Association of the SOD2 Polymorphism (Val16Ala) and SOD Activity with Vaso-occlusive Crisis and Acute Splenic Sequestration in Children with Sickle Cell Anemia
Isabela Cristina Cordeiro Farias1, Taciana Furtado Mendonça-Belmont1,2, Andreia Soares da Silva1, Kleyton Palmeira do Ó1, Felipe Ferreira3, Fernanda Silva Medeiros1, Luydson Richardson da Silva Vasconcelos4, Marcos André Cavalcanti Bezerra3,5, Aderson da Silva Araújo5, Patricia Muniz Mendes Freire de Moura1*, Betânia Lucena Domingues Hatzlhofer3, Ana Claudia Mendonça dos Anjos5 and Maria do Socorro de Mendonça Cavalcanti1,2
1 Biological Science Institute, University of Pernambuco Pernambuco, Brazil.
2 Post-Graduation Program in Biotechnology (RENORBIO), Federal Rural University of Pernambuco, Brazil.
3 Federal University of Pernambuco, Brazil.
4 Research Center Aggeu Magalhães (CPqAM), Oswaldo Cruz Foundation (Fiocruz), Brazil.
5 Hematology and Hemotherapy Foundation of Pernambuco (HEMOPE), Brazil.
Received: September 13, 2017
Accepted: January 15, 2018
Mediterr J Hematol Infect Dis 2018, 10(1): e2018012 DOI 10.4084/MJHID.2018.012
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Superoxide dismutase (SOD) is responsible for the first major cellular antioxidant defense, and it catalyzes the dismutation of the superoxide anion into hydrogen peroxide. Manganese superoxide dismutase (MnSOD) isoform is encoded by the SOD2 gene, which is addressed to the mitochondria. Its role in the cell’s defense against the deleterious effects of ROS is evident. The polymorphism -9 T>C (V16A) in the mitochondrial targeting sequence of the gene results in the substitution of valine by alanine. Studies in different diseases and populations revealed that the variant allele C of SOD2 reduces MnSOD catalytic activity.[4,6]
Patients with SCA (HbSS) presented reduced SOD activity when compared to the control (HbAA). In addition, Schacter et al. observed that patients with SCA presenting severe manifestations had lower SOD activity.
Because SOD2 has a wide range of allele frequencies depending on ethnicity, and the Brazilian population has mixed ancestry, our study aimed to investigate the frequency of SOD2 polymorphisms in the controls and in patients with SCA.
Materials and Methods
The patients selected for SOD determination were included randomly during the routine consultations at HEMOPE, and they were clinically stable, without the use of erythropoietin or hydroxyurea and/or without transfusion history in the last three months.
SOD2 polymorphism analysis (rs4880) was performed by real time PCR using the Rotor Gene 6000TM apparatus (Corbett Research Mortlake, Sydney, Australia) and Taqman Genotyping Assays (ID: C___8709053_10). SOD catalytic activity was determined in the plasma of patients using the Superoxide Dismutase Assay KIT according to the manufacturer’s protocol (Cayman Chemical, Ann Arbor, MI, USA).
The Hardy-Weinberg equilibrium test was performed using ARLEQUIN software (Geneva, Switzerland), and the differences of frequencies were analyzed using the Chi-square test with Yates’ correction using 2×2 contingency tables. The T-Student was used to see differences in SOD activity. The statistical analyses were performed using EPinfo (CDC, Atlanta, USA), with p<0.05 considered significant.
|Table 1. Genotipic frequencies of SOD2 polymorphism and its association with clinical events in children with sickle cell anemia treated in Hemope Foundation, Recife/Brazil.|
SOD activity was associated with the SOD2 polymorphism. TC (p=0.0321) and CC (p=0.0253) genotypes were related to decreased activity compared with TT (Figure 1). However, the SOD activity was not associated with VOC or ASS (p=0.7603; p=0.6909, respectively). On the other hand, a positive association was found between the genotypes (TC+CC) of SOD2, related to lower SOD activity, and the presence of one or more than one VOC or ASS episodes (p=0.0285; p=0.0090, respectively) (Table 1).
The present study found an association between SOD2 genotypes (TC+CC) and the presence of VOC and ASS. The association between the genotypes of decreased SOD activity (TC+CC) with ASS could be explained by the fact that macrophages in the spleen of patients with SCA would be highly activated promoting the phagocytosis of sickled cells, however, presenting diminished ability to control oxidative stress. Consequently, these macrophages could deregulate the homeostasis, contributing to the production of pro-inflammatory cytokines such as TNF-α found during VOC episodes, that induces SOD2 expression to protect cells from the TNF-α pro-inflammatory effects.
Human MnSOD precursor variants imported into rat liver mitochondria showed that the C allele precursor generated higher activity when compared to the T allele. It was demonstrated that the C allele seems to allow efficient import of MnSOD into the mitochondrial matrix, while the variant T allele appears to cause a partial arrest of the precursor within the inner membrane and a decreased formation of the active MnSOD homotetramer in the mitochondrial matrix.
On the other hand, Martin et al. showed that the C allele of the SOD2 polymorphism was associated with lower catalytic activity of MnSOD in cryopreserved hepatocytes. Bastaki et al. also found an association between the allele C and low activity of MnSOD in erythrocyte isolates of 231 healthy volunteers. In part, these reports are in accordance with our results, except that we determined the total SOD activity in the present work. The divergent effects of the allelic variants of SOD2 could be related to the experimental conditions of each study, indicating that the impact of the polymorphism could differ in regards to the species, tissue and organ compartment, such as plasma, spleen or liver.
Studies about the effects of SOD2 as marker of oxidative stress suggest a protective role of the T allele. Hong et al. observed increased formation of 8-OHdG, a common biomarker of DNA damage induced by ROS, in individuals carrying MnSOD TC/CC genotypes. Accordingly, Park et al. found that TC/CC genotypes modulate the effect of 1-OHP (a biomarker of exposure to PAHs), resulting in increased oxidative damage compared with the TT genotype. Thus, although these studies did not measure the functional enzyme activity, they support the idea that the T allele could be a marker for ROS protection.
Manfredini et al. showed increased SOD activity in hemolysates of patients with SCA when compared to the healthy individuals, indicating the activation of chronic oxidative stress in the patients with SCA. However, Schacter et al. showed association of lower SOD activity with severe manifestations in patients with SCA. Therefore, the individuals presenting genetic predisposition to have lower SOD activity would have difficulties to compensate the ROS triggered by sickling cells.
Our findings indicate that the SOD2 C allele may affect the SOD activity hampering innate cell response to oxidative stress, which plays an essential role in the occurrence of VOC and ASS. However, further functional studies should be conducted to clarify the role of the SOD2 polymorphism and its influence in SCA.
Therefore, the polymorphism of SOD2 could be considered as a genetic marker for predisposition of VOC and ASS. However, the genetic frequencies of SNPs should be limited to the studied population due to the small sample size. In addition, the combined analysis of SNPs and serum levels strongly suggests that these SNPs could have a significant influence in the variation of serum levels, which could influence the occurrence of VOC and ASS in SCA.
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