Novel Ca2+ signalling mechanisms in vascular myocytes:: symposium overview

被引:13
作者
Li, PL
Lee, HC
Nelson, MT
Meininger, GA
Van Breemen, C
机构
[1] Med Coll Wisconsin, Dept Pharmacol & Toxicol, Milwaukee, WI 53226 USA
[2] Univ Minnesota, Sch Med, Dept Pharmacol, Minneapolis, MN 55455 USA
[3] Univ Vermont, Sch Med, Dept Pharmacol, Burlington, VT 05405 USA
[4] Texas A&M Univ, Hlth Sci Ctr, Dept Physiol, College Stn, TX USA
[5] Univ British Columbia, Dept Pharmacol, Vancouver, BC V5Z 1M9, Canada
来源
ACTA PHYSIOLOGICA SCANDINAVICA | 2003年 / 179卷 / 04期
关键词
artery; integrin; mitochondria; ryanodine receptor; sarcoplasmic reticulum; signal transduction; smooth muscle;
D O I
10.1046/j.0001-6772.2003.01216.x
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
This commentary presents the proceedings of the symposium sponsored by Cardiovascular Section of American Physiological Society in San Diego, CA on 12 April 2003. The major focus of this symposium was on the actions and physiological relevance of several novel Ca2+ signalling mechanisms in vascular smooth muscle (VSM) cells. Five important topics were presented in this symposium including the discovery and roles of cyclic ADP-ribose (CADPR) and nicotinic acid adenine dinucleotide phosphate (NAADP) in mediating Ca2+ release, Ca2+ sparks and activation of plasma membrane K-Ca channels in VSM cells, the role of cADPR-mediated activation of ryanodine receptors in the control of vascular tone, the role of [Ca2+](i) in mechanotransduction in the arterioles, and interactions of mitochondrial Ca2+ release and SR Ca2+ mobilization. The purpose of this symposium was to promote discussions and exchange of ideas between scientists with interests in Ca2+ signalling mechanisms and those with interests in vascular physiology and pharmacology. The cross-fertilization of ideas is expected to greatly advance our understanding of the physiological and pharmacological relevance of these new Ca2+ signalling mechanisms.
引用
收藏
页码:339 / 352
页数:14
相关论文
共 103 条
[81]   RELAXATION OF ARTERIAL SMOOTH-MUSCLE BY CALCIUM SPARKS [J].
NELSON, MT ;
CHENG, H ;
RUBART, M ;
SANTANA, LF ;
BONEV, AD ;
KNOT, HJ ;
LEDERER, WJ .
SCIENCE, 1995, 270 (5236) :633-637
[82]   Cyclic ADP-ribose binds to FK506-binding protein 12.6 to release Ca2+ from islet microsomes [J].
Noguchi, N ;
Takasawa, S ;
Nata, K ;
Tohgo, A ;
Kato, I ;
Ikehata, F ;
Yonekura, H ;
Okamoto, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (06) :3133-3136
[83]   Cyclic ADP-ribose activates caffeine-sensitive calcium channels from sea urchin egg microsomes [J].
Pérez, CF ;
Marengo, JJ ;
Bull, R ;
Hidalgo, C .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1998, 274 (02) :C430-C439
[84]  
Petersen OH, 1996, NEWS PHYSIOL SCI, V11, P13
[85]   Microtubule-dependent regulation of vasomotor tone requires Rho-kinase [J].
Platts, SH ;
Martinez-Lemus, LA ;
Meininger, GA .
JOURNAL OF VASCULAR RESEARCH, 2002, 39 (02) :173-182
[86]   The comeback of mitochondria to calcium signalling [J].
Pozzan, T ;
Magalhaes, P ;
Rizzuto, R .
CELL CALCIUM, 2000, 28 (5-6) :279-283
[87]   Role of cyclic ADP-ribose in the regulation of [Ca2+]i in porcine tracheal smooth muscle [J].
Prakash, YS ;
Kannan, MS ;
Walseth, TF ;
Sieck, GC .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1998, 274 (06) :C1653-C1660
[88]   Crystal structure of Aplysia ADP ribosyl cyclase, a homologue of the bifunctional ectozyme CD38 [J].
Prasad, GS ;
McRee, DE ;
Stura, EA ;
Levitt, DG ;
Lee, HC ;
Stout, CD .
NATURE STRUCTURAL BIOLOGY, 1996, 3 (11) :957-964
[89]  
Qian Chen, 1992, Advances in Second Messenger and Phosphoprotein Research, V26, P335
[90]   CYCLIC ADP-RIBOSE COMPETES WITH ATP FOR THE ADENINE-NUCLEOTIDE BINDING-SITE ON THE CARDIAC RYANODINE RECEPTOR CA2+-RELEASE CHANNEL [J].
SITSAPESAN, R ;
MCGARRY, SJ ;
WILLIAMS, AJ .
CIRCULATION RESEARCH, 1994, 75 (03) :596-600