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肾脏管状上皮细胞中钙震荡的特征。

Characteristics of spontaneous calcium oscillations in renal tubular epithelial cells.

机构信息

Division of Kidney and Hypertension, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo, Japan.

出版信息

Clin Exp Nephrol. 2012 Jun;16(3):389-98. doi: 10.1007/s10157-012-0588-4. Epub 2012 Jan 26.

DOI:10.1007/s10157-012-0588-4
PMID:22278600
Abstract

BACKGROUND

The kidney is a major organ involved in calcium (Ca(2+)) metabolism. Ca(2+) is transported through renal tubular epithelial cells. The intracellular free calcium concentration (Ca(2+)) is tightly controlled at a low concentration, but transient increases and oscillations in Ca(2+) are induced by various conditions. In this study, we investigated the mechanisms underlying the spontaneous Ca(2+) oscillations observed in MDCK cells.

METHODS

Ca(2+) was monitored in fura-2-loaded Madin-Darby canine kidney (MDCK) cells using a calcium imaging system. We investigated the mechanism by which Ca(2+) changed by applying drugs or by changing the extracellular Ca(2+) concentration.

RESULTS

Spontaneous Ca(2+) oscillations occurred in MDCK cells. The oscillations occurred irregularly and were not transmitted to neighboring cells. Spontaneous Ca(2+) oscillations in MDCK cells were initiated by Ca(2+) release from ryanodine/IP(3)-sensitive intracellular calcium stores, and their frequency was largely unaffected by the extracellular Ca(2+) concentration. Moreover, the frequency of the oscillations was increased by extracellular nucleotide, but was decreased when the nucleotides were removed.

CONCLUSIONS

Our study suggested that Ca(2+) release from ryanodine/IP(3)-sensitive intracellular calcium stores mediates spontaneous Ca(2+) oscillations in MDCK cells. Calcium oscillations may be associated with the function of the renal tubular epithelial cells.

摘要

背景

肾脏是参与钙(Ca(2+))代谢的主要器官。Ca(2+) 通过肾小管上皮细胞进行转运。细胞内游离钙浓度(Ca(2+))被严格控制在低浓度,但Ca(2+)的瞬时增加和波动是由各种条件诱导的。在这项研究中,我们研究了观察到的 MDCK 细胞中自发的Ca(2+)波动的机制。

方法

使用钙成像系统监测负载 fura-2 的 Madin-Darby 犬肾(MDCK)细胞中的Ca(2+)。我们通过应用药物或改变细胞外 Ca(2+)浓度来研究Ca(2+)变化的机制。

结果

MDCK 细胞中发生自发的Ca(2+)波动。波动不规则发生,不会传递到相邻细胞。MDCK 细胞中的自发Ca(2+)波动是由 Ryanodine/IP(3)敏感的细胞内钙库中的 Ca(2+)释放引发的,其频率在很大程度上不受细胞外 Ca(2+)浓度的影响。此外,细胞外核苷酸增加了波动的频率,但当核苷酸被去除时,频率降低。

结论

我们的研究表明,Ryanodine/IP(3)敏感的细胞内钙库中的 Ca(2+)释放介导了 MDCK 细胞中的自发Ca(2+)波动。钙波动可能与肾小管上皮细胞的功能有关。

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