|
|
||||||||
VASCULAR BIOLOGY
Cardiovascular Division, Department of Internal Medicine, University of Virginia Health System, Charlottesville, Virginia
Submitted 7 June 2004 ; accepted in final form 21 October 2004
Increases in cyclic nucleotide levels induce smooth muscle relaxation by deactivation [reductions in myosin regulatory light chain (MRLC) phosphorylation (e.g., by reduced [Ca2+])] or force suppression (reduction in force without reduction in MRLC phosphorylation). Ser16-heat shock protein 20 (HSP20) phosphorylation is the proposed mediator of force suppression. We evaluated three potential hypotheses whereby Ser16-HSP20 phosphorylation could regulate smooth muscle force: 1) a threshold level of HSP20 phosphorylation could inactivate a thin filament as a whole, 2) phosphorylation of a single HSP20 could fully inactivate a small region of a thin filament, or 3) HSP20 phosphorylation could weakly inhibit myosin binding at either the thin- or thick-filament level. We tested these hypotheses by analyzing the dependence of force on Ser16-HSP20 phosphorylation in swine carotid media. First, we determined that swine HSP20 has a second phosphorylation site at Ser157. Ser157-HSP20 phosphorylation values were high and did not change during contractile activation or forskolin-induced relaxation. Forskolin significantly increased Ser16-HSP20 phosphorylation. The relationship between Ser16-HSP20 phosphorylation and force remained linear and was shifted downward in partially activated muscles relaxed with forskolin. Neither forskolin nor nitroglycerin induced actin depolymerization as detected using the F/G-actin ratio method in smooth muscle homogenates. These results suggest that force suppression does not occur in accordance with the first hypothesis (inactivation of a thin filament as a whole). Our data are more consistent with the second and third hypotheses that force suppression is mediated by full or partial inhibition of local myosin binding at the thin- or thick-filament level.
cAMP; cGMP; nitric oxide; vascular smooth muscle
This article has been cited by other articles:
![]() |
S. Chen, R. Wang, Q.-F. Li, and D. D. Tang Abl knockout differentially affects p130 Crk-associated substrate, vinculin, and paxillin in blood vessels of mice Am J Physiol Heart Circ Physiol, August 1, 2009; 297(2): H533 - H539. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. D. Tang p130 Crk-Associated Substrate (CAS) in Vascular Smooth Muscle Journal of Cardiovascular Pharmacology and Therapeutics, June 1, 2009; 14(2): 89 - 98. [Abstract] [PDF] |
||||
![]() |
D. D. Tang and Y. Anfinogenova Physiologic Properties and Regulation of the Actin Cytoskeleton in Vascular Smooth Muscle Journal of Cardiovascular Pharmacology and Therapeutics, June 1, 2008; 13(2): 130 - 140. [Abstract] [PDF] |
||||
![]() |
D. D. Tang Intermediate filaments in smooth muscle Am J Physiol Cell Physiol, April 1, 2008; 294(4): C869 - C878. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. M. Rembold, A. D. Tejani, M. L. Ripley, and S. Han Paxillin phosphorylation, actin polymerization, noise temperature, and the sustained phase of swine carotid artery contraction Am J Physiol Cell Physiol, September 1, 2007; 293(3): C993 - C1002. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. M. Rembold Force suppression and the crossbridge cycle in swine carotid artery Am J Physiol Cell Physiol, September 1, 2007; 293(3): C1003 - C1009. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Anfinogenova, R. Wang, Q.-f. Li, A. M. Spinelli, and D. D. Tang Abl Silencing Inhibits CAS-Mediated Process and Constriction in Resistance Arteries Circ. Res., August 17, 2007; 101(4): 420 - 428. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. J. Sandoval, E. R. Injeti, J. M. Williams, W. T. Georthoffer, and W. J. Pearce Myogenic contractility is more dependent on myofilament calcium sensitization in term fetal than adult ovine cerebral arteries Am J Physiol Heart Circ Physiol, July 1, 2007; 293(1): H548 - H556. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |