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1 Departments of Molecular Physiology and Biophysics and of Medicine, University of Vermont, Burlington, Vermont 05405; and 2 Department of Anatomy and Developmental Biology, Thomas Jefferson University, Philadelphia, Pennsylvania 19107
In this study, the expression of smooth muscle
actin and myosin was examined in cultures of rat tracheal smooth muscle
cells. Protein and mRNA analyses demonstrated that these cells express
- and
-smooth muscle actin and smooth muscle myosin and nonmuscle myosin-B heavy chains. The expression of the smooth muscle specific actin and myosin isoforms was regulated in the same direction when
growth conditions were changed. Thus, at confluency in 1 or 10%
serum-containing medium as well as for low-density cells (50-60%
confluent) deprived of serum, the expression of the smooth muscle forms
of actin and myosin was relatively high. Conversely, in rapidly
proliferating cultures at low density in 10% serum, smooth muscle
contractile protein expression was low. The expression of nonmuscle
myosin-B mRNA and protein was more stable and was upregulated only to a
small degree in growing cells. Our results provide new insight into the
molecular basis of differentiation and contractile function in airway
smooth muscle cells.
growth state
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