Proceedings of the Baltimore smooth muscle meeting: Identifying research frontiers and priorities for the lower urinary tract

被引:4
作者
Christ, GJ
Liebert, M
机构
[1] Wake Forest Univ, Wake Forest Inst Regenerat Med, Dept Urol, Cell Tissue Physiol Program, Winston Salem, NC 27157 USA
[2] Wake Forest Univ, Wake Forest Inst Regenerat Med, Dept Physiol & Pharmacol, Winston Salem, NC 27157 USA
[3] Amer Urol Assoc, Res Off, Linthicum, MD USA
关键词
urinary tract; urogenital system; muscle cells; muscle; smooth; physiopathology;
D O I
10.1097/01.ju.0000152289.23797.75
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose: The myocyte,is a major parenchymal cell of the lower urinary tract (LUT) in men and women. Significant phenotypic diversity ensures that myocytes subserve their important role in the physiologically distinct tissues and organs of the LUT, including the ureters, bladder, urethra, prostate, penis, vagina and myometrium. Coordinated contraction and relaxation of myocytes is required for normal organ function, while alterations in myocyte structure/function are implicated in the etiology of various LUT diseases/disorders. LUT diseases/disorders will continue to increase in an ever aging American population. The purpose of the Baltimore Smooth Muscle Meeting was to begin to identify some research frontiers and priorities. Materials and Methods: A 1-day conference of some of the leading world experts in smooth muscle research was held at American Urological Association headquarters. These experts gave presentations in their areas of expertise and extensively discussed their work. This report details those interactions. Results: There is astonishing diversity in the contribution of the myocyte to LUT physiology and dysfunction. Novel tools, technologies and ideas have produced increased understanding and identified new frontiers. Conclusions: An improved understanding of urogenital myocyte physiology, function and dysfunction is required better to elucidate disease mechanisms and develop novel therapeutics. The First Annual Baltimore Smooth Muscle Meeting provided the first step in this direction. More coordinated LUT myocyte funding initiatives, the further development of research resources, tools and technologies, and exploration of the urogenital system as a model system for studying systems biology and integrative physiology are among the highest research priorities.
引用
收藏
页码:1406 / 1409
页数:4
相关论文
共 20 条
[1]   Obstruction-induced changes in urinary bladder smooth muscle contractility: a role for Rho kinase [J].
Bing, W ;
Chang, SH ;
Hypolite, JA ;
DiSanto, ME ;
Zderic, SA ;
Rolf, L ;
Wein, AJ ;
Chacko, S .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2003, 285 (05) :F990-F997
[2]   Increased contractility of diabetic rabbit corpora smooth muscle in response to endothelin is mediated via Rho-kinase β [J].
Chang, S ;
Hypolite, J ;
Changolkar, A ;
Wein, AJ ;
Chacko, S ;
DiSanto, ME .
INTERNATIONAL JOURNAL OF IMPOTENCE RESEARCH, 2003, 15 (01) :53-62
[3]   Enhanced force generation by corpus cavernosum smooth muscle in rabbits with partial bladder outlet obstruction [J].
Chang, SH ;
Hypolite, JA ;
Zderic, SA ;
Wein, AJ ;
Chacko, S ;
DiSanto, ME .
JOURNAL OF UROLOGY, 2002, 167 (06) :2636-2644
[4]   Increased connexin43-mediated intercellular communication in a rat model of bladder overactivity in vivo [J].
Christ, GJ ;
Day, NS ;
Day, M ;
Zhao, WX ;
Persson, K ;
Pandita, RK ;
Andersson, KE .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2003, 284 (05) :R1241-R1248
[5]   Alteration in expression of myosin isoforms in detrusor smooth muscle following bladder outlet obstruction [J].
DiSanto, ME ;
Stein, R ;
Chang, SH ;
Hypolite, JA ;
Zheng, YM ;
Zderic, S ;
Wein, AJ ;
Chacko, S .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2003, 285 (06) :C1397-C1410
[6]   PHORBOL ESTER-INDUCED CONTRACTIONS OF SWINE CAROTID-ARTERY ARE SUPPORTED BY SLOWLY CYCLING CROSSBRIDGES WHICH ARE NOT DEPENDENT ON CALCIUM OR MYOSIN LIGHT-CHAIN PHOSPHORYLATION [J].
FULGINITI, J ;
SINGER, HA ;
MORELAND, RS .
JOURNAL OF VASCULAR RESEARCH, 1993, 30 (06) :315-322
[7]   Caldesmon phosphorylation is catalyzed by two kinases in permeabilized and intact vascular smooth muscle [J].
Gorenne, I ;
Su, XL ;
Moreland, R .
JOURNAL OF CELLULAR PHYSIOLOGY, 2004, 198 (03) :461-469
[8]   Ca2+-sensing transgenic mice -: Postsynaptic signaling in smooth muscle [J].
Ji, GJ ;
Feldman, ME ;
Deng, KY ;
Greene, KS ;
Wilson, J ;
Lee, JC ;
Johnston, RC ;
Rishniw, M ;
Tallini, Y ;
Zhang, J ;
Wier, WG ;
Blaustein, MP ;
Xin, HB ;
Nakai, J ;
Kotlikoff, MI .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (20) :21461-21468
[9]   RYR2 proteins contribute to the formation of Ca2+ sparks in smooth muscle [J].
Ji, GJ ;
Feldman, ME ;
Greene, KS ;
Sorrentino, V ;
Xin, HB ;
Kotlikoff, MI .
JOURNAL OF GENERAL PHYSIOLOGY, 2004, 123 (04) :377-386
[10]   Physiological roles for K+ channels and gap junctions in urogenital smooth muscle:: Implications for improved understanding of urogenital function, disease and therapy [J].
Karicheti, V ;
Christ, GJ .
CURRENT DRUG TARGETS, 2001, 2 (01) :1-20