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Expression of myosin heavy chain isoforms and myogenesis of intrafusal fibres in rat muscle spindles
Author(s) -
Soukup Tomáš,
PedrosaDomellöf Fatima,
Thornell LarsEric
Publication year - 1995
Publication title -
microscopy research and technique
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.536
H-Index - 118
eISSN - 1097-0029
pISSN - 1059-910X
DOI - 10.1002/jemt.1070300506
Subject(s) - myogenesis , myosin , gene isoform , biology , tonic (physiology) , myocyte , microbiology and biotechnology , immunocytochemistry , hindlimb , neuroscience , anatomy , gene , biochemistry , endocrinology
Abstract This review concerns the pattern of expression and regulation of myosin heavy chain (MHC) isoforms in intrafusal fibres of rat muscle spindles detected by immunocytochemistry. The three types of intrafusal fibres—nuclear bag 1 , nuclear bag 2 , and nuclear chain fibres—are unique in co‐expressing several MHCs including special isoforms such as slow tonic and α cardiac‐like MHC and isoforms typical of muscle development, such as embryonic and neonatal MHC. The distinct intrafusal fibre types appear sequentially during rat hind limb development, the nuclear bag 2 precursors being first identifiable at 17–18 days in utero as the only primary myotubes expressing slow tonic MHC. Sensory innervation is required for the expression of “spindle‐specific” MHC isoforms. Motor innervation contributes to the diversity in distribution of the different MHCs along the length of the nuclear bag fibres. It is suggested that unique populations of myoblasts are destined to become intrafusal fibres during development in the rat hind limb muscles and that the regional heterogeneity in MHC expression is related both to sensory and motor innervation and to the properties of the myoblast lineages. These distinct features make intrafusal fibres an attractive in situ model for investigating myogenesis, myofibrillogenesis, and the mechanisms regulating MHC expression. © 1995 Wiley‐Liss, Inc.