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Calcium Extrusion Pump PMCA4: A New Player in Renal Calcium Handling?

机译:钙挤出泵PMCA4:肾钙处理的新参与者?

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摘要

Calcium (Ca2+) is vital for multiple processes in the body, and maintenance of the electrolyte concentration is required for everyday physiological function. In the kidney, and more specifically, in the late distal convoluted tubule and connecting tubule, the fine-tuning of Ca2+ reabsorption from the pro-urine takes place. Here, Ca2+ enters the epithelial cell via the transient receptor potential vanilloid receptor type 5 (TRPV5) channel, diffuses to the basolateral side bound to calbindin-D28k and is extruded to the blood compartment via the Na+/Ca2+ exchanger 1 (NCX1) and the plasma membrane Ca2+ ATPase (PMCA). Traditionally, PMCA1 was considered to be the primary Ca2+ pump in this process. However, in recent studies TRPV5-expressing tubules were shown to highly express PMCA4. Therefore, PMCA4 may have a predominant role in renal Ca2+ handling. This study aimed to elucidate the role of PMCA4 in Ca2+ homeostasis by characterizing the Ca2+ balance, and renal and duodenal Ca2+-related gene expression in PMCA4 knockout mice. The daily water intake of PMCA4 knockout mice was significantly lower compared to wild type littermates. There was no significant difference in serum Ca2+ level or urinary Ca2+ excretion between groups. In addition, renal and duodenal mRNA expression levels of Ca2+-related genes, including TRPV5, TRPV6, calbindin-D28k, calbindin-D9k, NCX1 and PMCA1 were similar in wild type and knockout mice. Serum FGF23 levels were significantly increased in PMCA4 knockout mice. In conclusion, PMCA4 has no discernible role in normal renal Ca2+ handling as no urinary Ca2+ wasting was observed. Further investigation of the exact role of PMCA4 in the distal convoluted tubule and connecting tubule is required.
机译:钙(Ca 2 + )对于体内的多个过程至关重要,并且日常生理功能需要维持电解质浓度。在肾脏中,更具体地讲,在远端回旋小管和连接小管中,发生了尿中Ca 2 + 重吸收的微调。在这里,Ca 2 + 通过瞬态受体电位5类香草酸受体(TRPV5)通道进入上皮细胞,扩散到与calbindin-D28k结合的基底外侧,并通过Na进入血液腔室。 + / Ca 2 + 交换子1(NCX1)和质膜Ca 2 + ATPase(PMCA)。传统上,在此过程中,PMCA1被认为是主要的Ca 2 + 泵。但是,最近的研究表明,表达TRPV5的肾小管高表达PMCA4。因此,PMCA4可能在肾Ca 2 + 的处理中起主要作用。本研究旨在通过表征Ca 2 + 平衡以及肾脏和十二指肠Ca 2 + 的作用来阐明PMCA4在Ca 2 + 体内平衡中的作用。相关基因在PMCA4基因敲除小鼠中的表达。与野生型同窝仔相比,PMCA4敲除小鼠的每日饮水量明显降低。两组之间的血清Ca 2 + 水平或尿Ca 2 + 排泄量无显着差异。此外,在野生型和基因敲除小鼠中,Ca 2 + 相关基因的肾和十二指肠mRNA表达水平相似,包括TRPV5,TRPV6,calbindin-D28k,calbindin-D9k,NCX1和PMCA1。 PMCA4基因敲除小鼠的血清FGF23水平显着增加。总之,PMCA4在正常肾脏Ca 2 + 处理中没有明显的作用,因为未观察到尿Ca 2 + 的浪费。需要进一步研究PMCA4在远端回旋小管和连接小管中的确切作用。

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