Affiliation:
1. Laboratório de Imunofarmacologia Aplicada à Saúde, Fundação Oswaldo Cruz, FIOCRUZ-Rondônia, Rua da Beira, 7671 Br364, Km 3.5, 76812-245 Porto Velho, RO, Brazil
2. Centro de Biomoléculas Aplicadas à Saúde, FIOCRUZ-Rondônia e Departamento de Medicina, Universidade Federal de Rondônia (UNIR), Campus BR 364, Km 9.5, 76801-059 Porto Velho, RO, Brazil
Abstract
In the present study, we investigated thein vitroeffects of two basic myotoxic phospholipases A2(PLA2), BaTX-I, a catalytically inactive Lys-49 variant, and BaTX-II, a catalytically active Asp-49, and of one acidic myotoxic PLA2, BaPLA2, a catalytically active Asp-49, isolated fromBothrops atroxsnake venom, on the activation of J774A.1 macrophages. At noncytotoxic concentrations, the toxins did not affect the adhesion of the macrophages, nor their ability to detach. The data obtained showed that only BaTX-I stimulated complement receptor-mediated phagocytosis. However, BaTX-I, BaTX-II, and BaPLA2induced the release of the superoxide anion by J774A.1 macrophages. Additionally, only BaTX-I raised the lysosomal volume of macrophages after 15 min of incubation. After 30 min, all the phospholipases increased this parameter, which was not observed within 60 min. Moreover, BaTX-I, BaTX-II, and BaPLA2increased the number of lipid bodies on macrophages submitted to phagocytosis and not submitted to phagocytosis. However, BaTX-II and BaPLA2induced the release of TNF-αby J774A.1 macrophages. Taken together, the data show that, despite differences in enzymatic activity, the three toxins induced inflammatory events and whether the enzyme is acidic or basic does not seem to contribute to these effects.
Funder
Secretaria de Desenvolvimento do Estado de Rondonia
Subject
General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine