Abstract
By using acetylcholine-induced stimulation of [35S]guanosine-5′-O-(3-thio)triphosphate ([35S]GTPγS) binding to membrane G proteins as a functional assay of the cloned human m1–m4 muscarinic receptor subtypes stably expressed in Chinese hamster ovary cells, muscarinic toxin 3 (MT3) was found to block the m4 receptor with a potency (pA2 = 8.33) much higher than those displayed at the m1 (pA2 = 6.78), m3 (pA2 = 6.3), and m2 (pA2 < 6.3) subtypes. In N1E-115 cells, which have been reported to express m4 receptors coupled to inhibition of cAMP, MT3 potently antagonized the carbachol-induced inhibition of adenylyl cyclase with a pA2 of 8.81 and displayed monophasic inhibitory curves. Unexpectedly, in NG108-15 cells, known to express only m4 receptors, MT3 counteracted the carbachol inhibition of adenylyl cyclase with a lower potency (pA2 = 7.60) and showed a biphasic inhibitory curve, suggesting the participation of both m4 and m2 receptors. This possibility was supported by radioligand binding data showing that MT3 failed to completely displace the binding of [3H]N-methylscopolamine to NG108-15 cell membranes and by reverse transcription-polymerase chain reaction analysis, revealing the presence of mRNAs for both m4 and m2 receptor subtypes. These data demonstrate that MT3 possesses a high functional receptor selectivity for both the cloned and native m4 receptors and that in cell systems containing m4 and m2 receptors coupled to a common response, the toxin constitutes a powerful tool to resolve the relative contribution by each receptor subtype.
Footnotes
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Send reprint requests to: Pierluigi Onali, M.D., Section on Biochemical Pharmacology, Department of Neurosciences, University of Cagliari, via Porcell 4, 09124 Cagliari, Italy. E-mail:onali{at}unica.it.
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↵1 This work was supported by Grant CHRXCT940689 from the European Communities (to P.O.) and by MURST.
- Abbreviations:
- ACh
- acetylcholine chloride
- CCh
- carbachol chloride
- CHO
- Chinese hamster ovary
- BSA
- bovine serum albumin
- EGTA
- ethylene glycol bis(β-aminoethyl ether)-N,N,N′,N′-tetraacetic acid
- GTPγS
- guanosine-5′-O-(3-thio)triphosphate
- HEPES
- 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid
- MT3
- muscarinic toxin 3
- NMS
- N-methylscopolamine
- PACAP
- pituitary adenylate cyclase activating polypeptide
- RT
- reverse transcription
- PCR
- polymerase chain reaction
- Received April 15, 1998.
- Accepted June 25, 1998.
- The American Society for Pharmacology and Experimental Therapeutics
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