Defining human dendritic cell progenitors by multiparametric flow cytometry

被引:57
作者
Breton, Gaelle [1 ]
Lee, Jaeyop [2 ]
Liu, Kang [2 ]
Nussenzweig, Michel C. [1 ,3 ]
机构
[1] Rockefeller Univ, Lab Mol Immunol, New York, NY 10021 USA
[2] Columbia Univ, Med Ctr, Dept Microbiol & Immunol, New York, NY USA
[3] Howard Hughes Med Inst, Chevy Chase, MD USA
基金
美国国家卫生研究院;
关键词
MYELOID DC SUBSET; HUMAN CORD BLOOD; IDENTIFICATION; MACROPHAGES; HIERARCHY; REPRESENT; INNATE;
D O I
10.1038/nprot.2015.092
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Human dendritic cells (DCs) develop from progressively restricted bone marrow (BM) progenitors: these progenitor cells include granulocyte, monocyte and DC progenitor (GMDP) cells; monocyte and DC progenitor (MDP) cells; and common DC progenitor (CDP) and DC precursor (pre-DC) cells. These four DC progenitors can be defined on the basis of the expression of surface markers such as CD34 and hematopoietin receptors. In this protocol, we describe five multiparametric flow cytometry panels that can be used as a tool (i) to simultaneously detect or phenotype the four DC progenitors, (ii) to isolate DC progenitors to enable in vitro differentiation or (iii) to assess the in vitro differentiation and proliferation of DC progenitors. The entire procedure from isolation of cells to flow cytometry can be completed in 3-7 h. This protocol provides optimized antibody panels, as well as gating strategies, for immunostaining of BM and cord blood specimens to study human DC hematopoiesis in health, disease and vaccine settings.
引用
收藏
页码:1407 / 1422
页数:16
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