Although initially argued to be a feature of immature neurons with incomplete polarization, there is clear evidence that neurons in the peripheral nervous system retain the capacity for intra-axonal protein synthesis well into adulthood. This localized protein synthesis has been shown to contribute to injury signaling and axon regeneration in peripheral nerves. Recent works point to potential for protein synthesis in axons of the vertebrate central nervous system. mRNAs and protein synthesis machinery have now been documented in lamprey, mouse, and rat spinal cord axons. Intra-axonal protein synthesis appears to be activated in adult vertebrate spinal cord axons when they are regeneration-competent. Rat spinal cord axons regenerating into a peripheral nerve graft contain mRNAs and markers of activated translational machinery. Indeed, levels of some growth-associated mRNAs in these spinal cord axons are comparable to the regenerating sciatic nerve. Markers of active translation tend to decrease when these axons stop growing, but can be reactivated by a second axotomy. These emerging observations raise the possibility that mRNA transport into and translation within axons could be targeted to facilitate regeneration in both the peripheral and central nervous systems.
Intra-axonal protein synthesis - a new target for neural repair?
Creators
Jeffery L. Twiss - University of South Carolina
Ashley L. Kalinski - University of South Carolina
Rahul Sachdeva - Drexel University
John D. Houle - Drexel University
Publication Details
Neural regeneration research, v 11(9), pp 1365-1367
Publisher
Wolters Kluwer Medknow Publications
Number of pages
3
Grant note
R01-NS041596; R01-NS089663; P01-NS055976 / National Institutes of Health; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA
2011329 / US-Israel Binational Science Foundation
Dr. Miriam and Sheldon G. Adelson Medical Research Foundation
R01NS041596 / NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Institute of Neurological Disorders & Stroke (NINDS)
W81XWH-13-1-0308 / Department of Defense/Congressionally Mandated Research Program
MCB-1020970 / National Science Foundation; National Science Foundation (NSF)
Resource Type
Journal article
Language
English
Academic Unit
Neurobiology and Anatomy
Web of Science ID
WOS:000387768400001
Scopus ID
2-s2.0-84994850706
Other Identifier
991019168739004721
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