Akt-2 Is a Potential Therapeutic Target for Disseminated Candidiasis.
Ling HuangYilei MaHui GuoNa TangSong OuyangPatrick K Nuro-GyinaLijian TaoYusen LiuMatthew C O'BrienWallace Y LangdonJian ZhangPublished in: Journal of immunology (Baltimore, Md. : 1950) (2022)
Akt-1 and Akt-2 are the major isoforms of the serine/threonine Akt family that play a key role in controlling immune responses. However, the involvement of Akt-1 and Akt-2 isoforms in antifungal innate immunity is completely unknown. In this study, we show that Akt2 -/- , but not Akt1 -/- , mice are protected from lethal Candida albicans infection. Loss of Akt-2 facilitates the recruitment of neutrophils and macrophages to the spleen and increases reactive oxygen species expression in these cells. Treating C57BL/6 mice with a specific inhibitor for Akt-2, but not Akt-1, provides protection from lethal C. albicans infection. Our data demonstrate that Akt-2 inhibits antifungal innate immunity by hampering neutrophil and macrophage recruitment to spleens and suppressing oxidative burst, myeloperoxidase activity, and NETosis. We thus describe a novel role for Akt-2 in the regulation of antifungal innate immunity and unveil Akt-2 as a potential target for the treatment of fungal sepsis.
Keyphrases
- signaling pathway
- cell proliferation
- candida albicans
- induced apoptosis
- immune response
- pi k akt
- machine learning
- intensive care unit
- oxidative stress
- adipose tissue
- poor prognosis
- risk assessment
- acute kidney injury
- staphylococcus aureus
- insulin resistance
- long non coding rna
- binding protein
- smoking cessation
- human health
- cell wall