PTEC models, several human cell lines have been newly established over the last decade. In contrast, reliable mouse PTEC models are still unavailable. In this study, we established immortalized renal cortex tubule cell lines derived from p53 knockout mice and evaluated various PTEC characteristics toward the development of reliable mouse PTEC models. Here, we focus on MuRTE61, one of 13 newly established clonal cell lines. Albumin uptake in MuRTE61 cells was verified by incubation with fluorescent dye-labeled albumin. RT-PCR confirmed the expression of efflux transporter genes characteristic of PTECs in the MuRTE61 cells. MuRTE61 cells exhibited high sensitivity to treatment with cisplatin, a nephrotoxic agent, accompanied by upregulated expression of the uptake transporter Slc22a2 gene. Furthermore, MuRTE61 cells consistently formed spheroids with a lumen and apicobasal polarity in three-dimensional Matrigel cultures. Apical brush border microvilli were also observed in the spheroids by transmission electron microscopy. These data validate that MuRTE61 can be characterized as a reliable mouse PTEC line. In future, detailed analysis of reliable mouse and human PTEC lines will provide an accurate extrapolation of results of experiments using mice and humans, and may help resolve apparent inconsistencies between mouse and human nephrotoxicity.
尽管缺乏或低表达亲代近端肾小管上皮细胞(PTECs)特有的转运蛋白,但人类细胞系HK - 2在各种研究中最常被用作肾近端肾小管上皮细胞的模型。在过去十年中,为了开发可靠的PTEC模型,已经新建立了几种人类细胞系。相比之下,可靠的小鼠PTEC模型仍然无法获得。在本研究中,我们建立了源自p53基因敲除小鼠的永生化肾皮质肾小管细胞系,并评估了各种PTEC特征,以开发可靠的小鼠PTEC模型。在此,我们重点关注新建立的13个克隆细胞系之一的MuRTE61。通过与荧光染料标记的白蛋白孵育,验证了MuRTE61细胞对白蛋白的摄取。RT - PCR证实了MuRTE61细胞中PTECs特有的外排转运蛋白基因的表达。MuRTE61细胞对肾毒性药物顺铂治疗表现出高敏感性,同时摄取转运蛋白Slc22a2基因的表达上调。此外,MuRTE61细胞在三维基质胶培养中始终形成具有管腔和顶-基极性的球体。通过透射电子显微镜在球体中也观察到了顶端刷状缘微绒毛。这些数据证实MuRTE61可被表征为可靠的小鼠PTEC系。未来,对可靠的小鼠和人类PTEC系进行详细分析将为使用小鼠和人类进行实验的结果提供准确的外推,并可能有助于解决小鼠和人类肾毒性之间明显的不一致性。