The Rho-related protein Rnd1 inhibits Ca2+ sensitization of rat smooth muscle

被引:57
作者
Loirand, G [1 ]
Cario-Toumaniantz, C [1 ]
Chardin, P [1 ]
Pacaud, P [1 ]
机构
[1] CNRS, Inst Pharmacol Mol & Cellulaire, UPR 411, F-06560 Valbonne, France
来源
JOURNAL OF PHYSIOLOGY-LONDON | 1999年 / 516卷 / 03期
关键词
D O I
10.1111/j.1469-7793.1999.0825u.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
1. The small GTP-binding Rho proteins are involved in the agonist-induced Ca2+ sensitization of smooth muscle. The action and the expression of Rnd1, a new member of the Rho protein family constitutively bound to GTP, has been studied in rat smooth muscle. 2. Recombinant prenylated Rnd1 (0.01-0.1 mg ml(-1)) dose dependently inhibited carbachol- and GTP gamma S-induced Ca2+ sensitization in beta-escin-permeabilized ileal smooth muscle strips but had no effect on the tension at submaximal [Ca2+] (pCa 6.3). Rnd1 inhibited GTP gamma S-induced tension without shifting the dose-response curves to GTP gamma S. 3. pCa-tension relationships were not modified by Rnd1 and the rise in tension induced through the inhibition of myosin light chain phosphatase by calyculin A was not affected by Rnd1. 4. The C2+ sensitization induced by recombinant RhoA was completely abolished when RhoA and Rnd1 were applied together. 5. Rnd1 was expressed at a low level in membrane fractions prepared from intestinal or arterial smooth muscles. The expression of Rnd1 was strongly increased in ileal and aortic smooth muscle from rats treated with progesterone or oestrogen. Progesterone-treated ileal muscle strips showed a decrease in agonist-induced Ca2+ sensitization. 6. The present study shows that (i) Rnd1 inhibits agonist- and GTP gamma S-induced Ca2+ sensitization of smooth muscle by specifically interfering with a RhoA-dependent mechanism and (ii) an increase in Rnd1 expression may account, at least in part, for the steroid-induced decrease in agonist-induced C2+ sensitization.
引用
收藏
页码:825 / 834
页数:10
相关论文
共 42 条
[1]   Phosphorylation and activation of myosin by Rho-associated kinase (Rho-kinase) [J].
Amano, M ;
Ito, M ;
Kimura, K ;
Fukata, Y ;
Chihara, K ;
Nakano, T ;
Matsuura, Y ;
Kaibuchi, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (34) :20246-20249
[2]   GASTROINTESTINAL MOTILITY DISORDERS DURING PREGNANCY [J].
BARON, TH ;
RAMIREZ, B ;
RICHTER, JE .
ANNALS OF INTERNAL MEDICINE, 1993, 118 (05) :366-375
[3]   EFFECTS OF DIETHYLSTILBESTROL AND OVARIAN STEROIDS ON CONTRACTILE RESPONSES AND CALCIUM MOVEMENTS IN RAT UTERINE SMOOTH-MUSCLE [J].
BATRA, S ;
BENGTSSON, B .
JOURNAL OF PHYSIOLOGY-LONDON, 1978, 276 (MAR) :329-342
[4]   Nongenomic effects of progesterone on human intestinal smooth muscle cells [J].
Bielefeldt, K ;
Waite, L ;
Abboud, FM ;
Conklin, JL .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1996, 271 (02) :G370-G376
[5]   PROTEINS REGULATING RAS AND ITS RELATIVES [J].
BOGUSKI, MS ;
MCCORMICK, F .
NATURE, 1993, 366 (6456) :643-654
[6]   Protein prenyltransferases [J].
Casey, PJ ;
Seabra, MC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (10) :5289-5292
[7]   Impaired G protein function in gallbladder muscle from progesterone-treated guinea pigs [J].
Chen, Q ;
Chitinavis, V ;
Xiao, ZL ;
Yu, PR ;
Oh, S ;
Biancani, P ;
Behar, J .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1998, 274 (02) :G283-G289
[8]   Rho-stimulated contractility drives the formation of stress fibers and focal adhesions [J].
ChrzanowskaWodnicka, M ;
Burridge, K .
JOURNAL OF CELL BIOLOGY, 1996, 133 (06) :1403-1415
[9]   Inhibition of RhoA translocation and calcium sensitization by in vivo ADP-ribosylation with the chimeric toxin DC3B [J].
Fujihara, H ;
Walker, LA ;
Gong, MC ;
Lemichez, E ;
Boquet, P ;
Somlyo, AV ;
Somlyo, AP .
MOLECULAR BIOLOGY OF THE CELL, 1997, 8 (12) :2437-2447
[10]  
FUJITA A, 1995, J PHARMACOL EXP THER, V274, P555