点亮骨骼肌微管细胞骨架动力学。

IntraVital Pub Date : 2014-05-30 eCollection Date: 2014-01-01 DOI:10.4161/intv.29293
Andrius Masedunskas, Mark Appaduray, Peter W Gunning, Edna C Hardeman
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摘要

在过去的几十年里,活细胞显微镜技术与荧光标记相结合,为我们对细胞内部功能的了解提供了一个真正的爆炸。动态现象可以在活细胞内观察到,参与这些事件的单个分子的行为可以被记录下来。然而,我们对简单或容易的模型系统(如细胞培养)的偏好,是以追逐人工产物为代价的,并且错过了对复杂多细胞生物中发生的真实生物学的理解。我们现在正在进入一个新时代,在这个时代中,开发有意义的,而且易于处理的模型系统来动态研究哺乳动物体内的生物现象不仅是可能的;它将成为科学质量和转化潜力的黄金标准。Oddoux等人的一项研究描述了骨骼肌中微管(MT)细胞骨架的动力学,这是一个例子,证明了开发体内/离体模型的力量长期以来,MTs作为癌症治疗的靶点,以及最近作为杜氏肌营养不良的介质,一直备受关注肌纤维MT细胞骨架在肌膜下形成复杂的直线晶格,对肌肉的结构完整性至关重要。培养的细胞不会形成这样一个专门的细胞骨架组织,我们对它的理解来自于肌肉切片的静态快照在此背景下,Oddoux等人报告的方法和发现是向前迈出的重要一步。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Lighting up microtubule cytoskeleton dynamics in skeletal muscle.

In the past few decades, live cell microscopy techniques in combination with fluorescent tagging have provided a true explosion in our knowledge of the inner functioning of the cell. Dynamic phenomena can be observed inside living cells and the behavior of individual molecules participating in those events can be documented. However, our preference for simple or easy model systems such as cell culture, has come at a cost of chasing artifacts and missing out on understanding real biology as it happens in complex multicellular organisms. We are now entering a new era where developing meaningful, but also tractable model systems to study biological phenomenon dynamically in vivo in a mammal is not only possible; it will become the gold standard for scientific quality and translational potential.1,2 A study by Oddoux et al. describing the dynamics of the microtubule (MT) cytoskeleton in skeletal muscle is one example that demonstrates the power of developing in vivo/ex vivo models.3 MTs have long attracted attention as targets for cancer therapeutics 4 and more recently as mediators of Duchene muscular dystrophy.5 The muscle fiber MT cytoskeleton forms an intricate rectilinear lattice beneath the sarcolemma and is essential for the structural integrity of the muscle. Cultured cells do not develop such a specialized organization of the MT cytoskeleton and our understanding of it has come from static snapshots of muscle sections.6 In this context, the methodology and the findings reported by Oddoux et al. are a significant step forward.

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