Baer Patrick C, Bereiter-Hahn Jurgen, Schubert Ralf, Geiger Helmut
Division of Nephrology, Department of Internal Medicine III, J W Goethe University, Frankfurt/Main, Germany.
Cells Tissues Organs. 2006;184(1):16-22. doi: 10.1159/000096947.
The culture of human renal tubular cells of well-defined nephron origin is an important basis in the research of various physiological and pathophysiological mechanisms in the kidney. In vitro differentiation of cultured cells is affected by cell isolation and culture conditions. Our study describes in vitro differentiation of cultured human renal proximal and distal (thick ascending limb and early distal) tubular epithelial cells.
Proximal tubular cells (PTC) and early distal tubular cells (DTC) were isolated immunomagnetically and cultured. In vitro differentiation was assessed by Western blot analysis and reverse transcriptase polymerase chain reaction using characteristic markers. Morphologic characterization was shown by fluorescence and scanning electron microscopy.
E-cadherin was highly expressed in DTC, whereas expression was low in PTC. In contrast to DTC, in PTC, intercellular adhesion molecule 1 and aquaporin 1 were constitutively expressed at high levels. Both cell types expressed cytokeratin 18 and Na-K-ATPase but not alpha-smooth muscle actin. Morphological analysis showed that PTC develop long microvilli, whereas DTC formed short microvilli in culture, and both express the tight junction protein zona occludens protein 1.
We demonstrate differential expression of E-cadherin, intercellular adhesion molecule 1 and aquaporin 1 in cultured PTC and DTC as described for the renal tubule in vivo. We could show the in vitro differentiation of the cells, and thus, their usefulness as an in vitro model of the human proximal and early distal tubule.
源自明确肾单位的人肾小管细胞培养是研究肾脏各种生理和病理生理机制的重要基础。培养细胞的体外分化受细胞分离和培养条件影响。我们的研究描述了培养的人近端和远端(厚升支和早期远端)肾小管上皮细胞的体外分化。
通过免疫磁珠法分离并培养近端肾小管细胞(PTC)和早期远端肾小管细胞(DTC)。使用特征性标志物通过蛋白质印迹分析和逆转录聚合酶链反应评估体外分化。通过荧光和扫描电子显微镜进行形态学表征。
E-钙黏蛋白在DTC中高表达,而在PTC中表达较低。与DTC相反,在PTC中,细胞间黏附分子1和水通道蛋白1持续高水平表达。两种细胞类型均表达细胞角蛋白18和钠钾ATP酶,但不表达α-平滑肌肌动蛋白。形态学分析表明PTC形成长微绒毛,而DTC在培养中形成短微绒毛,并且两者均表达紧密连接蛋白闭合蛋白1。
我们证明了培养的PTC和DTC中E-钙黏蛋白、细胞间黏附分子1和水通道蛋白1的差异表达,这与体内肾小管的情况一致。我们能够展示细胞的体外分化,因此,它们作为人近端和早期远端小管的体外模型是有用的。