Literature DB >> 2924869

Tissue sections from the mature rat brain and spinal cord as substrates for neurite outgrowth in vitro: extensive growth on gray matter but little growth on white matter.

K A Crutcher1.   

Abstract

The failure of axons to regenerate within the brain and spinal cord of mature mammals has been attributed to the absence of growth-promoting substances, especially extracellular matrix components, or to the presence of growth-inhibiting substances, particularly components associated with CNS myelin. The ability of mature mammalian CNS tissue to support neurite regeneration was tested by growing explants of embryonic chick lumbar sympathetic ganglia on fresh frozen sections of the mature rat brain and spinal cord. The extent of neurite outgrowth was quantified using morphometric analysis for explants grown on sections that included most of the major anatomical divisions of the CNS. Extensive, but variable, regeneration was present on gray matter regions, whereas major white matter tracts showed poor support, if any, for neurite growth. The results are consistent with the presence of growth-inhibiting factors associated with CNS white matter but also indicate that most gray matter regions of the mature mammalian brain and spinal cord will support axonal regeneration in tissue culture in spite of the absence of known extracellular matrix components.

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Year:  1989        PMID: 2924869     DOI: 10.1016/0014-4886(89)90007-1

Source DB:  PubMed          Journal:  Exp Neurol        ISSN: 0014-4886            Impact factor:   5.330


  11 in total

1.  White matter of the CNS supports or inhibits neurite outgrowth in vitro depending on geometry.

Authors:  D B Pettigrew; K A Crutcher
Journal:  J Neurosci       Date:  1999-10-01       Impact factor: 6.167

Review 2.  Chondroitin sulphate proteoglycans: preventing plasticity or protecting the CNS?

Authors:  K E Rhodes; J W Fawcett
Journal:  J Anat       Date:  2004-01       Impact factor: 2.610

3.  Comparison of neurite outgrowth induced by intact and injured sciatic nerves: a confocal and functional analysis.

Authors:  E Agius; P Cochard
Journal:  J Neurosci       Date:  1998-01-01       Impact factor: 6.167

4.  p75NTR-dependent, myelin-mediated axonal degeneration regulates neural connectivity in the adult brain.

Authors:  Katya J Park; Carlos Ayala Grosso; Isabelle Aubert; David R Kaplan; Freda D Miller
Journal:  Nat Neurosci       Date:  2010-03-28       Impact factor: 24.884

5.  Enhanced neurotrophin-induced axon growth in myelinated portions of the CNS in mice lacking the p75 neurotrophin receptor.

Authors:  G S Walsh; K M Krol; K A Crutcher; M D Kawaja
Journal:  J Neurosci       Date:  1999-05-15       Impact factor: 6.167

6.  Neuronal cyclic AMP controls the developmental loss in ability of axons to regenerate.

Authors:  D Cai; J Qiu; Z Cao; M McAtee; B S Bregman; M T Filbin
Journal:  J Neurosci       Date:  2001-07-01       Impact factor: 6.167

7.  Absence of axonal sprouting following unilateral lesion in 125-day-old rat supraoptic nucleus may be due to age-dependent decrease in protein levels of ciliary neurotrophic factor receptor alpha.

Authors:  Jason M Askvig; John A Watt
Journal:  J Comp Neurol       Date:  2019-03-25       Impact factor: 3.215

8.  Lesioned corticospinal tract axons regenerate in myelin-free rat spinal cord.

Authors:  T Savio; M E Schwab
Journal:  Proc Natl Acad Sci U S A       Date:  1990-06       Impact factor: 11.205

9.  Myelin contributes to the parallel orientation of axonal growth on white matter in vitro.

Authors:  D B Pettigrew; K A Crutcher
Journal:  BMC Neurosci       Date:  2001-05-31       Impact factor: 3.288

10.  Disruption of spinal cord white matter and sciatic nerve geometry inhibits axonal growth in vitro in the absence of glial scarring.

Authors:  D B Pettigrew; K P Shockley; K A Crutcher
Journal:  BMC Neurosci       Date:  2001-05-31       Impact factor: 3.288

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