Abstract
l-Glutamate is the principal excitatory neurotransmitter in the vertebrate central nervous system, where it mediates many of its actions via G-protein-coupled metabotropic glutamate (mGlu) receptors. Since little is known about the dynamics of mGlu receptors at the plasma membrane, we have constructed a fusion protein comprising the mGlu receptor subtype 1alpha (mGlu1alpha) and green fluorescent protein (GFP). Using imaging of Ca2+ release from intracellular stores as a functional assay, the agonist pharmacology of this fluorescently tagged receptor was found to be similar to that of the wild-type receptor when expressed in HEK-293 cells. Receptor movement and function were measured simultaneously by combined imaging of Ca2+, using fura-red, and GFP fluorescence in single cells. Exposure to agonist induced a rapid loss of up to 30% of membrane-associated fluorescence, with a corresponding decrease in the functional response. Following removal of the agonist there was recovery of both the membrane fluorescence and the functional response. These data suggest that the surface expression of G-protein-coupled glutamate receptors might be rapidly regulated in response to agonist activation.
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- Abe T., Sugihara H., Nawa H., Shigemoto R., Mizuno N., Nakanishi S. Molecular characterization of a novel metabotropic glutamate receptor mGluR5 coupled to inositol phosphate/Ca2+ signal transduction. J Biol Chem. 1992 Jul 5;267(19):13361–13368. [PubMed] [Google Scholar]
- Aiba A., Chen C., Herrup K., Rosenmund C., Stevens C. F., Tonegawa S. Reduced hippocampal long-term potentiation and context-specific deficit in associative learning in mGluR1 mutant mice. Cell. 1994 Oct 21;79(2):365–375. doi: 10.1016/0092-8674(94)90204-6. [DOI] [PubMed] [Google Scholar]
- Aiba A., Kano M., Chen C., Stanton M. E., Fox G. D., Herrup K., Zwingman T. A., Tonegawa S. Deficient cerebellar long-term depression and impaired motor learning in mGluR1 mutant mice. Cell. 1994 Oct 21;79(2):377–388. [PubMed] [Google Scholar]
- Arvin B., Moncada C., Le Peillet E., Chapman A., Meldrum B. S. GYKI 52466 blocks the increase in extracellular glutamate induced by ischaemia. Neuroreport. 1992 Mar;3(3):235–238. doi: 10.1097/00001756-199203000-00004. [DOI] [PubMed] [Google Scholar]
- Barak L. S., Ferguson S. S., Zhang J., Caron M. G. A beta-arrestin/green fluorescent protein biosensor for detecting G protein-coupled receptor activation. J Biol Chem. 1997 Oct 31;272(44):27497–27500. doi: 10.1074/jbc.272.44.27497. [DOI] [PubMed] [Google Scholar]
- Barak L. S., Ferguson S. S., Zhang J., Martenson C., Meyer T., Caron M. G. Internal trafficking and surface mobility of a functionally intact beta2-adrenergic receptor-green fluorescent protein conjugate. Mol Pharmacol. 1997 Feb;51(2):177–184. doi: 10.1124/mol.51.2.177. [DOI] [PubMed] [Google Scholar]
- Barak L. S., Ménard L., Ferguson S. S., Colapietro A. M., Caron M. G. The conserved seven-transmembrane sequence NP(X)2,3Y of the G-protein-coupled receptor superfamily regulates multiple properties of the beta 2-adrenergic receptor. Biochemistry. 1995 Nov 28;34(47):15407–15414. doi: 10.1021/bi00047a003. [DOI] [PubMed] [Google Scholar]
- Batchelor A. M., Knöpfel T., Gasparini F., Garthwaite J. Pharmacological characterization of synaptic transmission through mGluRs in rat cerebellar slices. Neuropharmacology. 1997 Mar;36(3):401–403. doi: 10.1016/s0028-3908(97)00014-2. [DOI] [PubMed] [Google Scholar]
- Baude A., Nusser Z., Roberts J. D., Mulvihill E., McIlhinney R. A., Somogyi P. The metabotropic glutamate receptor (mGluR1 alpha) is concentrated at perisynaptic membrane of neuronal subpopulations as detected by immunogold reaction. Neuron. 1993 Oct;11(4):771–787. doi: 10.1016/0896-6273(93)90086-7. [DOI] [PubMed] [Google Scholar]
- Bordi F., Reggiani A., Conquet F. Regulation of synaptic plasticity by mGluR1 studied in vivo in mGluR1 mutant mice. Brain Res. 1997 Jun 27;761(1):121–126. doi: 10.1016/s0006-8993(97)00320-x. [DOI] [PubMed] [Google Scholar]
- Brakeman P. R., Lanahan A. A., O'Brien R., Roche K., Barnes C. A., Huganir R. L., Worley P. F. Homer: a protein that selectively binds metabotropic glutamate receptors. Nature. 1997 Mar 20;386(6622):284–288. doi: 10.1038/386284a0. [DOI] [PubMed] [Google Scholar]
- Brown E. M., Gamba G., Riccardi D., Lombardi M., Butters R., Kifor O., Sun A., Hediger M. A., Lytton J., Hebert S. C. Cloning and characterization of an extracellular Ca(2+)-sensing receptor from bovine parathyroid. Nature. 1993 Dec 9;366(6455):575–580. doi: 10.1038/366575a0. [DOI] [PubMed] [Google Scholar]
- Ciruela F., McIlhinney R. A. Differential internalisation of mGluR1 splice variants in response to agonist and phorbol esters in permanently transfected BHK cells. FEBS Lett. 1997 Nov 24;418(1-2):83–86. doi: 10.1016/s0014-5793(97)01353-7. [DOI] [PubMed] [Google Scholar]
- Clements J. D., Lester R. A., Tong G., Jahr C. E., Westbrook G. L. The time course of glutamate in the synaptic cleft. Science. 1992 Nov 27;258(5087):1498–1501. doi: 10.1126/science.1359647. [DOI] [PubMed] [Google Scholar]
- Conn P. J., Pin J. P. Pharmacology and functions of metabotropic glutamate receptors. Annu Rev Pharmacol Toxicol. 1997;37:205–237. doi: 10.1146/annurev.pharmtox.37.1.205. [DOI] [PubMed] [Google Scholar]
- Conquet F., Bashir Z. I., Davies C. H., Daniel H., Ferraguti F., Bordi F., Franz-Bacon K., Reggiani A., Matarese V., Condé F. Motor deficit and impairment of synaptic plasticity in mice lacking mGluR1. Nature. 1994 Nov 17;372(6503):237–243. doi: 10.1038/372237a0. [DOI] [PubMed] [Google Scholar]
- Feng X., Zhang J., Barak L. S., Meyer T., Caron M. G., Hannun Y. A. Visualization of dynamic trafficking of a protein kinase C betaII/green fluorescent protein conjugate reveals differences in G protein-coupled receptor activation and desensitization. J Biol Chem. 1998 Apr 24;273(17):10755–10762. doi: 10.1074/jbc.273.17.10755. [DOI] [PubMed] [Google Scholar]
- Georget V., Lobaccaro J. M., Terouanne B., Mangeat P., Nicolas J. C., Sultan C. Trafficking of the androgen receptor in living cells with fused green fluorescent protein-androgen receptor. Mol Cell Endocrinol. 1997 Apr 25;129(1):17–26. doi: 10.1016/s0303-7207(97)04034-3. [DOI] [PubMed] [Google Scholar]
- Henrich-Noack P., Hatton C. D., Reymann K. G. The mGlu receptor ligand (S)-4C3HPG protects neurons after global ischaemia in gerbils. Neuroreport. 1998 Apr 20;9(6):985–988. doi: 10.1097/00001756-199804200-00006. [DOI] [PubMed] [Google Scholar]
- Houamed K. M., Kuijper J. L., Gilbert T. L., Haldeman B. A., O'Hara P. J., Mulvihill E. R., Almers W., Hagen F. S. Cloning, expression, and gene structure of a G protein-coupled glutamate receptor from rat brain. Science. 1991 May 31;252(5010):1318–1321. doi: 10.1126/science.1656524. [DOI] [PubMed] [Google Scholar]
- John S. A., Monck J. R., Weiss J. N., Ribalet B. The sulphonylurea receptor SUR1 regulates ATP-sensitive mouse Kir6.2 K+ channels linked to the green fluorescent protein in human embryonic kidney cells (HEK 293). J Physiol. 1998 Jul 15;510(Pt 2):333–345. doi: 10.1111/j.1469-7793.1998.333bk.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kallal L., Gagnon A. W., Penn R. B., Benovic J. L. Visualization of agonist-induced sequestration and down-regulation of a green fluorescent protein-tagged beta2-adrenergic receptor. J Biol Chem. 1998 Jan 2;273(1):322–328. doi: 10.1074/jbc.273.1.322. [DOI] [PubMed] [Google Scholar]
- Kaupmann K., Huggel K., Heid J., Flor P. J., Bischoff S., Mickel S. J., McMaster G., Angst C., Bittiger H., Froestl W. Expression cloning of GABA(B) receptors uncovers similarity to metabotropic glutamate receptors. Nature. 1997 Mar 20;386(6622):239–246. doi: 10.1038/386239a0. [DOI] [PubMed] [Google Scholar]
- Koenig J. A., Edwardson J. M. Intracellular trafficking of the muscarinic acetylcholine receptor: importance of subtype and cell type. Mol Pharmacol. 1996 Feb;49(2):351–359. [PubMed] [Google Scholar]
- Koenig J. A., Edwardson J. M. Kinetic analysis of the trafficking of muscarinic acetylcholine receptors between the plasma membrane and intracellular compartments. J Biol Chem. 1994 Jun 24;269(25):17174–17182. [PubMed] [Google Scholar]
- Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
- Lujan R., Nusser Z., Roberts J. D., Shigemoto R., Somogyi P. Perisynaptic location of metabotropic glutamate receptors mGluR1 and mGluR5 on dendrites and dendritic spines in the rat hippocampus. Eur J Neurosci. 1996 Jul;8(7):1488–1500. doi: 10.1111/j.1460-9568.1996.tb01611.x. [DOI] [PubMed] [Google Scholar]
- Masu M., Tanabe Y., Tsuchida K., Shigemoto R., Nakanishi S. Sequence and expression of a metabotropic glutamate receptor. Nature. 1991 Feb 28;349(6312):760–765. doi: 10.1038/349760a0. [DOI] [PubMed] [Google Scholar]
- Mukhin A. G., Ivanova S. A., Faden A. I. mGluR modulation of post-traumatic neuronal death: role of NMDA receptors. Neuroreport. 1997 Jul 28;8(11):2561–2566. doi: 10.1097/00001756-199707280-00028. [DOI] [PubMed] [Google Scholar]
- Petralia R. S., Wang Y. X., Singh S., Wu C., Shi L., Wei J., Wenthold R. J. A monoclonal antibody shows discrete cellular and subcellular localizations of mGluR1 alpha metabotropic glutamate receptors. J Chem Neuroanat. 1997 Jul;13(2):77–93. doi: 10.1016/s0891-0618(97)00023-9. [DOI] [PubMed] [Google Scholar]
- Pin J. P., Duvoisin R. The metabotropic glutamate receptors: structure and functions. Neuropharmacology. 1995 Jan;34(1):1–26. doi: 10.1016/0028-3908(94)00129-g. [DOI] [PubMed] [Google Scholar]
- Rubio M. E., Wenthold R. J. Glutamate receptors are selectively targeted to postsynaptic sites in neurons. Neuron. 1997 Jun;18(6):939–950. doi: 10.1016/s0896-6273(00)80333-5. [DOI] [PubMed] [Google Scholar]
- Sakai N., Sasaki K., Ikegaki N., Shirai Y., Ono Y., Saito N. Direct visualization of the translocation of the gamma-subspecies of protein kinase C in living cells using fusion proteins with green fluorescent protein. J Cell Biol. 1997 Dec 15;139(6):1465–1476. doi: 10.1083/jcb.139.6.1465. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Seal A. J., Collingridge G. L., Henley J. M. In vitro translation and membrane topology of rat recombinant mGluR1 alpha. Neuropharmacology. 1994 Sep;33(9):1065–1070. doi: 10.1016/0028-3908(94)90144-9. [DOI] [PubMed] [Google Scholar]
- Tarasova N. I., Stauber R. H., Choi J. K., Hudson E. A., Czerwinski G., Miller J. L., Pavlakis G. N., Michejda C. J., Wank S. A. Visualization of G protein-coupled receptor trafficking with the aid of the green fluorescent protein. Endocytosis and recycling of cholecystokinin receptor type A. J Biol Chem. 1997 Jun 6;272(23):14817–14824. doi: 10.1074/jbc.272.23.14817. [DOI] [PubMed] [Google Scholar]
- Tu J. C., Xiao B., Yuan J. P., Lanahan A. A., Leoffert K., Li M., Linden D. J., Worley P. F. Homer binds a novel proline-rich motif and links group 1 metabotropic glutamate receptors with IP3 receptors. Neuron. 1998 Oct;21(4):717–726. doi: 10.1016/s0896-6273(00)80589-9. [DOI] [PubMed] [Google Scholar]
- Wessel D., Flügge U. I. A method for the quantitative recovery of protein in dilute solution in the presence of detergents and lipids. Anal Biochem. 1984 Apr;138(1):141–143. doi: 10.1016/0003-2697(84)90782-6. [DOI] [PubMed] [Google Scholar]
- Xiao B., Tu J. C., Petralia R. S., Yuan J. P., Doan A., Breder C. D., Ruggiero A., Lanahan A. A., Wenthold R. J., Worley P. F. Homer regulates the association of group 1 metabotropic glutamate receptors with multivalent complexes of homer-related, synaptic proteins. Neuron. 1998 Oct;21(4):707–716. doi: 10.1016/s0896-6273(00)80588-7. [DOI] [PubMed] [Google Scholar]
- von Zastrow M., Kobilka B. K. Antagonist-dependent and -independent steps in the mechanism of adrenergic receptor internalization. J Biol Chem. 1994 Jul 15;269(28):18448–18452. [PubMed] [Google Scholar]
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