微型多孔材料
材料科学
粒径
生物物理学
巨噬细胞极化
巨噬细胞
脂多糖
纳米技术
体外
细胞生物学
化学
复合材料
免疫学
生物
生物化学
物理化学
作者
Yining Liu,Alejandra Suarez‐Arnedo,Lindsay Riley,Tasman Miley,Jingyi Xia,Tatiana Segura
标识
DOI:10.1002/adhm.202300823
摘要
Macrophages are essential in the initiation, maintenance, and transition of inflammatory processes such as foreign body response and wound healing. Mounting evidence suggests that physical factors also modulate macrophage activation. 2D in vitro systems demonstrate that constraining macrophages to small areas or channels modulates their phenotypes and changes their responses to known inflammatory agents such as lipopolysaccharide. However, how dimensionality and pore size affect macrophage phenotype is less explored. In this work, the change in macrophage M1/M2 polarization when confined in microporous annealed particle (MAP) scaffolds is studied. Particles sizes (40, 70, and 130 µm) are selected using outputs from software LOVAMAP that analyzes the characteristics of 3D pores in MAP gels. As the size of building block particle correlates with pore size inside the scaffolds, the three types of scaffold allow us to study how the degree of spatial confinement modulates the behavior of embedded macrophages. Spatially confining macrophages in scaffolds with pore size on the scale of cells leads to a reduced level of the inflammatory response, which is correlated with a change in cell morphology and motility.
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