Activation of J77A.1 Macrophages by Three Phospholipases A2Isolated fromBothrops atroxSnake Venom
Author(s) -
Juliana L. Furtado,
George Azevedo de Oliveira,
Adriana S. Pontes,
Sulamita da Silva Setúbal,
Caroline V. Xavier,
Fabianne Lacouth-Silva,
Beatriz F. Lima,
Kayena Delaix Zaqueo,
Anderson M. Kayano,
Leonardo A. Calderón,
Rodrigo G. Stábeli,
Andreimar M. Soares,
Juliana P. Zuliani
Publication year - 2014
Publication title -
biomed research international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.772
H-Index - 126
eISSN - 2314-6141
pISSN - 2314-6133
DOI - 10.1155/2014/683123
Subject(s) - phagocytosis , bothrops , venom , snake venom , phospholipase , macrophage , superoxide , in vitro , enzyme , biochemistry , chemistry , biology , receptor , microbiology and biotechnology
In the present study, we investigated the in vitro effects of two basic myotoxic phospholipases A 2 (PLA 2 ), BaTX-I, a catalytically inactive Lys-49 variant, and BaTX-II, a catalytically active Asp-49, and of one acidic myotoxic PLA 2 , BaPLA 2 , a catalytically active Asp-49, isolated from Bothrops atrox snake 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 BaPLA 2 induced 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 BaPLA 2 increased the number of lipid bodies on macrophages submitted to phagocytosis and not submitted to phagocytosis. However, BaTX-II and BaPLA 2 induced the release of TNF- α by 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.
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