期刊
CURRENT OPINION IN NEUROBIOLOGY
卷 27, 期 -, 页码 53-60出版社
CURRENT BIOLOGY LTD
DOI: 10.1016/j.conb.2014.02.011
关键词
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资金
- National Institutes of Health
- Falk Medical Research Trust
- Swiss National Science Foundation
- Christopher and Dana Reeve Foundation
The expression of Nogo-A and the receptor NgR1 limits the recovery of adult mammals from central nervous system injury. Multiple studies have demonstrated efficacy from targeting this pathway for functional recovery and neural repair after spinal cord trauma, ischemic stroke, optic nerve injury and models of multiple sclerosis. Recent molecular studies have added Si PR2 as a receptor for the amino terminal domain of Nogo-A, and have demonstrated shared components for Nogo-A and CSPG signaling as well as novel Nogo antagonists. It has been recognized that neural repair involves plasticity, sprouting and regeneration. A physiologic role for Nogo-A and NgR1 has been documented in the restriction of experience-dependent plasticity with maturity, and the stability of synaptic, dendritic and axonal anatomy.
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