再生(生物学)
材料科学
细胞生物学
骨愈合
癌症研究
化学
医学
生物
解剖
作者
Zhiwei Zheng,Yahong Chen,Hao Hong,Yi Shen,Yun Wang,Jian Sun,Xiansong Wang
标识
DOI:10.1002/adhm.202000631
摘要
Abstract Tissue regeneration driven by immunomodulatory agents has emerged as a potential solution for repairing bone defects. However, the therapeutic benefits are compromised by disturbances in the pro‐ and anti‐inflammatory balance. Here, using magnesium nanoparticles (MgNPs) as a template, magnesium‐enriched graphene oxide nanoscrolls (MgNPs@GNSs) designed for combinational modulation of the inflammatory response are reported. First, the different effects of graphene oxide (GO) and magnesium ions (Mg 2+ ) on Raw264.7 macrophage phenotype transformation are screened. The results reveal that GO activates inflammatory M1 macrophages, and that Mg 2+ facilitates repolarization of M1 macrophages to the pro‐healing M2 phenotype. With sustained release of Mg 2+ , the MgNPs@GNS nanoplatform can orchestrate harmonious type 1 and type 2 inflammatory responses. Mg 2+ decrease the internalization of GO and downregulate the nuclear factor kappa‐B pathway, which is profoundly involved in the inflammatory process. A series of experiments show that the ordered inflammatory response induced by MgNPs@GNSs stimulates in vitro angiogenesis and osteogenesis through chemotactic, mitogenic, and morphogenic actions. Obvious vascularized bone regeneration is achieved in a rat cranial bone defect model via MgNPs@GNS deposited decellularized bone matrix scaffold. Therefore, the potential of using inherently therapeutic nanomedicine to modulate biomaterial‐induced immune responses and thus enhance bone regeneration is demonstrated.
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