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</script>doi: 10.1038/35014065
pmid: 10854329
Here we have used gene-targeting to eliminate expression of smooth-muscle myosin heavy chain. Elimination of this gene does not affect expression of non-muscle myosin heavy chain, and knockout individuals typically survive for three days. Prolonged activation, by KCl depolarisation, of intact bladder preparations from wild-type neonatal mice produces an initial transient state (phase 1) of high force generation and maximal shortening velocity, which is followed by a sustained state (phase 2) characterized by low force generation and maximal shortening velocity. Similar preparations from knockout neonatal mice do not undergo phase 1, but exhibit a normal phase 2. We propose that, in neonatal smooth muscle phase 1 is generated by recruitment of smooth-muscle myosin heavy chain, whereas phase 2 can be generated by activation of non-muscle myosin heavy chain. We conclude that phase 1 becomes indispensable for survival and normal growth soon after birth, particularly for functions such as homeostasis and circulation.
Male, Mice, Knockout, Myosin Heavy Chains, Body Weight, Fluorescent Antibody Technique, Blood Pressure, Muscle, Smooth, In Vitro Techniques, Potassium Chloride, Intestines, Isoenzymes, Mice, Animals, Newborn, Mutation, Animals, Protein Isoforms, Female, Ductus Arteriosus, Patent, Cells, Cultured, Muscle Contraction
Male, Mice, Knockout, Myosin Heavy Chains, Body Weight, Fluorescent Antibody Technique, Blood Pressure, Muscle, Smooth, In Vitro Techniques, Potassium Chloride, Intestines, Isoenzymes, Mice, Animals, Newborn, Mutation, Animals, Protein Isoforms, Female, Ductus Arteriosus, Patent, Cells, Cultured, Muscle Contraction
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