Blood monocytes consist of two principal subsets with distinct migratory properties.
By F. Geissmann, Steffen Jung, Dan R. Littman. Immunity, 2003
3,609 citations recorded by the source corpus.
Subfields: Immunology, Oncology
View Paper: https://www.semanticscholar.org/paper/3cf100f9958337f12575ab261a96900ad737270f
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Citations in the corpus
- Monocyte recruitment during infection and inflammation (2011, background): “Monocyte subsets and chemokine receptors Monocytes are divided into subsets on the basis of chemokine receptor expression and the presence of specific surface molecule”
- Use of Ly6G‐specific monoclonal antibody to deplete neutrophils in mice (2008, background): “As reported by others, 1A8 (anti-Ly6G) identified blood neutrophils but not blood monocytes or blood lymphocytes [12]; RB6-8C5 (anti-Gr-1) identified blood neutrophils and a subpopulation of blood monocytes [18, 19].”
- Identification of a Unique TGF-β Dependent Molecular and Functional Signature in Microglia (2013, positive): “…in order to determine whether there was similar expression of these genes in human microglia, we performed qPCR in both fetal and adult human CNS-derived microglia and human blood-derived CD14 + CD16 − and CD14 + CD16 + monocytes which are analogous to murine Ly6C Hi and Ly6C Low subsets 13 .”
- The Identification of Markers of Macrophage Differentiation in PMA-Stimulated THP-1 Cells and Monocyte-Derived Macrophages (2010, background): “Macrophage heterogeneity is influenced by differentiation state, with marked differences between monocytes and macrophages [1,40].”
- The chemokine system in innate immunity. (2015, neutral): “1) (Geissmann et al. 2003).”
- Visualizing stromal cell dynamics in different tumor microenvironments by spinning disk confocal microscopy (2008, positive): “Based on our FACS data, the fast migratory cfms+/Gr1+ cell population in the tumor stroma probably consists of granulocytes, MDSCs or monocytes (Geissmann et al., 2003).”
- Subpopulations of Mouse Blood Monocytes Differ in Maturation Stage and Inflammatory Response1 (2004, background): “monocytes indicated that CX3CR1 low (our Ly-6C) monocytes correspond to the classical CD14CD16 monocytes, whereas CX3CR1 high (our Ly-6C ) monocytes resemble CD14CD16 cells (14).”
- Immune cell migration in inflammation: present and future therapeutic targets (2005, background): “Macrophage subsets are less well defined than T cell subsets, although studies have identified a CCR2 hi CX3CR1 lo inflammatory subset and a CCR2 lo CX3CR1 hi homeostatic subse”
- AS04, an Aluminum Salt- and TLR4 Agonist-Based Adjuvant System, Induces a Transient Localized Innate Immune Response Leading to Enhanced Adaptive Immunity1 (2009, background): “Monocytes have the capacity to differentiate into DCs (27, 30) and such a differentiated population can be detected by the expression of the cell surface markers Ly6C, CD11b, and F4/80 (31, 32).”