Truncated Milk Fat Globule-EGF-like Factor 8 Ameliorates Liver Fibrosis via Inhibition of Integrin-TGFβ Receptor Interaction.
Geun Ho AnJaehun LeeXiong JinJinwoo ChungJoon-Chul KimJung-Hyuck ParkMinkyung KimChoongseong HanJong-Hoon KimDong-Hun WooPublished in: Biomedicines (2021)
Milk fat globule-EGF factor 8 (MFG-E8) protein is known as an immunomodulator in various diseases, and we previously demonstrated the anti-fibrotic role of MFG-E8 in liver disease. Here, we present a truncated form of MFG-E8 that provides an advanced therapeutic benefit in treating liver fibrosis. The enhanced therapeutic potential of the modified MFG-E8 was demonstrated in various liver fibrosis animal models, and the efficacy was further confirmed in human hepatic stellate cells and a liver spheroid model. In the subsequent analysis, we found that the modified MFG-E8 more efficiently suppressed transforming growth factor β (TGF-β) signaling than the original form of MFG-E8, and it deactivated the proliferation of hepatic stellate cells in the liver disease environment through interfering with the interactions between integrins (αvβ3 & αvβ5) and TGF-βRI. Furthermore, the protein preferentially delivered in the liver after administration, and the safety profiles of the protein were demonstrated in male and female rat models. Therefore, in conclusion, this modified MFG-E8 provides a promising new therapeutic strategy for treating fibrotic diseases.
Keyphrases
- liver fibrosis
- transforming growth factor
- epithelial mesenchymal transition
- induced apoptosis
- cell cycle arrest
- adipose tissue
- signaling pathway
- binding protein
- protein protein
- amino acid
- growth factor
- systemic sclerosis
- oxidative stress
- endothelial cells
- endoplasmic reticulum stress
- fatty acid
- small molecule
- cell death
- mouse model
- data analysis