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The Drosophila indirect flight muscle myosin heavy chain isoform is insufficient to transform the jump muscle into a highly stretch-activated muscle type

机译:果蝇间接飞行肌肉肌球蛋白重链同种型不足以将跳跃肌肉转化为高度拉伸激活的肌肉型

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Stretch activation (SA) is a delayed increase in force that enables high power and efficiency from a cyclically contracting muscle. SA exists in various degrees in almost all muscle types. In Drosophila, the indirect flight muscle (IFM) displays exceptionally high SA force production (FSa), whereas the jump muscle produces only minimal Fsa- We previously found that expressing an embryonic (EMB) myosin heavy chain (MHC) isoform in the jump muscle transforms it into a moderately SA muscle type and enables positive cyclical power generation. To investigate whether variation in MHC isoforms is sufficient to produce even higher FSa, we substituted the IFM MHC isoform (IFI) into the jump muscle. Surprisingly, we found that IFI only caused a 1.7-fold increase in Fsa, less than half the increase previously observed with EMB, and only at a high Pi concentration, 16 mM. This IFI-induced Fsa is much less than what occurs in IFM, relative to isometric tension, and did not enable positive cyclical power generation by the jump muscle. Both isometric tension and Fsa of control fibers decreased with increasing Pi concentration. However, for IFI-express-ing fibers, only isometric tension decreased. The rate of FSa generation was ~1.5-fold faster for IFI fibers than control fibers, and both rates were Pi dependent. We conclude that MHC isoforms can alter FSa and hence cyclical power generation but that isoforms can only endow a muscle type with moderate FSa- Highly SA muscle types, such as IFM, likely use a different or additional mechanism.
机译:拉伸激活(SA)是从循环收缩肌肉中实现高功率和效率的延迟增加。 SA几乎存在于各种肌肉类型的程度上。在果蝇中,间接飞行肌肉(IFM)显示出极高的SA力量生产(FSA),而跳跃肌肉仅产生最小的FSA-我们以前发现表达胚胎(EMB)肌蛋白重链(MHC)同种型在跳跃肌肉中表达胚胎将其转化为适度的SA肌肉类型,并实现正循环发电。为了研究MHC同种型的变异是否足以产生更高的FSA,我们将IFM MHC同种型(IFI)取代为跳跃肌肉。令人惊讶的是,我们发现IFI只引起FSA的1.7倍,小于先前观察到的胚胎增加的一半,并且仅以高pi浓度为16毫米。这种IFI诱导的FSA远小于IFM,相对于等距张力发生的东西,并且没有通过跳跃肌肉实现正循环发电。随着PI浓度的增加,对照纤维的等距张力和FSA均降低。然而,对于IFI-Express-ing纤维,只有等距张力降低。对于IFI纤维的FSA生成速率比对照纤维更快,而且两个速率都是PI依赖性的。我们得出结论,MHC同种型可以改变FSA,因此可以改变循环发电,但同种型只能赋予肌肉型以适度的FSA-高度SA肌肉类型,例如IFM,可能使用不同或其他机制。

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