Abstract
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.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Animals, Newborn
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Blood Pressure / physiology
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Body Weight
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Cells, Cultured
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Ductus Arteriosus, Patent / physiopathology
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Female
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Fluorescent Antibody Technique
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In Vitro Techniques
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Intestines / abnormalities
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Intestines / physiology
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Isoenzymes / deficiency
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Isoenzymes / genetics
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Isoenzymes / metabolism
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Male
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Mice
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Mice, Knockout
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Muscle Contraction / drug effects
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Muscle Contraction / physiology*
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Muscle, Smooth / abnormalities
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Muscle, Smooth / cytology
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Muscle, Smooth / drug effects
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Muscle, Smooth / physiology*
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Mutation / genetics
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Myosin Heavy Chains / analysis
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Myosin Heavy Chains / deficiency
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Myosin Heavy Chains / genetics
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Myosin Heavy Chains / physiology*
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Potassium Chloride / pharmacology
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Protein Isoforms / analysis
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Protein Isoforms / deficiency
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Protein Isoforms / genetics
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Protein Isoforms / physiology
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RNA, Messenger / analysis
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RNA, Messenger / genetics
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Renin / blood
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Urinary Bladder / abnormalities
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Urinary Bladder / cytology
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Urinary Bladder / drug effects
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Urinary Bladder / physiology
Substances
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Isoenzymes
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Protein Isoforms
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RNA, Messenger
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Potassium Chloride
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Renin
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Myosin Heavy Chains