Diadenosine polyphosphates as extracellular signal molecules

被引:67
作者
Hoyle, CHV
Hilderman, RH
Pintor, JJ
Schlüter, H
King, BF
机构
[1] Royal Free & Univ Coll Med Sch, Dept Physiol, London NW3 2PF, England
[2] UCL, Dept Anat & Dev Biol, London, England
[3] Clemson Univ, Dept Biochem, Clemson, SC USA
[4] Univ Complutense, Dept Biochem, E-28040 Madrid, Spain
[5] Univ Klin Marienhosp, Berlin, Germany
关键词
dinucleotide; diadenosine polyphosphate; nucleotide; nucleoside; receptor agonist; extracellular signalling;
D O I
10.1002/ddr.1123
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Dinucleoside polyphosphates are an interesting group of signalling molecules that control numerous physiological functions. Diadenosine compounds, with a backbone of anything from two to seven phosphates, are known to occur naturally Some of them have been isolated from cerebral nerve terminals and, acting via nucleoside (P1), nucleotide (P2), or dinucleotide receptors, can affect central nervous system function. Many of them have been isolated from human blood platelet secretory granules acid are potentially involved in haemostatic mechanisms and peripheral control of vascular tone. Many visceral organs respond to the application of adenine dinucleotides and, although they act on receptors in the periphery that can be mainly defined as either P1 or P2, evidence is now accumulating for discrete dinucleotide receptors. In the periphery adenine dinucleotides can be potent agonists, with diverse functions, causing contraction or relaxation of smooth muscle. Many P2X receptor proteins and P2Y receptors have been cloned and adenine dinucleotides have a variable pharmacological profile at these receptors and may be useful tools for characterising subtypes of P2X and P2Y receptors. This review provides a broad description of the many extracellular roles of diadenosine polyphosphates as emerging, yet increasingly important, natural ligands for a plethora of structurally diverse mononucleotide and dinucleotide receptors. Drug Dev. Res. 52:260-273, 2001. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:260 / 273
页数:14
相关论文
共 137 条
[1]  
AMBROSE E J, 1967, Ciba Symposium, P101
[2]   EFFECTS OF SURAMIN ON CONTRACTIONS OF THE GUINEA-PIG VAS-DEFERENS INDUCED BY ANALOGS OF ADENOSINE 5'-TRIPHOSPHATE [J].
BAILEY, SJ ;
HOURANI, SMO .
BRITISH JOURNAL OF PHARMACOLOGY, 1995, 114 (06) :1125-1132
[3]  
Berry DA, 1999, ELECTROPHORESIS, V20, P2059, DOI 10.1002/(SICI)1522-2683(19990701)20:10<2059::AID-ELPS2059>3.0.CO
[4]  
2-T
[5]   Pharmacological characterization of recombinant human and rat P2X receptor subtypes [J].
Bianchi, BR ;
Lynch, KJ ;
Touma, E ;
Niforatos, W ;
Burgard, EC ;
Alexander, KM ;
Park, HS ;
Yu, HX ;
Metzger, R ;
Kowaluk, E ;
Jarvis, MF ;
van Biesen, T .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1999, 376 (1-2) :127-138
[6]   Characterization of ATP and P2 agonists binding to the cardiac plasma membrane P1,P4-diadenosine 5′-tetraphosphate receptor [J].
Blouse, GE ;
Liu, G ;
Hilderman, RH .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1998, 1375 (1-2) :61-72
[7]   A P2X PURINOCEPTOR CDNA CONFERRING A NOVEL PHARMACOLOGICAL PROFILE [J].
BO, XN ;
ZHANG, Y ;
NASSAR, M ;
BURNSTOCK, G ;
SCHOEPFER, R .
FEBS LETTERS, 1995, 375 (1-2) :129-133
[8]   Molecular cloning and characterization of rat P2Y4 nucleotide receptor [J].
Bogdanov, YD ;
Wildman, SS ;
Clements, MP ;
King, BF ;
Burnstock, G .
BRITISH JOURNAL OF PHARMACOLOGY, 1998, 124 (03) :428-430
[9]   NEW STRUCTURAL MOTIF FOR LIGAND-GATED ION CHANNELS DEFINED BY AN IONOTROPIC ATP RECEPTOR [J].
BRAKE, AJ ;
WAGENBACH, MJ ;
JULIUS, D .
NATURE, 1994, 371 (6497) :519-523
[10]   An antagonist-insensitive P-2X receptor expressed in epithelia and brain [J].
Buell, G ;
Lewis, C ;
Collo, G ;
North, RA ;
Surprenant, A .
EMBO JOURNAL, 1996, 15 (01) :55-62