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The Effects of Paracoccidioides brasiliensis Infection on GM-CSF- and M-CSF-Induced Mouse Bone Marrow-Derived Macrophage from Resistant and Susceptible Mice Strains.

Abstract
Considering the importance of macrophages as the first line of defense against fungal infection and the different roles played by the two M1- and M2-like polarized macrophages, we decided to evaluate the effects of Paracoccidioides brasiliensis infection on GM-CSF- and M-CSF-induced bone marrow-derived macrophages (BMM) from the A/J and B10.A mouse strains, an established model of resistance/susceptibility to PCM, respectively. Upon differentiation, the generated GM- or M-BMMs were characterized by morphological analyses, gene expression profiles, and cytokines production. Our main results demonstrate that GM-BMMs derived from A/J and B.10 produced high levels of pro- and anti-inflammatory cytokines that may contribute to generate an unbalanced early immune response. In accordance with the literature, the B10.A susceptible mice lineage has an innate tendency to polarize into M1-like phenotype, whereas the opposite phenotype occurs in A/J resistance mice. In this context, our data support that susceptibility and resistance are strongly correlated with M1 and M2 polarization, respectively.
AuthorsCalliandra de Souza Silva, Aldo Henrique Tavares, Marcio Sousa Jeronimo, Yasmin Soares de Lima, Lorena da Silveira Derengowski, Anamélia Lorenzetti Bocca, Ildinete Silva-Pereira
JournalMediators of inflammation (Mediators Inflamm) Vol. 2015 Pg. 605450 ( 2015) ISSN: 1466-1861 [Electronic] United States
PMID26543326 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Chemokines
  • Cytokines
  • Macrophage Colony-Stimulating Factor
  • Granulocyte-Macrophage Colony-Stimulating Factor
Topics
  • Animals
  • Bone Marrow Cells (metabolism)
  • Cell Adhesion
  • Cell Differentiation
  • Cells, Cultured
  • Chemokines (metabolism)
  • Cytokines (metabolism)
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Granulocyte-Macrophage Colony-Stimulating Factor (metabolism)
  • Inflammation
  • Macrophage Colony-Stimulating Factor (metabolism)
  • Macrophages (metabolism)
  • Male
  • Mice
  • Paracoccidioides
  • Paracoccidioidomycosis (metabolism)
  • Phagocytosis
  • Phenotype
  • Real-Time Polymerase Chain Reaction
  • Signal Transduction

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