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条件性永生化小鼠肾小球内皮细胞系的分离与鉴定

Isolation and characterization of conditionally immortalized mouse glomerular endothelial cell lines.

作者信息

Rops Angelique L, van der Vlag Johan, Jacobs Cor W, Dijkman Henry B, Lensen Joost F, Wijnhoven Tessa J, van den Heuvel Lambert P, van Kuppevelt Toin H, Berden Jo H

机构信息

Division of Nephrology, Department of Pathology, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands.

出版信息

Kidney Int. 2004 Dec;66(6):2193-201. doi: 10.1111/j.1523-1755.2004.66009.x.

Abstract

BACKGROUND

The culture and establishment of glomerular cell lines has proven to be an important tool for the understanding of glomerular cell functions in glomerular physiology and pathology. Especially, the recent establishment of a conditionally immortalized visceral epithelial cell line has greatly boosted the research on podocyte biology.

METHODS

Glomeruli were isolated from H-2Kb-tsA58 transgenic mice that contain a gene encoding a temperature-sensitive variant of the SV40 large tumor antigen, facilitating proliferative growth at 33 degrees C and differentiation at 37 degrees C. Glomerular endothelial cells were isolated from glomerular outgrowth by magnetic beads loaded with CD31, CD105, GSL I-B4, and ULEX. Clonal cell lines were characterized by immunofluorescence staining with antibodies/lectins specific for markers of endothelial cells, podocytes, and mesangial cells. Putative glomerular endothelial cell lines were analyzed for (1) cytokine-induced expression of adhesion molecules; (2) tube formation on Matrigel coating; and (3) the presence of fenestrae.

RESULTS

As judged by immunostaining for Wilms tumor-1, smooth muscle actin (SMA), podocalyxin, and von Willebrand factor (vWF), we obtained putative endothelial, podocyte and mesangial cell lines. The mouse glomerular endothelial cell clone #1 (mGEnC-1) was positive for vWF, podocalyxin, CD31, CD105, VE-cadherin, GSL I-B4, and ULEX, internalized acetylated-low-density lipoprotein (LDL), and showed increased expression of adhesion molecules after activation with proinflammatory cytokines. Furthermore, mGEnC-1 formed tubes and contained nondiaphragmed fenestrae.

CONCLUSION

The mGEnC-1 represents a conditionally immortalized cell line with various characteristics of differentiated glomerular endothelial cells when cultured at 37 degrees C. Most important, mGEnC-1 contains nondiaphragmed fenestrae, which is a unique feature of glomerular endothelial cells.

摘要

背景

肾小球细胞系的培养与建立已被证明是理解肾小球生理和病理过程中肾小球细胞功能的重要工具。特别是,最近建立的条件永生化内脏上皮细胞系极大地推动了足细胞生物学的研究。

方法

从含有编码SV40大肿瘤抗原温度敏感变体基因的H-2Kb-tsA58转基因小鼠中分离肾小球,该基因便于在33℃增殖生长以及在37℃分化。通过负载有CD31、CD105、GSL I-B4和荆豆凝集素的磁珠从肾小球生长物中分离肾小球内皮细胞。用针对内皮细胞、足细胞和系膜细胞标志物的抗体/凝集素进行免疫荧光染色来鉴定克隆细胞系。对假定的肾小球内皮细胞系进行以下分析:(1)细胞因子诱导的黏附分子表达;(2)在基质胶包被上形成管腔;(3)窗孔的存在情况。

结果

通过对肾母细胞瘤-1、平滑肌肌动蛋白(SMA)、足细胞标记蛋白和血管性血友病因子(vWF)进行免疫染色判断,我们获得了假定的内皮细胞、足细胞和系膜细胞系。小鼠肾小球内皮细胞克隆#1(mGEnC-1)对vWF、足细胞标记蛋白、CD31、CD105、血管内皮钙黏蛋白、GSL I-B4和荆豆凝集素呈阳性,内化乙酰化低密度脂蛋白(LDL),并且在用促炎细胞因子激活后黏附分子表达增加。此外,mGEnC-1形成管腔并含有无隔膜窗孔。

结论

mGEnC-1代表一种条件永生化细胞系,在37℃培养时具有分化的肾小球内皮细胞的各种特征。最重要的是,mGEnC-1含有无隔膜窗孔,这是肾小球内皮细胞的独特特征。

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