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“微小梁概念”后来怎么样了?

Whatever happened to the 'microtrabecular concept'?

作者信息

Heuser John

机构信息

Department of Cell Biology and Physiology, Washington University School of Medicine, St Louis, Missouri 63110, USA.

出版信息

Biol Cell. 2002 Dec;94(9):561-96. doi: 10.1016/s0248-4900(02)00013-8.

Abstract

Keith Porter culminated his stellar career as the founding father of biological electron microscopy by acquiring, in the late 1970s, a high-voltage electron microscope (HVEM). With this magnificent instrument he examined whole-mounts of cultured cells, and perceived within them a structured cytoplasmic matrix he named the "microtrabecular lattice". Over the next decade Porter published a series of studies, together with a team of outstanding young colleagues, which elaborated his broader "microtrabecular concept." This concept posited that microtrabeculae were real physical entities that represented the fundamental organization the cytoplasm, and that they were the physical basis of cytoplasmic motility and of cell-shape determination. The present review presents Porter's original images of microtrabeculae, after conversion to a more interpretable "digital-anaglyph" form, and discusses the rise and fall of the microtrabecular concept. Further, it explains how the HVEM images of microtrabeculae finally came to be considered as an artifact of the preparative methods Porter used to prepare whole cells for HVEM. Still, Keith's "microtrabecular concept" foretold of our current appreciation of the complexity and pervasiveness of the cytoskeleton, which has now been found by more modern methods of EM to actually be the fundamental organizing principle of the cytoplasmic matrix. During the impending eclipse of Porter's microtrabecular concept in the late 1980s, many of Keith's colleagues fondly described the cell as being filled, not with protoplasm, but with "Porterplasm." Despite the fact that Keith's view was clouded by the methods of his time, it would be fitting and apt to retain this name, still today, for the ordered matrix of cytoskeletal macromolecules that exists in the living cell. In the end, the story of what happened to Porter's microtrabecular concept should be an object lesson in scientific hubris that should humble and inform all of us in cell biology, even today--particularly when we begin to think that our most recent methods and observations are achieving "the last word".

摘要

基思·波特在20世纪70年代末购置了一台高压电子显微镜(HVEM),以此作为生物电子显微镜的开创者,达到了他辉煌职业生涯的顶峰。借助这台了不起的仪器,他观察了培养细胞的整装标本,并在其中察觉到一种有结构的细胞质基质,他将其命名为“微梁晶格”。在接下来的十年里,波特与一群杰出的年轻同事共同发表了一系列研究,阐述了他更广泛的“微梁概念”。这个概念假定微梁是真实的物理实体,代表了细胞质的基本组织形式,并且它们是细胞质运动和细胞形状确定的物理基础。本综述展示了波特微梁的原始图像,这些图像已转换为更易于解读的“数字立体图”形式,并讨论了微梁概念的兴衰。此外,它解释了微梁的HVEM图像最终如何被认为是波特用于为HVEM制备全细胞的制备方法所产生的假象。尽管如此,基思的“微梁概念”预示了我们目前对细胞骨架复杂性和普遍性的认识,现在通过更现代的电子显微镜方法已经发现,细胞骨架实际上是细胞质基质的基本组织原则。在20世纪80年代末波特的微梁概念即将失宠之际,基思的许多同事亲切地将细胞描述为充满了“波特质”,而不是原生质。尽管基思的观点受到当时方法所限,但即便在今天,用这个名字来称呼活细胞中存在的细胞骨架大分子的有序基质仍然恰当合适。最后,波特的微梁概念的故事应该成为一个关于科学傲慢的教训,即使在今天,它也应该让我们细胞生物学领域的所有人保持谦逊并从中得到启示——尤其是当我们开始认为我们最新的方法和观察结果是“最终定论”的时候。

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