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The promotion of neural regeneration in an extreme rat spinal cord injury model using a collagen scaffold containing a collagen binding neuroprotective protein and an egfr neutralizing antibody
Han, Qianqian2,3; Jin, Wei1; Xiao, Zhifeng2; Ni, Hongbin1; Wang, Jinhuan4; Kong, Jie1; Wu, Jun1; Liang, Weibang1; Chen, Lei2; Zhao, Yannan2
刊名Biomaterials
2010-12-01
卷号31期号:35页码:9212-9220
关键词Collagen Egfr neutralizing antibody Spinal cord injury Nerve regeneration
ISSN号0142-9612
DOI10.1016/j.biomaterials.2010.08.040
通讯作者Liang, weibang(lwbnj@yahoo.com.cn)
英文摘要In the treatment of spinal cord injury, implantation of scaffolding biomaterials and the addition of neuroprotective factors will promote neural regeneration. it has been demonstrated in our previous work that linear ordered collagen scaffold (locs) will bridge neural regeneration after the injury of spinal cord hemisection, and bdnf fused with a collagen binding domain (cbd-bdnf) can bind to collagen specifically to exert the neuroprotective effect. besides neuroprotective factors, the lack of axon regeneration of the injured spinal cord has been attributed partially to regeneration inhibitors such as myelin associated proteins and chondroitin sulfate proteoglycans (cspgs). epidermal growth factor receptor (egfr) activation is downstream of the signaling pathways of these inhibitors. here, the monoclonal antibody, 151igg that inhibits signaling of egfr was used to neutralize egfr. 151igg was cross-linked to locs and cbd-bdnf bound to locs to make a triple-functional biomaterial for neural regeneration (bridging, prompting growth and neutralizing growth inhibitors). this triple-functional device was tested in a 6 mm transected sci model. results showed that this collagen scaffold with the addition of 151igg and cbd-bdnf provided effective bridging and stimulation effects for neural regeneration, recovery of electrical transmission of synapses and preventing the formation of glial scars in the extreme transected rat sci model. (c) 2010 elsevier ltd. all rights reserved.
WOS关键词MYELIN-ASSOCIATED GLYCOPROTEIN ; EPIDERMAL-GROWTH-FACTOR ; CENTRAL-NERVOUS-SYSTEM ; AXON REGENERATION ; FUNCTIONAL RECOVERY ; NEURITE OUTGROWTH ; ADULT-RAT ; MONOCLONAL-ANTIBODY ; WHITE-MATTER ; RECEPTOR
WOS研究方向Engineering ; Materials Science
WOS类目Engineering, Biomedical ; Materials Science, Biomaterials
语种英语
出版者ELSEVIER SCI LTD
WOS记录号WOS:000284393300008
内容类型期刊论文
URI标识http://www.corc.org.cn/handle/1471x/2413338
专题中国科学院大学
通讯作者Liang, Weibang
作者单位1.Nanjing Univ, Dept Neurosurg, Affiliated Drum Tower Hosp, Sch Med, Nanjing 210008, Peoples R China
2.Chinese Acad Sci, Key Lab Mol Dev Biol, Inst Genet & Dev Biol, Beijing 100080, Peoples R China
3.Chinese Acad Sci, Grad Sch, Beijing 100080, Peoples R China
4.Tianjing Huanhu Hosp, Inst Neurosurg, Tianjin 300060, Peoples R China
推荐引用方式
GB/T 7714
Han, Qianqian,Jin, Wei,Xiao, Zhifeng,et al. The promotion of neural regeneration in an extreme rat spinal cord injury model using a collagen scaffold containing a collagen binding neuroprotective protein and an egfr neutralizing antibody[J]. Biomaterials,2010,31(35):9212-9220.
APA Han, Qianqian.,Jin, Wei.,Xiao, Zhifeng.,Ni, Hongbin.,Wang, Jinhuan.,...&Dai, Jianwu.(2010).The promotion of neural regeneration in an extreme rat spinal cord injury model using a collagen scaffold containing a collagen binding neuroprotective protein and an egfr neutralizing antibody.Biomaterials,31(35),9212-9220.
MLA Han, Qianqian,et al."The promotion of neural regeneration in an extreme rat spinal cord injury model using a collagen scaffold containing a collagen binding neuroprotective protein and an egfr neutralizing antibody".Biomaterials 31.35(2010):9212-9220.
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