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Phosphatidylinositol 3-Kinase γ is required for the development of experimental cerebral malaria.

Abstract
Experimental cerebral malaria (ECM) is characterized by a strong immune response, with leukocyte recruitment, blood-brain barrier breakdown and hemorrhage in the central nervous system. Phosphatidylinositol 3-kinase γ (PI3Kγ) is central in signaling diverse cellular functions. Using PI3Kγ-deficient mice (PI3Kγ-/-) and a specific PI3Kγ inhibitor, we investigated the relevance of PI3Kγ for the outcome and the neuroinflammatory process triggered by Plasmodium berghei ANKA (PbA) infection. Infected PI3Kγ-/- mice had greater survival despite similar parasitemia levels in comparison with infected wild type mice. Histopathological analysis demonstrated reduced hemorrhage, leukocyte accumulation and vascular obstruction in the brain of infected PI3Kγ-/- mice. PI3Kγ deficiency also presented lower microglial activation (Iba-1+ reactive microglia) and T cell cytotoxicity (Granzyme B expression) in the brain. Additionally, on day 6 post-infection, CD3+CD8+ T cells were significantly reduced in the brain of infected PI3Kγ-/- mice when compared to infected wild type mice. Furthermore, expression of CD44 in CD8+ T cell population in the brain tissue and levels of phospho-IkB-α in the whole brain were also markedly lower in infected PI3Kγ-/- mice when compared with infected wild type mice. Finally, AS605240, a specific PI3Kγ inhibitor, significantly delayed lethality in infected wild type mice. In brief, our results indicate a pivotal role for PI3Kγ in the pathogenesis of ECM.
AuthorsNorinne Lacerda-Queiroz, Fatima Brant, David Henrique Rodrigues, Juliana Priscila Vago, Milene Alvarenga Rachid, Lirlândia Pires Sousa, Mauro Martins Teixeira, Antonio Lucio Teixeira
JournalPloS one (PLoS One) Vol. 10 Issue 3 Pg. e0119633 ( 2015) ISSN: 1932-6203 [Electronic] United States
PMID25775137 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • 5-quinoxalin-6-ylmethylenethiazolidine-2,4-dione
  • Phosphoinositide-3 Kinase Inhibitors
  • Quinoxalines
  • Thiazolidinediones
  • Class Ib Phosphatidylinositol 3-Kinase
  • Pik3cg protein, mouse
Topics
  • Animals
  • Brain (immunology)
  • Class Ib Phosphatidylinositol 3-Kinase (genetics, metabolism)
  • Disease Models, Animal
  • Extracellular Matrix (immunology, parasitology)
  • Female
  • Humans
  • Lung (enzymology, parasitology)
  • Malaria, Cerebral (enzymology, immunology, parasitology, pathology)
  • Mice
  • Phosphoinositide-3 Kinase Inhibitors
  • Plasmodium berghei (immunology)
  • Quinoxalines (pharmacology)
  • Survival Analysis
  • Thiazolidinediones (pharmacology)

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