Interleukin-4-Loaded Heparin Hydrogel Regulates Macrophage Polarization to Promote Osteogenic Differentiation.
Yuhao ZhaoXiaofei FengZhenrui ZhaoZhengdong SongWenji WangHaiyan ZhaoPublished in: ACS biomaterials science & engineering (2024)
In bone tissue engineering, biological scaffolds are designed with structural and functional properties that closely resemble the extracellular environment, aiming to establish a microenvironment conducive to osteogenesis. Macrophages hold significant potential for promoting osteogenesis and modulating the biological behavior of tumor cells. Multiple coculture experiments of macrophages and osteoblasts have demonstrated that macrophage polarization significantly impacts osteogenesis. Therefore, exploring bone biomaterials that can modulate macrophage polarization holds great clinical significance. In this study, heparin was modified with maleimide and was used as a raw material to form a hydrogel with 4-am-PEG-SH. The compound was used to polarize macrophages and promote osteogenesis after combining with interleukin 4 (IL-4) by taking advantage of the electronegativity of heparin. The results revealed overexpressed M2 macrophage-related phenotypic genes and cocultivation with MC3T3-E1 cells demonstrated the osteogenesis-promoting effect of the loaded IL-4 heparin hydrogel. Previous research reported that hydrogel loaded with IL-4 can be used as a biomaterial for osteogenesis promotion. Heparin materials used in this paper are derived from clinically anticoagulant drugs and feature a simple operation. The synthesized hydrogel effectively binds cytokines, regulates macrophages to induce osteogenesis and has many potential clinical applications.
Keyphrases
- tissue engineering
- drug delivery
- bone regeneration
- venous thromboembolism
- wound healing
- growth factor
- cancer therapy
- bone mineral density
- stem cells
- induced apoptosis
- mesenchymal stem cells
- machine learning
- deep learning
- climate change
- signaling pathway
- risk assessment
- human health
- cell death
- dna methylation
- oxidative stress
- gene expression
- cell cycle arrest
- cell proliferation
- postmenopausal women
- bone loss