Expansion and differentiation of CD14+CD16− and CD14++CD16+ human monocyte subsets from cord blood CD34+ hematopoietic progenitors
Cord blood
CD16
Monocyte
CD163
DOI:
10.1189/jlb.0207117
Publication Date:
2007-06-27T00:54:16Z
AUTHORS (7)
ABSTRACT
Abstract To determine whether monocytes can be generated from CD34+ hematopoietic progenitors in large numbers, cord blood cells were first expanded for 3–10 days X-VIVO 10 medium supplemented with FCS, stem cell factor (SCF), thrombopoietin (TPO), and Flt-3 Ligand (Flt-3L), then differentiated IMDM SCF, Flt-3L, IL-3 M-CSF 7–14 days. These two step cultures resulted up to a 600-fold mean increase of total CD14+ cells. Using this approach, subpopulations obtained: CD14+CD16− CD14++CD16+ occurring at 2:1 ratio. 1.25(OH)2 Vitamin D3 added the differentiation altered ratio by decreasing proportion monocytes. In comparison CD14+CD16−, showed different morphology an enhanced expression CD11b, CD33, CD40, CD64, CD86, CD163, HLA-DR, CCR5. Both secreted TNF IL-12p40 but little or no IL-10. released significantly more IL-12p40, better stimulators MLR less S. aureus phagocytosis. are clearly those present may novel monocyte subsets that represent stages distinct biological function.
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