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Spatiotemporal distribution of chondroitin sulfate proteoglycans after optic nerve injury in rodents.
Pearson, Craig S; Solano, Andrea G; Tilve, Sharada M; Mencio, Caitlin P; Martin, Keith R; Geller, Herbert M.
Afiliación
  • Pearson CS; Laboratory of Developmental Neurobiology, National Heart, Lung, Blood Institute, National Institutes of Health, Bethesda, MD, USA; Department of Clinical Neurosciences, University of Cambridge, United Kingdom.
  • Solano AG; Laboratory of Developmental Neurobiology, National Heart, Lung, Blood Institute, National Institutes of Health, Bethesda, MD, USA.
  • Tilve SM; Laboratory of Developmental Neurobiology, National Heart, Lung, Blood Institute, National Institutes of Health, Bethesda, MD, USA.
  • Mencio CP; Laboratory of Developmental Neurobiology, National Heart, Lung, Blood Institute, National Institutes of Health, Bethesda, MD, USA.
  • Martin KR; Department of Clinical Neurosciences, University of Cambridge, United Kingdom.
  • Geller HM; Laboratory of Developmental Neurobiology, National Heart, Lung, Blood Institute, National Institutes of Health, Bethesda, MD, USA. Electronic address: gellerh@nhlbi.nih.gov.
Exp Eye Res ; 190: 107859, 2020 01.
Article en En | MEDLINE | ID: mdl-31705897
The accumulation of chondroitin sulfate proteoglycans (CSPGs) in the glial scar following acute damage to the central nervous system (CNS) limits the regeneration of injured axons. Given the rich diversity of CSPG core proteins and patterns of GAG sulfation, identifying the composition of these CSPGs is essential for understanding their roles in injury and repair. Differential expression of core proteins and sulfation patterns have been characterized in the brain and spinal cord of mice and rats, but a comprehensive study of these changes following optic nerve injury has not yet been performed. Here, we show that the composition of CSPGs in the optic nerve and retina following optic nerve crush (ONC) in mice and rats exhibits an increase in aggrecan, brevican, phosphacan, neurocan and versican, similar to changes following spinal cord injury. We also observe an increase in inhibitory 4-sulfated (4S) GAG chains, which suggests that the persistence of CSPGs in the glial scar opposes the growth of CNS axons, thereby contributing to the failure of regeneration and recovery of function.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Nervio Óptico / Retina / Traumatismos del Nervio Óptico / Lesiones por Aplastamiento Idioma: En Revista: Exp Eye Res Año: 2020 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Nervio Óptico / Retina / Traumatismos del Nervio Óptico / Lesiones por Aplastamiento Idioma: En Revista: Exp Eye Res Año: 2020 Tipo del documento: Article