Neuronal connectivity is reshaped by use – in health and disease
P. Andersen,
P. Andersen
Institute for Basic Medical Sciences, University of Oslo
Search for more papers by this authorP. Andersen,
P. Andersen
Institute for Basic Medical Sciences, University of Oslo
Search for more papers by this authorFirst published: 02 January 2002
References
- 1 Ramon y Cajal S. Estudios sobre la degeración y regeración del sistema nervioso. 1913–1914. Madrid, 2 vol.
- 2 Bray GM, Villegas-Perez MP, Vidal-Sanz M & Aguayo AJ. The use of peripheral nerve grafts to enhance neuronal survival, promote growth and permit terminal reconnections in the central nervous system of adult rats. J Exp Biol 1987; 102: 5–19.
- 3 Davies SJA, Fitch MT, Memberg SP, Hall AK, Raisman G & Silver J. Regeneration of adult axons in white matter tracts of the central nervous system. Nature 1997; 390: 680–683.
- 4 Schnell L & Schwab ME. Axonal regeneration in the rat spinal cord produced by an antibody against myelin-associ-ated neurite growth inhibitors. Nature 1990; 343: 269–272.
- 5 Chen MS, Huber AB & Van Der Haar ME et al. Nogo-A is a myelin-associated neurite outgrowth inhibitor and an anti-gen for monoclonal antibody IN-1. Nature 2000; 403: 434–439.
- 6 GrandPré T, Nakamura F, Vartanian T & Strittmatter SM. Identification of the Nogo inhibitor of axon regeneration as a Reticulon protein. Nature 2000; 403: 439–444.
- 7 Prinjha R, Moore SE & Vinson M et al. Inhibitor of neurite outgrowth in humans. Nature 2000; 403: 383–384.
- 8 Fawcett JW & Asher RA. The glial scar and central nervous system repair. Brain Res Bull 1999; 49: 377–391.
- 9 Pasterkamp RJ, Giger RJ & Ruitenberg MJ et al. Expression of the gene encoding the chemorepellent semaphorin III is induced in the fibroblast component of neural scar tissue formed following injuries of adult but not neonatal CNS. Mol Cell Neurosci 1999; 13: 143–166.
- 10 Miranda JD, White LA, Marcillo AE, Willson CA, Jagid J & Whittemore SR. Induction of Eph B3 after spinal cord injury. Exp Neurol 1999; 156: 218–222.
- 11 Trommald M, Hulleberg G & Andersen P. Long-term poten-tiation is associated with new excitatory spine syn-apses on rat dentate granule cells. Learning & Memory 1996; 3: 218–228.
- 12 Engert F & Bonhoeffer T. Dendritic spine changes associated with hippocampal long-term synaptic plasticity. Nature 1999; 399: 66–70.
- 13 Maletic-Savatic M, Malinow R & Svoboda K. Rapid dendritic morphogenesis in CA 1 hippocampal dendrites induced by synaptic activity. Science 1999; 283: 1923–1927.
- 14 Korkotian E & Segal M. Fast confocal imaging of calcium released from stores in dendritic spines. Eur J Neurosci 1998; 10: 2076–2084.
- 15 Kaas JH. Plasticity of sensory and motor maps in adult mammals. Ann Rev Neurosci 1991; 14: 137–167.
- 16 Nudo RJ, Wise BM, SiFuentes F & Milliken G. Neural sub-strates for the effects of rehabilitative training on motor recovery after ischemic infarct. Science 1996; 272: 1791–1794.
- 17 Klinke R, Kral A, Heid S, Tillein J & Hartmann R. Recruit-ment of the auditory cortex in congenitally deaf cats by long-term cochlear electrostimulation. Science 1999; 285: 1729–1733.
- 18 Cheng H, Cao Y & Olson L. Spinal cord repair in adult paraplegic rats: partial restoration of hind limb function. Science 1996; 273: 510–513.
- 19 Li Y, Field PM & Raisman G. Regeneration of adult rat corticospinal axons induced by transplanted olfactory ensheating cells. J Neurosci 1998; 18: 10514–10524.
- 20 Eriksson PS, Perfilieva E & Björk-Eriksson T et al. Neurogenesis in the adult human hippocampus. Nature Med 1998; 4: 1313–1317.
- 21 Clarke DL, Johansson CB & Wilbertz J et al. Generalised potential of adult neural stem cells. Science 2000; 288: 1660–1663.
- 22
Björklund A.
The use of neural stem cells for gene therapy in the central nervous system.
J Gene Med
1999; 1: 223–226.
10.1002/(SICI)1521-2254(199905/06)1:3<223::AID-JGM38>3.0.CO;2-0 CAS PubMed Web of Science® Google Scholar
