» Articles » PMID: 7651381

Expression of Calcium-binding Protein Regucalcin MRNA in the Kidney Cortex of Rats: the Stimulation by Calcium Administration

Overview
Publisher Springer
Specialty Biochemistry
Date 1995 May 10
PMID 7651381
Citations 20
Authors
Affiliations
Soon will be listed here.
Abstract

The expression of calcium-binding protein regucalcin mRNA in the kidney cortex of rats was investigated. The change of regucalcin mRNA levels was analyzed by Northern blotting using liver regucalcin complementary DNA (0.9 kb of open-reading frame). Regucalcin mRNA was expressed in the kidney cortex, and this expression was clearly increased by a single intraperitoneal administration of calcium chloride solution (5-15 mg Ca/100 g body weight) in rats; this increase was remarkable at 60-120 min after the administration. Thyroparathyroidectomy (TPTX) caused a slight decrease of regucalcin mRNA levels in the kidney cortex. However, the administration of calcium (10 mg/100 g) in TPTX rats produced a clear increase of regucalcin mRNA levels in the kidney cortex. The subcutaneous administration of calcitonin (10-100 MRC mU/100 g) or parathyroid hormone [1-34] (1-10 U/100 g) in TPTX rats which received calcium (10 mg/100 g) administration did not cause an appreciable alteration of regucalcin mRNA levels in the kidney cortex, suggesting that the mRNA expression is not stimulated by calcium-regulating hormones. The administration of trifluoperazine (TFP; 5 mg/100 g), an inhibitor of Ca2+/calmodulin action, completely blocked the expression of regucalcin mRNA stimulated by calcium administration. Now, calcium content in the kidney cortex was significantly elevated by a single intraperitneal administration of calcium (10 mg/100 g) in rats. The present study clearly demonstrates that the expression of regucalcin mRNA in the kidney cortex is stimulated by calcium administration in rats. This expression may be mediated through Ca2+/calmodulin action in the kidney cortex.

Citing Articles

Extracellular Regucalcin: A Potent Suppressor in the Cancer Cell Microenvironment.

Yamaguchi M Cancers (Basel). 2025; 17(2).

PMID: 39858022 PMC: 11763602. DOI: 10.3390/cancers17020240.


Induction of renal senescence marker protein-30 (SMP30) expression by testosterone and its contribution to urinary calcium absorption in male rats.

Lin P, Jian C, Chou J, Chen C, Chen C, Soong C Sci Rep. 2016; 6:32085.

PMID: 27553527 PMC: 4995462. DOI: 10.1038/srep32085.


5α-Dihydrotestosterone regulates the expression of L-type calcium channels and calcium-binding protein regucalcin in human breast cancer cells with suppression of cell growth.

Marques R, Peres C, Vaz C, Gomes I, Figueira M, Cairrao E Med Oncol. 2015; 32(9):228.

PMID: 26255063 DOI: 10.1007/s12032-015-0676-x.


The diverse roles of calcium-binding protein regucalcin in cell biology: from tissue expression and signalling to disease.

Marques R, Maia C, Vaz C, Correia S, Socorro S Cell Mol Life Sci. 2013; 71(1):93-111.

PMID: 23519827 PMC: 11113322. DOI: 10.1007/s00018-013-1323-3.


Regucalcin and cell regulation: role as a suppressor protein in signal transduction.

Yamaguchi M Mol Cell Biochem. 2011; 353(1-2):101-37.

PMID: 21431902 DOI: 10.1007/s11010-011-0779-4.


References
1.
Yamaguchi M, Mori S . Effect of calcium-binding protein regucalcin on hepatic protein synthesis: inhibition of aminoacyl-tRNA synthetase activity. Mol Cell Biochem. 1990; 99(1):25-32. DOI: 10.1007/BF01261390. View

2.
Cheung W . Calmodulin plays a pivotal role in cellular regulation. Science. 1980; 207(4426):19-27. DOI: 10.1126/science.6243188. View

3.
Yamaguchi M, Mori S . Inhibitory effect of calcium-binding protein regucalcin on protein kinase C activity in rat liver cytosol. Biochem Med Metab Biol. 1990; 43(2):140-6. DOI: 10.1016/0885-4505(90)90019-w. View

4.
Van Os C . Transcellular calcium transport in intestinal and renal epithelial cells. Biochim Biophys Acta. 1987; 906(2):195-222. DOI: 10.1016/0304-4157(87)90012-8. View

5.
Yamaguchi M, Takei Y, Yamamoto T . Effect of thyrocalcitonin on calcium concentration in liver of intact and thyroparathyroidectomized rats. Endocrinology. 1975; 96(4):1004-8. DOI: 10.1210/endo-96-4-1004. View