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. 1998 Jul 15;333(Pt 2):301–308. doi: 10.1042/bj3330301

Acute desensitization of phospholipase C-coupled muscarinic M3 receptors but not gonadotropin-releasing hormone receptors co-expressed in alphaT3-1 cells: implications for mechanisms of rapid desensitization.

G B Willars 1, C A McArdle 1, S R Nahorski 1
PMCID: PMC1219586  PMID: 9657969

Abstract

In the present study we have expressed the muscarinic M3 receptor in an immortalized mouse pituitary cell line (alphaT3-1), which expresses an endogenous gonadotropin-releasing hormone (GnRH) receptor, to examine potential differences in acute receptor regulation. Both of these receptors couple to the activation of phosphoinositide-specific phospholipase C (PLC) in these cells and we demonstrate that, despite expression in the same cell background, acute desensitization is a feature of muscarinic M3 receptors but not of GnRH receptors. We show that, when the concentrations of GnRH and methacholine are matched to give approximately equivalent maximal elevations of Ins(1,4,5)P3, the GnRH receptor is able to sustain PLC activity at the initial rate, whereas the muscarinic M3 receptor cannot. Thus PLC-activating G-protein-coupled receptors are able to undergo rapid desensitization in this cell line, indicating that the desensitization profile is receptor-specific rather than cell-specific. This argues strongly that post-receptor regulatory features do not have a prominent role in mediating rapid desensitization in these cells. Furthermore GnRH receptor-mediated PLC activity is sustained despite a marked and persistent depletion in the steady-state level of PtdIns(4,5)P2. In contrast, activation of muscarinic receptors is not sustained despite only a transient decrease in PtdIns(4,5)P2 concentration. Thus, whereas the contribution of PtdIns(4,5)P2 depletion to the temporal profile of receptor-mediated PLC signalling has been difficult to assess, the present results demonstrate that this is unlikely to be of importance in these cells. We suggest that unique structural features of the GnRH receptor result in a lack of appropriate regulatory phospho-acceptor sites and that the absence of agonist-dependent phosphorylation might underlie the lack of acute regulation.

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Selected References

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  1. Alblas J., van Etten I., Khanum A., Moolenaar W. H. C-terminal truncation of the neurokinin-2 receptor causes enhanced and sustained agonist-induced signaling. Role of receptor phosphorylation in signal attenuation. J Biol Chem. 1995 Apr 14;270(15):8944–8951. doi: 10.1074/jbc.270.15.8944. [DOI] [PubMed] [Google Scholar]
  2. Arora K. K., Sakai A., Catt K. J. Effects of second intracellular loop mutations on signal transduction and internalization of the gonadotropin-releasing hormone receptor. J Biol Chem. 1995 Sep 29;270(39):22820–22826. doi: 10.1074/jbc.270.39.22820. [DOI] [PubMed] [Google Scholar]
  3. Barr A. J., Watson S. P. Protein kinase C mediates delayed inhibitory feedback regulation of human neurokinin type 1 receptor activation of phospholipase C in UC11 astrocytoma cells. Mol Pharmacol. 1994 Aug;46(2):266–273. [PubMed] [Google Scholar]
  4. Burford N. T., Tobin A. B., Nahorski S. R. Differential coupling of m1, m2 and m3 muscarinic receptor subtypes to inositol 1,4,5-trisphosphate and adenosine 3',5'-cyclic monophosphate accumulation in Chinese hamster ovary cells. J Pharmacol Exp Ther. 1995 Jul;274(1):134–142. [PubMed] [Google Scholar]
  5. Challiss R. A., Chilvers E. R., Willcocks A. L., Nahorski S. R. Heterogeneity of [3H]inositol 1,4,5-trisphosphate binding sites in adrenal-cortical membranes. Characterization and validation of a radioreceptor assay. Biochem J. 1990 Jan 15;265(2):421–427. doi: 10.1042/bj2650421. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Davidson J. S., Wakefield I. K., Millar R. P. Absence of rapid desensitization of the mouse gonadotropin-releasing hormone receptor. Biochem J. 1994 Jun 1;300(Pt 2):299–302. doi: 10.1042/bj3000299. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Eason M. G., Moreira S. P., Liggett S. B. Four consecutive serines in the third intracellular loop are the sites for beta-adrenergic receptor kinase-mediated phosphorylation and desensitization of the alpha 2A-adrenergic receptor. J Biol Chem. 1995 Mar 3;270(9):4681–4688. doi: 10.1074/jbc.270.9.4681. [DOI] [PubMed] [Google Scholar]
  8. Fisher S. K. Homologous and heterologous regulation of receptor-stimulated phosphoinositide hydrolysis. Eur J Pharmacol. 1995 Feb 15;288(3):231–250. doi: 10.1016/0922-4106(95)90035-7. [DOI] [PubMed] [Google Scholar]
  9. Fisher S. K., Slowiejko D. M., McEwen E. L. A rapid attenuation of muscarinic agonist stimulated phosphoinositide hydrolysis precedes receptor sequestration in human SH-SY-5Y neuroblastoma cells. Neurochem Res. 1994 May;19(5):549–554. doi: 10.1007/BF00971329. [DOI] [PubMed] [Google Scholar]
  10. Fredericks Z. L., Pitcher J. A., Lefkowitz R. J. Identification of the G protein-coupled receptor kinase phosphorylation sites in the human beta2-adrenergic receptor. J Biol Chem. 1996 Jun 7;271(23):13796–13803. doi: 10.1074/jbc.271.23.13796. [DOI] [PubMed] [Google Scholar]
  11. Gray D. W., Challiss R. A., Nahorski S. R. Differential effects of lithium on muscarinic cholinoceptor-stimulated CMP-phosphatidate accumulation in cerebellar granule cells, CHO-M3 cells, and SH-SY5Y neuroblastoma cells. J Neurochem. 1994 Oct;63(4):1354–1360. doi: 10.1046/j.1471-4159.1994.63041354.x. [DOI] [PubMed] [Google Scholar]
  12. Horn F., Bilezikjian L. M., Perrin M. H., Bosma M. M., Windle J. J., Huber K. S., Blount A. L., Hille B., Vale W., Mellon P. L. Intracellular responses to gonadotropin-releasing hormone in a clonal cell line of the gonadotrope lineage. Mol Endocrinol. 1991 Mar;5(3):347–355. doi: 10.1210/mend-5-3-347. [DOI] [PubMed] [Google Scholar]
  13. Jenkinson S., Nahorski S. R., Challiss R. A. Disruption by lithium of phosphatidylinositol-4,5-bisphosphate supply and inositol-1,4,5-trisphosphate generation in Chinese hamster ovary cells expressing human recombinant m1 muscarinic receptors. Mol Pharmacol. 1994 Dec;46(6):1138–1148. [PubMed] [Google Scholar]
  14. Jewell-Motz E. A., Liggett S. B. An acidic motif within the third intracellular loop of the alpha2C2 adrenergic receptor is required for agonist-promoted phosphorylation and desensitization. Biochemistry. 1995 Sep 19;34(37):11946–11953. doi: 10.1021/bi00037a036. [DOI] [PubMed] [Google Scholar]
  15. Koréh K., Monaco M. E. The relationship of hormone-sensitive and hormone-insensitive phosphatidylinositol to phosphatidylinositol 4,5-bisphosphate in the WRK-1 cell. J Biol Chem. 1986 Jan 5;261(1):88–91. [PubMed] [Google Scholar]
  16. Kurose H., Lefkowitz R. J. Differential desensitization and phosphorylation of three cloned and transfected alpha 2-adrenergic receptor subtypes. J Biol Chem. 1994 Apr 1;269(13):10093–10099. [PubMed] [Google Scholar]
  17. 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]
  18. Lattion A. L., Diviani D., Cotecchia S. Truncation of the receptor carboxyl terminus impairs agonist-dependent phosphorylation and desensitization of the alpha 1B-adrenergic receptor. J Biol Chem. 1994 Sep 9;269(36):22887–22893. [PubMed] [Google Scholar]
  19. Liggett S. B., Freedman N. J., Schwinn D. A., Lefkowitz R. J. Structural basis for receptor subtype-specific regulation revealed by a chimeric beta 3/beta 2-adrenergic receptor. Proc Natl Acad Sci U S A. 1993 Apr 15;90(8):3665–3669. doi: 10.1073/pnas.90.8.3665. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Lohse M. J. Molecular mechanisms of membrane receptor desensitization. Biochim Biophys Acta. 1993 Nov 7;1179(2):171–188. doi: 10.1016/0167-4889(93)90139-g. [DOI] [PubMed] [Google Scholar]
  21. McArdle C. A., Forrest-Owen W., Willars G., Davidson J., Poch A., Kratzmeier M. Desensitization of gonadotropin-releasing hormone action in the gonadotrope-derived alpha T3-1 cell line. Endocrinology. 1995 Nov;136(11):4864–4871. doi: 10.1210/endo.136.11.7588218. [DOI] [PubMed] [Google Scholar]
  22. McArdle C. A., Schomerus E., Gröner I., Poch A. Estradiol regulates gonadotropin-releasing hormone receptor number, growth and inositol phosphate production in alpha T3-1 cells. Mol Cell Endocrinol. 1992 Sep;87(1-3):95–103. doi: 10.1016/0303-7207(92)90237-z. [DOI] [PubMed] [Google Scholar]
  23. McArdle C. A., Willars G. B., Fowkes R. C., Nahorski S. R., Davidson J. S., Forrest-Owen W. Desensitization of gonadotropin-releasing hormone action in alphaT3-1 cells due to uncoupling of inositol 1,4,5-trisphosphate generation and Ca2+ mobilization. J Biol Chem. 1996 Sep 27;271(39):23711–23717. doi: 10.1074/jbc.271.39.23711. [DOI] [PubMed] [Google Scholar]
  24. Menniti F. S., Takemura H., Oliver K. G., Putney J. W., Jr Different modes of regulation for receptors activating phospholipase C in the rat pancreatoma cell line AR4-2J. Mol Pharmacol. 1991 Nov;40(5):727–733. [PubMed] [Google Scholar]
  25. Nahorski S. R., Ragan C. I., Challiss R. A. Lithium and the phosphoinositide cycle: an example of uncompetitive inhibition and its pharmacological consequences. Trends Pharmacol Sci. 1991 Aug;12(8):297–303. doi: 10.1016/0165-6147(91)90581-c. [DOI] [PubMed] [Google Scholar]
  26. Nakanishi S., Catt K. J., Balla T. A wortmannin-sensitive phosphatidylinositol 4-kinase that regulates hormone-sensitive pools of inositolphospholipids. Proc Natl Acad Sci U S A. 1995 Jun 6;92(12):5317–5321. doi: 10.1073/pnas.92.12.5317. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Neill J. D., Sellers J. C., Musgrove L. C., Duck L. W. Epitope-tagged gonadotropin-releasing hormone receptors heterologously-expressed in mammalian (COS-1) and insect (Sf9) cells. Mol Cell Endocrinol. 1997 Mar 28;127(2):143–154. doi: 10.1016/s0303-7207(96)04003-8. [DOI] [PubMed] [Google Scholar]
  28. Palmer T. M., Benovic J. L., Stiles G. L. Molecular basis for subtype-specific desensitization of inhibitory adenosine receptors. Analysis of a chimeric A1-A3 adenosine receptor. J Biol Chem. 1996 Jun 21;271(25):15272–15278. doi: 10.1074/jbc.271.25.15272. [DOI] [PubMed] [Google Scholar]
  29. Rana R. S., Hokin L. E. Role of phosphoinositides in transmembrane signaling. Physiol Rev. 1990 Jan;70(1):115–164. doi: 10.1152/physrev.1990.70.1.115. [DOI] [PubMed] [Google Scholar]
  30. Tobin A. B., Keys B., Nahorski S. R. Identification of a novel receptor kinase that phosphorylates a phospholipase C-linked muscarinic receptor. J Biol Chem. 1996 Feb 16;271(7):3907–3916. doi: 10.1074/jbc.271.7.3907. [DOI] [PubMed] [Google Scholar]
  31. Tsutsumi M., Zhou W., Millar R. P., Mellon P. L., Roberts J. L., Flanagan C. A., Dong K., Gillo B., Sealfon S. C. Cloning and functional expression of a mouse gonadotropin-releasing hormone receptor. Mol Endocrinol. 1992 Jul;6(7):1163–1169. doi: 10.1210/mend.6.7.1324422. [DOI] [PubMed] [Google Scholar]
  32. Willars G. B., Challiss R. A., Nahorski S. R. Acute regulation of the receptor-mediated phosphoinositide signal transduction pathway. J Lipid Mediat Cell Signal. 1996 Sep;14(1-3):157–168. doi: 10.1016/0929-7855(96)00521-4. [DOI] [PubMed] [Google Scholar]
  33. Willars G. B., Nahorski S. R. Quantitative comparisons of muscarinic and bradykinin receptor-mediated Ins (1,4,5)P3 accumulation and Ca2+ signalling in human neuroblastoma cells. Br J Pharmacol. 1995 Mar;114(6):1133–1142. doi: 10.1111/j.1476-5381.1995.tb13325.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Wilson D. B., Neufeld E. J., Majerus P. W. Phosphoinositide interconversion in thrombin-stimulated human platelets. J Biol Chem. 1985 Jan 25;260(2):1046–1051. [PubMed] [Google Scholar]
  35. Wojcikiewicz R. J., Tobin A. B., Nahorski S. R. Desensitization of cell signalling mediated by phosphoinositidase C. Trends Pharmacol Sci. 1993 Jul;14(7):279–285. doi: 10.1016/0165-6147(93)90131-3. [DOI] [PubMed] [Google Scholar]
  36. Wojcikiewicz R. J., Tobin A. B., Nahorski S. R. Muscarinic receptor-mediated inositol 1,4,5-trisphosphate formation in SH-SY5Y neuroblastoma cells is regulated acutely by cytosolic Ca2+ and by rapid desensitization. J Neurochem. 1994 Jul;63(1):177–185. doi: 10.1046/j.1471-4159.1994.63010177.x. [DOI] [PubMed] [Google Scholar]

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