TY - JOUR
T1 - Single-cell RNA-seq reveals new types of human blood dendritic cells, monocytes, and progenitors
AU - Villani, Alexandra Chloé
AU - Satija, Rahul
AU - Reynolds, Gary
AU - Sarkizova, Siranush
AU - Shekhar, Karthik
AU - Fletcher, James
AU - Griesbeck, Morgane
AU - Butler, Andrew
AU - Zheng, Shiwei
AU - Lazo, Suzan
AU - Jardine, Laura
AU - Dixon, David
AU - Stephenson, Emily
AU - Nilsson, Emil
AU - Grundberg, Ida
AU - McDonald, David
AU - Filby, Andrew
AU - Li, Weibo
AU - De Jager, Philip L.
AU - Rozenblatt-Rosen, Orit
AU - Lane, Andrew A.
AU - Haniffa, Muzlifah
AU - Regev, Aviv
AU - Hacohen, Nir
N1 - Funding Information:
Harvard University Center for AIDS Research (CFAR), an NIH-funded program (5 P30 AI060354-10)
PY - 2017/4/21
Y1 - 2017/4/21
N2 - 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.
AB - 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.
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U2 - 10.1126/science.aah4573
DO - 10.1126/science.aah4573
M3 - Article
C2 - 28428369
AN - SCOPUS:85018582872
SN - 0036-8075
VL - 356
JO - Science
JF - Science
IS - 6335
M1 - eaah4573
ER -