Targeting Neurotrophins to Specific Populations of Neurons: NGF, BDNF, and NT-3 and Their Relevance for Treatment of Spinal Cord Injury
Genre
Journal articleDate
2017-03-03Author
Keefe, Kathleen M.Sheikh, Imran S.
Smith, George M.
Group
Shriners Hospital Pediatric Research Center, Center for Neural Repair and Rehabilitation (Temple University)Subject
Spinal cord injuryNeurotrophic factors
Nerve growth factor
Brain-derived neurotrophic factor
Neurotrophin-3
Neuroprotection
Plasticity
Regeneration
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http://hdl.handle.net/20.500.12613/8789
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https://doi.org/10.3390/ijms18030548Abstract
Neurotrophins are a family of proteins that regulate neuronal survival, synaptic function, and neurotransmitter release, and elicit the plasticity and growth of axons within the adult central and peripheral nervous system. Since the 1950s, these factors have been extensively studied in traumatic injury models. Here we review several members of the classical family of neurotrophins, the receptors they bind to, and their contribution to axonal regeneration and sprouting of sensory and motor pathways after spinal cord injury (SCI). We focus on nerve growth factor (NGF), brain derived neurotrophic factor (BDNF), and neurotrophin-3 (NT-3), and their effects on populations of neurons within diverse spinal tracts. Understanding the cellular targets of neurotrophins and the responsiveness of specific neuronal populations will allow for the most efficient treatment strategies in the injured spinal cord.Citation
Keefe KM, Sheikh IS, Smith GM. Targeting Neurotrophins to Specific Populations of Neurons: NGF, BDNF, and NT-3 and Their Relevance for Treatment of Spinal Cord Injury. International Journal of Molecular Sciences. 2017; 18(3):548. https://doi.org/10.3390/ijms18030548Citation to related work
MDPIHas part
International Journal of Molecular Sciences, Vol. 18, Iss. 3, Special issue: Neurotrophic Factors - Historical Perspective and New DirectionsADA compliance
For Americans with Disabilities Act (ADA) accommodation, including help with reading this content, please contact scholarshare@temple.eduae974a485f413a2113503eed53cd6c53
http://dx.doi.org/10.34944/dspace/8753