Literature DB >> 2671041

Immunocytochemical analysis of the perinatal development of cat masseter muscle using anti-myosin antibodies.

J F Hoh1, S Hughes.   

Abstract

The developmental changes in myosin gene expression in the masseter muscle of embryonic and juvenile kittens were examined immunocytochemically using anti-myosin heavy chain antibodies of various specificities. In the mature cat, this muscle contains only two phenotypes, the majority of fibres are superfast, the rest being slow fibres. In foetal tissues, the histological appearance of bundles of myotubes, comprising a large central myotube surrounded by a rosette of smaller myotubes, strongly suggest the existence in the jaw muscle of primary and secondary fibres during development. Immunocytochemical data are consistent with the hypothesis that there are four types of fibre; two types of primary fibre as well as two types of secondary fibre. (1) Slow primaries stain strongly with an anti-slow myosin antibody throughout the period under study. These fibres transiently express embryonic but not foetal myosin. (2) Superfast primaries stain for embryonic/foetal and slow myosins in the perinatal period but progressively replace these myosins with superfast myosin during postnatal development. (3) Superfast secondaries initially express embryonic/foetal myosins, but later, beginning around the time of birth progressively replace these myosins with superfast myosin. These fibres do not express slow myosin. (4) Slow secondaries, which initially also express embryonic/foetal myosins, but which postnatally express slow or slow and superfast myosins and express only slow myosin in the adult. These four types of fibres are homologous to the four isotypes of limb muscle fibres and may be derived from distinct lineages of myoblasts.

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Year:  1989        PMID: 2671041     DOI: 10.1007/bf01758427

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


  17 in total

1.  Immunocytochemical and electrophoretic analyses of changes in myosin gene expression in cat posterior temporalis muscle during postnatal development.

Authors:  J F Hoh; S Hughes; C Chow; P T Hale; R B Fitzsimons
Journal:  J Muscle Res Cell Motil       Date:  1988-02       Impact factor: 2.698

2.  Rabbit skeletal myosin isoenzymes from fetal, fast-twitch and slow-twitch muscles.

Authors:  J F Hoh; G P Yeoh
Journal:  Nature       Date:  1979-07-26       Impact factor: 49.962

3.  Selective synthesis and degradation of slow skeletal myosin heavy chains in developing muscle fibers.

Authors:  G K Dhoot
Journal:  Muscle Nerve       Date:  1986-02       Impact factor: 3.217

4.  Developmental origins of skeletal muscle fibers: clonal analysis of myogenic cell lineages based on expression of fast and slow myosin heavy chains.

Authors:  J B Miller; F E Stockdale
Journal:  Proc Natl Acad Sci U S A       Date:  1986-06       Impact factor: 11.205

5.  Embryonic growth and innervation of rat skeletal muscles. I. Neural regulation of muscle fibre numbers.

Authors:  A J Harris
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1981-07-16       Impact factor: 6.237

6.  The sequential replacement of myosin subunit isoforms during muscle type transformation induced by long term electrical stimulation.

Authors:  W E Brown; S Salmons; R G Whalen
Journal:  J Biol Chem       Date:  1983-12-10       Impact factor: 5.157

7.  The fibre-type composition of the first branchial arch muscles in Carnivora and Primates.

Authors:  A Rowlerson; F Mascarello; A Veggetti; E Carpene
Journal:  J Muscle Res Cell Motil       Date:  1983-08       Impact factor: 2.698

8.  Temporal separation of the migration of distinct myogenic precursor populations into the developing chick wing bud.

Authors:  J Seed; S D Hauschka
Journal:  Dev Biol       Date:  1984-12       Impact factor: 3.582

9.  The organogenesis of murine striated muscle: a cytoarchitectural study.

Authors:  M Ontell; K Kozeka
Journal:  Am J Anat       Date:  1984-10

10.  The histogenesis of rat intercostal muscle.

Authors:  A M Kelly; S I Zacks
Journal:  J Cell Biol       Date:  1969-07       Impact factor: 10.539

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  9 in total

1.  Expression of masticatory-specific isoforms of myosin heavy-chain, myosin-binding protein-C and tropomyosin in muscle fibers and satellite cell cultures of cat masticatory muscle.

Authors:  Lucia H D Kang; Agita Rughani; Matthew L Walker; Rosa Bestak; Joseph F Y Hoh
Journal:  J Histochem Cytochem       Date:  2010-03-30       Impact factor: 2.479

2.  Expression of extraocular myosin heavy chain in rabbit laryngeal muscle.

Authors:  C A Lucas; A Rughani; J F Hoh
Journal:  J Muscle Res Cell Motil       Date:  1995-08       Impact factor: 2.698

3.  An immunocytochemical marker for early type I muscle fibers in the developing rat hindlimb.

Authors:  J Kucera; J M Walro
Journal:  Anat Embryol (Berl)       Date:  1995-08

4.  Sequences of intrafusal fiber formation are muscle-dependent in rat hindlimbs.

Authors:  J Kucera; J M Walro
Journal:  Anat Embryol (Berl)       Date:  1994-09

5.  Impact of post-synaptic block of neuromuscular transmission, muscle unloading and mechanical ventilation on skeletal muscle protein and mRNA expression.

Authors:  H Norman; J Nordquist; P Andersson; T Ansved; X Tang; B Dworkin; L Larsson
Journal:  Pflugers Arch       Date:  2006-07-26       Impact factor: 3.657

6.  Comparison of the foetal development of fibre types in four bovine muscles.

Authors:  B Picard; J Robelin; F Pons; Y Geay
Journal:  J Muscle Res Cell Motil       Date:  1994-08       Impact factor: 2.698

7.  Myosin heavy chain expression in rabbit masseter muscle during postnatal development.

Authors:  J J Bredman; W A Weijs; H A Korfage; P Brugman; A F Moorman
Journal:  J Anat       Date:  1992-04       Impact factor: 2.610

8.  Myosin isoform transitions during development of extra-ocular and masticatory muscles in the fetal rat.

Authors:  F Mascarello; A M Rowlerson
Journal:  Anat Embryol (Berl)       Date:  1992

9.  Transient expression of a slow-tonic MHC isoform by extrafusal fibers in the developing rat.

Authors:  J Kucera; J M Walro
Journal:  Anat Embryol (Berl)       Date:  1993-10
  9 in total

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