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Inflammation-induced modulation of cellular galectin-1 and -3 expression in a model of rat peritonitis
Authors:C. D. Gil  D. Cooper  G. Rosignoli  M. Perretti  S. M. Oliani
Affiliation:2. Department of Anatomy, Faculty of Medicine (FAMERP), Av. Brigadeiro Faria Lima 5416, 15090-000, S?o José do Rio Preto, SP, Brazil
3. Post-Graduation in Morphology, S?o Paulo School of Medicine – UNIFESP, Rua Botucatu 740, 04023-900, S?o Paulo, SP, Brazil
4. The William Harvey Research Institute, Queen Mary School of Medicine and Dentistry, Charterhouse Square, London, EC1M 6BQ, UK
1. Department of Biology, Instituto de Biociências, Letras e Ciências Exatas (IBILCE), University of S?o Paulo State (UNESP), Rua Cristóv?o Colombo 2265, 15054-000, S?o José do Rio Preto, SP, Brazil
Abstract:
Objective and design: To investigate the effect of galectin-1 (Gal-1) and −3 (Gal-3) on leukocyte migration and analyze the expression of both galectins in inflammatory cells using a model of rat peritonitis. Material or Subjects: Sprague-Dawley rats (n = 4 per group). Treatment: Peritonitis was induced in animals through intraperitoneal injection of carrageenin (1.5 mg/kg) and rat mesenteries were analyzed at different time points (0, 4, 24 and 48h). For pharmacological treatment, rats received intravenous injection of Gal-1 or -3 (3μg/kg) followed by carrageenin. Methods: Western blotting and immunoelectron microscopy analysis. Statistical analysis was performed using ANOVA followed by Bonferroni test. Results: Pharmacological treatment with Gal-1, but not Gal-3, inhibited (~50 %) leukocyte recruitment into the peritoneal cavity at 4 h time-point. In this early phase, immunogold staining of mesenteries showed a diminished Gal-3 expression in degranulated mast cells and Gal-1 in transmigrated neutrophils (~20 % reduction compared to intravascular cells). In the later phases (24 and 48h), leukocyte turnover was associated with augmented Gal-1 expression in neutrophils and macrophages and Gal-3 in mast cells and macrophages. Conclusions: These results point to a balanced expression of cell-associated-Gal-1/Gal-3 and might impact on the development of new therapeutic strategies for inflammatory diseases. Received 2 September 2005; returned for revision 28 October 2005; returned for final revision 22 November 2005; accepted by M. Parnham 23 November 2005
Keywords:In vivo inflammation  Mast cell  Neutrophil  Endothelial cell  Macrophage
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