Single-cell RNA-seq reveals new types of human blood dendritic cells, monocytes, and progenitors.
Alexandra-Chloé VillaniRahul SatijaGary ReynoldsSiranush SarkizovaKarthik ShekharJames FletcherMorgane GriesbeckAndrew W ButlerShiwei ZhengSuzan LazoLaura JardineDavid DixonEmily StephensonEmil NilssonIda GrundbergDavid McDonaldAndrew FilbyWeibo LiPhilip L De JagerOrit Rozenblatt-RosenAndrew A LaneMuzlifah A HaniffaAviv RegevNir HacohenPublished in: Science (New York, N.Y.) (2017)
Dendritic cells (DCs) and monocytes play a central role in pathogen sensing, phagocytosis, and antigen presentation and consist of multiple specialized subtypes. However, their identities and interrelationships are not fully understood. Using unbiased single-cell RNA sequencing (RNA-seq) of ~2400 cells, we identified six human DCs and four monocyte subtypes in human blood. Our study reveals a new DC subset that shares properties with plasmacytoid DCs (pDCs) but potently activates T cells, thus redefining pDCs; a new subdivision within the CD1C+ subset of DCs; the relationship between blastic plasmacytoid DC neoplasia cells and healthy DCs; and circulating progenitor of conventional DCs (cDCs). Our revised taxonomy will enable more accurate functional and developmental analyses as well as immune monitoring in health and disease.
Keyphrases
- dendritic cells
- single cell
- rna seq
- endothelial cells
- immune response
- regulatory t cells
- high throughput
- induced apoptosis
- induced pluripotent stem cells
- healthcare
- pluripotent stem cells
- public health
- palliative care
- high grade
- high resolution
- risk assessment
- signaling pathway
- endoplasmic reticulum stress
- case report