C3 peptide enhances recovery from spinal cord injury by improved regenerative growth of descending fiber tracts

Author:

Boato Francesco1,Hendrix Sven12,Huelsenbeck Stefanie C.3,Hofmann Fred3,Große Gisela4,Djalali Susann4,Klimaschewski Lars5,Auer Maria5,Just Ingo3,Ahnert-Hilger Gudrun4,Höltje Markus4

Affiliation:

1. Center for Anatomy, Institute of Cell Biology and Neurobiology, Charité-Universitätsmedizin Berlin, Charitéplatz 1, D-10117 Berlin, Germany

2. Department of Morphology and BIOMED Institute, Hasselt University, Agoralaangebouw A, B-3590 Diepenbeek, Belgium

3. Institute of Toxicology, Hannover Medical School (MHH), Carl-Neuberg-Straße 1, D-30625 Hannover, Germany

4. Center for Anatomy, Functional Cell Biology, Charité-Universitätsmedizin Berlin, Charitéplatz 1, D-10117 Berlin, Germany

5. Division of Neuroanatomy, Department of Anatomy, Histology and Embryology, Innsbruck Medical University, Müllerstraße 59, A-6020 Innsbruck, Austria

Abstract

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 C3bot154-182. 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, C3bot154-182 stimulated regenerative growth of raphespinal fibers and improved serotonergic input to lumbar α-motoneurons. These in vivo data were confirmed by in vitro data, showing an enhanced axon outgrowth of α-motoneurons and hippocampal neurons cultivated on normal or growth-inhibitory substrates after application of C3bot154-182. 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, C3bot154-182 did not induce neurite outgrowth in primary cultures of dorsal root ganglion cells. In conclusion, C3bot154-182 represents a novel, promising tool to foster axonal protection and/or repair, as well as functional recovery after traumatic CNS injury.

Publisher

The Company of Biologists

Subject

Cell Biology

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