Published online Jan 14, 2018. doi: 10.3748/wjg.v24.i2.216
Peer-review started: September 12, 2017
First decision: October 18, 2017
Revised: November 3, 2017
Accepted: November 22, 2017
Article in press: November 22, 2017
Published online: January 14, 2018
Processing time: 125 Days and 1.2 Hours
Lipopolysaccharide (LPS)-induced liver injury serves as the pathological basis of varied hepatic diseases. LPS does not directly harm hepatocytes, while Kupffer cells serve as the key components of LPS-induced injury through secretion of pro-inflammatory cytokines such as TNF-α, IL-6, and IL-1β. β-arrestin 2 is a protein that plays an important role in regulating the TLR4/NF-κB signaling pathway, which plays a critical role in inflammation. However, the role of β-arrestin 2 in LPS-induced liver injury remains unclear.
The inhibition of LPS-induced inflammation via regulation of the TLR4/NF-κB signaling pathway may be a therapeutic method for modulating LPS-induced injury. β-arrestin 2 is a protein that plays an important role in regulating the TLR4/NF-κB signaling pathway. Therefore, we hypothesized that β-arrestin 2 can play a role in the prevention of LPS-induced liver injury.
The objective of this study was to investigate the role and the possible mechanism of β-arrestin 2 in LPS-induced liver injury in vivo and in vitro. This is the first study to show that β-arrestin 2 attenuated LPS-induced liver injury in a mouse model induced by injection of pure LPS. β-arrestin 2 may serve as a therapeutic target for the prevention and treatment of LPS-induced liver injury.
The animal model was established via intraperitoneal injection of LPS or physiological sodium chloride solution in male β-arrestin 2+/+ and β-arrestin 2-/- C57BL/6J mice. Blood samples and liver tissues were collected for analysis of liver injury and levels of pro-inflammatory cytokines. Extracts from the cultured mouse macrophage cell line RAW264.7 treated with various conditions were collected to analyze the production of pro-inflammatory cytokines and expression of key molecules involved in the TLR4/NF-κB signaling pathway.
The β-arrestin 2 knockout mice displayed more severe LPS-induced liver injury and significantly higher levels of pro-inflammatory cytokines, including IL-1β, IL-6, TNF-α, and IL-10, than the wild-type mice. Compared with the control group, pro-inflammatory cytokines, including IL-1β, IL-6, TNF-α, and IL-10, produced by the β-arrestin 2 siRNA-treated RAW264.7 cells were significantly higher at 6 h after treatment with LPS. The key molecules involved in the TLR4/NF-κB signaling pathway were also increased, including phospho-IκBα and phosho-p65.
We hypothesized that β-arrestin 2 could protect liver tissue from LPS-induced injury via inhibition of TLR4/NF-κB-mediated inflammation. This hypothesis was proven using an animal model of LPS-induced liver injury in male β-arrestin 2+/+ and β-arrestin 2-/- C57BL/6J mice and a cell model using the mouse macrophage cell line RAW264.7. These findings may be helpful for the prevention and treatment of LPS-induced liver injury in future clinical practice via strengthening the function of β-arrestin 2. However, further study on the exact role and possible mechanism is still needed.
Studies of the role of β-arrestin 2 agonists and methods of up-regulation of β-arrestin 2 in the prevention and treatment of LPS-induced liver injury should be performed.