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Regulation of the smooth muscle contractile phenotype by nonmuscle myosin

机译:非肌肉肌球蛋白对平滑肌收缩表型的调节

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摘要

The contractile phenotype of a smooth muscle can broadly be classified as phasic or tonic. Following activation, phasic smooth muscle exhibits an initial period of rapid force activation, following which force falls to a lower steady state level. In contrast, force generated by tonic smooth muscle rises slowly to a sustained steady state. The differences in contractile patterns cannot be explained by the time course of either the Ca2+ transient or phosphorylation of the 20-kDa regulatory myosin light chain (MLC20). Therefore, a molecular marker that defines tonic and phasic smooth muscle contractile properties remains elusive. Further, smooth muscle can maintain force at low levels of MLC20 phosphorylation; often referred to as the latch state. The mechanism for the latch state is unknown and has been hypothesized to be due to a number of mechanisms including the formation of slowly cycling dephosphorylated or latch cross-bridges (Hai and Murphy, Am J Physiol 253:H1365–H1371, 1988). This review will focus evidence suggesting that nonmuscle myosin IIB (NMIIB) are the latch cross-bridges in smooth muscle and NMIIB content could define the tonic contractile phenotype.
机译:平滑肌的收缩表型可大致分为阶段性或强直性。激活后,阶段性平滑肌表现出快速的力量激活的初始阶段,此后力量下降到较低的稳态水平。相反,由滋补平滑肌产生的力缓慢上升至持续的稳定状态。收缩模式的差异无法通过20kDa调节性肌球蛋白轻链(MLC20 )的Ca2 +瞬变或磷酸化的时间过程来解释。因此,定义强直和阶段性平滑肌收缩特性的分子标记仍然难以捉摸。此外,平滑肌可以在低水平的MLC20 磷酸化作用下维持力量。通常称为闩锁状态。闩锁状态的机制尚不清楚,据推测是由于许多机制引起的,包括形成缓慢循环的去磷酸化或闩锁横桥(Hai和Murphy,Am J Physiol 253:H1365–H1371,1988)。这篇综述将集中证据表明非肌肉肌球蛋白IIB(NMIIB)是平滑肌的闩锁交叉桥,而NMIIB的含量可以定义强直收缩表型。

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