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AAV vector-mediated secretion of chondroitinase provides a sensitive tracer for axonal arborisations.
Alves, João Nuno; Muir, Elizabeth M; Andrews, Melissa R; Ward, Anneliese; Michelmore, Nicholas; Dasgupta, Debayan; Verhaagen, Joost; Moloney, Elizabeth B; Keynes, Roger J; Fawcett, James W; Rogers, John H.
Afiliación
  • Alves JN; John van Geest Centre for Brain Repair, Forvie Site, Robinson Way, Cambridge CB2 0PY, UK; Department of Physiology Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB2 3EG, UK.
  • Muir EM; Department of Physiology Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB2 3EG, UK.
  • Andrews MR; John van Geest Centre for Brain Repair, Forvie Site, Robinson Way, Cambridge CB2 0PY, UK.
  • Ward A; Department of Physiology Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB2 3EG, UK.
  • Michelmore N; Department of Physiology Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB2 3EG, UK.
  • Dasgupta D; Department of Physiology Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB2 3EG, UK.
  • Verhaagen J; Laboratory for Neuroregeneration, Netherlands Institute for Neuroscience, Meibergdreef 47, 1105BA Amsterdam, Netherlands.
  • Moloney EB; Laboratory for Neuroregeneration, Netherlands Institute for Neuroscience, Meibergdreef 47, 1105BA Amsterdam, Netherlands.
  • Keynes RJ; Department of Physiology Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB2 3EG, UK.
  • Fawcett JW; John van Geest Centre for Brain Repair, Forvie Site, Robinson Way, Cambridge CB2 0PY, UK.
  • Rogers JH; Department of Physiology Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB2 3EG, UK. Electronic address: jhr11@cam.ac.uk.
J Neurosci Methods ; 227: 107-20, 2014 Apr 30.
Article en En | MEDLINE | ID: mdl-24583077
ABSTRACT
As part of a project to express chondroitinase ABC (ChABC) in neurons of the central nervous system, we have inserted a modified ChABC gene into an adeno-associated viral (AAV) vector and injected it into the vibrissal motor cortex in adult rats to determine the extent and distribution of expression of the enzyme. A similar vector for expression of green fluorescent protein (GFP) was injected into the same location. For each vector, two versions with minor differences were used, giving similar results. After 4 weeks, the brains were stained to show GFP and products of chondroitinase digestion. Chondroitinase was widely expressed, and the AAV-ChABC and AAV-GFP vectors gave similar expression patterns in many respects, consistent with the known projections from the directly transduced neurons in vibrissal motor cortex and adjacent cingulate cortex. In addition, diffusion of vector to deeper neuronal populations led to labelling of remote projection fields which was much more extensive with AAV-ChABC than with AAV-GFP. The most notable of these populations are inferred to be neurons of cortical layer 6, projecting widely in the thalamus, and neurons of the anterior pole of the hippocampus, projecting through most of the hippocampus. We conclude that, whereas GFP does not label the thinnest axonal branches of some neuronal types, chondroitinase is efficiently secreted from these arborisations and enables their extent to be sensitively visualised. After 12 weeks, chondroitinase expression was undiminished.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Axones / Condroitina ABC Liasa / Vectores Genéticos / Neuronas Tipo de estudio: Diagnostic_studies Límite: Animals Idioma: En Revista: J Neurosci Methods Año: 2014 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Axones / Condroitina ABC Liasa / Vectores Genéticos / Neuronas Tipo de estudio: Diagnostic_studies Límite: Animals Idioma: En Revista: J Neurosci Methods Año: 2014 Tipo del documento: Article País de afiliación: Reino Unido