Literature DB >> 1665860

Effects of putative modulators of relaxation microinjected into intact amphibian smooth muscle cells.

F S Fay1, W C Granger, H H Shelvin, S R Taylor.   

Abstract

1. Single smooth muscle cells were isolated intact from the stomach of the toad Bufo marinus. The relaxation of cells following cessation of electrical stimulation was compared with those relaxed by pressure microinjection of either metal ion chelators or cyclic nucleotides. 2. Injection of either a Ca2+ chelator or 3',5'-cyclic AMP slowed or halted shortening and promoted re-extension of a cell or collapse of membrane evaginations (blebs) in a manner similar to that following cessation of electrical stimulation. Collapse of blebs occurred first and was then followed smoothly by the next stage with cells re-extending at maximum rates in one of three ranges at 22 degrees C. These rates, in order of increasing speed, were 0.005, 0.009 and 0.03 cell lengths s-1 after electrical stimulation, 3',5'-cyclic AMP and EDTA injection, respectively. On the other hand, shortening began at a maximum rate of about 0.1 cell lengths s-1 unless a Ca2+ chelator or 3',5'-cyclic AMP was injected about 30 s or less before electrical stimulation. Injection of these agents reduced the speed of shortening by about half. 3. Injection of a liquid per se (e.g. 140 mM-KCl) neither altered action potentials nor duplicated the changes produced by the aforementioned relaxing agents. Large, sustained injections of substances that were not relaxing agents (e.g. dilute KCl) ruptured the membrane without producing any bleb collapse or re-extension of a contracted cell. Blebs not only collapsed rapidly when a relaxing agent was injected but bleb collapse was a much more sensitive indication of relaxation than cell re-extension; small injections of relaxing agents could clearly collapse blebs with no associated measurable change in cell length. This supports the idea previously inferred from fixed or permeabilized cells, that filaments in smooth muscle are organized to produce force over short distances at points along the cell membrane, in addition to shortening along the long axis. 4. Physiological relaxation of smooth muscle can evidently be mimicked by 3',5'-cyclic AMP elevation. Restoring forces may develop during shortening of isolated smooth muscle cells in elements of their cytoskeleton, surface membrane, or contractile filaments. However, these putative forces may not be able to produce physiological re-extension in the absence of a rise in cyclic AMP and/or a fall in [Ca2+].

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Year:  1991        PMID: 1665860      PMCID: PMC1179891          DOI: 10.1113/jphysiol.1991.sp018795

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  16 in total

1.  Aequorin luminescence during activation of single isolated smooth muscle cells.

Authors:  F S Fay; H H Shlevin; W C Granger; S R Taylor
Journal:  Nature       Date:  1979-08-09       Impact factor: 49.962

2.  Cyclic AMP-dependent inhibition of smooth muscle actomyosin.

Authors:  U Mrwa; M Troschka; J C Rüegg
Journal:  FEBS Lett       Date:  1979-11-15       Impact factor: 4.124

3.  The multiple membrane spanning topography of the beta 2-adrenergic receptor. Localization of the sites of binding, glycosylation, and regulatory phosphorylation by limited proteolysis.

Authors:  H G Dohlman; M Bouvier; J L Benovic; M G Caron; R J Lefkowitz
Journal:  J Biol Chem       Date:  1987-10-15       Impact factor: 5.157

4.  Mechanism of beta-adrenergic relaxation of smooth muscle.

Authors:  C R Scheid; T W Honeyman; F S Fay
Journal:  Nature       Date:  1979-01-04       Impact factor: 49.962

5.  Regulation of calcium concentration in voltage-clamped smooth muscle cells.

Authors:  P L Becker; J J Singer; J V Walsh; F S Fay
Journal:  Science       Date:  1989-04-14       Impact factor: 47.728

6.  Graded contractions in muscle strips and single cells from Bufo marinus stomach.

Authors:  R M Bagby; B A Fisher
Journal:  Am J Physiol       Date:  1973-07

7.  Contraction of isolated smooth-muscle cells--structural changes.

Authors:  F S Fay; C M Delise
Journal:  Proc Natl Acad Sci U S A       Date:  1973-03       Impact factor: 11.205

8.  Calcium in excitation--contraction coupling of skeletal muscle.

Authors:  S R Taylor; H H Shlevin; J R López
Journal:  Biochem Soc Trans       Date:  1979-08       Impact factor: 5.407

9.  Adenosine 3',5'-monophosphate: electrophysiological evidence for a role in synaptic transmission.

Authors:  D A McAfee; P Greengard
Journal:  Science       Date:  1972-10       Impact factor: 47.728

10.  Effects of modulators of myosin light-chain kinase activity in single smooth muscle cells.

Authors:  T Itoh; M Ikebe; G J Kargacin; D J Hartshorne; B E Kemp; F S Fay
Journal:  Nature       Date:  1989-03-09       Impact factor: 49.962

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