Extracellular nucleotide signaling along the renal epithelium

被引:143
作者
Schwiebert, EM
Kishore, BK
机构
[1] Univ Alabama Birmingham, Dept Physiol & Biophys, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Dept Cell Biol, Birmingham, AL 35294 USA
[3] Univ Cincinnati, Med Ctr, Dept Internal Med, Div Nephrol & Hypertens, Cincinnati, OH 45267 USA
关键词
purinergic; adeonsine 5 '-triphosphate; kidney; receptors; epithelia;
D O I
10.1152/ajprenal.2001.280.6.F945
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
During the past two decades, several cell membrane receptors, which preferentially bind extracellular nucleotides, and their analogs have been identified. These receptors, collectively known as nucleotide receptors or "purinergic" receptors, have been characterized and classified on the basis of their biological actions, their pharmacology, their molecular biology, and their tissue and cell distribution. For these receptors to have biological and physiological relevance, nucleotides must be released from cells. The field of extracellular ATP release and signaling is exploding, as assays to detect this biological process increase in number and ingenuity. Studies of ATP release have revealed a myriad of roles in local regulatory (autocrine or paracrine) processes in almost every tissue in the body. The regulatory mechanisms that these receptors control or modulate have physiological and pathophysiological roles and potential therapeutic applications. Only recently, however, have ATP release and nucleotide receptors been identified along the renal epithelium of the nephron. This work has set the stage for the study of their physiological and pathophysiological roles in the kidney. This review provides a comprehensive presentation of these issues, with a focus on the renal epithelium.
引用
收藏
页码:F945 / F963
页数:19
相关论文
共 154 条
[31]   Localization of P2X1 purinoceptors by autoradiography and immunohistochemistry in rat kidneys [J].
Chan, CM ;
Unwin, RJ ;
Bardini, M ;
Oglesby, IB ;
Ford, APDW ;
Townsend-Nicholson, A ;
Burnstock, G .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1998, 274 (04) :F799-F804
[32]  
CHURCHILL PC, 1993, J PHARMACOL EXP THER, V266, P160
[33]  
CORNFIELD LJ, 1992, J PHARMACOL EXP THER, V263, P552
[34]   ATP stimulates Cl- secretion and reduces amiloride-sensitive Na+ absorption in M-1 mouse cortical collecting duct cells [J].
Cuffe, JE ;
Bielfeld-Ackermann, A ;
Thomas, J ;
Leipziger, J ;
Korbmacher, C .
JOURNAL OF PHYSIOLOGY-LONDON, 2000, 524 (01) :77-90
[35]  
DALZIEL HH, 1994, PHARMACOL REV, V46, P449
[36]  
Deetjen P, 2000, J AM SOC NEPHROL, V11, P1798, DOI 10.1681/ASN.V11101798
[37]   ADENINE-NUCLEOTIDE METABOLISM DURING CARDIAC-HYPERTROPHY AND ISCHEMIA IN RATS [J].
DEGENRING, FH ;
RUBIO, R ;
BERNE, RM .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1975, 7 (02) :105-113
[38]   UTP inhibits Na+ absorption in wild-type and ΔF508 CFTR-expressing human bronchial epithelia [J].
Devor, DC ;
Pilewski, JM .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1999, 276 (04) :C827-C837
[39]   PURINERGIC REGULATION OF BASAL AND ARGININE VASOPRESSIN-STIMULATED HYDRAULIC CONDUCTIVITY IN RABBIT CORTICAL COLLECTING TUBULE [J].
DILLINGHAM, MA ;
ANDERSON, RJ .
JOURNAL OF MEMBRANE BIOLOGY, 1985, 88 (03) :277-281
[40]   The structure of the potassium channel:: Molecular basis of K+ conduction and selectivity [J].
Doyle, DA ;
Cabral, JM ;
Pfuetzner, RA ;
Kuo, AL ;
Gulbis, JM ;
Cohen, SL ;
Chait, BT ;
MacKinnon, R .
SCIENCE, 1998, 280 (5360) :69-77