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Expression and anti-inflammatory role of activin receptor-interacting protein 2 in lipopolysaccharide-activated
1Department of Immunology, College of Basic Medical Sciences, Jilin University, Changchun, China.
Abstract:
The bacterial endotoxin lipopolysaccharide (LPS), a key pathogenic stimulator, can induce the activation of macrophages. Activin receptor-interacting protein 2 (ARIP2), an intracellular signaling protein, has a wide histological distribution, however, whether ARIP2 is involved in regulation of activation of macrophages was not well characterized. Here, by immunocytochemical staining, we found that ARIP2 protein existed in monocyte-macrophage cell line RAW264.7 cells and peritoneal macrophages of mouse, and ARIP2 expression in RAW264.7 cells was up-regulated by LPS. Furthermore, the results revealed that ARIP2 overexpression in the LPS-activated RAW264.7 cells inhibited the productions of IL-1β and TNFα, phagocytic activities and CD14 expression, whereas did not alter expressions of MyD88, TLR2 and TLR4. Additionally, in vivo ARIP2 overexpression also reduced the productions of IL-1β and TNFα from the LPS-stimulated peritoneal macrophages of mouse. These data suggest that ARIP2 may play an anti-inflammatory role in macrophages via inhibiting CD14 expression.
Insights
Activin receptor-interacting protein 2 (ARIP2) is upregulated by lipopolysaccharide (LPS) in macrophages. ARIP2 overexpression inhibits inflammatory cytokine production and phagocytosis, suggesting an anti-inflammatory role in macrophage activation.
Area of Science:
- Immunology
- Cell Biology
- Molecular Biology
Background:
- Lipopolysaccharide (LPS) activates macrophages, key immune cells.
- The role of Activin receptor-interacting protein 2 (ARIP2) in macrophage activation is unclear.
Purpose of the Study:
- To investigate the role of ARIP2 in macrophage activation induced by LPS.
- To determine if ARIP2 influences inflammatory responses and phagocytic activity.
Main Methods:
- Immunocytochemical staining to detect ARIP2 expression in RAW264.7 cells and mouse peritoneal macrophages.
- Overexpression of ARIP2 in LPS-activated macrophages.
- Measurement of cytokine production (IL-1β, TNFα), phagocytic activity, and CD14 expression.
- Assessment of MyD88, TLR2, and TLR4 expression.
Main Results:
- ARIP2 protein is present in macrophages and its expression is increased by LPS.
- ARIP2 overexpression inhibited IL-1β and TNFα production, phagocytosis, and CD14 expression in LPS-activated macrophages.
- ARIP2 overexpression did not affect MyD88, TLR2, or TLR4 expression.
- In vivo ARIP2 overexpression reduced inflammatory cytokine production in LPS-stimulated mouse macrophages.
Conclusions:
- ARIP2 plays an anti-inflammatory role in macrophages.
- ARIP2 may exert its anti-inflammatory effects by inhibiting CD14 expression during LPS-induced activation.
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