Collagen/heparin sulfate scaffolds fabricated by a 3D bioprinter improved mechanical properties and neurological function after spinal cord injury in rats

被引:102
作者
Chen, Chong [1 ,2 ]
Zhao, Ming-liang [1 ,2 ]
Zhang, Ren-kun [1 ,2 ]
Lu, Gang [2 ,3 ]
Zhao, Chang-yu [1 ,2 ]
Fu, Feng [1 ,2 ]
Sun, Hong-tao [1 ,2 ]
Zhang, Sai [1 ,2 ]
Tu, Yue [1 ,2 ]
Li, Xiao-hong [1 ,2 ]
机构
[1] Logist Univ Chinese Peoples Armed Police Forces, Inst Traumat Brain Injury & Neurol, Pingjin Hosp, Logist Univ, Tianjin 300162, Peoples R China
[2] Key Lab Neurotrauma Repair Tianjin, Tianjin 300162, Peoples R China
[3] Logist Univ Chinese Peoples Armed Police Forces, Pingjin Hosp, Dept Radiol, Tianjin 300162, Peoples R China
关键词
spinal cord injury; collagen; heparin sulfate; 3D bioprinter; mechanical properties; IN-VIVO EVALUATION; BONE MORPHOGENETIC PROTEIN-2; HEPARIN-CONJUGATED FIBRIN; CROSS-LINKING; REGENERATION; STRATEGIES; BIOCOMPATIBILITY; RECOVERY; SYSTEM; MATRIX;
D O I
10.1002/jbm.a.36011
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Effective treatments promoting axonal regeneration and functional recovery for spinal cord injury (SCI) are still in the early stages of development. Most approaches have been focused on providing supportive substrates for guiding neurons and overcoming the physical and chemical barriers to healing that arise after SCI. Although collagen has become a promising natural substrate with good compatibility, its low mechanical properties restrict its potential applications. The mechanical properties mainly rely on the composition and pore structure of scaffolds. For the composition of a scaffold, we used heparin sulfate to react with collagen by crosslinking. For the structure, we adopted a three-dimensional (3D) printing technology to fabricate a scaffold with a uniform pore distributions. We observed that the internal structure of the scaffold printed with a 3D bioprinter was regular and porous. We also found that both the compression modulus and strengths of the scaffold were significantly enhanced by the collagen/heparin sulfate composition compared to a collagen scaffold. Meanwhile, the collagen/heparin sulfate scaffold presented good biocompatibility when it was co-cultured with neural stem cells in vitro. We also demonstrated that heparin sulfate modification significantly improved bFGF immobilization and absorption to the collagen by examining the release kinetics of bFGF from scaffolds. Two months after implantating the scaffold into transection lesions in T10 of the spinal cord in rats, the collagen/heparin sulfate group demonstrated significant recovery of locomotor function and according to electrophysiological examinations. Parallel to functional recovery, collagen/heparin sulfate treatment further ameliorated the pathological process and markedly increased the number of neurofilament (NF) positive cells compared to collagen treatment alone. These data suggested that a collagen/heparin sulfate scaffold fabricated by a 3D bioprinter could enhance the mechanical properties of collagen and provide continuous guidance channels for axons, which would improve the neurological function after SCI. (C) 2017 Wiley Periodicals, Inc.
引用
收藏
页码:1324 / 1332
页数:9
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