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PMID: 11673466 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Rho-dependent agonist-induced spatio-temporal change in myosin phosphorylation in smooth muscle cells.

The Journal of biological chemistry ·Vol. 277 ·No. 1 ·2002-01-04 ·Pages 725-34

Miyazaki K, Yano T, Schmidt DJ, Tokui T, Shibata M, Lifshitz LM, Kimura S, Tuft RA, Ikebe M

Abstract

Agonist-induced translocation of RhoA and the spatio-temporal change in myosin regulatory light chain (MLC20) phosphorylation in smooth muscle was clarified at the single cell level. We expressed green fluorescent protein-tagged RhoA in the differentiated tracheal smooth muscle cells and visualized the translocation of RhoA in a living cell with three-dimensional digital imaging analysis. The stimulation of the cells by carbachol initiated the translocation of green fluorescent protein-tagged wild type RhoA to the plasma membrane within a minute. The change in MLC20 phosphorylation level after carbachol stimulation was monitored by using phospho-Ser-19-specific antibody recognizing the phosphorylated MLC20 in single cells. Cells expressing the dominant negative form (T19N) of RhoA significantly suppressed sustained MLC20 phosphorylation during the prolonged phase (>300 s), whereas the maximum phosphorylation level (reached at 10 s after stimulation) of these cells was not significantly different from the control cells. The kinetics of RhoA translocation was consistent with that of sustained myosin phosphorylation, suggesting the involvement of a RhoA pathway. Carbachol stimulation increased myosin phosphorylation within a minute both at the cortical and the central region. On the other hand, during prolonged phase, myosin phosphorylation was sustained at the cortical region of the cells but not at the central fibers. A myosin light chain kinase-specific inhibitor, ML-9, diminished myosin phosphorylation at the central region of the cells after the stimulation but not at the cortical area. On the other hand, Y-27632, a Rho kinase-specific inhibitor, diminished myosin phosphorylation at the cortical region but not the central region. The results clearly show that the myosin light chain kinase pathway and the Rho pathway distinctly change myosin phosphorylation in smooth muscle cells in both a temporal and spatial manner.

MeSH Terms
Animals Biological Transport COS Cells Carbachol/pharmacology Cells, Cultured Muscle, Smooth/cytology,metabolism Myosin-Light-Chain Kinase/physiology Myosins/metabolism Phosphorylation Swine Trachea/cytology,metabolism rhoA GTP-Binding Protein/metabolism
Chemicals
Carbachol Myosin-Light-Chain Kinase Myosins rhoA GTP-Binding Protein
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Miyazaki Koji
Department of Physiology and Biomedical Imaging Group, University of Massachusetts Medical School, Worcester, Massachusetts 01655, USA.
Yano Takeo
Schmidt David J
Tokui Toshiya
Shibata Masao
Lifshitz Lawrence M
Kimura Satoshi
Tuft Richard A
Ikebe Mitsuo
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2002-01-04
Epub
2001-00-22
Pages
725-34
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NHLBI NIH HHS · HL60831 · United States
NHLBI NIH HHS · HL61426 · United States
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