Abstract
Muscarinic acetylcholine receptors expression and signaling in the human Jurkat T cell line were investigated. Semiquantitative real-time PCR and radioligand binding studies, using a wide set of antagonist compounds, showed the co-existence of M(3), M(4), and M(5) subtypes. Stimulation of these subpopulations caused a concentration and time- dependent activation of second messengers and ERK signaling pathways, with a major contribution of the M(3) subtype in a G(q/11)-mediated response. In addition, we found that T-cell stimulation leads to increased expression of M(3) and M(5) both at transcriptional and protein levels in a PLC/PKCθ dependent manner. Our data clarifies the functional role of AChR subtypes in Jurkat cells and pave the way to future studies on the potential cross-talk among these subpopulations and their regulation of T lymphocytes immune function.
Copyright © 2011 Elsevier B.V. All rights reserved.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Humans
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Jurkat Cells
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Muscarinic Antagonists / pharmacology
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Receptor, Muscarinic M1 / biosynthesis
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Receptor, Muscarinic M1 / genetics
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Receptor, Muscarinic M2 / biosynthesis
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Receptor, Muscarinic M2 / genetics
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Receptor, Muscarinic M3 / biosynthesis
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Receptor, Muscarinic M3 / genetics
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Receptor, Muscarinic M4 / biosynthesis
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Receptor, Muscarinic M4 / genetics
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Receptor, Muscarinic M5 / biosynthesis
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Receptor, Muscarinic M5 / genetics
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Receptors, Muscarinic / biosynthesis
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Receptors, Muscarinic / genetics*
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Receptors, Muscarinic / physiology
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Signal Transduction / drug effects
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Signal Transduction / genetics
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Signal Transduction / physiology*
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T-Lymphocytes / drug effects
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T-Lymphocytes / immunology
Substances
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Muscarinic Antagonists
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Receptor, Muscarinic M1
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Receptor, Muscarinic M2
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Receptor, Muscarinic M3
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Receptor, Muscarinic M4
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Receptor, Muscarinic M5
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Receptors, Muscarinic