TY - JOUR
T1 - Akt-2 Is a Potential Therapeutic Target for Disseminated Candidiasis
AU - Huang, Ling
AU - Ma, Yilei
AU - Guo, Hui
AU - Tang, Na
AU - Ouyang, Song
AU - Nuro-Gyina, Patrick
AU - Tao, Lijian
AU - Liu, Yusen
AU - O'Brien, Matthew C.
AU - Langdon, Wallace Y.
AU - Zhang, Jian
PY - 2022/9
Y1 - 2022/9
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85136480439&partnerID=8YFLogxK
U2 - 10.4049/jimmunol.2101003
DO - 10.4049/jimmunol.2101003
M3 - Article
C2 - 36130126
AN - SCOPUS:85136480439
SN - 0022-1767
VL - 209
SP - 991
EP - 1000
JO - Journal of Immunology
JF - Journal of Immunology
IS - 5
ER -