Abstract
Monoclonal antibodies raised against purified acetylcholine receptor from muscle and electric organ were tested for cross-reaction with surface components on chicken ciliary ganglion neurons. Indirect immunofluorescence indicated that antibodies to a determinant in the "main immunogenic region" of the receptor bind to the neurons in culture. Ultrastructural studies on 16-day embryonic ganglia, using horseradish peroxidase-conjugated monoclonal antibody, revealed that most of the conjugate labeling was associated with synaptic membrane on the neurons. A lesser amount of labeling was associated with the short processes extending from the neuronal somata in the region of preganglionic innervation. The labeling was blocked by coincubation with unlabeled antibodies of appropriate specificity and not by nonimmune serum. The pattern of labeling was clearly different from that previously found for a horseradish peroxidase conjugate of alpha-bungarotoxin: the toxin conjugate bound extensively to the short processes but not to synaptic membrane on the neurons. The synaptic antigen identified here by the cross-reacting antibodies is a candidate for the synaptic acetylcholine receptor on chicken ciliary ganglion neurons.
MeSH Terms
Animals
Antibodies, Monoclonal
Antigen-Antibody Complex
Cells, Cultured
Chick Embryo
Electrophorus
Epitopes/analysis
Fluorescent Antibody Technique
Immunoenzyme Techniques
Microscopy, Electron
Microscopy, Fluorescence
Neurons/analysis,ultrastructure
Receptors, Nicotinic/analysis
Retina/analysis
Retinal Ganglion Cells/analysis,ultrastructure
Species Specificity
Synapses/analysis
Chemicals
Antibodies, Monoclonal
Antigen-Antibody Complex
Epitopes
Receptors, Nicotinic
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Jacob M H
Berg D K
Lindstrom J M
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29 references, click to expand
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