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肌联蛋白依赖性生物力学反馈使肌节适应昆虫的特殊肌肉功能。

Titin-dependent biomechanical feedback tailors sarcomeres to specialized muscle functions in insects.

作者信息

Loreau Vincent, Koolhaas Wouter H, Chan Eunice HoYee, De Boissier Paul, Brouilly Nicolas, Avosani Sabina, Sane Aditya, Pitaval Christophe, Reiter Stefanie, Luis Nuno Miguel, Mangeol Pierre, von Philipsborn Anne C, Rupprecht Jean-François, Görlich Dirk, Habermann Bianca H, Schnorrer Frank

机构信息

Aix Marseille University, CNRS, IBDM, Turing Centre for Living Systems, Marseille, France.

Max Planck Institute of Biochemistry, Martinsried, Germany.

出版信息

Sci Adv. 2025 May 9;11(19):eads8716. doi: 10.1126/sciadv.ads8716.

Abstract

Sarcomeres are the universal contractile units of muscles that enable animals to move. Insect muscles display a remarkable functional diversity: they operate at extremely different contraction frequencies (ranging from ~1 to 1000 hertz) and amplitudes during flying, walking, and crawling. This is puzzling because sarcomeres are built from essentially the same actin-myosin components. Here, we address how functionally different sarcomeres are made. We show that the giant protein titin and the regulation of developmental contractility are key for the sarcomere specializations. I-band titin spans and determines the length of the sarcomeric I-band in a muscle type-specific manner. Unexpectedly, I-band titin also rules the length of the force-generating myosin filament using a feedback mechanism that is modulated by myosin contractility. We propose a model of how sarcomere specializations in insects are tuned, provide evidence for this model, and discuss its validity beyond insects.

摘要

肌节是肌肉的通用收缩单位,使动物能够运动。昆虫肌肉表现出显著的功能多样性:在飞行、行走和爬行过程中,它们以极其不同的收缩频率(范围从约1赫兹到1000赫兹)和幅度进行运作。这令人困惑,因为肌节基本上是由相同的肌动蛋白 - 肌球蛋白成分构成。在这里,我们探讨功能不同的肌节是如何形成的。我们表明,巨大的肌联蛋白和发育收缩性的调节是肌节特化的关键。I带肌联蛋白以肌肉类型特异性的方式跨越并决定肌节I带的长度。出乎意料的是,I带肌联蛋白还通过一种由肌球蛋白收缩性调节的反馈机制来控制产生力量的肌球蛋白丝的长度。我们提出了一个关于昆虫肌节特化如何调节的模型,为该模型提供了证据,并讨论了其在昆虫之外的有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db9e/12063666/fa3bea077cda/sciadv.ads8716-f1.jpg

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