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Volume 270,
Number 24,
Issue of June 16, pp. 14366-14375, 1995
©1995 by The American Society for Biochemistry and Molecular Biology, Inc.
Acetylcholine
Differentially Affects Intracellular Calcium via Nicotinic and
Muscarinic Receptors on the Same Population of Neurons
Margaret M.
Rathouz
,
Sukumar
Vijayaraghavan
,
Darwin K.
Berg
Multiple receptor subtypes activated by the same ligand but
coupled to different second messengers can produce divergent signaling
in a cell, while receptors activated by different ligands but sharing
the same second messenger can produce convergent signaling. We show
here that chick ciliary ganglion neurons have three classes of
receptors activated by the same neurotransmitter, acetylcholine, and
that all three regulate the same second messenger, intracellular free
calcium. Activation of muscarinic receptors on the neurons stimulates
phosphatidylinositol turnover and induces calcium oscillations that are
initiated and maintained by calcium release from
caffeine/ryanodine-insensitive intracellular stores. Extracellular
calcium is required to sustain the oscillations, while cadmium
abolishes them. Activation of either of two classes of nicotinic
receptors, distinguished both by location on the neurons and by subunit
composition, induces a single, rapid elevation in intracellular calcium
without inducing phosphatidylinositol turnover. The nicotinic responses
are entirely dependent on extracellular calcium, show no dependence on
release from internal stores, and do not display oscillations. Low
concentrations of the native agonist, acetylcholine, induce repetitive
calcium spikes in the neurons characteristic of muscarinic receptors,
while higher concentrations induce nonoscillating increases in
intracellular calcium that include contributions from nicotinic
receptors. The three classes of receptors also differ in the
acetylcholine concentration required to elicit a response. These
differences, together with differences in receptor location and sources
of calcium mobilized, may enable the receptor subtypes to target
different sets of calcium-dependent processes for regulation.

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Copyright © 1995 by the American Society for Biochemistry and Molecular Biology.
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