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豹蛙颌部肌肉中的神经肌肉重塑与肌纤维更新

Neuromuscular remodeling and myofiber turnover in Rana pipiens' jaw muscles.

作者信息

Alley K E, Omerza F F

机构信息

Departments of Oral Biology, Cell Biology, Neurobiology and Anatomy, Ohio State University, Columbus 43210, USA.

出版信息

Cells Tissues Organs. 1999;164(1):46-58. doi: 10.1159/000016642.

Abstract

Larval jaw myofibers in Rana pipiens degenerate during metamorphosis and are replaced by a second wave of myogenesis that provides for adult jaw function. Trigeminal motoneurons that innervate larval myofibers transfer their preterminal axons to these adult successors where they establish new motor endplates. Silver/acetyl-cholinesterase histochemistry was used to compare innervation patterns in the larval and adult jaw adductor muscles and to plot the time course over which these changes occur. Innervation patterns differ substantially on the pre- and postmetamorphic myofiber populations. Jaw myofibers in the tadpole were unique by virtue of their exceedingly high level of distributed and focal polyinnervation. Each myofiber was innervated by approximately 10 small, junctional zones, most containing multiple axons, diffusely distributed over the length excepting small junctional free zones at either end of the muscle. In juvenile frogs, immediately following redeployment, the replacement myofibers had a polyinnervation pattern that mirrors that observed in the larvae. However, by 12 weeks after metamorphosis there was a clear condensation of the end plates into multiple zones. Moreover, jaw myofibers in adult frogs had a reduced level of distributed and focal polyinnervation, less than 15% show signs of polyinnervation. The pattern of polyinnervation, axonal redeployment and myofiber degeneration is consistent with the hypothesis that the larval jaw muscles serve as a population of primary myofibers, ensuring survival of the trigeminal motoneurons through the prolonged period of larval development, while also providing a scaffold on which secondary jaw myofibers are constructed.

摘要

牛蛙蝌蚪的幼体颌部肌纤维在变态发育过程中退化,并被第二轮肌生成所取代,后者为成年颌部功能提供支持。支配幼体肌纤维的三叉神经运动神经元将其终末前轴突转移至这些成年后继者,在那里建立新的运动终板。采用银/乙酰胆碱酯酶组织化学方法比较幼体和成体颌部内收肌的神经支配模式,并绘制这些变化发生的时间进程。变态前后的肌纤维群体的神经支配模式存在显著差异。蝌蚪的颌部肌纤维具有独特性,其分布式和局灶性多神经支配水平极高。每条肌纤维由大约10个小的连接区支配,大多数连接区含有多个轴突,除了肌肉两端的小连接游离区外,沿肌纤维长度呈弥散分布。在幼蛙中,重新部署后,替代肌纤维的多神经支配模式与在蝌蚪中观察到的模式相似。然而,变态后12周,终板明显聚集形成多个区域。此外,成年蛙的颌部肌纤维的分布式和局灶性多神经支配水平降低,不到15%表现出多神经支配迹象。多神经支配、轴突重新部署和肌纤维退化的模式与以下假设一致:幼体颌部肌肉作为一群初级肌纤维,确保三叉神经运动神经元在漫长的幼体发育过程中存活,同时也提供一个支架,在其上构建次级颌部肌纤维。

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