细胞生物学
树突状细胞
免疫系统
生物
PI3K/AKT/mTOR通路
安普克
代谢途径
作者
Juraj Adamik,Paul V. Munson,Felix J. Hartmann,Alexis J. Combes,Philippe Pierre,Matthew F. Krummel,Sean C. Bendall,Rafael J. Argüello,Lisa H. Butterfield
标识
DOI:10.1038/s41467-022-32849-1
摘要
Abstract Cellular metabolism underpins immune cell functionality, yet our understanding of metabolic influences in human dendritic cell biology and their ability to orchestrate immune responses is poorly developed. Here, we map single-cell metabolic states and immune profiles of inflammatory and tolerogenic monocytic dendritic cells using recently developed multiparametric approaches. Single-cell metabolic pathway activation scores reveal simultaneous engagement of multiple metabolic pathways in distinct monocytic dendritic cell differentiation stages. GM-CSF/IL4-induce rapid reprogramming of glycolytic monocytes and transient co-activation of mitochondrial pathways followed by TLR4-dependent maturation of dendritic cells. Skewing of the mTOR:AMPK phosphorylation balance and upregulation of OXPHOS, glycolytic and fatty acid oxidation metabolism underpin metabolic hyperactivity and an immunosuppressive phenotype of tolerogenic dendritic cells, which exhibit maturation-resistance and a de-differentiated immune phenotype marked by unique immunoregulatory receptor signatures. This single-cell dataset provides important insights into metabolic pathways impacting the immune profiles of human dendritic cells.
科研通智能强力驱动
Strongly Powered by AbleSci AI