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Macrophage activation in vitro by Parachartergus fraternus venom.
Muller, Jéssica de Araujo Isaias; Lencina, Joyce Dos Santos; Souza, Maria Inês Lenz; Mortari, Márcia Renata; Toffoli-Kadri, Mônica Cristina.
Afiliação
  • Muller JAI; Laboratory of Pharmacology and Inflammation, FACFAN/Federal University of Mato Grosso do Sul, Brazil; PhD Student of the Multicenter Program of Post-Graduation in Biochemistry and Molecular Biology, INBIO/Federal University of Mato Grosso do Sul, Brazil.
  • Lencina JDS; Laboratory of Pharmacology and Inflammation, FACFAN/Federal University of Mato Grosso do Sul, Brazil; Master of Science Student of the Program of Post-Graduation in Pharmacy, FACFAN/ Federal University of Mato Grosso do Sul, Brazil.
  • Souza MIL; Laboratory of Biophysiopharmacology, INBIO/ Federal University of Mato Grosso do Sul, Brazil, CB/University of Brasilia, Brazil.
  • Mortari MR; Laboratory of Neuropharmacology, ICB/University of Brasilia, Brazil.
  • Toffoli-Kadri MC; Laboratory of Pharmacology and Inflammation, FACFAN/Federal University of Mato Grosso do Sul, Brazil. Electronic address: monica.kadri@ufms.br.
Toxicon ; 198: 48-53, 2021 Jul 30.
Article em En | MEDLINE | ID: mdl-33940047
Parachartergus fraternus wasp induces inflammation with a predominance of mononuclear cells, that can acquire macrophage functions at the sting site, amplifying the response. These cells can be activated by venomous animals and are involved in destruction of injurious agents and release of inflammatory mediators. The objective of this work was to evaluate the activity of P. fraternus venom (Pfv) on isolated murine macrophage function. The cells were obtained from peritoneal cavity of Swiss male mice and incubated with Pfv (2.5, 5 and 10 µg/mL). Cytotoxicity was determined using MTT assay. Adhesion and detachment were evaluated using violet crystal dye. Spreading was evaluated based on morphological parameters. Phagocytosis was performed with opsonized zymosan. Production of hydrogen peroxide (H2O2) and nitric oxide (NO) were quantified using the phenol red and Griess assays, respectively. Pfv at concentrations evaluated was not cytotoxic in MTT assay and did not cause macrophage detachment in cell culture plates. However, it increased adhesion of macrophage, spreading and phagocytosis of opsonized zymosan, as well as induced production of H2O2 and NO. Therefore, Pfv induces macrophage activation in vitro and the response of these cells can be correlated with the previously reported inflammatory process triggered by this wasp.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vespas / Ativação de Macrófagos Limite: Animals Idioma: En Revista: Toxicon Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Brasil País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vespas / Ativação de Macrófagos Limite: Animals Idioma: En Revista: Toxicon Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Brasil País de publicação: Reino Unido