Human dendritic cells (DCs) are derived from distinct circulating precursors that are precommitted to become CD1c+ or CD141+ DCs.
Human dendritic cells (DCs) are derived from distinct circulating precursors that are precommitted to become CD1c+ or CD141+ DCs.
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DOI:
10.1084/jem.20161135
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发表时间:
2016-12-12
期刊:
影响因子:
--
通讯作者:
Nussenzweig MC
中科院分区:
文献类型:
--
作者:
Breton G;Zheng S;Valieris R;Tojal da Silva I;Satija R;Nussenzweig MC
Breton et al. identify CD172a as a lineage marker that distinguishes human cDC precursor (pre-cDC) subpopulations committed to the CD1c+ lineage (CD172a+ pre-cDCs) or CD141+ lineage (CD172a− pre-cDCs). In humans, conventional dendritic cells (cDCs) exist as two unique populations characterized by expression of CD1c and CD141. cDCs arise from increasingly restricted but well-defined bone marrow progenitors that include the common DC progenitor that differentiates into the pre-cDC, which is the direct precursor of cDCs. In this study, we show that pre-cDCs in humans are heterogeneous, consisting of two distinct populations of precursors that are precommitted to become either CD1c+ or CD141+ cDCs. The two groups of lineage-primed precursors can be distinguished based on differential expression of CD172a. Both subpopulations of pre-cDCs arise in the adult bone marrow and can be found in cord blood and adult peripheral blood. Gene expression analysis revealed that CD172a+ and CD172a− pre-cDCs represent developmentally discrete populations that differentially express lineage-restricted transcription factors. A clinical trial of Flt3L injection revealed that this cytokine increases the number of both CD172a− and CD172a+ pre-cDCs in human peripheral blood.
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影响因子:
64.8
作者:
Shalek, Alex K.;Satija, Rahul;Shuga, Joe;Trombetta, John J.;Gennert, Dave;Lu, Diana;Chen, Peilin;Gertner, Rona S.;Gaublomme, Jellert T.;Yosef, Nir;Schwartz, Schraga;Fowler, Brian;Weaver, Suzanne;Wang, Jing;Wang, Xiaohui;Ding, Ruihua;Raychowdhury, Raktima;Friedman, Nir;Hacohen, Nir;Park, Hongkun;May, Andrew P.;Regev, Aviv
通讯作者:
Regev, Aviv
DOI:
10.1093/bioinformatics/btu638
发表时间:
2015-01-15
期刊:
Bioinformatics (Oxford, England)
影响因子:
--
作者:
Anders S;Pyl PT;Huber W
通讯作者:
Huber W
影响因子:
30.5
作者:
Grajales-Reyes GE;Iwata A;Albring J;Wu X;Tussiwand R;Kc W;Kretzer NM;Briseño CG;Durai V;Bagadia P;Haldar M;Schönheit J;Rosenbauer F;Murphy TL;Murphy KM
通讯作者:
Murphy KM
影响因子:
8.7
作者:
Manicassamy S;Pulendran B
通讯作者:
Pulendran B
DOI:
10.1084/jem.20141441
发表时间:
2015-03-09
期刊:
The Journal of experimental medicine
影响因子:
--
作者:
Breton G;Lee J;Zhou YJ;Schreiber JJ;Keler T;Puhr S;Anandasabapathy N;Schlesinger S;Caskey M;Liu K;Nussenzweig MC
通讯作者:
Nussenzweig MC