Impact of neural cell adhesion molecule deletion on regeneration after mouse spinal cord injury

Autor: Melitta Schachner, Gabriele Loers, Igor Jakovcevski, Vedangana Saini, Gurcharan Kaur
Rok vydání: 2016
Předmět:
0301 basic medicine
Genetically modified mouse
Nervous system
medicine.medical_specialty
Genotype
metabolism [Axons]
Biology
metabolism [Spinal Cord Injuries]
Mice
03 medical and health sciences
0302 clinical medicine
Injury Site
Cell Movement
Internal medicine
medicine
genetics [Neural Cell Adhesion Molecules]
Animals
ddc:610
Neural Cell Adhesion Molecules
Spinal cord injury
Cells
Cultured

Spinal Cord Injuries
physiology [Axons]
metabolism [Astrocytes]
Glial fibrillary acidic protein
genetics [Spinal Cord Injuries]
General Neuroscience
physiology [Astrocytes]
medicine.disease
Spinal cord
Axons
Nerve Regeneration
Mice
Inbred C57BL

metabolism [Neural Cell Adhesion Molecules]
030104 developmental biology
medicine.anatomical_structure
Endocrinology
nervous system
Astrocytes
biology.protein
Female
Neural cell adhesion molecule
Neuroscience
Locomotion
030217 neurology & neurosurgery
Astrocyte
Zdroj: European journal of neuroscience 44(1), 1734-1746 (2016). doi:10.1111/ejn.13271
ISSN: 0953-816X
DOI: 10.1111/ejn.13271
Popis: The neural cell adhesion molecule (NCAM) plays important functional roles in development of the nervous system. We investigated the influence of a constitutive ablation of NCAM on the outcome of spinal cord injury. Transgenic mice lacking NCAM (NCAM-/-) were subjected to severe compression injury of the lower thoracic spinal cord using wild-type (NCAM+/+) littermates as controls. According to the single-frame motion analysis, the NCAM-/- mice showed reduced locomotor recovery in comparison to control mice at 3 and 6 weeks after injury, indicating an overall positive impact of NCAM on recovery after injury. Also the Basso Mouse Scale score was lower in NCAM-/- mice at 3 weeks after injury, whereas at 6 weeks after injury the difference between genotypes was not statistically significant. Worse locomotor function was associated with decreased monoaminergic and cholinergic innervation of the spinal cord caudal to the injury site and decreased axonal regrowth/sprouting at the site of injury. Astrocytic scar formation at the injury site, as assessed by immunohistology for glial fibrillary acidic protein at and around the lesion site was increased in NCAM-/- compared with NCAM+/+ mice. Migration of cultured monolayer astrocytes from NCAM-/- mice was reduced as assayed by scratch wounding. Numbers of Iba-1 immunopositive microglia were not different between genotypes. We conclude that constitutive NCAM deletion in young adult mice reduces recovery after spinal cord injury, validating the hypothesized beneficial role of this molecule in recovery after injury.
Databáze: OpenAIRE