Xerogel Interfaced Nanofibers Stimulate Bone Regeneration Through the Activation of Integrin and Bone Morphogenetic Protein Pathways

被引:13
|
作者
Lee, Yoo-Mi [1 ,2 ]
Yun, Hyung-Mun [1 ,2 ]
Lee, Hye-Young [4 ,7 ]
Lee, Jung-Hwan [4 ,7 ]
Lim, Hyun-Chang [3 ]
Lee, Hae-Hyoung [5 ,6 ,7 ]
Kim, Hae-Won [4 ,5 ,6 ,7 ]
Kim, Eun-Cheol [1 ,2 ]
机构
[1] Kyung Hee Univ, Sch Dent, Dept Oral & Maxillofacial Pathol, Seoul 02447, South Korea
[2] Kyung Hee Univ, Sch Dent, Res Ctr Tooth & Periodontal Regenerat MRC, Seoul 02447, South Korea
[3] Kyung Hee Univ, Sch Dent, Dept Periodontol, Seoul 02447, South Korea
[4] Dankook Univ, Inst Tissue Regenerat Engn ITREN, Cheonan 31116, South Korea
[5] Dankook Univ, Dept Nanobiomed Sci, Cheonan 31116, South Korea
[6] Dankook Univ, PLUS NBM Global Res Ctr Regenerat Med BK21, Cheonan 31116, South Korea
[7] Dankook Univ, Coll Dent, Dept Biomat Sci, Cheonan 31116, South Korea
基金
新加坡国家研究基金会;
关键词
Xerogel; Interface; Core-Shell; Nanofibrous Scaffold; Bone Regeneration; Integrin Signaling; BMP Signaling; CALCIUM-PHOSPHATE PHASES; DENTAL-PULP CELLS; OSTEOBLAST DIFFERENTIATION; MECHANICAL-PROPERTIES; HYBRID; MINERALIZATION; SCAFFOLDS; ENHANCE; SHELL; BMP;
D O I
10.1166/jbn.2017.2329
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A xerogel was interfaced onto biopolymer nanofibers though a core-shell electrospinning design for bone regeneration. The xerogel-interfaced biopolymer nanofibrous matrix was bioactive and highly hydrophilic, with a significant decrease in the water contact angle. The matrix showed excellent in vitro responses of primary osteoblasts in terms of adhesion, proliferation, and migration. Furthermore, the osteoblastic differentiation of cells, including alkaline phosphatase activity, mineralization, and gene expression, was significantly upregulated by the xerogel interface. In vivo animal tests in a critical-sized calvarial defect confirmed the new bone formation ability of the xerogel-surfaced nanofiber matrices. The underlying signaling mechanisms of the stimulation were implied to be integrin and bone morphogenetic protein (BMP) pathways, as demonstrated by the activation of integrin (alpha 2 beta 1) and downstream signaling molecules (FAK, paxillin, RhoA, MAPK, and NF-kappa B), as well as the BMPs and the downstream transcription factor Smad1/5/8. Taking these findings together, the xerogel-surfaced biopolymer nanofibers are proposed to be a promising scaffold candidate for bone regeneration.
引用
收藏
页码:180 / 191
页数:12
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