Literature DB >> 402082

Reorientation of myofilaments during contraction of a vertebrate smooth muscle.

B A Fisher, R M Bagby.   

Abstract

The purpose of the investigation was to determine whether filaments within smooth muscle cells changed their orientation (with respect to the main axis of the cell) during contraction. The stomach muscle of Bufo marinus was used, since its cells may be easily isolated, enabling direct observation in living cells. In addition to still micrography, cinemicrography was used to record continuously during contraction. Polarization microscopy revealed a change in birefringence after contraction, with relaxed cells exhibiting uniform birefringence while contracted cells displayed a discontinuous pattern. Movies revealed a progressive change in orientation of birefringent elements from nearly parallel to the cell's main axis in relaxed cells to increasingly larger angles to the cell's axis as contraction progressed. Phase-contrast microscopy revealed a change in filamentous components, from being parallel to the cell's axis in relaxed cells to being in an undulating or helical pattern during concentration. Cell shape tended to follow the configuration of the filamentous component. Electron microscopy of muscle strips corroborated the observations of living cells and substantiated the conclusion that filaments change their orientation from parallel to oblique (with respect to the cell's axis) during shortening with an undulating or helical pattern of filaments in shortened muscles.

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Year:  1977        PMID: 402082     DOI: 10.1152/ajpcell.1977.232.1.C5

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  12 in total

1.  Identification and characterization of major ionic currents in isolated smooth muscle cells using the voltage-clamp technique.

Authors:  J V Walsh; J J Singer
Journal:  Pflugers Arch       Date:  1987-02       Impact factor: 3.657

2.  Structural limits on force production and shortening of smooth muscle.

Authors:  Marion J Siegman; Sandra Davidheiser; Susan U Mooers; Thomas M Butler
Journal:  J Muscle Res Cell Motil       Date:  2012-12-12       Impact factor: 2.698

3.  Analysis of the birefringence of the smooth muscle anococcygeus of the rat, at rest and in contraction. I.

Authors:  A Godfraind-De Becker; J M Gillis
Journal:  J Muscle Res Cell Motil       Date:  1988-02       Impact factor: 2.698

4.  High shortening velocity of isolated single arterial muscle cells.

Authors:  K Hermsmeyer
Journal:  Experientia       Date:  1979-12-15

5.  A method for isolating smooth muscle cells from pig urinary bladder with low concentrations of collagenase and papain: the relation between calcium concentration and isolated cell length.

Authors:  R Schot; E van Asselt; R van Mastrigt
Journal:  Urol Res       Date:  1993-01

6.  Mechanical properties of smooth muscle cells in the walls of arterial resistance vessels.

Authors:  W Halpern; M J Mulvany; D M Warshaw
Journal:  J Physiol       Date:  1978-02       Impact factor: 5.182

7.  Double-immunofluorescent staining of isolated smooth muscle cells. I. preparation of anti-chicken gizzard alpha-actinin and its use with anti-chicken gizzard myosin for co-localization of alpha-actinin and myosin in chicken gizzard cells.

Authors:  R M Bagby
Journal:  Histochemistry       Date:  1980

8.  Action potentials and net membrane currents of isolated smooth muscle cells (urinary bladder of the guinea-pig).

Authors:  U Klöckner; G Isenberg
Journal:  Pflugers Arch       Date:  1985-12       Impact factor: 3.657

9.  Supercontracted state of vertebrate smooth muscle cell fragments reveals myofilament lengths.

Authors:  J V Small; M Herzog; M Barth; A Draeger
Journal:  J Cell Biol       Date:  1990-12       Impact factor: 10.539

10.  Geometry of actin-membrane attachments in the smooth muscle cell: the localisations of vinculin and alpha-actinin.

Authors:  J V Small
Journal:  EMBO J       Date:  1985-01       Impact factor: 11.598

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