Angiogenesis-promoted bone repair with silicate-shelled hydrogel fiber scaffolds

被引:51
作者
Dashnyam, Khandmaa [1 ,2 ,3 ]
Buitrago, Jennifer O. [1 ,2 ,3 ]
Bold, Tsendmaa [1 ,2 ,3 ]
Mandakhbayar, Nandin [1 ,2 ,3 ]
Perez, Roman A. [1 ,2 ,3 ,4 ]
Knowles, Jonathan C. [5 ,6 ,7 ,8 ]
Lee, Jung-Hwan [1 ,2 ,3 ,5 ,8 ]
Kim, Hae-Won [1 ,2 ,3 ,5 ,8 ]
机构
[1] Dankook Univ, Inst Tissue Regenerat Engn ITREN, Cheonan 31116, South Korea
[2] Dankook Univ, Dept Nanobiomed Sci, Cheonan 31116, South Korea
[3] Dankook Univ, BK21 PLUS Global Res Ctr Regenerat Med, Cheonan 31116, South Korea
[4] Univ Int Catalunya, Regenerat Med Res Inst, Barcelona, Spain
[5] Dankook Univ, UCL Eastman Korea Dent Med Innovat Ctr, Cheonan 31116, South Korea
[6] UCL, Eastman Dent Inst, Div Biomat & Tissue Engn, London, England
[7] UCL, Eastman Dent Inst, Discoveries Ctr Regenerat & Precis Med, London, England
[8] 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
OSTEOGENIC DIFFERENTIATION; DESIGNED SCAFFOLDS; CO-DELIVERY; PROLIFERATION; NANOPARTICLES; PHOSPHATE; DRUG; CUES; ION;
D O I
10.1039/c9bm01103j
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Promoting angiogenesis is a key strategy for stimulating the repair of damaged tissues, including bone. Among other proangiogenic factors, ions have recently been considered a potent element that can be incorporated into biomaterials and then released at therapeutic doses. Silicate-based biomaterials have been reported to induce neovascularization through vascular endothelial growth factor signaling pathway, potentiating acceleration of bone regeneration. Here, we designed a silicate-shelled hydrogel fiber scaffold with a hard/soft layered structure to investigate the possibility of silicate coating on biopolymer for enhancing biological properties. An alginate hydrogel was injected to form a fiber scaffold with shape-tunability that was then coated with a thin silicate layer with various sol-gel compositions. The silicate/alginate scaffold could release calcium and silicate ions, and in particular, silicate ion release was highly sustainable for over one week at therapeutically relevant levels. The ionic release was highly effective in stimulating the mRNA expression of angiogenic markers (VEGF, KDR, eNOS, bFGF, and HIF1-alpha) in endothelial cells (HUVECs). Moreover, the in vitro tubular networking of cells was significantly enhanced (1.5 times). In vivo implantation in subcutaneous tissue revealed more pronounced blood vessel formation around the silicate-shelled scaffolds than around silicate-free scaffolds. The presence of a silicate shell was also shown to accelerate acellular mineral (hydroxyapatite) formation. The cellular osteogenesis potential of the silicate/alginate scaffold was further proven by the enhanced expression of osteogenic genes (Col1a1, ALP and OCN). When implanted in a rat calvarium defect, the silicate-shelled scaffold demonstrated significantly improved bone formation (2-3 times higher in bone volume and density) with a concurrent sign of proangiogenesis. This work highlights that the surface-layering of silicate composition is an effective approach for improving the bone regeneration capacity of polymeric hydrogel scaffolds by stimulating ion-induced angiogenesis and providing bone bioactivity to the surface.
引用
收藏
页码:5221 / 5231
页数:11
相关论文
共 51 条
[1]   A calcium-induced signaling cascade leading to osteogenic differentiation of human bone marrow-derived mesenchymal stromal cells [J].
Barradas, Ana M. C. ;
Fernandes, Hugo A. M. ;
Groen, Nathalie ;
Chai, Yoke Chin ;
Schrooten, Jan ;
van de Peppel, Jeroen ;
van Leeuwen, Johannes P. T. M. ;
van Blitterswijk, Clemens A. ;
de Boer, Jan .
BIOMATERIALS, 2012, 33 (11) :3205-3215
[2]   Bioactive silica-based nanoparticles stimulate bone-forming osteoblasts, suppress bone-resorbing osteoclasts, and enhance bone mineral density in vivo [J].
Beck, George R., Jr. ;
Ha, Shin-Woo ;
Camalier, Corinne E. ;
Yamaguchi, Masayoshi ;
Li, Yan ;
Lee, Jin-Kyu ;
Weitzmann, M. Neale .
NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2012, 8 (06) :793-803
[3]   Dual-ion delivery for synergistic angiogenesis and bactericidal capacity with silica-based microsphere [J].
Boldbaatar, Khaliun ;
Dashnyam, Khandmaa ;
Knowles, Jonathan C. ;
Lee, Hae-Hyoung ;
Lee, Jung-Hwan ;
Kim, Hae-Won .
ACTA BIOMATERIALIA, 2019, 83 :322-333
[4]   Design principles for therapeutic angiogenic materials [J].
Briquez, Priscilla S. ;
Clegg, Lindsay E. ;
Martino, Mikal M. ;
Mac Gabhann, Feilim ;
Hubbell, Jeffrey A. .
NATURE REVIEWS MATERIALS, 2016, 1 (01)
[5]   Enhancing microvascular formation and vessel maturation through temporal control over multiple pro-angiogenic and pro-maturation factors [J].
Brudno, Yevgeny ;
Ennett-Shepard, Alessandra B. ;
Chen, Ruth R. ;
Aizenberg, Michael ;
Mooney, David J. .
BIOMATERIALS, 2013, 34 (36) :9201-9209
[6]   Core-shell fibrous stem cell carriers incorporating osteogenic nanoparticulate cues for bone tissue engineering [J].
Buitrago, Jennifer Olmos ;
Perez, Roman A. ;
El-Fiqi, Ahmed ;
Singh, Rajendra K. ;
Kim, Joong-Hyun ;
Kim, Hae-Won .
ACTA BIOMATERIALIA, 2015, 28 :183-192
[7]   Angiogenesis in life, disease and medicine [J].
Carmeliet, P .
NATURE, 2005, 438 (7070) :932-936
[8]   Angiogenesis in health and disease [J].
Carmeliet, P .
NATURE MEDICINE, 2003, 9 (06) :653-660
[9]   Epithelial Protein Lost In Neoplasm (EPLIN) Interacts with α-Catenin and Actin Filaments in Endothelial Cells and Stabilizes Vascular Capillary Network in Vitro [J].
Chervin-Petinot, Adeline ;
Courcon, Marie ;
Almagro, Sebastien ;
Nicolas, Alice ;
Grichine, Alexei ;
Grunwald, Didier ;
Prandini, Marie-Helene ;
Huber, Philippe ;
Gulino-Debrac, Danielle .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2012, 287 (10) :7556-7572
[10]   A mini review focused on the proangiogenic role of silicate ions released from silicon-containing biomaterials [J].
Dashnyam, Khandmaa ;
El-Fiqi, Ahmed ;
Buitrago, Jennifer O. ;
Perez, Roman A. ;
Knowles, Jonathan C. ;
Kim, Hae-Won .
JOURNAL OF TISSUE ENGINEERING, 2017, 8