Key result
Lower force per cross bridge in rat diaphragm fibers expressing slow and neonatal myosin heavy chain isoforms contributes to the lower maximum specific force seen in early postnatal development.
The study demonstrates that lower force per cross bridge in fibers expressing slow and neonatal MHC isoforms contributes to lower maximum specific force in early postnatal development of rat diaphragm muscle.
Informs mechanisms of postnatal rat diaphragm weakness; hypothesis-generating for human neonatal respiratory muscle development.
It has been found that maximum specific force (F(max); force per cross-sectional area) of rat diaphragm muscle doubles from birth to 84 days (adult). We hypothesize that this developmental change in F(max) reflects an increase in myosin heavy chain (MHC) content per half-sarcomere (an estimate of the number of cross bridges in parallel) and/or a greater force per cross bridge in fibers expressing fast MHC isoforms compared with slow and neonatal MHC isoforms (MHC(slow) and MHC(neo), respectively). Single Triton 100-X-permeabilized fibers were activated at a pCa of 4.0. MHC isoform expression was determined by SDS-PAGE. MHC content per half-sarcomere was determined by densitometric analysis and comparison to a standard curve of known MHC concentrations. MHC content per half-sarcomere progressively increased during early postnatal development. When normalized for MHC content per half-sarcomere, fibers expressing MHC(slow) and coexpressing MHC(neo) produced less force than fibers expressing fast MHC isoforms. We conclude that lower force per cross bridge in fibers expressing MHC(slow) and MHC(neo) contributes to the lower F(max) seen in early postnatal development.
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Geiger et al. (2001) studied Rat diaphragm muscle development. Myosin heavy chain (MHC) isoform expression vs. Fast MHC isoforms was evaluated on Maximum specific force (F(max)) and MHC content per half-sarcomere. Lower force per cross bridge in rat diaphragm fibers expressing slow and neonatal myosin heavy chain isoforms contributes to the lower maximum specific force seen in early postnatal development.
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