Related Experiment Video
Updated: Jan 26, 2026

Studying the Stoichiometry of Epidermal Growth Factor Receptor in Intact Cells using Correlative Microscopy
Published on: September 11, 2015
Milk Fat Globule-Epidermal Growth Factor-Factor 8 Reverses Lipopolysaccharide-Induced Microglial Oxidative Stress
Jie Li1, Xiaotian Xu2, Xiaoying Cai3
1Department of Neurology, Zengcheng District People's Hospital of Guangzhou, Guangzhou, China.
Abstract:
Oxidative stress plays an important role in various neurological disorders. Milk fat globule-epidermal growth factor-factor 8 (MFG-E8) is a regulatory protein for microglia. However, its involvement in microglial oxidative stress has not been established. In this study, we observed microglial oxidative stress in response to lipopolysaccharide (LPS) both in vitro and in vivo. LPS induced significant elevation of TNF-α, IL-6, MDA, and ROS and reduction of GSH and SOD in the mouse brains and primary microglia, which were reversed by MFG-E8 pretreatment. MFG-E8 induced the expression of Nrf-2 and HO-1 that was reduced by LPS incubation. Moreover, LPS-increased Keap-1 expression was reversed by MFG-E8. But the above tendencies were not seen when MFG-E8 was applied alone. The current study established the involvement of MFG-E8 in antioxidant effects during neuroinflammation. It may achieve the effects through the regulation of Keap-1/Nrf-2/HO-1 pathways.
Insights
Milk fat globule-epidermal growth factor-factor 8 (MFG-E8) protects against microglial oxidative stress in neuroinflammation. MFG-E8 reverses lipopolysaccharide-induced damage by regulating the Keap-1/Nrf-2/HO-1 pathway.
Area of Science:
- Neuroscience
- Molecular Biology
- Immunology
Background:
- Oxidative stress is implicated in neurological disorders.
- Microglia play a key role in neuroinflammation.
- The function of MFG-E8 in microglial oxidative stress is unknown.
Purpose of the Study:
- To investigate the role of MFG-E8 in microglial oxidative stress.
- To elucidate the underlying molecular mechanisms.
Main Methods:
- In vitro and in vivo models of microglial oxidative stress induced by lipopolysaccharide (LPS).
- Assessment of oxidative stress markers (TNF-α, IL-6, MDA, ROS, GSH, SOD).
- Analysis of the Keap-1/Nrf-2/HO-1 pathway components.
Main Results:
- LPS induced oxidative stress in mouse brains and primary microglia.
- MFG-E8 pretreatment reversed LPS-induced oxidative stress markers.
- MFG-E8 modulated the expression of Keap-1, Nrf-2, and HO-1.
Conclusions:
- MFG-E8 exhibits antioxidant effects in neuroinflammation.
- MFG-E8 may exert its protective effects via the Keap-1/Nrf-2/HO-1 pathway.
More Related Videos
Related Concept Videos
Role of Hematopoietic Growth Factors
Thrombopoietin (TPO), mainly released by the liver,...
Factors Influencing Microbial Growth: pH
Transcription Factors
Factors Influencing Microbial Growth: Temperature
Factors Influencing Microbial Growth: Osmolarity
Factors Affecting Solubility

