Literature DB >> 20554312

A functional matrix metalloproteinase (MMP)-9 polymorphism modifies plasma MMP-9 levels in subjects environmentally exposed to mercury.

Anna L B Jacob-Ferreira1, Carlos J S Passos, Raquel F Gerlach, Fernando Barbosa, Jose E Tanus-Santos.   

Abstract

Mercury (Hg) exposure causes health problems including cardiovascular diseases. Although precise mechanisms have not been precisely defined yet, matrix metalloproteinases (MMPs) may be involved. The gene encoding MMP-9 presents genetic polymorphisms which affect the expression and activity level of this enzyme. Two polymorphisms in the promoter region [C(-1562)T and (CA)(n)] are functionally relevant, and are implicated in several diseases. This study aimed at examining how these polymorphisms affect the circulating MMP-9 levels and its endogenous inhibitor, the tissue inhibitor of metalloproteinase-1 (TIMP-1) in 266 subjects environmentally exposed to Hg. Blood and plasma Hg concentrations were determined by inductively coupled plasma-mass spectrometry (ICP-MS). MMP-9 and TIMP-1 concentrations were measured in plasma samples by gelatin zymography and ELISA, respectively. Genotypes for the C(-1562)T and the microsatellite (CA)(n) polymorphisms were determined. We found a positive association (P<0.05) between plasma Hg concentrations and MMP-9/TIMP-1 ratio (an index of net MMP-9 activity). When the subjects were divided into tertiles with basis on their plasma Hg concentrations, we found that the (CA)(n) polymorphism modified MMP-9 concentrations and MMP-9/TIMP-1 ratio in subjects with the lowest Hg concentrations (first tertile), with the highest MMP-9 levels being found in subjects with genotypes including alleles with 21 or more CA repeats (H alleles) (P<0.05). Conversely, this polymorphism had no effects on subjects with intermediate or high plasma Hg levels (second and third tertiles, respectively). The C(-1562)T polymorphism had no effects on MMP-9 levels. These findings suggest a significant interaction between the (CA)(n) polymorphism and low levels of Hg exposure, possibly increasing the risk of developing diseases in subjects with H alleles. Copyright 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 20554312     DOI: 10.1016/j.scitotenv.2010.05.036

Source DB:  PubMed          Journal:  Sci Total Environ        ISSN: 0048-9697            Impact factor:   7.963


  2 in total

Review 1.  Genetic Aspects of Susceptibility to Mercury Toxicity: An Overview.

Authors:  Virginia Andreoli; Francesca Sprovieri
Journal:  Int J Environ Res Public Health       Date:  2017-01-18       Impact factor: 3.390

2.  Genetic Susceptibility to Neurodegeneration in Amazon: Apolipoprotein E Genotyping in Vulnerable Populations Exposed to Mercury.

Authors:  Gabriela P F Arrifano; Rosa C R Martín-Doimeadios; María Jiménez-Moreno; Sergio Fernández-Trujillo; Marcus Augusto-Oliveira; José R Souza-Monteiro; Barbarella M Macchi; Jacqueline I Alvarez-Leite; José L M do Nascimento; Marcos T Amador; Sidney Santos; Ândrea Ribeiro-Dos-Santos; Liz C Silva-Pereira; Reinaldo B Oriá; Maria E Crespo-Lopez
Journal:  Front Genet       Date:  2018-07-27       Impact factor: 4.599

  2 in total

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