4.8 Article

Stratified-structural hydrogel incorporated with magnesium-ion-modified black phosphorus nanosheets for promoting neuro-vascularized bone regeneration

期刊

BIOACTIVE MATERIALS
卷 16, 期 -, 页码 271-284

出版社

KEAI PUBLISHING LTD
DOI: 10.1016/j.bioactmat.2022.02.024

关键词

Angiogenesis; Neurogenesis; Bone regeneration; Hydrogel; Black phosphorus

资金

  1. National Key Research and Devel-opment Program of China [2017YFC1103800]

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Angiogenesis and neurogenesis play important roles in bone repair. This study focuses on the development of a bilayer hydrogel that mimics the periosteum and incorporates magnesium-ion-modified black phosphorus nanosheets to enhance neurovascularized bone regeneration. The results demonstrate that this bilayer hydrogel platform can significantly promote angiogenesis and neurogenesis, as well as enhance the activity and osteogenic differentiation of bone marrow mesenchymal stem cells. Furthermore, in vivo experiments show that the bilayer hydrogel scaffolds effectively enhance early vascularization and neurogenesis, leading to successful bone regeneration and remodeling.
Angiogenesis and neurogenesis play irreplaceable roles in bone repair. Although biomaterial implantation that mimics native skeletal tissue is extensively studied, the nerve-vascular network reconstruction is neglected in the design of biomaterials. Our goal here is to establish a periosteum-simulating bilayer hydrogel and explore the efficiency of bone repair via enhancement of angiogenesis and neurogenesis. In this contribution, we designed a bilayer hydrogel platform incorporated with magnesium-ion-modified black phosphorus (BP) nanosheets for promoting neuro-vascularized bone regeneration. Specifically, we incorporated magnesium-ion-modified black phosphorus (BP@Mg) nanosheets into gelatin methacryloyl (GelMA) hydrogel to prepare the upper hydrogel, whereas the bottom hydrogel was designed as a double-network hydrogel system, consisting of two interpenetrating polymer networks composed of GelMA, PEGDA, and p-TCP nanocrystals. The magnesium ion modification process was developed to enhance BP nanosheet stability and provide a sustained release platform for bioactive ions. Our results demonstrated that the upper layer of hydrogel provided a bionic periosteal structure, which significantly facilitated angiogenesis via induction of endothelial cell migration and presented multiple advantages for the upregulation of nerve-related protein expression in neural stem cells (NSCs). Moreover, the bottom layer of the hydrogel significantly promoted bone marrow mesenchymal stem cells (BMSCs) activity and osteogenic differentiation. We next employed the bilayer hydrogel structure to correct rat skull defects. Based on our radiological and histological examinations, the bilayer hydrogel scaffolds markedly enhanced early vascularization and neurogenesis, which prompted eventual bone regeneration and remodeling. Our current strategy paves way for designing nerve-vascular network biomaterials for bone regeneration.

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