Back to Search
Start Over
Human CD14dim monocytes patrol and sense nucleic acids and viruses via TLR7 and TLR8 receptors.
- Source :
-
Immunity [Immunity] 2010 Sep 24; Vol. 33 (3), pp. 375-86. Date of Electronic Publication: 2010 Sep 09. - Publication Year :
- 2010
-
Abstract
- Monocytes are effectors of the inflammatory response to microbes. Human CD14(+) monocytes specialize in phagocytosis and production of reactive oxygen species and secrete inflammatory cytokines in response to a broad range of microbial cues. Here, we have characterized the functions of human monocytes that lack CD14 (CD14(dim)) and express CD16. CD14(dim) monocytes were genetically distinct from natural killer cells. Gene expression analyses indicated similarities with murine patrolling Gr1(dim) monocytes, and they patrolled the endothelium of blood vessels after adoptive transfer, in a lymphocyte function-associated antigen-1-dependent manner. CD14(dim) monocytes were weak phagocytes and did not produce ROS or cytokines in response to cell-surface Toll-like receptors. Instead, they selectively produced TNF-α, IL-1β, and CCL3 in response to viruses and immune complexes containing nucleic acids, via a proinflammatory TLR7-TLR 8-MyD88-MEK pathway. Thus, CD14(dim) cells are bona fide monocytes involved in the innate local surveillance of tissues and the pathogenesis of autoimmune diseases.<br /> (Copyright © 2010 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Antigen Presentation
Cytokines biosynthesis
GPI-Linked Proteins
HLA-DR Antigens analysis
Humans
Lupus Erythematosus, Systemic immunology
Mice
Myeloid Differentiation Factor 88 physiology
Reactive Oxygen Species metabolism
Receptors, IgG analysis
Lipopolysaccharide Receptors physiology
Monocytes physiology
Nucleic Acids physiology
Toll-Like Receptor 7 physiology
Toll-Like Receptor 8 physiology
Viruses immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1097-4180
- Volume :
- 33
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Immunity
- Publication Type :
- Academic Journal
- Accession number :
- 20832340
- Full Text :
- https://doi.org/10.1016/j.immuni.2010.08.012