Receptor for the pain modulatory neuropeptides FF and AF is an orphan G protein-coupled receptor

被引:235
作者
Elshourbagy, NA
Ames, RS
Fitzgerald, LR
Foley, JJ
Chambers, JK
Szekeres, PG
Evans, NA
Schmidt, DB
Buckley, PT
Dytko, GM
Murdock, PR
Milligan, G
Groarke, DA
Tan, KB
Shabon, U
Nuthulaganti, P
Wang, DY
Wilson, S
Bergsma, DJ
Sarau, HM
机构
[1] SmithKline Beecham Pharmaceut, Dept Biol Mol, King Of Prussia, PA 19406 USA
[2] SmithKline Beecham Pharmaceut, Dept Renal Pharmacol, King Of Prussia, PA 19406 USA
[3] SmithKline Beecham Pharmaceut, Dept Pulm Biol, King Of Prussia, PA 19406 USA
[4] SmithKline Beecham Pharmaceut, Dept Vasc Biol, King Of Prussia, PA 19406 USA
[5] SmithKline Beecham Pharmaceut, Dept Gene Express Sci, King Of Prussia, PA 19406 USA
[6] Univ Glasgow, Mol Pharmacol Grp, Div Biochem & Mol Biol, Inst Biomed & Life Sci, Glasgow G12 8QQ, Lanark, Scotland
关键词
D O I
10.1074/jbc.M004515200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Opiate tolerance and dependence are major clinical and social problems. The anti-opiate neuropeptides FF and AF (NPFF and NPAF) have been implicated in pain modulation as well as in opioid tolerance and may play a critical role in this process, although their mechanism of action has remained unknown. Here we describe a cDNA encoding a novel neuropeptide Y-like human orphan G protein-coupled receptor (GPCR), referred to as HLWAR77 for which NPAF and NPFF have high affinity. Cells transiently or stably expressing HLWAR77 bind and respond in a concentration-dependent manner to NPAF and NPFF and are also weakly activated by FMRF-amide (Phe-Met-Arg-Phe-amide) and a variety of related peptides. The high affinity and potency of human NPFF and human NPAF for HLWAR77 strongly suggest that these are the cognate ligands for this receptor. Expression of HLWAR77 was demonstrated in brain regions associated with opiate activity, consistent with the pain-modulating activity of these peptides, whereas the expression in adipose tissue suggests other physiological and pathophysiological activities for FMRF-amide neuropeptides. The discovery that the anti-opiate neuropeptides are the endogenous ligands for HLWAR77 will aid in defining the physiological role(s) of these ligands and facilitate the identification of receptor agonists and antagonists.
引用
收藏
页码:25965 / 25971
页数:7
相关论文
共 30 条
  • [1] COMPLEMENTARY-DNA SEQUENCING - EXPRESSED SEQUENCE TAGS AND HUMAN GENOME PROJECT
    ADAMS, MD
    KELLEY, JM
    GOCAYNE, JD
    DUBNICK, M
    POLYMEROPOULOS, MH
    XIAO, H
    MERRIL, CR
    WU, A
    OLDE, B
    MORENO, RF
    KERLAVAGE, AR
    MCCOMBIE, WR
    VENTER, JC
    [J]. SCIENCE, 1991, 252 (5013) : 1651 - 1656
  • [2] A beta-arrestin green fluorescent protein biosensor for detecting G protein-coupled receptor activation
    Barak, LS
    Ferguson, SSG
    Zhang, J
    Caron, MG
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (44) : 27497 - 27500
  • [3] Melanin-concentrating hormone is the cognate ligand for the orphan G-protein-coupled receptor SLC-1
    Chambers, J
    Ames, RS
    Bergsma, D
    Muir, A
    Fitzgerald, LR
    Hervieu, G
    Dytko, GM
    Foley, JJ
    Martin, J
    Liu, WS
    Park, J
    Ellis, C
    Ganguly, S
    Konchar, S
    Cluderay, J
    Leslie, R
    Wilson, S
    Sarau, HM
    [J]. NATURE, 1999, 400 (6741) : 261 - 265
  • [4] A G protein-coupled receptor for UDP-glucose
    Chambers, JK
    Macdonald, LE
    Sarau, HM
    Ames, RS
    Freeman, K
    Foley, JJ
    Zhu, Y
    McLaughlin, MM
    Murdock, P
    McMillan, L
    Trill, J
    Swift, A
    Aiyar, N
    Taylor, P
    Vawter, L
    Naheed, S
    Szekeres, P
    Hervieu, G
    Scott, C
    Watson, JM
    Murphy, AJ
    Duzic, E
    Klein, C
    Bergsma, DJ
    Wilson, S
    Livi, GP
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (15) : 10767 - 10771
  • [5] Sequence and tissue distribution of a novel G-protein-coupled receptor expressed prominently in human placenta
    Cikos, S
    Gregor, P
    Koppel, J
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 256 (02) : 352 - 356
  • [6] SUBSTITUTION OF 3 AMINO-ACIDS SWITCHES RECEPTOR SPECIFICITY OF G(Q)ALPHA TO THAT OF G(I)ALPHA
    CONKLIN, BR
    FARFEL, Z
    LUSTIG, KD
    JULIUS, D
    BOURNE, HR
    [J]. NATURE, 1993, 363 (6426) : 274 - 276
  • [7] Chimeric G proteins allow a high-throughput signaling assay of Gi-coupled receptors
    Coward, P
    Chan, SDH
    Wada, HG
    Humphries, GM
    Conklin, BR
    [J]. ANALYTICAL BIOCHEMISTRY, 1999, 270 (02) : 242 - 248
  • [8] CHARACTERIZATION OF A POTENT AGONIST FOR NPFF RECEPTORS - BINDING STUDY ON RAT SPINAL-CORD MEMBRANES
    DEVILLERS, JP
    MAZARGUIL, H
    ALLARD, M
    DICKENSON, AH
    ZAJAC, JM
    SIMONNET, G
    [J]. NEUROPHARMACOLOGY, 1994, 33 (05) : 661 - 669
  • [9] Measurement of responses from Gi-, Gs-, or Gq-coupled receptors by a multiple response element/cAMP response element-directed reporter assay
    Fitzgerald, LR
    Mannan, IJ
    Dytko, GM
    Wu, HL
    Nambi, P
    [J]. ANALYTICAL BIOCHEMISTRY, 1999, 275 (01) : 54 - 61
  • [10] ANTINOCICEPTIVE EFFECTS OF INTRATHECALLY ADMINISTERED F8FAMIDE AND FMRFAMIDE IN THE RAT
    GOUARDERES, C
    SUTAK, M
    ZAJAC, JM
    JHAMANDAS, K
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1993, 237 (01) : 73 - 81