Protein Variants | Comment | Organism |
---|---|---|
additional information | generation of PI3Kgamma-deficient mice | Mus musculus |
Inhibitors | Comment | Organism | Structure |
---|---|---|---|
AS605240 | a specific PI3Kgamma inhibitor, significantly delays lethality in Plasmodium berghei-infected wild-type micer | Mus musculus |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Mus musculus | - |
isozyme PI3Kgamma | - |
Mus musculus C57BL/6 | - |
isozyme PI3Kgamma | - |
Source Tissue | Comment | Organism | Textmining |
---|---|---|---|
brain | - |
Mus musculus | - |
T-lymphocyte | - |
Mus musculus | - |
Synonyms | Comment | Organism |
---|---|---|
phosphatidylinositol 3-kinase gamma | - |
Mus musculus |
PI3Kgamma | - |
Mus musculus |
General Information | Comment | Organism |
---|---|---|
malfunction | Plasmodium berghei ANKA-infected PI3Kgamm knockout mice show greater survival despite similar parasitemia levels in comparison with infected wild-type mice. Histopathological analysis demonstrates reduced hemorrhage, leukocyte accumulation and vascular obstruction in the brain of infected PI3Kgamma null mice. PI3Kgamma deficiency also causes lower microglial activation and T cell cytotoxicity in the brain. On day 6 post-infection, CD3+/CD8+ T cells are significantly reduced in the brain of infected PI3Kgamma null mice when compared to infected wild-type mice and expression of CD44 in CD8+ T cell population in the brain tissue and levels of phospho-IkappaB-alpha in the whole brain are also markedly lower in infected PI3Kgamma null mice, phenotype, overview | Mus musculus |
physiological function | phosphatidylinositol 3-kinase gamma is central in signaling diverse cellular functions. Relevance of isozyme PI3Kgamma for the outcome and the neuroinflammatory process triggered by Plasmodium berghei ANKA infection | Mus musculus |