分子生物学
IVD分子诊断
细胞培养与分析
蛋白研究
细胞因子
重组蛋白
抗体
高通量测序建库
病原检测UCF系列
生物医药
工具酶
抑制剂激活剂与常用试剂
仪器
耗材

Accelerated bone defect regeneration through sequential activation of the M1 and M2 phenotypes of macrophages by a composite BMP-2@SIS hydrogel: An immunomodulatory perspective

Jie Tan, Qing-Yi Zhang, Yu-Ting Song, Kai Huang, Yan-Lin Jiang, Jun Chen, Rui Wang, Chen-Yu Zou, Qian-Jin Li, Bo-Quan Qin, Ning Sheng, Rong Nie, Zi-Yuan Feng, Da-Zhi Yang, Wei-Hong Yi, Hui-Qi Xie

Journal:COMPOSITES PART B-ENGINEERING

IF:11.32

DOI:10.1016/j.compositesb.2022.110149

PMID:

Published:2022-07-31

research field:分子生物学药理学细胞生物学癌症生物学

Abstract

The immune response of the host towards foreign body, especially in the form of giant cell reaction against the implanted materials, is a vital factor for determining the repair outcome of bone defect. Biomaterials with good immunomodulatory capacity and suitable degradation may promote the regeneration of bone defect and osteointegration with the host. Small intestine submucosa (SIS), a decellularized material, has been shown to possess a property for inducing the M2 phenotype of macrophages. Our findings suggested that the SIS hydrogel could induce the macrophages to polarize into mixed M1/M2 phenotypes, and such phenotypes have enhanced the migration and tube formation of angiogenesis-associated cells in vitro , whilst having a mild effect on osteoclastogenesis and osteogenesis. Experiment with a rat model for critical-sized bone defect regeneration further demonstrated that the composite [email protected] hydrogel could sequentially activate M1 and M2 macrophages and promote early-stage angiogenesis, which altogether expedited final bone defect regeneration.

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