Modified porous scaffolds of silk fibroin with mimicked microenvironment based on decellularized pulp/fibronectin for designed performance biomaterials in maxillofacial bone defect

被引:19
作者
Sangkert, Supaporn [1 ]
Kamonmattayakul, Suttatip [2 ]
Chai, Wen Lin [3 ]
Meesane, Jirut [1 ]
机构
[1] Prince Songkla Univ, Fac Med, Inst Biomed Engn, Hat Yai 90110, Songkhla, Thailand
[2] Prince Songkla Univ, Fac Dent, Dept Prevent Dent, Hat Yai 90110, Songkhla, Thailand
[3] Univ Malaya, Fac Dent, Dept Gen Dent Practice & Oral & Maxillofacial Ima, Kuala Lumpur, Malaysia
关键词
silk fibroin; bone tissue engineering; scaffolds; microenvironment; mimicking; EXTRACELLULAR-MATRIX PROTEINS; BIOMIMETIC MATERIALS; ADIPOSE-TISSUE; DENTAL-PULP; DIFFERENTIATION; HYDROXYAPATITE; FIBRONECTIN; PROLIFERATION; CELLS;
D O I
10.1002/jbm.a.35983
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Maxillofacial bone defect is a critical problem for many patients. In severe cases, the patients need an operation using a biomaterial replacement. Therefore, to design performance biomaterials is a challenge for materials scientists and maxillofacial surgeons. In this research, porous silk fibroin scaffolds with mimicked microenvironment based on decellularized pulp and fibronectin were created as for bone regeneration. Silk fibroin scaffolds were fabricated by freeze-drying before modification with three different components: decellularized pulp, fibronectin, and decellularized pulp/fibronectin. The morphologies of the modified scaffolds were observed by scanning electron microscopy. Existence of the modifying components in the scaffolds was proved by the increase in weights and from the pore size measurements of the scaffolds. The modified scaffolds were seeded with MG-63 osteoblasts and cultured. Testing of the biofunctionalities included cell viability, cell proliferation, calcium content, alkaline phosphatase activity (ALP), mineralization and histological analysis. The results demonstrated that the modifying components organized themselves into aggregations of a globular structure. They were arranged themselves into clusters of aggregations with a fibril structure in the porous walls of the scaffolds. The results showed that modified scaffolds with a mimicked microenvironment of decellularized pulp/fibronectin were suitable for cell viability since the cells could attach and spread into most of the pores of the scaffold. Furthermore, the scaffolds could induce calcium synthesis, mineralization, and ALP activity. The results indicated that modified silk fibroin scaffolds with a mimicked microenvironment of decellularized pulp/fibronectin hold promise for use in tissue engineering in maxillofacial bone defects. (c) 2017 Wiley Periodicals, Inc
引用
收藏
页码:1624 / 1636
页数:13
相关论文
共 52 条
[1]   Engineered Microenvironments for Controlled Stem Cell Differentiation [J].
Burdick, Jason A. ;
Vunjak-Novakovic, Gordana .
TISSUE ENGINEERING PART A, 2009, 15 (02) :205-219
[2]   Porous silk scaffolds can be used for tissue engineering annulus fibrosus [J].
Chang, G. ;
Kim, H. -J. ;
Kaplan, D. ;
Vunjak-Novakovic, G. ;
Kandel, R. A. .
EUROPEAN SPINE JOURNAL, 2007, 16 (11) :1848-1857
[3]   An overview of tissue and whole organ decellularization processes [J].
Crapo, Peter M. ;
Gilbert, Thomas W. ;
Badylak, Stephen F. .
BIOMATERIALS, 2011, 32 (12) :3233-3243
[4]   Preparation of bi-continuous macroporous polyamide copolymer membranes for cell culture [J].
Don, Trong-Ming ;
Hsu, Yi-Chun ;
Tai, Hung-Yin ;
Fu, Earl ;
Cheng, Liao-Ping .
JOURNAL OF MEMBRANE SCIENCE, 2012, 415 :784-792
[5]   Gradient nanofibrous chitosan/poly ε-caprolactone scaffolds as extracellular microenvironments for vascular tissue engineering [J].
Du, Fengyi ;
Wang, Hao ;
Zhao, Wei ;
Li, Dong ;
Kong, Deling ;
Yang, Jun ;
Zhang, Yuanyuan .
BIOMATERIALS, 2012, 33 (03) :762-770
[6]   The use of decellularized adipose tissue to provide an inductive microenvironment for the adipogenic differentiation of human adipose-derived stem cells [J].
Flynn, L. E. .
BIOMATERIALS, 2010, 31 (17) :4715-4724
[7]   Decellularization of tissues and organs [J].
Gilbert, TW ;
Sellaro, TL ;
Badylak, SF .
BIOMATERIALS, 2006, 27 (19) :3675-3683
[8]   Cells and extracellular matrices of dentin and pulp: A biological basis for repair and tissue engineering [J].
Goldberg, M ;
Smith, AJ .
CRITICAL REVIEWS IN ORAL BIOLOGY & MEDICINE, 2004, 15 (01) :13-27
[9]   Basic Components of Connective Tissues and Extracellular Matrix: Elastin, Fibrillin, Fibulins, Fibrinogen, Fibronectin, Laminin, Tenascins and Thrombospondins [J].
Halper, Jaroslava ;
Kjaer, Michael .
PROGRESS IN HERITABLE SOFT CONNECTIVE TISSUE DISEASES, 2014, 802 :31-47
[10]   Expression of Extracellular Matrix Proteins in Human Dental Pulp Stem Cells Depends on the Donor Tooth Conditions [J].
Harumi Miyagi, Sueli Patricia ;
Kerkis, Irina ;
da Costa Maranduba, Carlos Magno ;
Gomes, Cicera Maria ;
Martins, Manoela Domingues ;
Marques, Marcia Martins .
JOURNAL OF ENDODONTICS, 2010, 36 (05) :826-831