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Modulation of telomerase gene expression of activated peripheral | 27204
Journal of Cell Science & Therapy

Journal of Cell Science & Therapy
Open Access

ISSN: 2157-7013

+44 1300 500008

Modulation of telomerase gene expression of activated peripheral blood mononuclear cells is influenced by Ala16Val-Sod2 gene polymorphism


5th World Congress on Cell & Stem Cell Research

March 23-25, 2015 DoubleTree by Hilton Chicago - North Shore, USA

Fernanda Barbisan?, Dianni Capelleto, Veronica Azzolin, Eduardo Bortoluzzi Dornelles1, Francine Carla Cadona1, Alencar Kolinski Machado1, Cybele Ferreira Teixeira1,Glauber Wagner2, Euler Esteves Ribeiro1, Ivana Beatrice M�nica da Cruz1

Posters: J Cell Sci Ther

Abstract :

The activation process of T and B-lymphocytes involves the increase in cellular proliferation and upregulation of telomerase activity, comparable to those observed in stem cells and transformed cell lines. However, aging decline of total number of T and B-lymphocytes(immunosenescence) due decrease in the telomerase activity that is responsible to telomeric DNA region restoration. As immunosenescence is a process that present individuals variation, the influence of genetic alteration of oxidative stress metabolism on telomerase gene expression of activated lymphocytes, need to be elucidated. Human beings present a superoxide dismutase manganese dependent (SOD2) single nucleotide polymorphism (SNP) (rs4880 in 16 codon (Ala16Val-SOD2) generating three genotypes. Both homozygous genotypes create imbalance in O-2? H2O2 levels due change in SOD2 efficiency (VV = low efficiency; AA= high efficiency) and has been associated with chronic diseases and differential response to drug and toxicants exposition.Therefore, we evaluated the effect of SOD2-SNP cell expansion, viability and telomerase expression of peripheral blood mononuclear cells (PBMCs) from subjects with different Ala16Val-SOD2 genotypes (n=12). PBMCs were cultured in RPMI 1340 in controlled conditions (CO2 5%-37oC) and the viability/cells proliferation was evaluated by MTT assay and flow cytometry (cell cycle and apoptosis induction) after 1, 3, 7 and 14 days. The telomerase modulation was analyzed by qRT-PCR and telomere shortening by ELISA immunoassay. Whereas, after 3 three days exposition AA-PBMCs presented high proliferative rate than other genotypes, from this period also occur a fast loss of proliferation and apoptosis processes. After 15 days just VV genotype presented up regulation of telomerase gene.The present study corroborate the hypothesis that proliferation-imunosenescence is broadly regulated by O-2? H2O2 mitochondrial levels.

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