Toutain H, Fillastre J P, Morin J P
Institut National de la Santé et de la Recherche Médicale U. 295, U.E.R. de Médecine de Rouen, Saint Etienne de Rouvray, France.
Eur J Cell Biol. 1989 Aug;49(2):274-80.
High voltage free flow electrophoresis is a carrier-free method used for analytical and preparative cell separation, based on charge surface properties of cells. Two cell populations from the proximal tubule of the rabbit kidney were isolated by free flow electrophoresis from a suspension of pure proximal cells. This single-cell suspension was obtained through an original method by the combination of a Ca-binder action and gentle mechanical treatment associated with several shifting steps, on a pure suspension of isolated proximal tubules. Before the electrophoretic separation, the proximal cell origin was confirmed by enzymatic marker measurements, and the metabolic capacity was assessed by the cell respiratory activity. The isolated cells were very poor in distal tubule marker enzymes and were enriched in proximal tubule marker enzymes. Respiratory measurement showed a high cell metabolic capacity. After the electrophoretic separation, the origin of the cell populations was assessed by measuring specific marker enzymes. The cells in the slow-moving electrophoresis fractions had a high gamma-glutamyl transpeptidase activity and a low glucose-6-phosphatase activity. The fast moving cells showed a high glucose-6-phosphatase content and a poor gamma-glutamyl transpeptidase activity. Cells isolated by free flow electrophoresis were shown to possess long microvilli. This new methodology, allowed for the first time, the separation of a fast-moving cell population originating from the convoluted portion of the proximal tubule and a slow-moving cell population originating from the straight part of the proximal tubule of the rabbit kidney.
高压自由流动电泳是一种基于细胞表面电荷特性的无载体方法,用于分析性和制备性细胞分离。通过自由流动电泳从兔肾近端小管的纯近端细胞悬液中分离出两个细胞群体。这种单细胞悬液是通过一种原始方法获得的,该方法是将钙结合剂作用与温和的机械处理相结合,并进行了几个转移步骤,作用于分离出的近端小管的纯悬液。在进行电泳分离之前,通过酶标记物测量确认近端细胞的来源,并通过细胞呼吸活性评估代谢能力。分离出的细胞远端小管标记酶含量极低,近端小管标记酶含量丰富。呼吸测量显示细胞具有高代谢能力。电泳分离后,通过测量特定标记酶来评估细胞群体的来源。在慢速电泳组分中的细胞具有高γ-谷氨酰转肽酶活性和低葡萄糖-6-磷酸酶活性。快速移动的细胞显示出高葡萄糖-6-磷酸酶含量和低γ-谷氨酰转肽酶活性。通过自由流动电泳分离出的细胞显示出具有长微绒毛。这种新方法首次实现了对源自兔肾近端小管曲部的快速移动细胞群体和源自近端小管直部的慢速移动细胞群体的分离。