Abstract
1. Smooth muscle fragments from the longitudinal layer of the small intestine of the guinea-pig were permeabilized with Staphylococcus aureus alpha toxin (alpha-toxin) and used to investigate the role of G-protein activation in the regulation of muscarinic acetylcholine receptor (AChR)-stimulated inositol phospholipid hydrolysis. 2. The efficiency of alpha-toxin permeabilization was estimated by the release of [3H]-2-deoxyglucose ([3H]-2DG) after prior loading or lactate dehydrogenase (LDH) enzyme release from the smooth muscle fragments. 3. In alpha-toxin-permeabilized smooth muscle, but not in non-permeabilized muscle, GTP gamma S induced time- and concentration-dependent increases in labelled inositol phosphates. Carbachol (CCh) increased labelled inositol phosphates in both permeabilized and non-permeabilized muscle, although the increases were greater in non-permeabilized smooth muscle. The response to 100 microM CCh was severely reduced by 0.5 microM atropine. 4. In permeabilized muscle the effects of GTP gamma S or CCh on inositol phosphate levels were reduced by treatment with pertussis toxin (PTX) and completely inhibited by GDP beta S. 5. GTP gamma S caused a concentration-dependent inhibition of the CCh-induced increases in the levels of labelled inositol phosphates. Dibutyryl cyclic AMP or Sp-cAMPs (adenosine-3',5'-cyclic phosphorothiolate-Sp) reduced the effects of CCh on inositol phosphate levels. 6. The results suggest that muscarinic AChR activation induces inositol phospholipid hydrolysis via more than one G-protein in this smooth muscle and that several mechanisms may contribute to the modulation of both stimulatory and inhibitory responses observed.
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Selected References
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- Ashkenazi A., Peralta E. G., Winslow J. W., Ramachandran J., Capon D. J. Functionally distinct G proteins selectively couple different receptors to PI hydrolysis in the same cell. Cell. 1989 Feb 10;56(3):487–493. doi: 10.1016/0092-8674(89)90251-1. [DOI] [PubMed] [Google Scholar]
- Barocelli E., Chiavarini M., Ballabeni V., Bordi F., Impicciatore M. Interaction of selective compounds with muscarinic receptors at dispersed intestinal smooth muscle cells. Br J Pharmacol. 1993 Feb;108(2):393–397. doi: 10.1111/j.1476-5381.1993.tb12815.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Batty I. R., Nahorski S. R., Irvine R. F. Rapid formation of inositol 1,3,4,5-tetrakisphosphate following muscarinic receptor stimulation of rat cerebral cortical slices. Biochem J. 1985 Nov 15;232(1):211–215. doi: 10.1042/bj2320211. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Best L., Bolton T. B. Depolarisation of guinea-pig visceral smooth muscle causes hydrolysis of inositol phospholipids. Naunyn Schmiedebergs Arch Pharmacol. 1986 May;333(1):78–82. doi: 10.1007/BF00569664. [DOI] [PubMed] [Google Scholar]
- Bhakdi S., Tranum-Jensen J. Damage to mammalian cells by proteins that form transmembrane pores. Rev Physiol Biochem Pharmacol. 1987;107:147–223. doi: 10.1007/BFb0027646. [DOI] [PubMed] [Google Scholar]
- Bizzarri C., Di Girolamo M., D'Orazio M. C., Corda D. Evidence that a guanine nucleotide-binding protein linked to a muscarinic receptor inhibits directly phospholipase C. Proc Natl Acad Sci U S A. 1990 Jun;87(12):4889–4893. doi: 10.1073/pnas.87.12.4889. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Burnstock G., Campbell G., Satchell D., Smythe A. Evidence that adenosine triphosphate or a related nucleotide is the transmitter substance released by non-adrenergic inhibitory nerves in the gut. Br J Pharmacol. 1970 Dec;40(4):668–688. doi: 10.1111/j.1476-5381.1970.tb10646.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Casey P. J., Gilman A. G. G protein involvement in receptor-effector coupling. J Biol Chem. 1988 Feb 25;263(6):2577–2580. [PubMed] [Google Scholar]
- Cattaneo M. G., Vicentini L. M. Differential mechanisms of inositol phosphate generation at the receptors for bombesin and platelet-derived growth factor. Biochem J. 1989 Sep 1;262(2):665–668. doi: 10.1042/bj2620665. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cockcroft S., Gomperts B. D. Role of guanine nucleotide binding protein in the activation of polyphosphoinositide phosphodiesterase. Nature. 1985 Apr 11;314(6011):534–536. doi: 10.1038/314534a0. [DOI] [PubMed] [Google Scholar]
- Downes C. P., Michell R. H. The polyphosphoinositide phosphodiesterase of erythrocyte membranes. Biochem J. 1981 Jul 15;198(1):133–140. doi: 10.1042/bj1980133. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fermum R., Kosche D., Möritz K. U. Membrane-associated signal transduction modulates contractile responses to Ca2+ in saponin-skinned coronary smooth muscle. Naunyn Schmiedebergs Arch Pharmacol. 1991 Feb;343(2):209–216. doi: 10.1007/BF00168612. [DOI] [PubMed] [Google Scholar]
- Füssle R., Bhakdi S., Sziegoleit A., Tranum-Jensen J., Kranz T., Wellensiek H. J. On the mechanism of membrane damage by Staphylococcus aureus alpha-toxin. J Cell Biol. 1981 Oct;91(1):83–94. doi: 10.1083/jcb.91.1.83. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gutowski S., Smrcka A., Nowak L., Wu D. G., Simon M., Sternweis P. C. Antibodies to the alpha q subfamily of guanine nucleotide-binding regulatory protein alpha subunits attenuate activation of phosphatidylinositol 4,5-bisphosphate hydrolysis by hormones. J Biol Chem. 1991 Oct 25;266(30):20519–20524. [PubMed] [Google Scholar]
- Hohman R. J. Aggregation of IgE receptors induces degranulation in rat basophilic leukemia cells permeabilized with alpha-toxin from Staphylococcus aureus. Proc Natl Acad Sci U S A. 1988 Mar;85(5):1624–1628. doi: 10.1073/pnas.85.5.1624. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Honkanen R. E., Abdel-Latif A. A. Muscarinic-agonist and guanine nucleotide stimulation of myo-inositol trisphosphate formation in membranes isolated from bovine iris sphincter smooth muscle: effects of short-term cholinergic desensitization. Membr Biochem. 1989;8(1):39–59. doi: 10.3109/09687688909025825. [DOI] [PubMed] [Google Scholar]
- Irvine R. F., Anggård E. E., Letcher A. J., Downes C. P. Metabolism of inositol 1,4,5-trisphosphate and inositol 1,3,4-trisphosphate in rat parotid glands. Biochem J. 1985 Jul 15;229(2):505–511. doi: 10.1042/bj2290505. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Itoh T., Kuriyama H., Suzuki H. Differences and similarities in the noradrenaline- and caffeine-induced mechanical responses in the rabbit mesenteric artery. J Physiol. 1983 Apr;337:609–629. doi: 10.1113/jphysiol.1983.sp014645. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jafferji S. S., Michell R. H. Muscarinic cholinergic stimulation of phosphatidylinositol turnover in the longitudinal smooth muscle of guinea-pig ileum. Biochem J. 1976 Mar 15;154(3):653–657. doi: 10.1042/bj1540653. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Katada T., Gilman A. G., Watanabe Y., Bauer S., Jakobs K. H. Protein kinase C phosphorylates the inhibitory guanine-nucleotide-binding regulatory component and apparently suppresses its function in hormonal inhibition of adenylate cyclase. Eur J Biochem. 1985 Sep 2;151(2):431–437. doi: 10.1111/j.1432-1033.1985.tb09120.x. [DOI] [PubMed] [Google Scholar]
- Katz A., Wu D., Simon M. I. Subunits beta gamma of heterotrimeric G protein activate beta 2 isoform of phospholipase C. Nature. 1992 Dec 17;360(6405):686–689. doi: 10.1038/360686a0. [DOI] [PubMed] [Google Scholar]
- Kitazawa T., Gaylinn B. D., Denney G. H., Somlyo A. P. G-protein-mediated Ca2+ sensitization of smooth muscle contraction through myosin light chain phosphorylation. J Biol Chem. 1991 Jan 25;266(3):1708–1715. [PubMed] [Google Scholar]
- Knight D. E., Scrutton M. C. Gaining access to the cytosol: the technique and some applications of electropermeabilization. Biochem J. 1986 Mar 15;234(3):497–506. doi: 10.1042/bj2340497. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
- Lee S. B., Shin S. H., Hepler J. R., Gilman A. G., Rhee S. G. Activation of phospholipase C-beta 2 mutants by G protein alpha q and beta gamma subunits. J Biol Chem. 1993 Dec 5;268(34):25952–25957. [PubMed] [Google Scholar]
- Litosch I., Wallis C., Fain J. N. 5-Hydroxytryptamine stimulates inositol phosphate production in a cell-free system from blowfly salivary glands. Evidence for a role of GTP in coupling receptor activation to phosphoinositide breakdown. J Biol Chem. 1985 May 10;260(9):5464–5471. [PubMed] [Google Scholar]
- Logothetis D. E., Kim D. H., Northup J. K., Neer E. J., Clapham D. E. Specificity of action of guanine nucleotide-binding regulatory protein subunits on the cardiac muscarinic K+ channel. Proc Natl Acad Sci U S A. 1988 Aug;85(16):5814–5818. doi: 10.1073/pnas.85.16.5814. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Low M. G., Carroll R. C., Cox A. C. Characterization of multiple forms of phosphoinositide-specific phospholipase C purified from human platelets. Biochem J. 1986 Jul 1;237(1):139–145. doi: 10.1042/bj2370139. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Michel A. D., Whiting R. L. The binding of [3H]4-diphenylacetoxy-N-methylpiperidine methiodide to longitudinal ileal smooth muscle muscarinic receptors. Eur J Pharmacol. 1990 Feb 6;176(2):197–205. doi: 10.1016/0014-2999(90)90528-e. [DOI] [PubMed] [Google Scholar]
- Nishimura J., Khalil R. A., Drenth J. P., van Breemen C. Evidence for increased myofilament Ca2+ sensitivity in norepinephrine-activated vascular smooth muscle. Am J Physiol. 1990 Jul;259(1 Pt 2):H2–H8. doi: 10.1152/ajpheart.1990.259.1.H2. [DOI] [PubMed] [Google Scholar]
- Nishimura J., Kolber M., van Breemen C. Norepinephrine and GTP-gamma-S increase myofilament Ca2+ sensitivity in alpha-toxin permeabilized arterial smooth muscle. Biochem Biophys Res Commun. 1988 Dec 15;157(2):677–683. doi: 10.1016/s0006-291x(88)80303-6. [DOI] [PubMed] [Google Scholar]
- Obara K., Yamada T. Some properties of chemically skinned single smooth muscle cells. Jpn J Physiol. 1984;34(6):1089–1104. doi: 10.2170/jjphysiol.34.1089. [DOI] [PubMed] [Google Scholar]
- Olefsky J. M. Mechanisms of the ability of insulin to activate the glucose-transport system in rat adipocytes. Biochem J. 1978 Apr 15;172(1):137–145. doi: 10.1042/bj1720137. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ono T., Mita M., Suga O., Hashimoto T., Oishi K., Uchida M. K. Receptor-coupled shortening of alpha-toxin-permeabilized single smooth muscle cells from the guinea-pig stomach. Br J Pharmacol. 1992 Jul;106(3):539–543. doi: 10.1111/j.1476-5381.1992.tb14371.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Otero A. D. Transphosphorylation and G protein activation. Biochem Pharmacol. 1990 May 1;39(9):1399–1404. doi: 10.1016/0006-2952(90)90420-p. [DOI] [PubMed] [Google Scholar]
- Pacaud P., Bolton T. B. Relation between muscarinic receptor cationic current and internal calcium in guinea-pig jejunal smooth muscle cells. J Physiol. 1991 Sep;441:477–499. doi: 10.1113/jphysiol.1991.sp018763. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Park D., Jhon D. Y., Lee C. W., Lee K. H., Rhee S. G. Activation of phospholipase C isozymes by G protein beta gamma subunits. J Biol Chem. 1993 Mar 5;268(7):4573–4576. [PubMed] [Google Scholar]
- Prestwich S. A., Bolton T. B. G-protein involvement in muscarinic receptor-stimulation of inositol phosphates in longitudinal smooth muscle from the small intestine of the guinea-pig. Br J Pharmacol. 1995 Jan;114(1):119–126. doi: 10.1111/j.1476-5381.1995.tb14915.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Prestwich S. A., Bolton T. B. Measurement of picomole amounts of any inositol phosphate isomer separable by h.p.l.c. by means of a bioluminescence assay. Biochem J. 1991 Mar 15;274(Pt 3):663–672. doi: 10.1042/bj2740663. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ross E. M., Gilman A. G. Biochemical properties of hormone-sensitive adenylate cyclase. Annu Rev Biochem. 1980;49:533–564. doi: 10.1146/annurev.bi.49.070180.002533. [DOI] [PubMed] [Google Scholar]
- Ryu S. H., Lee S. Y., Lee K. Y., Rhee S. G. Catalytic properties of inositol trisphosphate kinase: activation by Ca2+ and calmodulin. FASEB J. 1987 Nov;1(5):388–393. doi: 10.1096/fasebj.1.5.2824270. [DOI] [PubMed] [Google Scholar]
- Smellie F. W., Davis C. W., Daly J. W., Wells J. N. Alkylxanthines: inhibition of adenosine-elicited accumulation of cyclic AMP in brain slices and of brain phosphodiesterase activity. Life Sci. 1979 Jun 25;24(26):2475–2482. doi: 10.1016/0024-3205(79)90458-2. [DOI] [PubMed] [Google Scholar]
- Smith C. D., Lane B. C., Kusaka I., Verghese M. W., Snyderman R. Chemoattractant receptor-induced hydrolysis of phosphatidylinositol 4,5-bisphosphate in human polymorphonuclear leukocyte membranes. Requirement for a guanine nucleotide regulatory protein. J Biol Chem. 1985 May 25;260(10):5875–5878. [PubMed] [Google Scholar]
- Somlyo A. V., Bond M., Somlyo A. P., Scarpa A. Inositol trisphosphate-induced calcium release and contraction in vascular smooth muscle. Proc Natl Acad Sci U S A. 1985 Aug;82(15):5231–5235. doi: 10.1073/pnas.82.15.5231. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sternweis P. C., Gilman A. G. Aluminum: a requirement for activation of the regulatory component of adenylate cyclase by fluoride. Proc Natl Acad Sci U S A. 1982 Aug;79(16):4888–4891. doi: 10.1073/pnas.79.16.4888. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sternweis P. C., Smrcka A. V. Regulation of phospholipase C by G proteins. Trends Biochem Sci. 1992 Dec;17(12):502–506. doi: 10.1016/0968-0004(92)90340-f. [DOI] [PubMed] [Google Scholar]
- Uhing R. J., Prpic V., Jiang H., Exton J. H. Hormone-stimulated polyphosphoinositide breakdown in rat liver plasma membranes. Roles of guanine nucleotides and calcium. J Biol Chem. 1986 Feb 15;261(5):2140–2146. [PubMed] [Google Scholar]
- Van Geet C., Deckmyn H., Kienast J., Wittevrongel C., Vermylen J. Guanine nucleotide-dependent inhibition of phospholipase C in human endothelial cells. J Biol Chem. 1990 May 15;265(14):7920–7926. [PubMed] [Google Scholar]
- Woods N. M., Cuthbertson K. S., Cobbold P. H. Phorbol-ester-induced alterations of free calcium ion transients in single rat hepatocytes. Biochem J. 1987 Sep 15;246(3):619–623. doi: 10.1042/bj2460619. [DOI] [PMC free article] [PubMed] [Google Scholar]