细胞生物学
体内
脚手架
再生(生物学)
脂多糖
归巢(生物学)
PLGA公司
炎症
材料科学
巨噬细胞
化学
免疫系统
骨愈合
体外
生物物理学
生物医学工程
生物化学
免疫学
生物
医学
解剖
生态学
生物技术
作者
Jinhui Huang,Jiawei Wei,Xue Xia,Shiqi Xiao,Shue Jin,Qin Zou,Yi Zuo,Yubao Li,Jidong Li
标识
DOI:10.1016/j.mtbio.2024.101063
摘要
Effective tissue repair relies on the orchestration of different macrophage phenotypes, both the M2 phenotype (promotes tissue repair) and M1 phenotype (pro-inflammatory) deserve attention. In this study, we propose a sequential immune activation strategy to mediate bone regeneration, by loading lipopolysaccharide (LPS) onto the surface of a strontium (Sr) ions -contained composite scaffold, which was fabricated by combining Sr-doped micro/nano-hydroxyapatite (HA) and dual degradable matrices of polycaprolactone (PCL) and poly (lactic-co-glycolic acid) (PLGA). Our strategy involves the sequential release of LPS to promote macrophage homing and induce the expression of the pro-inflammatory M1 phenotype, followed by the release of Sr ions to suppress inflammation. In vitro and in vivo experiments demonstrated that, the appropriate pro-inflammatory effects at the initial stage of implantation, along with the anti-inflammatory effects at the later stage, as well as the structural stability of the scaffolds conferred by the composition, can synergistically promote the regeneration and repair of bone defects.
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