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Hippo kinases Mst1 and Mst2 maintain NK cell homeostasis by orchestrating metabolic state and transcriptional activity.
- Source :
-
Cell death & disease [Cell Death Dis] 2024 Jun 19; Vol. 15 (6), pp. 430. Date of Electronic Publication: 2024 Jun 19. - Publication Year :
- 2024
-
Abstract
- Natural killer (NK) cells play a crucial role in immune response against viral infections and tumors. However, further investigation is needed to better understand the key molecules responsible for determining the fate and function of NK cells. In this study, we made an important discovery regarding the involvement of the Hippo kinases Mst1 and Mst2 as novel regulators in maintaining mouse NK cell homeostasis. The presence of high Mst1 and Mst2 (Mst1/2) activity in NK cells is essential for their proper development, survival and function in a canonical Hippo signaling independent mode. Mechanistically, Mst1/2 induce cellular quiescence by regulating the processes of proliferation and mitochondrial metabolism, thereby ensuring the development and survival of NK cells. Furthermore, Mst1/2 effectively sense IL-15 signaling and facilitate the activation of pSTAT3-TCF1, which contributes to NK cell homeostasis. Overall, our investigation highlights the crucial role of Mst1/2 as key regulators in metabolic reprogramming and transcriptional regulation for mouse NK cell survival and function, emphasizing the significance of cellular quiescence during NK cell development and functional maturation.<br /> (© 2024. The Author(s).)
- Subjects :
- Animals
Humans
Mice
AMP-Activated Protein Kinases
Cell Proliferation
Cell Survival
Hippo Signaling Pathway
Interleukin-15 metabolism
Mice, Inbred C57BL
Mitochondria metabolism
Proto-Oncogene Proteins metabolism
Proto-Oncogene Proteins genetics
Signal Transduction
STAT3 Transcription Factor metabolism
Transcription, Genetic
Homeostasis
Killer Cells, Natural metabolism
Killer Cells, Natural immunology
Protein Serine-Threonine Kinases metabolism
Protein Serine-Threonine Kinases genetics
Serine-Threonine Kinase 3
Subjects
Details
- Language :
- English
- ISSN :
- 2041-4889
- Volume :
- 15
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Cell death & disease
- Publication Type :
- Academic Journal
- Accession number :
- 38898027
- Full Text :
- https://doi.org/10.1038/s41419-024-06828-x