Injection of duck recombinant follistatin fusion protein into duck muscle tissues stimulates satellite cell proliferation and muscle fiber hypertrophy
Follistatin ( FST ) can inhibit the expression of myostatin , which is a predominant inhibitor of muscle development. The potential application of myostatin -based technology has been prompted in different ways in agriculture. We previously constructed an expression vector of duck FST and isolated t...
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Veröffentlicht in: | Applied microbiology and biotechnology 2012-06, Vol.94 (5), p.1255-1263 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Follistatin
(
FST
) can inhibit the expression of
myostatin
, which is a predominant inhibitor of muscle development. The potential application of
myostatin
-based technology has been prompted in different ways in agriculture. We previously constructed an expression vector of
duck
FST and isolated the FST fusion protein. After the protein was purified and refolded, it was added to the medium of
duck
myoblasts cultured in vitro. The results show that the 3-(4,5-dimethylthiazol-2-
yl
)-2, 5-diphenyltetrazolium bromide value of the myoblasts in the
duck
FST treatment group is higher than that in the control group, which indicates that the
duck
FST fusion protein exhibits the biological activities that can accelerate myoblast proliferation. To further investigate the roles of
duck FST
on muscle development, we injected the protein into the
duck
muscle tissues in vivo. The results show that both the
duck
muscle fiber cross-sectional area and the satellite cell activation frequency are influenced more in the
FST
treatment group than they are in the control group. In addition to these phenomena, expression of
MyoD
and
Myf5
were increased, and the expression of
myostatin
was decreased. Together, these results suggest the potential for using
duck FST
fusion protein to inhibit
myostatin
activity and subsequently to enhance muscle growth in vivo. The mechanism by which
FST
regulates muscle development in the
duck
is similar to that in mammals and fishes. |
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ISSN: | 0175-7598 1432-0614 |
DOI: | 10.1007/s00253-012-3908-4 |