C3 peptide enhances recovery from spinal cord injury by improved regenerative growth of descending fiber tracts
Author(s) -
Francesco Boato,
Sven Hendrix,
Stefanie C. Huelsenbeck,
Fred Hofmann,
G Grosse,
Susann Djalali,
Lars Klimaschewski,
Maria Auer,
Ingo Just,
Gudrun AhnertHilger,
Markus Höltje
Publication year - 2010
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.066050
Subject(s) - biology , spinal cord injury , corticospinal tract , neurite , spinal cord , axon , regeneration (biology) , retrograde tracing , dorsal root ganglion , microbiology and biotechnology , neuroscience , serotonergic , anatomy , in vitro , central nervous system , biochemistry , serotonin , medicine , radiology , diffusion mri , magnetic resonance imaging , receptor
Functional recovery and regeneration of corticospinal tract (CST) fibers following spinal cord injury by compression or dorsal hemisection in mice was monitored after application of the enzyme-deficient Clostridium botulinum C3-protein-derived 29-amino-acid fragment C3bot(154-182). This peptide significantly improved locomotor restoration in both injury models as assessed by the open-field Basso Mouse Scale for locomotion test and Rotarod treadmill experiments. These data were supported by tracing studies showing an enhanced regenerative growth of CST fibers in treated animals as visualized by anterograde tracing. Additionally, C3bot(154-182) stimulated regenerative growth of raphespinal fibers and improved serotonergic input to lumbar alpha-motoneurons. These in vivo data were confirmed by in vitro data, showing an enhanced axon outgrowth of alpha-motoneurons and hippocampal neurons cultivated on normal or growth-inhibitory substrates after application of C3bot(154-182). The observed effects were probably caused by a non-enzymatic downregulation of active RhoA by the C3 peptide as indicated by pull-down experiments. By contrast, C3bot(154-182) did not induce neurite outgrowth in primary cultures of dorsal root ganglion cells. In conclusion, C3bot(154-182) represents a novel, promising tool to foster axonal protection and/or repair, as well as functional recovery after traumatic CNS injury.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom