Suppr超能文献

利用过表达纤连蛋白的马-达二氏犬肾细胞阐明晶体-细胞相互作用的机制。

Elucidation of the mechanism of crystal-cell interaction using fibronectin-overexpressing Madin-Darby canine kidney cells.

作者信息

Tsujikawa Kozo, Tsujihata Masao, Tei Norihide, Yoshimura Kazuhiro, Nonomura Norio, Okuyama Akihiko

机构信息

Department of Urology, Osaka University Graduate School of Medicine, Osaka, Japan.

出版信息

Urol Int. 2007;79(2):157-63. doi: 10.1159/000106331.

Abstract

INTRODUCTION

Attachment of newly formed crystals to renal epithelial cells is considered to be a critical step in stone formation. Previously, we reported that exogenous fibronectin (FN; 220-240 kDa) had an inhibitory effect against renal tubular cell injury in Madin-Darby canine kidney (MDCK) cells. However, the exact mechanism of FN is not fully understood. To examine the role of FN in crystal-cell interaction, we generated stably transfected MDCK cells that overexpress FN.

MATERIALS AND METHODS

MDCK cells were transfected with rat FN cDNA. First, we assessed cell injury by addition of calcium oxalate monohydrate (COM) crystals. Next, we examined the effect of FN on the adhesion of COM crystals. Finally, we studied the association of COM crystals by scanning electron microscopy.

RESULTS

Cell injury was significantly reduced in the transfected cells relative to control MDCK cells. In the inhibitory assay, crystal adhesion decreased markedly as compared with control MDCK cells. Morphological study showed that few crystals were attached to the surface of the transfected cells.

CONCLUSIONS

We elucidated the relationship between crystal-cell interaction and FN by using FN-overexpressing MDCK cells. We suppose that FN inhibits the adhesion of crystals to cells by coating the renal tubular epithelial cells.

摘要

引言

新形成的晶体附着于肾上皮细胞被认为是结石形成的关键步骤。此前,我们报道外源性纤连蛋白(FN;220 - 240 kDa)对麦迪逊-达比犬肾(MDCK)细胞的肾小管细胞损伤具有抑制作用。然而,FN的确切机制尚未完全明确。为研究FN在晶体 - 细胞相互作用中的作用,我们构建了稳定转染且过表达FN的MDCK细胞。

材料与方法

用大鼠FN cDNA转染MDCK细胞。首先,通过添加一水合草酸钙(COM)晶体评估细胞损伤。接下来,检测FN对COM晶体黏附的影响。最后,通过扫描电子显微镜研究COM晶体的结合情况。

结果

与对照MDCK细胞相比,转染细胞的细胞损伤显著降低。在抑制试验中,与对照MDCK细胞相比,晶体黏附明显减少。形态学研究表明,很少有晶体附着于转染细胞表面。

结论

我们通过使用过表达FN的MDCK细胞阐明了晶体 - 细胞相互作用与FN之间的关系。我们推测FN通过覆盖肾小管上皮细胞来抑制晶体与细胞的黏附。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验