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原代兔肾近端小管细胞培养物在激素限定的无血清培养基中培养时可维持分化功能。

Primary rabbit kidney proximal tubule cell cultures maintain differentiated functions when cultured in a hormonally defined serum-free medium.

作者信息

Taub M L, Yang I S, Wang Y

机构信息

Biochemistry Department, State University of New York, Buffalo 14214.

出版信息

In Vitro Cell Dev Biol. 1989 Sep;25(9):770-5. doi: 10.1007/BF02623659.

Abstract

A primary rabbit kidney epithelial cell culture system has been developed which retains differentiated functions of the renal proximal tubule. In addition, the cells have a distinctive metabolism and spectrum of hormone responses. The primary cells were observed to retain in vitro a Na+-dependent sugar transport system (distinctive of the proximal segment of the nephron) and a Na+-dependent phosphate transport system. Both of these transport processes are localized on the apical membrane of proximal tubule cells in vivo. In addition, probenicid-sensitive p-aminohippurate (PAH) uptake was observed in basolateral membranes of the primary tubule cells, and the PAH uptake by these vesicles occurred at a rate that was very similar to that observed with membranes derived from the original tissue. Several other characteristics of the primary cells were examined, including hormone-sensitive cyclic AMP production and phosphoenolpyruvate carboxykinase (PEPCK) activity. Like the cells in vivo, the primary proximal tubule cells were observed to produce significant cyclic AMP in response to parathyroid hormone, but not in response to arginine vasopressin or salmon calcitonin. Significant PEPCK activity was observed in the particulate fraction derived from a homogenate of primary rabbit kidney proximal tubule cells.

摘要

已开发出一种原代兔肾上皮细胞培养系统,该系统保留了肾近端小管的分化功能。此外,这些细胞具有独特的代谢和激素反应谱。观察到原代细胞在体外保留了一种依赖钠的糖转运系统(这是肾单位近端段所特有的)和一种依赖钠的磷酸盐转运系统。这两种转运过程在体内均定位于近端小管细胞的顶膜上。此外,在原代小管细胞的基底外侧膜中观察到丙磺舒敏感的对氨基马尿酸(PAH)摄取,并且这些囊泡对PAH的摄取速率与从原始组织获得的膜所观察到的速率非常相似。还检查了原代细胞的其他几个特征,包括激素敏感的环磷酸腺苷(cAMP)产生和磷酸烯醇丙酮酸羧激酶(PEPCK)活性。与体内细胞一样,观察到原代近端小管细胞对甲状旁腺激素有显著的cAMP产生,但对精氨酸加压素或鲑鱼降钙素无反应。在原代兔肾近端小管细胞匀浆的微粒部分中观察到显著水平的PEPCK活性。

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