Literature DB >> 1694445

Loss of channel modulation by transmitter and protein kinase C during innervation of an identified leech neuron.

P Drapeau1.   

Abstract

When serotonergic Retzius (R) neurons of the leech contact pressure-sensitive (P) neurons in culture, P cells selectively lose a protein kinase C-dependent cationic response to serotonin and the R cell reforms the inhibitory, chloride-dependent synapse seen in vivo. In P cells not contacted by R cells, cell-attached patches contained single cation channels sensitive to serotonin and phorbol ester with characteristic properties and high incidence (present in about one-half of the patches). P cells paired with R cells had a cation channel with similar biophysical properties and incidence, but channel activity was not stimulated by serotonin and phorbol ester. These results suggest that the early clearing of the non-synaptic (excitatory) response to serotonin is due to the loss of activation by protein kinase C (and not the number) of cation channels as a prelude to inhibitory synapse formation.

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Year:  1990        PMID: 1694445     DOI: 10.1016/0896-6273(90)90140-b

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


  4 in total

1.  Requirement for tyrosine phosphatase during serotonergic neuromodulation by protein kinase C.

Authors:  S Catarsi; P Drapeau
Journal:  J Neurosci       Date:  1997-08-01       Impact factor: 6.167

2.  Selection of transmitter responses at sites of neurite contact during synapse formation between identified leech neurons.

Authors:  S Ching; S Catarsi; P Drapeau
Journal:  J Physiol       Date:  1993-08       Impact factor: 5.182

3.  Modulation and selection of neurotransmitter responses during synapse formation between identified leech neurons.

Authors:  S Catarsi; P Drapeau
Journal:  Cell Mol Neurobiol       Date:  1996-12       Impact factor: 5.046

4.  Tyrosine phosphorylation during synapse formation between identified leech neurons.

Authors:  S Catarsi; S Ching; D C Merz; P Drapeau
Journal:  J Physiol       Date:  1995-06-15       Impact factor: 5.182

  4 in total

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