» Articles » PMID: 23475213

Calcium Oxalate Nephrolithiasis and Expression of Matrix GLA Protein in the Kidneys

Overview
Journal World J Urol
Specialty Urology
Date 2013 Mar 12
PMID 23475213
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

Objectives: Polymorphism of the gene for matrix GLA protein (MGP), a calcification inhibitor, is associated with nephrolithiasis. However, experimental investigations of MGP role in stone pathogenesis are limited. We determined the effect of renal epithelial exposure to oxalate (Ox), calcium oxalate (CaOx) monohydrate (COM) or hydroxyapatite (HA) crystal on the expression of MGP.

Methods: MDCK cells in culture were exposed to 0.3, 0.5 or 1 mM Ox and 33, 66 or 133-150 μg/cm(2) of COM/HA for 3-72 h. MGP expression and production were determined by Western blotting and densitometric analysis. Enzyme-linked immunosorbent assay was performed to determine MGP release into the medium. Hyperoxaluria was induced in male Sprague-Dawley rats by feeding hydroxyl-L-proline. Immunohistochemistry was performed to detect renal MGP expression.

Results: Exposure to Ox and crystals led to time- and concentration-dependent increase in expression of MGP in MDCK cells. Cellular response was quicker to crystal exposure than to the Ox, expression being significantly higher after 3-h exposure to COM or HA crystals and more than 6 h of exposure to Ox. MGP expression was increased in kidneys of hyperoxaluric rats particularly in renal peritubular vessels.

Conclusion: We demonstrate increased expression of MGP in renal tubular epithelial cells exposed to Ox or CaOx crystals as well as the HA crystals. The most significant finding of this study is the increased staining seen in renal peritubular vessels of the hyperoxaluric rats, indicating involvement of renal endothelial cells in the synthesis of MGP.

Citing Articles

Advances in the mechanism of urinary proteins in calcium oxalate kidney stone formation.

Shi M, Su X, Xiang H, Song Q, Yang S Urolithiasis. 2025; 53(1):27.

PMID: 39932538 DOI: 10.1007/s00240-025-01703-6.


Vitamins as regulators of calcium-containing kidney stones - new perspectives on the role of the gut microbiome.

Chmiel J, Stuivenberg G, Al K, Akouris P, Razvi H, Burton J Nat Rev Urol. 2023; 20(10):615-637.

PMID: 37161031 PMC: 10169205. DOI: 10.1038/s41585-023-00768-5.


Renal tubular epithelial cells treated with calcium oxalate up-regulate S100A8 and S100A9 expression in M1-polarized macrophages via interleukin 6.

Wang Q, Zhang J, Chen X, Sun F, Jiang K Iran J Basic Med Sci. 2023; 26(5):603-608.

PMID: 37051106 PMC: 10083839. DOI: 10.22038/IJBMS.2023.69202.15080.


Identification of Protein-Coding Gene Structure and Protein-Related Genes and Their Splicing Sites in Kidney Stone Disease: A Protein Big Data Analysis.

Wang S, Chen X Appl Biochem Biotechnol. 2023; 195(10):6020-6031.

PMID: 36763230 DOI: 10.1007/s12010-023-04322-2.


Crosstalk between Renal and Vascular Calcium Signaling: The Link between Nephrolithiasis and Vascular Calcification.

Liu C, Cheng C, Tsai Y, Huang H Int J Mol Sci. 2021; 22(7).

PMID: 33808324 PMC: 8036726. DOI: 10.3390/ijms22073590.


References
1.
Khan S, Glenton P, Byer K . Modeling of hyperoxaluric calcium oxalate nephrolithiasis: experimental induction of hyperoxaluria by hydroxy-L-proline. Kidney Int. 2006; 70(5):914-23. DOI: 10.1038/sj.ki.5001699. View

2.
OConnor P, Cowley Jr A . Modulation of pressure-natriuresis by renal medullary reactive oxygen species and nitric oxide. Curr Hypertens Rep. 2010; 12(2):86-92. PMC: 3722865. DOI: 10.1007/s11906-010-0094-6. View

3.
Cola C, Almeida M, Li D, Romeo F, Mehta J . Regulatory role of endothelium in the expression of genes affecting arterial calcification. Biochem Biophys Res Commun. 2004; 320(2):424-7. DOI: 10.1016/j.bbrc.2004.05.181. View

4.
Gao B, Yasui T, Itoh Y, Tozawa K, Hayashi Y, Kohri K . A polymorphism of matrix Gla protein gene is associated with kidney stones. J Urol. 2007; 177(6):2361-5. DOI: 10.1016/j.juro.2007.01.118. View

5.
Stoller M, Meng M, Abrahams H, Kane J . The primary stone event: a new hypothesis involving a vascular etiology. J Urol. 2004; 171(5):1920-4. DOI: 10.1097/01.ju.0000120291.90839.49. View