Abstract |
During the resolution of inflammation macrophages undergo functional changes upon exposure to pro-resolving agents in their microenvironment. Primarily, engulfment of apoptotic polymorphonuclear (PMN) cells promotes conversion of macrophages toward a pro-resolving phenotype characterized by reduced CD11b expression. These macrophages are not phagocytic, do not respond to TLR ligands, and express relatively high levels of the pro-resolving enzyme 12/ 15-lipoxygenase (LO). Here, we report that the immuno-regulatory lectin galectin-1 is selectively expressed by CD11b(high), but not CD11b(low) macrophages. Upon exposure in vivo and ex vivo, galectin-1 directly promoted macrophage conversion from a CD11b(high) to a CD11b(low) phenotype and up-regulated the expression and activity of 12/15-LO. Moreover, galectin-1 treatment in vivo promoted the loss of phagocytic capacity (efferocytic satiation) in peritoneal macrophages and down-regulated secretion of TNF-α, IL-1β, and IL-10 upon LPS exposure. Our results suggest that galectin-1 could be an essential mediator in the control of macrophage function during the resolution of inflammation.
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Authors | Ran Rostoker, Hiba Yaseen, Sagie Schif-Zuck, Rachel G Lichtenstein, Gabriel A Rabinovich, Amiram Ariel |
Journal | Prostaglandins & other lipid mediators
(Prostaglandins Other Lipid Mediat)
Vol. 107
Pg. 85-94
(Dec 2013)
ISSN: 1098-8823 [Print] United States |
PMID | 23954858
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2013 Elsevier Inc. All rights reserved. |
Chemical References |
- CD11 Antigens
- Cytokines
- Galectin 1
- Lipopolysaccharides
- Arachidonate 12-Lipoxygenase
- Arachidonate 15-Lipoxygenase
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Topics |
- Animals
- Apoptosis
- Arachidonate 12-Lipoxygenase
(genetics, metabolism)
- Arachidonate 15-Lipoxygenase
(genetics, metabolism)
- CD11 Antigens
(metabolism)
- Cells, Cultured
- Cytokines
(metabolism)
- Enzyme Induction
- Galectin 1
(physiology)
- Inflammation
(enzymology)
- Lipopolysaccharides
(pharmacology)
- Macrophages, Peritoneal
(enzymology, immunology, metabolism)
- Male
- Mice
- Mice, Inbred C57BL
- Phenotype
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