Cargando…

Cytotoxic and inflammatory potential of a phospholipase A(2) from Bothrops jararaca snake venom

BACKGROUND: Snake venom phospholipases A(2) (PLA(2)s) have been reported to induce myotoxic, neurotoxic, hemolytic, edematogenic, cytotoxic and proinflammatory effects. This work aimed at the isolation and functional characterization of a PLA(2) isolated from Bothrops jararaca venom, named BJ-PLA(2)...

Descripción completa

Detalles Bibliográficos
Autores principales: Cedro, Rafhaella C. A., Menaldo, Danilo L., Costa, Tássia R., Zoccal, Karina F., Sartim, Marco A., Santos-Filho, Norival A., Faccioli, Lúcia H., Sampaio, Suely V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251196/
https://www.ncbi.nlm.nih.gov/pubmed/30498509
http://dx.doi.org/10.1186/s40409-018-0170-y
Descripción
Sumario:BACKGROUND: Snake venom phospholipases A(2) (PLA(2)s) have been reported to induce myotoxic, neurotoxic, hemolytic, edematogenic, cytotoxic and proinflammatory effects. This work aimed at the isolation and functional characterization of a PLA(2) isolated from Bothrops jararaca venom, named BJ-PLA(2)-I. METHODS AND RESULTS: For its purification, three consecutive chromatographic steps were used (Sephacryl S-200, Source 15Q and Mono Q 5/50 GL). BJ-PLA(2)-I showed acidic characteristics, with pI~ 4.4 and molecular mass of 14.2 kDa. Sequencing resulted in 60 amino acid residues that showed high similarity to other Bothrops PLA(2)s, including 100% identity with BJ-PLA(2), an Asp49 PLA(2) previously isolated from B. jararaca venom. Being an Asp49 PLA(2), BJ-PLA(2)-I showed high catalytic activity, and also inhibitory effects on the ADP-induced platelet aggregation. Its inflammatory characterization showed that BJ-PLA(2)-I was able to promote leukocyte migration in mice at different concentrations (5, 10 and 20 μg/mL) and also at different response periods (2, 4 and 24 h), mainly by stimulating neutrophil infiltration. Furthermore, increased levels of total proteins, IL-6, IL-1β and PGE(2) were observed in the inflammatory exudate induced by BJ-PLA(2)-I, while nitric oxide, TNF-α, IL-10 and LTB(4) levels were not significantly altered. This toxin was also evaluated for its cytotoxic potential on normal (PBMC) and tumor cell lines (HL-60 and HepG2). Overall, BJ-PLA(2)-I (2.5–160 μg/mL) promoted low cytotoxicity, with cell viabilities mostly varying between 70 and 80% and significant values obtained for HL-60 and PBMC only at the highest concentrations of the toxin evaluated. CONCLUSIONS: BJ-PLA(2)-I was characterized as an acidic Asp49 PLA(2) that induces acute local inflammation and low cytotoxicity. These results should contribute to elucidate the action mechanisms of snake venom PLA(2)s.