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DESCRIPTION (provided by applicant): Class 3 semaphores (Sema3) are repulsive cues that are involved axon guidance during development of the nervous system. Their continued expression in the adult central nervous system (CMS) as well as their upregulation at the lesion site after spinal cord injury (SCI) raises the possibility that they may contribute to the failure of axonal regeneration after SCI. We will investigate this possibility by using mutant mice that lack the signal transducing moiety of SemaS receptor complex, namely the Plexin A3 and A4 subtypes. The specific aims of this proposal are as follows: 1) Investigate the effect of disrupting class 3 semaphorin signaling on regeneration of the corticospinal, serotonergic, and ascending sensory axons after a complete mid-thoracic transection. 2) Investigate the effect of disrupting class 3 semaphorin signaling on the formation the astrocyte-meningeal fibroblast border. 3) Generate a conditional Plexin A4 knockout mouse and analyze the regenerative phenotype of its 5-HT axons after acute deletion of Plexin A4 in astrocytes. This research will aid in better understanding how chemorepellents can contribute to axon regeneration failure, and how overcoming this inhibitory barrier may be used to treat spinal cord injured patients. The results of this research will increase our understanding of how molecules that are important for repelling axons during development can negatively affect axonal regeneration in the adult mammalian central nervous system. Overcoming this inhibitory barrier to enhance axonal regeneration can have significant therapeutic implications for patients who suffer from spinal cord injury.
期刊论文(4)
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DOI: 10.1016/j.expneurol.2011.05.001
发表时间: 2012-05
期刊: EXPERIMENTAL NEUROLOGY
影响因子: 5.3
作者: [Lee, Jae K., Zheng, Binhai]
通讯作者: Zheng, Binhai
Axon regeneration after spinal cord injury: insight from genetically modified mouse models.
脊髓损伤后轴突再生:来自转基因小鼠模型的见解。
DOI: --
发表时间: 2008
期刊: Restorative neurology and neuroscience
影响因子: 2.8
作者: [Lee,JaeK, Zheng,Binhai]
通讯作者: Zheng,Binhai
DOI: 10.1523/jneurosci.1864-09.2009
发表时间: 2009-07-08
期刊: The Journal of neuroscience : the official journal of the Society for Neuroscience
影响因子: --
作者: [Lee JK, Chan AF, Luu SM, Zhu Y, Ho C, Tessier-Lavigne M, Zheng B]
通讯作者: Zheng B
DOI: 10.1523/jneurosci.2269-10.2010
发表时间: 2010-08-11
期刊: The Journal of neuroscience : the official journal of the Society for Neuroscience
影响因子: --
作者: [Lee JK, Chow R, Xie F, Chow SY, Tolentino KE, Zheng B]
通讯作者: Zheng B
Regeneration-permissive glia after spinal cord injury
RAP as a therapeutic compound for neuronal regeneration after spinal cord injury
  • 批准号:
    8898661
  • 项目类别:
  • 资助金额:
    $2.5万
  • 财政年份:
    2014
  • 负责人:
    Jae K Lee
  • 依托单位:
RAP as a therapeutic compound for neuronal regeneration after spinal cord injury
  • 批准号:
    8781972
  • 项目类别:
  • 资助金额:
    $22.5万
  • 财政年份:
    2014
  • 负责人:
    Jae K Lee
  • 依托单位:
Translational Profile of Perivascular Fibroblasts after Spinal Cord Injury
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