Blackburn J G, Hazen-Martin D J, Detrisac C J, Sens D A
Department of Pathology, Medical University of South Carolina, Charleston.
Kidney Int. 1988 Feb;33(2):508-16. doi: 10.1038/ki.1988.27.
The present study was undertaken to determine if cultures of human proximal tubule cells would retain in vivo properties inherent to this segment in the intact nephron. Ussing chamber studies demonstrated that these cultured cells generated transepithelial potential differences of approximately -2.0 mV and resistances of 0.310 K omega.cm2, supporting the concept that the proximal tubule is a "leaky" epithelium. The electrical properties did not change when the cells were exposed to amiloride (10(-4) M), but did respond to acetazolamide (10(-4) M), consistent with responses known to occur in proximal tubules. Ultrastructural analysis of these cells demonstrated features indicative of proximal tubule cells. When grown on permeable supports, where apical and basolateral growth medium compartments were maintained separate from each other, the cells were noted to undergo increased differentiation with morphological evidence of cell polarity. Freeze fracture analysis demonstrated well-formed tight junction strands and segregation of unique numbers of intramembranous particles in apical, lateral, and basal membranes. The replicas also demonstrated the presence of aggregates though to represent gap junctions, structures which occur exclusively in the proximal segment of the human nephron. These observations provide evidence that this human cell culture model originates from the human proximal tubule and retains, in culture, many of the properties associated with proximal tubule cell function and structure in vivo.
本研究旨在确定人近端小管细胞培养物是否会保留完整肾单位中该节段固有的体内特性。尤斯灌流小室研究表明,这些培养细胞产生的跨上皮电位差约为-2.0 mV,电阻为0.310 KΩ·cm2,支持近端小管是“渗漏性”上皮的概念。当细胞暴露于氨氯吡脒(10^(-4) M)时,电特性未发生变化,但对乙酰唑胺(10^(-4) M)有反应,这与近端小管中已知的反应一致。对这些细胞的超微结构分析显示出近端小管细胞的特征。当在可渗透支持物上生长时,顶端和基底外侧生长培养基隔室彼此保持分离,观察到细胞发生了分化增加,并有细胞极性的形态学证据。冷冻断裂分析显示形成良好的紧密连接链,以及顶端、侧面和基底膜中独特数量的膜内颗粒的分离。复制品还显示存在聚集体,推测代表间隙连接,这种结构仅存在于人类肾单位的近端节段。这些观察结果提供了证据,表明这种人类细胞培养模型起源于人近端小管,并在培养中保留了许多与体内近端小管细胞功能和结构相关的特性。