Literature DB >> 1551477

Mechanisms of nascent fiber formation during avian skeletal muscle hypertrophy.

K M McCormick1, E Schultz.   

Abstract

This study examined two putative mechanisms of new fiber formation in postnatal skeletal muscle, namely longitudinal fragmentation of existing fibers and de novo formation. The relative contributions of these two mechanisms to fiber formation in hypertrophying anterior latissimus dorsi (ALD) muscle were assessed by quantitative analysis of their nuclear populations. Muscle hypertrophy was induced by wing-weighting for 1 week. All nuclei formed during the weighting period were labeled by continuous infusion of 5-bromo-2'-deoxyuridine (BrdU), a thymidine analog, and embryonic-like fibers were identified using an antibody to ventricular-like embryonic (V-EMB) myosin. The number of BrdU-labeled and unlabeled nuclei in V-EMB-positive fibers were counted. Wing-weighting resulted in significant muscle enlargement and the appearance of many V-EMB+ fibers. The majority of V-EMB+ fibers were completely independent of mature fibers and had a nuclear density characteristics of developing fibers. Furthermore, nearly 100% of the nuclei in independent V-EMB+ fibers were labeled. These findings strongly suggest that most V-EMB+ fibers were nascent fibers formed de novo during the weighting period by satellite cell activation and fusion. Nascent fibers were found primarily in the space between fascicles where they formed a complex anastomosing network of fibers running at angles to one another. Although wing-weighting induced an increase in the number of branched fibers, there was no evidence that V-EMB+ fibers were formed by longitudinal fragmentation. The location of newly formed fibers in wing-weighted and regenerating ALD muscle was compared to determine whether satellite cells in the ALD muscle were unusual in that, if stimulated to divide, they would form fibers in the inter- and intrafascicular space. In contrast to wing-weighted muscle, nascent fibers were always found closely associated with necrotic fibers. These results suggest that wing-weighting is not simply another model of regeneration, but rather produces a unique environment which induces satellite cell migration and subsequent fiber formation in the interfascicular space. De novo fiber formation is apparently the principal mechanism for the hyperplasia reported to occur in the ALD muscle undergoing hypertrophy induced by wing-weighting.

Entities:  

Keywords:  NASA Discipline Musculoskeletal; Non-NASA Center

Mesh:

Substances:

Year:  1992        PMID: 1551477     DOI: 10.1016/0012-1606(92)90245-c

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  11 in total

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2.  Comparative analysis of satellite cell properties in heavy- and lightweight strains of turkey.

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3.  Effective fiber hypertrophy in satellite cell-depleted skeletal muscle.

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Journal:  Development       Date:  2011-09       Impact factor: 6.868

4.  Skeletal muscle morphology in power-lifters with and without anabolic steroids.

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5.  An electron microscopic investigation into the possible source of new muscle fibres in teleost fish.

Authors:  W Stoiber; A M Sänger
Journal:  Anat Embryol (Berl)       Date:  1996-12

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7.  High concentrations of HGF inhibit skeletal muscle satellite cell proliferation in vitro by inducing expression of myostatin: a possible mechanism for reestablishing satellite cell quiescence in vivo.

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Review 8.  The identification of myogenic cells in skeletal muscle, with emphasis on the use of tritiated thymidine autoradiography and desmin antibodies.

Authors:  M J Lawson-Smith; J K McGeachie
Journal:  J Anat       Date:  1998-02       Impact factor: 2.610

9.  Presence of embryonic myosin in normal postural muscles of the adult rat.

Authors:  L J Wanek; M H Snow
Journal:  Cell Tissue Res       Date:  1995-06       Impact factor: 5.249

10.  Adaptation in myosin expression of avian skeletal muscle after weighting and unweighting.

Authors:  S E Alway; J A Carson; W J Roman
Journal:  J Muscle Res Cell Motil       Date:  1995-04       Impact factor: 2.698

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