Tissue engineering in spinal cord regeneration

组织工程在脊髓再生中的应用

• 批准号: 8792737
• 负责人: XUEJUN WEN
• 金额: $ 15.99万
• 依托单位: VIRGINIA COMMONWEALTH UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-04-01 至 2014-09-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8792737
• 关键词: Tissue; engineering; spinal; cord; regeneration

DESCRIPTION (provided by applicant): A damaging or pathological process that disrupts the continuity of axons in the adult mammalian central nervous system (CMS) often results in permanent disability due to the failure of injured axons to regenerate. Current therapeutic interventions are short of eliciting a robust regenerative response that leads to a decent degree of functional recovery. Recently, the emergence of neuronal bridging devices based upon tissue engineering principles offers new hope for the treatment and manipulation of CMS injuries and diseases. By engineering a controlled environment at the lesion site, neural bridging devices awaken the intrinsic ability of CMS axons to regenerate across and beyond the site of injury to reach their appropriate targets. The combined use of material scaffolds containing guidance cues with adhesive molecules and cells of selective properties further confers vitality and resilience to the devices. Our long-term goal is to develop a clinically applicable tissue-engineered neuronal bridging device to repair damaged CNS nerve tracts. The proposed project aims to construct and evaluate a tissue-engineered bridging device based upon a multi-filament entubulation approach in which bundles of ultra-thin filaments are entubulated into a semi- permeable biodegradable hollow fiber membrane sleeve. Our hypothesis is that such a bridging device will convey strong unidirectional guidance cues and define a well-controlled environment for regenerating axons, and therefore promote and guide axonal regeneration following spinal cord injury, leading to a greater degree of functional recovery compared to conventional neuronal bridging strategies. Aim #1 is to evaluate the effect of the packing density of the filament bundles within the HFM entubulation sleeve on the directional outgrowth length and directionality of axons in vitro. Aim #2 is to examine the efficiency of multifilament bridging device in promoting axonal outgrowth using a spinal cord hemisection model in vivo. Aim #3 is to determine whether a combined strategy aimed at 1) enhancing directional regeneration across the lesion gap, and 2) inhibiting glial scar formation at the device-host interface will further promote axonal growth to the lumbar central pattern generator (CPG; an intact neural circuit located within the L1-2 segment that responsible for hindlimb locomotor function), resulting in both anatomical reconnection and functional recovery.

描述（由申请人提供）：破坏成年哺乳动物中枢神经系统（CMS）中轴突连续性的损伤或病理过程通常由于受伤轴突无法再生而导致永久性残疾。目前的治疗干预措施缺乏引发强大的再生反应，导致适当程度的功能恢复。近年来，基于组织工程原理的神经桥接装置的出现为CMS损伤和疾病的治疗和操作提供了新的希望。通过在损伤部位设计一个可控的环境，神经桥接装置唤醒CMS轴突的内在能力，使其在损伤部位内外再生，到达适当的目标。结合使用含有粘附分子和选择性细胞的引导线索的材料支架，进一步赋予设备活力和弹性。我们的长期目标是开发一种临床应用的组织工程神经元桥接装置来修复受损的中枢神经束。该项目旨在构建和评估一种基于多丝膨化方法的组织工程桥接装置，其中超薄纤维束被膨化成半透可生物降解的中空纤维膜套。我们的假设是，这种桥接装置将传递强大的单向引导信号，并为轴突的再生定义一个良好的控制环境，从而促进和引导脊髓损伤后轴突的再生，与传统的神经元桥接策略相比，导致更大程度的功能恢复。目的1是评估HFM扩管套内长丝束的填充密度对体外轴突定向生长长度和方向性的影响。目的2：利用活体脊髓半切模型研究多丝桥接装置促进轴突生长的效率。目的#3是确定旨在1)增强病变间隙的定向再生和2)抑制装置-宿主界面胶质瘢痕形成的联合策略是否会进一步促进腰椎中枢模式发生器（CPG；位于L1-2节段内负责后肢运动功能的完整神经回路）的轴突生长，从而导致解剖重连和功能恢复。

项目成果

Improve the viability of transplanted neural cells with appropriate sized neurospheres coated with mesenchymal stem cells.

• DOI: 10.1016/j.mehy.2012.05.010
• 发表时间: 2012-08
• 期刊: Medical hypotheses
• 影响因子: 4.7
• 作者: Xiaowei Li;Xiaoyan Liu;Yu-Yan Tan;V. Tran;Ning Zhang;X. Wen

Effects of substrate stiffness on adipogenic and osteogenic differentiation of human mesenchymal stem cells.

• DOI: 10.1016/j.msec.2014.03.048
• 发表时间: 2014-07
• 期刊: Materials science & engineering. C, Materials for biological applications
• 作者: Wen Zhao;Xiaowei Li;Xiaoyan Liu;Ning Zhang;X. Wen

Polymer nanofibrous structures: Fabrication, biofunctionalization, and cell interactions.

• DOI: 10.1016/j.progpolymsci.2010.03.003
• 发表时间: 2010-07-01
• 期刊: Progress in polymer science
• 影响因子: 27.1
• 作者: Beachley V;Wen X
• 通讯作者: Wen X

Formation of well-defined embryoid bodies from dissociated human induced pluripotent stem cells using microfabricated cell-repellent microwell arrays.

• DOI: 10.1038/srep07402
• 发表时间: 2014-12-10
• 期刊: Scientific reports
• 影响因子: 4.6
• 作者: Pettinato G;Wen X;Zhang N
• 通讯作者: Zhang N

Biphasic bisperoxovanadium administration and Schwann cell transplantation for repair after cervical contusive spinal cord injury.

• DOI: 10.1016/j.expneurol.2014.12.002
• 发表时间: 2015-02
• 期刊: EXPERIMENTAL NEUROLOGY
• 影响因子: 5.3
• 作者: Walker, Chandler L.;Wang, Xiaofei;Bullis, Carli;Liu, Nai-Kui;Lu, Qingbo;Fry, Colin;Deng, Lingxiao;Xu, Xiao-Ming
• 通讯作者: Xu, Xiao-Ming