Rembold C M, Murphy R A
Department of Internal Medicine, University of Virginia Health Sciences Center, Charlottesville 22908.
J Muscle Res Cell Motil. 1993 Jun;14(3):325-34. doi: 10.1007/BF00123097.
The mechanism responsible for formation of attached, dephosphorylated crossbridges (latchbridges) in smooth muscle is controversial. Myosin light chain phosphorylation may be obligatory for crossbridge attachment; if this were the case, latchbridges would arise solely by dephosphorylation of attached, phosphorylated crossbridges. Alternatively, the presence of attached crossbridges could induce cooperative activation by allowing dephosphorylated crossbridges to attach to the thin filament. We evaluated whether four-state models based on dephosphorylation and/or cooperativity-regulated attachment could quantitatively predict smooth muscle contractile behaviour. Five quantitative models for transitions between crossbridge states were developed. Mechanisms for latchbridge formation included: (1) dephosphorylation, (2) cooperativity-regulated attachment dependent only on attached, phosphorylated crossbridges, (3) cooperativity-regulated attachment dependent on all attached crossbridges, (4) dephosphorylation and cooperativity-regulated attachment dependent only on attached, phosphorylated crossbridges, and (5) dephosphorylation and cooperativity-regulated attachment dependent on all attached crossbridges. All five models approximated the time course of contraction and the dependence of steady-state stress on myosin phosphorylation in the swine carotid artery. In the two models that had cooperative attachment regulated by all attached crossbridges, small increases in the rate constant for cooperativity-regulated attachment resulted in positive feedback and irreversible contraction. We suggest that a number of four-state crossbridge models can predict contractile behaviour in arterial smooth muscle. Potentially, latchbridges could be formed by both dephosphorylation and cooperativity-regulated attachment. If cooperativity-regulated latchbridge attachment does exist in smooth muscle, we suggest that it should be dependent only on the number of phosphorylated crossbridges rather than all attached crossbridges.
平滑肌中负责形成附着的、去磷酸化的横桥(闭锁桥)的机制存在争议。肌球蛋白轻链磷酸化对于横桥附着可能是必需的;如果是这种情况,闭锁桥将仅通过附着的、磷酸化的横桥去磷酸化而产生。或者,附着横桥的存在可通过允许去磷酸化的横桥附着于细肌丝来诱导协同激活。我们评估了基于去磷酸化和/或协同调节附着的四态模型是否能够定量预测平滑肌的收缩行为。开发了五个横桥状态转变的定量模型。闭锁桥形成的机制包括:(1)去磷酸化,(2)仅依赖附着的、磷酸化的横桥的协同调节附着,(3)依赖所有附着横桥的协同调节附着,(4)仅依赖附着的、磷酸化的横桥的去磷酸化和协同调节附着,以及(5)依赖所有附着横桥的去磷酸化和协同调节附着。所有五个模型都近似于猪颈动脉收缩的时间进程以及稳态应力对肌球蛋白磷酸化的依赖性。在两个由所有附着横桥调节协同附着的模型中,协同调节附着速率常数的小幅增加导致正反馈和不可逆收缩。我们认为许多四态横桥模型可以预测动脉平滑肌的收缩行为。潜在地,闭锁桥可通过去磷酸化和协同调节附着两者形成。如果平滑肌中确实存在协同调节的闭锁桥附着,我们认为它应仅依赖于磷酸化横桥的数量而非所有附着横桥的数量。