Europium-doped mesoporous silica nanosphere as an immune-modulating osteogenesis/angiogenesis agent

被引:158
作者
Shi, Mengchao [1 ,2 ]
Xia, Lunguo [3 ]
Chen, Zetao [4 ]
Lv, Fang [5 ,6 ]
Zhu, Huiying [1 ]
Wei, Fei [4 ]
Han, Shengwei [4 ]
Chang, Jiang [1 ,2 ]
Xiao, Yin [2 ,4 ]
Wu, Chengtie [1 ,2 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Ceram, State Key Lab High Performance Ceram & Superfine, Shanghai 200050, Peoples R China
[2] Queensland Univ Technol, Australia China Ctr Tissue Engn & Regenerat Med, Brisbane, Qld 4059, Australia
[3] Shanghai Jiao Tong Univ, Sch Med, Peoples Hosp 9, Ctr Craniofacial Orthodont,Dept Oral & Cranio Max, Shanghai 200011, Peoples R China
[4] Queensland Univ Technol, Inst Hlth & Biomed Innovat, Brisbane, Qld 4059, Australia
[5] East China Normal Univ, Shanghai Key Lab Regulatory Biol, Inst Biomed Sci, Shanghai 200241, Peoples R China
[6] East China Normal Univ, Sch Life Sci, Shanghai 200241, Peoples R China
关键词
Mesoporous silica nanospheres; Osteogenesis; Angiogenesis; Bone tissue engineering; MARROW STROMAL CELLS; ENDOTHELIAL GROWTH-FACTOR; BIOACTIVE GLASSES; OSTEOGENIC DIFFERENTIATION; ANGIOGENESIS; NANOPARTICLES; LUMINESCENT; DRUG; IONS; BIOCERAMICS;
D O I
10.1016/j.biomaterials.2017.08.027
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Although much research has gone into the design of nanomaterials, inflammatory response still impedes the capacity of nanomaterial-induced tissue regeneration. In-situ incorporation of nutrient elements in silica-based biomaterials has emerged as a new option to endow the nanomaterials modulating biological reactions. In this work, europium-doped mesoporous silica nanospheres (Eu-MSNs) were successfully synthesized via a one-pot method. The nanospheres (size of 280-300 nm) possess uniformly spherical morphology and mesoporous structure, and well distributed Eu elements. The nanospheres show distinct fluorescent property at 615 nm for potential bio-labeling. Noticeably, the Eu-MSNs stimulate pro-inflammatory response of macrophages and induce a modulated immune microenvironment, which further activates the osteogenic differentiation of bone marrow stromal cells (BMSCs) as well as angiogenic activity of human umbilical vein endothelial cells (HUVECs). During the process, osteogenesis-related genes (e.g. ALP, OCN, OPN and COL-I) of BMSCs, and angiogenesis-related genes (e.g. CD31, MMP9, VEGFR1/2, and PDGFR alpha/beta) of HUVECs were significantly upregulated by Eu-MSNs modulating immune environment of macrophages. The in vivo study further demonstrated that the Eu-MSNs could not only stimulate osteogenesis by accelerating the new bone formation at critical-sized cranial defect site, but also support the blood vessel formation as well as collagen deposition and re-epithelialization at chronic skin wound sites, showing an improved angiogenesis activity when comparing with MSNs alone. Given the easy handling characteristics and extensive application potential, the results suggest that Eu-MSNs could be used as immunity-modulated osteogenesis/angiogenesis agent for skin and bone regeneration. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:176 / 187
页数:12
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