학술논문

Distinct metabolic states guide maturation of inflammatory and tolerogenic dendritic cells
Document Type
article
Source
Nature Communications. 13(1)
Subject
Biochemistry and Cell Biology
Biomedical and Clinical Sciences
Biological Sciences
Immunology
Vaccine Related
Underpinning research
2.1 Biological and endogenous factors
Aetiology
1.1 Normal biological development and functioning
Inflammatory and immune system
Metabolic and endocrine
Cell Differentiation
Dendritic Cells
Glycolysis
Humans
Monocytes
Oxidative Phosphorylation
Language
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.