scholarly journals Sequential accumulation of mRNAs encoding different myosin heavy chain isoforms during skeletal muscle development in vivo detected with a recombinant plasmid identified as coding for an adult fast myosin heavy chain from mouse skeletal muscle.

1983 ◽  
Vol 258 (22) ◽  
pp. 13867-13874
Author(s):  
A Weydert ◽  
P Daubas ◽  
M Caravatti ◽  
A Minty ◽  
G Bugaisky ◽  
...  
Keyword(s):  
Skeletal Muscle ◽  
Myosin Heavy Chain ◽  
Heavy Chain ◽  
Recombinant Plasmid ◽  
Muscle Development ◽  
Myosin Heavy Chain Isoforms ◽  
Skeletal Muscle Development ◽  
Fast Myosin ◽  
Fast Myosin Heavy Chain

Evidence for three adult fast myosin heavy chain isoforms in type II skeletal muscle fibers in pigs.

1998 ◽  
Vol 76 (6) ◽  
pp. 1584 ◽  
Author(s):  
L Lefaucheur ◽  
R K Hoffman ◽  
D E Gerrard ◽  
C S Okamura ◽  
N Rubinstein ◽  
...  
Keyword(s):  
Skeletal Muscle ◽  
Myosin Heavy Chain ◽  
Heavy Chain ◽  
Muscle Fibers ◽  
Myosin Heavy Chain Isoforms ◽  
Type Ii ◽  
Fast Myosin ◽  
Skeletal Muscle Fibers ◽  
Fast Myosin Heavy Chain

scholarly journals Slow and fast myosin heavy chain content defines three types of myotubes in early muscle cell cultures.

1985 ◽  
Vol 101 (5) ◽  
pp. 1643-1650 ◽  
Author(s):  
J B Miller ◽  
M T Crow ◽  
F E Stockdale
Keyword(s):  
Myosin Heavy Chain ◽  
Heavy Chain ◽  
Pectoral Muscle ◽  
Myosin Heavy Chain Isoforms ◽  
Fiber Formation ◽  
Single Type ◽  
Fast Myosin ◽  
Slow Myosin Heavy Chain ◽  
Fast Myosin Heavy Chain ◽  
Different Populations

We prepared monoclonal antibodies specific for fast or slow classes of myosin heavy chain isoforms in the chicken and used them to probe myosin expression in cultures of myotubes derived from embryonic chicken myoblasts. Myosin heavy chain expression was assayed by gel electrophoresis and immunoblotting of extracted myosin and by immunostaining of cultures of myotubes. Myotubes that formed from embryonic day 5-6 pectoral myoblasts synthesized both a fast and a slow class of myosin heavy chain, which were electrophoretically and immunologically distinct, but only the fast class of myosin heavy chain was synthesized by myotubes that formed in cultures of embryonic day 8 or older myoblasts. Furthermore, three types of myotubes formed in cultures of embryonic day 5-6 myoblasts: one that contained only a fast myosin heavy chain, a second that contained only a slow myosin heavy chain, and a third that contained both a fast and a slow heavy chain. Myotubes that formed in cultures of embryonic day 8 or older myoblasts, however, were of a single type that synthesized only a fast class of myosin heavy chain. Regardless of whether myoblasts from embryonic day 6 pectoral muscle were cultured alone or mixed with an equal number of myoblasts from embryonic day 12 muscle, the number of myotubes that formed and contained a slow class of myosin was the same. These results demonstrate that the slow class of myosin heavy chain can be synthesized by myotubes formed in cell culture, and that three types of myotubes form in culture from pectoral muscle myoblasts that are isolated early in development, but only one type of myotube forms from older myoblasts; and they suggest that muscle fiber formation probably depends upon different populations of myoblasts that co-exist and remain distinct during myogenesis.

scholarly journals De-phosphorylation of MyoD is linking nerve-evoked activity to fast myosin heavy chain expression in rodent adult skeletal muscle

2007 ◽  
Vol 584 (2) ◽  
pp. 637-650 ◽  
Author(s):  
Merete Ekmark ◽  
Zaheer Ahmad Rana ◽  
Greg Stewart ◽  
D. Grahame Hardie ◽  
Kristian Gundersen
Keyword(s):  
Skeletal Muscle ◽  
Myosin Heavy Chain ◽  
Heavy Chain ◽  
Adult Skeletal Muscle ◽  
Fast Myosin ◽  
Fast Myosin Heavy Chain ◽  
Evoked Activity

Enhancement of hybrid-fiber types in rat soleus muscle after clenbuterol administration during hindlimb unloading

2004 ◽  
Vol 82 (5) ◽  
pp. 311-318 ◽  
Author(s):  
F Picquet ◽  
L De-Doncker ◽  
M Falempin
Keyword(s):  
Myosin Heavy Chain ◽  
Heavy Chain ◽  
Fiber Type ◽  
Myosin Heavy Chain Isoforms ◽  
Hindlimb Unloading ◽  
Fiber Types ◽  
Myosin Isoforms ◽  
Fast Myosin ◽  
Contractile Parameters ◽  
Fast Myosin Heavy Chain

Our objective was to determine the effects of a clenbuterol (CB) treatment orally administered (2 mg per kg) to rats submitted to 14 days of hindlimb unloading (HU). The morphological and the contractile properties as well as the myosin heavy chain isoforms contained in each fiber type were determined in whole soleus muscles. As classically described after HU, a decrease in muscle wet weight and in body mass associated with a loss of muscular force, an evolution of the contractile parameters towards those of a fast muscle type, and the emergence of fast myosin heavy chain isoforms were observed. The CB treatment in the HU rats helped reduce the decrease in 1) muscle and body weights, 2) force and 3) the proportion of slow fibers, without preventing the emergence of fast myosin isoforms. Clenbuterol induced a complex remodelling of the muscle typing promoting the combination of both slow and fast myosin isoforms within one fiber. To conclude, our data demonstrate that CB administration partially counteracts the effects produced by HU, and they allow us to anticipate advances in the treatment of muscular atrophy.Key words: β2 agonist, clenbuterol, soleus, contractile parameters, myosin, immunohistochemistry, simulated microgravity, countermeasure.

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