Literature DB >> 7069464

Reversible developmental change in the ability of ciliary ganglion neurons to extend neurites in culture.

F Collins, M R Lee.   

Abstract

From stages 35 to 40 in the chicken embryo, ciliary ganglion neurons undergo a developmental change which is detected in our assay system as a marked decline in the ability to extend neurites when placed in culture. This developmental loss is observed when the neurons are placed in culture as single, dissociated cells or as undissociated ganglion explants. The loss of the ability to extend neurites in culture is not a transitory phenomenon, for no recovery of this ability is observed during the rest of embryonic development or posthatching. There is a close temporal correlation between the embryonic period during which the ability of ciliary ganglion neurons to extend neurites declines and the period (stages 35 to 40) when these neurons form functional peripheral synapses in the embryo. The ability to extend neurites rapidly is not recovered during normal development as long as the ganglion and its connections within the organism remain intact. However, if the ciliary ganglia are removed from a stage 40 embryo and cultured for 3 to 4 days before being dissociated, the neurons have largely recovered their ability to initiate neurite outgrowth rapidly. This recovery after removal from the embryo is also presumably responsible for the eventual dense outgrowth of neurites from stage 40 ganglion explants after a 3- to 4-day delay in culture. Our results, in conjunction with similar results from other systems, suggest a cause and effect relationship between the establishment or disruption of peripheral connections and the loss or recovery, respectively, of the ability to extend neurites rapidly.

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Mesh:

Year:  1982        PMID: 7069464      PMCID: PMC6564250     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  6 in total

1.  A transcription-dependent switch controls competence of adult neurons for distinct modes of axon growth.

Authors:  D S Smith; J H Skene
Journal:  J Neurosci       Date:  1997-01-15       Impact factor: 6.167

2.  Embryonic neural retinal cell response to extracellular matrix proteins: developmental changes and effects of the cell substratum attachment antibody (CSAT).

Authors:  D E Hall; K M Neugebauer; L F Reichardt
Journal:  J Cell Biol       Date:  1987-03       Impact factor: 10.539

3.  Expression and in vitro function of beta 1-integrin laminin receptors in the developing avian ciliary ganglion.

Authors:  C D Weaver; C K Yoshida; I de Curtis; L F Reichardt
Journal:  J Neurosci       Date:  1995-07       Impact factor: 6.167

4.  N-Cadherin and integrins: two receptor systems that mediate neuronal process outgrowth on astrocyte surfaces.

Authors:  Louis F Reichardt
Journal:  Neuron       Date:  2008-11-06       Impact factor: 17.173

5.  Changes in the number of chick ciliary ganglion neuron processes with time in cell culture.

Authors:  L W Role; G D Fischbach
Journal:  J Cell Biol       Date:  1987-02       Impact factor: 10.539

6.  Identification of the major proteins that promote neuronal process outgrowth on Schwann cells in vitro.

Authors:  J L Bixby; J Lilien; L F Reichardt
Journal:  J Cell Biol       Date:  1988-07       Impact factor: 10.539

  6 in total

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