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Distinct metabolic states guide maturation of inflammatory and tolerogenic dendritic cells
- Source :
- Nature Communications, Nature Communications, 2022, 13, ⟨10.1038/s41467-022-32849-1⟩, Nature communications, vol 13, iss 1
- Publication Year :
- 2022
- Publisher :
- Springer Science and Business Media LLC, 2022.
-
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.
- Subjects :
- Cell biology
Multidisciplinary
1.1 Normal biological development and functioning
Inflammatory and immune system
[SDV]Life Sciences [q-bio]
Translational immunology
General Physics and Astronomy
Cell Differentiation
Dendritic Cells
General Chemistry
Monocytes
Oxidative Phosphorylation
General Biochemistry, Genetics and Molecular Biology
[SDV] Life Sciences [q-bio]
Vaccine Related
Underpinning research
2.1 Biological and endogenous factors
Humans
Aetiology
Glycolysis
Metabolic and endocrine
Subjects
Details
- ISSN :
- 20411723
- Volume :
- 13
- Database :
- OpenAIRE
- Journal :
- Nature Communications
- Accession number :
- edsair.doi.dedup.....08713b67702d6df21a8943bdc1c265d9
- Full Text :
- https://doi.org/10.1038/s41467-022-32849-1