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1 Medicine, McGill University, Meakins-Christie Laboratories, Montreal, Canada
2 Sacre-Coeur Hospital, Universite de Montreal, Research Centre, Montreal, Canada
* To whom correspondence should be addressed. E-mail: anne-marie.lauzon{at}mcgill.ca.
Four smooth muscle myosin heavy chain (SMMHC) isoforms are generated by alternative mRNA splicing of a single gene. Two of these isoforms differ by the presence [(+)insert] or absence [(-)insert] of a 7 amino acid insert in the motor domain. The rate of actin filament propulsion of the (+)insert SMMHC isoform, as measured in the in vitro motility assay, is 2-fold greater than that of the (-)insert isoform. We hypothesized that a greater expression of the (+)insert SMMHC isoform and greater regulatory light chain (LC20) phosphorylation contribute to airway hyperresponsiveness. We measured airway responsiveness to methacholine in the Fisher hyperresponsive and Lewis normoresponsive rats and determined SMMHC isoform mRNA and protein expression, as well as essential light chain (LC17) isoforms, h-caldesmon and 
-actin protein expression in their tracheae. We also measured tracheal muscle strip contractility in response to methacholine and corresponding LC20 phosphorylation. We found that Fisher rats have more (+)insert mRNA (69.4±2.0%) (mean±SE) than Lewis rats (53.0±2.4%; p<0.05) and a 44% greater content of (+)insert isoform relative to total myosin protein. No difference was found for LC17 isoform, h-caldesmon, and -actin expression. The contractility experiments revealed a greater isometric force for Fisher trachealis segments (4.2±0.8mN) than Lewis (1.9±0.4mN; p<0.05) and greater LC20 phosphorylation level in Fisher (55.1±6.4) than in Lewis (41.4±6.1; p<0.05) rats. These results further support the contention that innate airway hyperresponsiveness is a multifactorial disorder in which increased expression of the fast (+)insert SMMHC isoform and greater activation of LC20 lead to smooth muscle hypercontractility.
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