Skip to main content
Biochemical Journal logoLink to Biochemical Journal
. 1987 Jun 15;244(3):647–653. doi: 10.1042/bj2440647

Homologous desensitization of substance-P-induced inositol polyphosphate formation in rat parotid acinar cells.

H Sugiya 1, K A Tennes 1, J W Putney Jr 1
PMCID: PMC1148045  PMID: 2451500

Abstract

Maximal concentrations of substance P and methacholine induced a rapid increase in [3H]inositol trisphosphate ([3H]IP3) formation. After about 1 min, the [3H]IP3 in the substance-P-treated cells ceased to increase further, whereas in the methacholine-treated cells [3H]IP3 continued to increase. Addition of methacholine to the substance-P-treated cells caused a rapid increase in [3H]IP3, whereas a second addition of a 10-fold excess of substance P had no effect. Pretreatment of cells with substance P, followed by removal of the substance P by washing, resulted in a decreased response to a second application of substance P. A similar protocol involving pretreatment with methacholine had no effect on subsequent responsiveness to substance P. Analysis of [3H]substance P binding to substance-P-treated cells indicated that the number of receptors for substance P was decreased, but the affinity of the receptors for substance P was unaffected. After substance P pretreatment, a prolonged incubation (2 h) restored responsiveness of the cells to substance P, measured as [3H]IP3 formation, and restored the number of binding sites to control values. These findings indicate that, in the rat parotid gland, substance P induces a homologous desensitization of its receptor, which involves a slowly reversible down-regulation or sequestration of substance-P-binding sites.

Full text

PDF
647

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Aub D. L., Putney J. W., Jr Metabolism of inositol phosphates in parotid cells: implications for the pathway of the phosphoinositide effect and for the possible messenger role of inositol trisphosphate. Life Sci. 1984 Apr 2;34(14):1347–1355. doi: 10.1016/0024-3205(84)90006-7. [DOI] [PubMed] [Google Scholar]
  2. Aub D. L., Putney J. W., Jr Properties of receptor-controlled inositol trisphosphate formation in parotid acinar cells. Biochem J. 1985 Jan 1;225(1):263–266. doi: 10.1042/bj2250263. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Berridge M. J., Dawson R. M., Downes C. P., Heslop J. P., Irvine R. F. Changes in the levels of inositol phosphates after agonist-dependent hydrolysis of membrane phosphoinositides. Biochem J. 1983 May 15;212(2):473–482. doi: 10.1042/bj2120473. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Berridge M. J. Inositol trisphosphate and diacylglycerol as second messengers. Biochem J. 1984 Jun 1;220(2):345–360. doi: 10.1042/bj2200345. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Berridge M. J., Irvine R. F. Inositol trisphosphate, a novel second messenger in cellular signal transduction. Nature. 1984 Nov 22;312(5992):315–321. doi: 10.1038/312315a0. [DOI] [PubMed] [Google Scholar]
  6. Bone E. A., Michell R. H. Accumulation of inositol phosphates in sympathetic ganglia. Effects of depolarization and of amine and peptide neurotransmitters. Biochem J. 1985 Apr 1;227(1):263–269. doi: 10.1042/bj2270263. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Burgess G. M., McKinney J. S., Irvine R. F., Putney J. W., Jr Inositol 1,4,5-trisphosphate and inositol 1,3,4-trisphosphate formation in Ca2+-mobilizing-hormone-activated cells. Biochem J. 1985 Nov 15;232(1):237–243. doi: 10.1042/bj2320237. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Bury R. W., Mashford M. L. A pharmacological investigation of synthetic substance P on the isolated guinea-pig ileum. Clin Exp Pharmacol Physiol. 1977 Sep-Oct;4(5):453–461. doi: 10.1111/j.1440-1681.1977.tb02409.x. [DOI] [PubMed] [Google Scholar]
  9. Downes C. P., Hawkins P. T., Irvine R. F. Inositol 1,3,4,5-tetrakisphosphate and not phosphatidylinositol 3,4-bisphosphate is the probable precursor of inositol 1,3,4-trisphosphate in agonist-stimulated parotid gland. Biochem J. 1986 Sep 1;238(2):501–506. doi: 10.1042/bj2380501. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Friedman Z. Y., Selinger Z. A transient release of potassium mediated by the action of substance P on rat parotid slices. J Physiol. 1978 May;278:461–469. doi: 10.1113/jphysiol.1978.sp012317. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Friedman Z. Y., Wormser U., Rubini E., Chorev M., Gilon C., Selinger Z. Desensitization of substance P-induced K+ release in rat parotid. Eur J Pharmacol. 1985 Nov 19;117(3):323–328. doi: 10.1016/0014-2999(85)90005-6. [DOI] [PubMed] [Google Scholar]
  12. Gallacher D. V. Substance P is a functional neurotransmitter in the rat parotid gland. J Physiol. 1983 Sep;342:483–498. doi: 10.1113/jphysiol.1983.sp014864. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Hanley M. R., Lee C. M., Michell R. H., Jones L. M. Similar effects of substance P and related peptides on salivation and on phosphatidylinositol turnover in rat salivary glands. Mol Pharmacol. 1980 Jul;18(1):78–83. [PubMed] [Google Scholar]
  14. 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]
  15. Irvine R. F., Letcher A. J., Heslop J. P., Berridge M. J. The inositol tris/tetrakisphosphate pathway--demonstration of Ins(1,4,5)P3 3-kinase activity in animal tissues. Nature. 1986 Apr 17;320(6063):631–634. doi: 10.1038/320631a0. [DOI] [PubMed] [Google Scholar]
  16. Irvine R. F., Letcher A. J., Lander D. J., Downes C. P. Inositol trisphosphates in carbachol-stimulated rat parotid glands. Biochem J. 1984 Oct 1;223(1):237–243. doi: 10.1042/bj2230237. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Konishi S., Otsuka M. The effects of substance P and other peptides on spinal neurons of the frog. Brain Res. 1974 Jan 18;65(3):397–410. doi: 10.1016/0006-8993(74)90231-5. [DOI] [PubMed] [Google Scholar]
  18. Leeb-Lundberg L. M., Cotecchia S., Lomasney J. W., DeBernardis J. F., Lefkowitz R. J., Caron M. G. Phorbol esters promote alpha 1-adrenergic receptor phosphorylation and receptor uncoupling from inositol phospholipid metabolism. Proc Natl Acad Sci U S A. 1985 Sep;82(17):5651–5655. doi: 10.1073/pnas.82.17.5651. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Leeman S. E., Hammerschlag R. Stimulation of salivary secretion by a factor extracted from hypothalamic tissue. Endocrinology. 1967 Oct;81(4):803–810. doi: 10.1210/endo-81-4-803. [DOI] [PubMed] [Google Scholar]
  20. Liang T., Cascieri M. A. Specific binding of an immunoreactive and biologically active 125I-labeled N(1)acylated substance P derivative to parotid cells. Biochem Biophys Res Commun. 1980 Oct 31;96(4):1793–1799. doi: 10.1016/0006-291x(80)91382-0. [DOI] [PubMed] [Google Scholar]
  21. Liang T., Cascieri M. A. Substance P receptor on parotid cell membranes. J Neurosci. 1981 Oct;1(10):1133–1141. doi: 10.1523/JNEUROSCI.01-10-01133.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Liang T., Cascieri M. A. Substance P stimulation of amylase release by isolated parotid cells and inhibition of substance P induction of salivation by vasoactive peptides. Mol Cell Endocrinol. 1979 Sep;15(3):151–162. doi: 10.1016/0303-7207(79)90035-2. [DOI] [PubMed] [Google Scholar]
  23. Lynch C. J., Charest R., Bocckino S. B., Exton J. H., Blackmore P. F. Inhibition of hepatic alpha 1-adrenergic effects and binding by phorbol myristate acetate. J Biol Chem. 1985 Mar 10;260(5):2844–2851. [PubMed] [Google Scholar]
  24. Ogata N. Substance P causes direct depolarisation of neurones of guinea pig interpeduncular nucleus in vitro. Nature. 1979 Feb 8;277(5696):480–481. doi: 10.1038/277480a0. [DOI] [PubMed] [Google Scholar]
  25. Phillis J. W., Limacher J. J. Substance P excitation of cerebral cortical Betz cells. Brain Res. 1974 Mar 29;69(1):158–163. doi: 10.1016/0006-8993(74)90383-7. [DOI] [PubMed] [Google Scholar]
  26. Putney J. W., Jr, Aub D. L., Taylor C. W., Merritt J. E. Formation and biological action of inositol 1,4,5-trisphosphate. Fed Proc. 1986 Oct;45(11):2634–2638. [PubMed] [Google Scholar]
  27. Putney J. W., Jr, McKinney J. S., Aub D. L., Leslie B. A. Phorbol ester-induced protein secretion in rat parotid gland. Relationship to the role of inositol lipid breakdown and protein kinase C activation in stimulus-secretion coupling. Mol Pharmacol. 1984 Sep;26(2):261–266. [PubMed] [Google Scholar]
  28. Putney J. W., Jr Muscarinic, alpha-adrenergic and peptide receptors regulate the same calcium influx sites in the parotid gland. J Physiol. 1977 Jun;268(1):139–149. doi: 10.1113/jphysiol.1977.sp011851. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Putney J. W., Jr, Van de Walle C. M., Wheeler C. S. Binding of 125I-physalaemin to rat parotid acinar cells. J Physiol. 1980 Apr;301:205–212. doi: 10.1113/jphysiol.1980.sp013199. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Putney J. W., Jr, VanDeWalle C. M., Leslie B. A. Receptor control of calcium influx in parotid acinar cells. Mol Pharmacol. 1978 Nov;14(6):1046–1053. [PubMed] [Google Scholar]
  31. Sibley D. R., Lefkowitz R. J. Molecular mechanisms of receptor desensitization using the beta-adrenergic receptor-coupled adenylate cyclase system as a model. Nature. 1985 Sep 12;317(6033):124–129. doi: 10.1038/317124a0. [DOI] [PubMed] [Google Scholar]
  32. Strasser R. H., Sibley D. R., Lefkowitz R. J. A novel catecholamine-activated adenosine cyclic 3',5'-phosphate independent pathway for beta-adrenergic receptor phosphorylation in wild-type and mutant S49 lymphoma cells: mechanism of homologous desensitization of adenylate cyclase. Biochemistry. 1986 Mar 25;25(6):1371–1377. doi: 10.1021/bi00354a027. [DOI] [PubMed] [Google Scholar]
  33. Tennes K. A., McKinney J. S., Putney J. W., Jr Metabolism of inositol 1,4,5-trisphosphate in guinea-pig hepatocytes. Biochem J. 1987 Mar 15;242(3):797–802. doi: 10.1042/bj2420797. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Toews M. L., Waldo G. L., Harden T. K., Perkins J. P. Comparison of binding of 125I-iodopindolol to control and desensitized cells at 37 degrees and on ice. J Cyclic Nucleotide Protein Phosphor Res. 1986;11(1):47–62. [PubMed] [Google Scholar]
  35. Tregear G. W., Niall H. D., Potts J. T., Jr, Leeman S. E., Chang M. M. Synthesis of substance P. Nat New Biol. 1971 Jul 21;232(29):87–89. doi: 10.1038/newbio232087a0. [DOI] [PubMed] [Google Scholar]
  36. Vicentini L. M., Di Virgilio F., Ambrosini A., Pozzan T., Meldolesi J. Tumor promoter phorbol 12-myristate, 13-acetate inhibits phosphoinositide hydrolysis and cytosolic Ca2+ rise induced by the activation of muscarinic receptors in PC12 cells. Biochem Biophys Res Commun. 1985 Feb 28;127(1):310–317. doi: 10.1016/s0006-291x(85)80160-1. [DOI] [PubMed] [Google Scholar]
  37. Watson S. P., Downes C. P. Substance P induced hydrolysis of inositol phospholipids in guinea-pig ileum and rat hypothalamus. Eur J Pharmacol. 1983 Sep 30;93(3-4):245–253. doi: 10.1016/0014-2999(83)90144-9. [DOI] [PubMed] [Google Scholar]
  38. Watson S. P., Lapetina E. G. 1,2-Diacylglycerol and phorbol ester inhibit agonist-induced formation of inositol phosphates in human platelets: possible implications for negative feedback regulation of inositol phospholipid hydrolysis. Proc Natl Acad Sci U S A. 1985 May;82(9):2623–2626. doi: 10.1073/pnas.82.9.2623. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Watson S. P. The action of substance P on contraction, inositol phospholipids and adenylate cyclase in rat small intestine. Biochem Pharmacol. 1984 Dec 1;33(23):3733–3737. doi: 10.1016/0006-2952(84)90033-9. [DOI] [PubMed] [Google Scholar]
  40. Weiss S. J., McKinney J. S., Putney J. W., Jr Receptor-mediated net breakdown of phosphatidylinositol 4,5-bisphosphate in parotid acinar cells. Biochem J. 1982 Sep 15;206(3):555–560. doi: 10.1042/bj2060555. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Weiss S. J., Putney J. W., Jr The relationship of phosphatidylinositol turnover to receptors and calcium-ion channels in rat parotid acinar cells. Biochem J. 1981 Feb 15;194(2):463–468. doi: 10.1042/bj1940463. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Womack M. D., Hanley M. R., Jessell T. M. Functional substance P receptors on a rat pancreatic acinar cell line. J Neurosci. 1985 Dec;5(12):3370–3378. doi: 10.1523/JNEUROSCI.05-12-03370.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Biochemical Journal are provided here courtesy of The Biochemical Society

RESOURCES