Literature DB >> 2523410

Fibre types in Limulus telson muscles: morphology and histochemistry.

R J Levine1, S Davidheiser, A M Kelly, R W Kensler, J Leferovich, R E Davies.   

Abstract

Using a variety of techniques, we have demonstrated the presence of at least two fibre types in Limulus median telson levator muscle. By light and electron microscopy, large (2,156 microns 2 mean cross-sectional area) fibres have A-bands of 4.1 microns, one-half I bands of 2.15 microns and Z lines less than or equal to 0.5 microns in width. Few mitochondria are found in these fibres, which comprise 54% of those present in a given microscope field and which occupy 82% of the total cross-sectional area. Small fibres (484 microns 2 mean cross-sectional area) have A bands of 6.3 microns, one-half I bands of 3.1 microns and Z lines between 0.5 and 1.0 microns in width and are rich in mitochondria. Although small fibres comprise nearly one-half (46%) of the fibres in a field, they occupy only 18% of the total cross-sectional area. Histochemical staining for alkaline-stable myofibrillar ATPase activity and mitochondrial reduced beta-nicotinamide adenine nucleotide (beta-NADH) tetrazolium reductase activity confirms the presence of two fibre types. The large fibres react positively for the myofibrillar ATPase activity and negatively for the mitochondrial enzyme activity. The reverse is seen with the small fibres. Some fibres of intermediate size, having intermediate staining characteristics, were also observed. Native gel electrophoresis of both myofibrillar and purified myosin preparations supports the observed differences in myofibrillar ATPase activity in that two myosin isozymes are resolved on pyrophosphate gels. Although the thick filaments isolated from unstimulated small fibres are longer (greater than 6.0 microns) than those isolated from unstimulated large fibres (4.26 microns), all have a similar appearance with respect to the arrangement of myosin heads on their surfaces, and similar diameters. The implications of the observed heterogeneity of fibre types is discussed with reference to previously reported phenomena in Limulus telson muscle, including changes in length of thick filaments on fibre stimulation and the shape of the length-tension curve obtained from fibre bundles.

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Year:  1989        PMID: 2523410     DOI: 10.1007/bf01739856

Source DB:  PubMed          Journal:  J Muscle Res Cell Motil        ISSN: 0142-4319            Impact factor:   2.698


  25 in total

1.  The specificity of the histochemical method for adenosine triphosphatase.

Authors:  H A PADYKULA; E HERMAN
Journal:  J Histochem Cytochem       Date:  1955-05       Impact factor: 2.479

2.  The A and IB and lengths in stretched or contracted horseshoe crab skeletal muscle.

Authors:  G W DE VILLAFRANCA
Journal:  J Ultrastruct Res       Date:  1961-04

3.  Some comments on the histochemical characterization of muscle adenosine triphosphatase.

Authors:  M H Brooke; K K Kaiser
Journal:  J Histochem Cytochem       Date:  1969-06       Impact factor: 2.479

4.  Arrangement of the heads of myosin in relaxed thick filaments from tarantula muscle.

Authors:  R A Crowther; R Padrón; R Craig
Journal:  J Mol Biol       Date:  1985-08-05       Impact factor: 5.469

5.  Structure of Limulus telson muscle thick filaments.

Authors:  M Stewart; R W Kensler; R J Levine
Journal:  J Mol Biol       Date:  1981-12-15       Impact factor: 5.469

6.  Phosphorylation-dependent regulation of Limulus myosin.

Authors:  J R Sellers
Journal:  J Biol Chem       Date:  1981-09-10       Impact factor: 5.157

7.  Changes in thick filament length in Limulus striated muscle.

Authors:  M M Dewey; B Walcott; D E Colflesh; H Terry; R J Levine
Journal:  J Cell Biol       Date:  1977-11       Impact factor: 10.539

8.  Electron microscopic and optical diffraction analysis of the structure of scorpion muscle thick filaments.

Authors:  R W Kensler; R J Levine; M Stewart
Journal:  J Cell Biol       Date:  1985-08       Impact factor: 10.539

9.  Three-dimensional reconstruction of thick filaments from Limulus and scorpion muscle.

Authors:  M Stewart; R W Kensler; R J Levine
Journal:  J Cell Biol       Date:  1985-08       Impact factor: 10.539

10.  Connectin filaments in stretched skinned fibers of frog skeletal muscle.

Authors:  K Maruyama; H Sawada; S Kimura; K Ohashi; H Higuchi; Y Umazume
Journal:  J Cell Biol       Date:  1984-10       Impact factor: 10.539

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  4 in total

1.  Mechanism of phosphorylation of the regulatory light chain of myosin from tarantula striated muscle.

Authors:  C Hidalgo; R Craig; M Ikebe; R Padrón
Journal:  J Muscle Res Cell Motil       Date:  2001       Impact factor: 2.698

2.  Analysis of tarantula skeletal muscle protein sequences and identification of transcriptional isoforms.

Authors:  Jingui Zhu; Yongqiao Sun; Fa-Qing Zhao; Jun Yu; Roger Craig; Songnian Hu
Journal:  BMC Genomics       Date:  2009-03-19       Impact factor: 3.969

3.  The effect of calcium activation of skinned fiber bundles on the structure of Limulus thick filaments.

Authors:  R J Levine; J L Woodhead; H A King
Journal:  J Cell Biol       Date:  1991-05       Impact factor: 10.539

4.  Effects of phosphorylation by myosin light chain kinase on the structure of Limulus thick filaments.

Authors:  R J Levine; P D Chantler; R W Kensler; J L Woodhead
Journal:  J Cell Biol       Date:  1991-05       Impact factor: 10.539

  4 in total

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