Title of article
Comparative Analysis of the Morphological, Cytochemical, Immunophenotypical, and Functional Characteristics of Normal Human Peripheral Blood Lineage−/CD16+/HLA-DR+/CD14−/lo Cells, CD14+ Monocytes, and CD16− Dendritic Cells
Author/Authors
Almeida، نويسنده , , Julia and Bueno، نويسنده , , Clara and Alguer?، نويسنده , , Ma Carmen and Sanchez، نويسنده , , Ma Luz and de Santiago، نويسنده , , Ma and Escribano، نويسنده , , Luis and D?́az-Agust?́n، نويسنده , , Beatriz and Vaquero، نويسنده , , Jose Miguel and Laso، نويسنده , , F.Javier and San Miguel، نويسنده , , Jesus F. and Orfao، نويسنده , , Alberto، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2001
Pages
14
From page
325
To page
338
Abstract
Human peripheral blood (PB) CD14lo/HLA-DR+ cells were initially described as a subset of mature monocytes. Recently, it has been suggested that these represent a part of a new subset of dendritic cells (DC), characterized by the coexpression of MDC-8/HLA-DR/CD16. The aim of the present paper was to analyze the morphological, cytochemical, phenotypical, and functional characteristics of PB CD16+/HLA-DR+ cells compared to both PB CD14+ monocytes and CD16− DC. In contrast to CD14+ monocytes, purified CD16+/HLA-DR+ cells displayed cytoplasmic veils and lacked cytoplasmic myeloperoxidase and α-naphthyl acetate esterase. Normal human PB CD16+/HLA-DR+ cells also displayed phenotypic characteristics different from those of CD14+ monocytes: they lacked the CD64 Fcγ receptor, showed lower levels of CD32, and expressed higher amounts of CD16 compared to CD14+ monocytes. They also displayed a different pattern of expression of other antigens, including CD14, HLA-DR, CD45RA, CD45RO, complement receptors and complement regulatory surface proteins, adhesion and costimulatory molecules, and cytokine receptors, among others. When compared to CD16− DC, CD16+/HLA-DR+ cells showed reactivity for CD16, dim positivity for CD14, higher expression of both Ig- and complement-receptors and lower reactivity for HLA-DR, adhesion, and costimulatory molecules (with the exception of CD86). The CD16+/HLA-DR+ cell subset displayed a higher Ig/complement-mediated phagocytic/oxidative activity than CD16− DC, although this activity was significantly lower than that of mature monocytes. Regarding cytokine production at the single cell level, LPS plus IFN-γ-stimulated PB CD16+/HLA-DR+ cells produced significant amounts of IL1β, IL6, IL12, TNFα, and IL8; however, the percentage of cytokine-producing cells and the amount of cytokine/cell were lower in CD16+/HLA-DR+ cells than in CD14+ monocytes. In addition, upon comparing CD16+/HLA-DR+ cells with CD33+++/CD16− DC, we found that the percentage of cytokine-producing cells and the amount of cytokine/cell were significantly different in both cell subsets. In summary, our results show that CD16+/HLA-DR+ cells clearly display different morphologic, cytochemical, immunophenotypical, and functional characteristics compared to both mature monocytes and CD16− DC. Interestingly, these cells are more frequent than other DC in normal human adult PB and cord blood samples, while they are less represented in normal bone marrow.
Keywords
human dendritic cell subsets , flow cytometry , Immunophenotype , phagocytic/oxidative burst activity , cytokines
Journal title
Clinical Immunology
Serial Year
2001
Journal title
Clinical Immunology
Record number
1848845
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