Stretching arterial smooth muscle induces myosin light chain phosphorylation via intracellular calcium release, independent of active contraction.
Challenges view that contraction is prerequisite for myosin phosphorylation; leaves open translation to human vascular mechanobiology.
Stretching to 1.7 times the resting length of porcine carotid arteries reversibly prevents active tension development by K+ or norepinephrine stimulation. The 20,000-dalton light chain of myosin was maximally phosphorylated in the stretched noncontracting muscles, equal to that in the nonstretched contracting muscles challenged with K+ or norepinephrine. These results show that the contractile event is not a prerequisite for phosphorylation. Furthermore, stretching alone also induced maximal light chain phosphorylation even in the absence of K+ or norepinephrine. The stretch-induced light chain phosphorylation was not affected by exhaustive washing of the muscle with Ca2+-free physiological salt solution, treatment of the muscle with verapamil, or by a short exposure to ethylene glycol bis(beta-aminoethyl ether)-N,N,N',N'-tetraacetic acid (EGTA). Prolonged EGTA treatment abolished the stretch-induced light chain phosphorylation. All evidence suggests that upon stretch, Ca2+ is released from intracellular sources and this Ca2+ activates the myosin light chain kinase producing phosphorylation of the light chain.
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Ledvora et al. (1983) studied this question.
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