{"title":"Wavelike motions of cytoskeletal fibrils and their mechanics.","authors":"R Jarosch","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Actin filaments and microtubules can slide and translocate particles along as it is well known. Moreover, bendings, corners, regions of branching and crossbridges can move in a wavelike manner along bundles of cytoskeletal elements. This has been demonstrated by microcinematography e.g. of ringlike closed F-actin bundles (\"waving polygons\") in cytoplasmic drops squeezed out of characean internodial cells (Jarosch 1960) and by microtubule bundles of axostyles of Pyrsonympha (Langford and Inoué 1979), or by the rootlet fibril (costa) of Trichomonas (Amos et al. 1979). Single isolated microtubules from squid giant axons that become visible by video-enhanced interference contrast microscopy can glide on glass slides and start a kind of \"fishtailing\" when gliding is prevented by an obstacle (Allen et al. 1985). The described wavelike motions cannot be explained by the power-stroke or rowing-stroke model of myosin-, kinesin-, or dynein-crossbridges between filaments or microtubules--thus the problem of proper coordination and localization of the single power-strokes is unsolved. The motions can be explained and simulated in detail by macroscopic models with rotating steel helices. This indicates the existence of quickly rotating cytoskeletal elements. Two types of mechanisms are possible: 1) The propagation of angles and corners may depend on the close contact between the rotating elements of the bundle, e.g., by mutual winding and unwinding of actin-associated filaments or microtubule-associated filaments (characean polygons, axostyles of Pyrsonympha). 2) The rotating elements of the bundle form superhelices, and their rotation results in microscopic helical waves (bacterial flagella, helical filopodia, \"corkscrewing\" of a helical bundle). Eucaryotic flagella transform the latent helical waves of their helically shaped doublet microtubules and the central singlet helix to large helical or uniplanar bending waves by a most intricate mechanical coil-coil interaction that is demonstrated in a simplified manner by model experiments.</p>","PeriodicalId":7002,"journal":{"name":"Acta histochemica. Supplementband","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1991-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta histochemica. Supplementband","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Actin filaments and microtubules can slide and translocate particles along as it is well known. Moreover, bendings, corners, regions of branching and crossbridges can move in a wavelike manner along bundles of cytoskeletal elements. This has been demonstrated by microcinematography e.g. of ringlike closed F-actin bundles ("waving polygons") in cytoplasmic drops squeezed out of characean internodial cells (Jarosch 1960) and by microtubule bundles of axostyles of Pyrsonympha (Langford and Inoué 1979), or by the rootlet fibril (costa) of Trichomonas (Amos et al. 1979). Single isolated microtubules from squid giant axons that become visible by video-enhanced interference contrast microscopy can glide on glass slides and start a kind of "fishtailing" when gliding is prevented by an obstacle (Allen et al. 1985). The described wavelike motions cannot be explained by the power-stroke or rowing-stroke model of myosin-, kinesin-, or dynein-crossbridges between filaments or microtubules--thus the problem of proper coordination and localization of the single power-strokes is unsolved. The motions can be explained and simulated in detail by macroscopic models with rotating steel helices. This indicates the existence of quickly rotating cytoskeletal elements. Two types of mechanisms are possible: 1) The propagation of angles and corners may depend on the close contact between the rotating elements of the bundle, e.g., by mutual winding and unwinding of actin-associated filaments or microtubule-associated filaments (characean polygons, axostyles of Pyrsonympha). 2) The rotating elements of the bundle form superhelices, and their rotation results in microscopic helical waves (bacterial flagella, helical filopodia, "corkscrewing" of a helical bundle). Eucaryotic flagella transform the latent helical waves of their helically shaped doublet microtubules and the central singlet helix to large helical or uniplanar bending waves by a most intricate mechanical coil-coil interaction that is demonstrated in a simplified manner by model experiments.
众所周知,肌动蛋白丝和微管可以滑动和转移颗粒。此外,弯曲、角落、分支区域和交叉桥可以沿着细胞骨架元素束以波浪形的方式移动。这已经通过显微摄影技术得到证实,例如从特征性节间细胞中挤出的细胞质液滴中的环状封闭的f -肌动蛋白束(“波形体”)(Jarosch 1960),以及pysonympha轴柱的微管束(Langford and inou 1979),或毛滴虫的根细纤维(costa) (Amos et al. 1979)。通过视频增强干涉对比显微镜可以看到的来自乌贼巨大轴突的单个分离微管可以在玻片上滑动,并且当滑动被障碍物阻止时开始一种“鱼尾”(Allen et al. 1985)。所描述的波状运动不能用肌凝蛋白、动力蛋白或动力蛋白在细丝或微管之间的交叉桥的动力冲程或划船冲程模型来解释,因此单个动力冲程的适当协调和定位问题没有得到解决。这些运动可以用带有旋转钢螺旋的宏观模型来详细解释和模拟。这表明存在快速旋转的细胞骨架元件。角度和角的传播可能有两种机制:1)角度和角的传播可能取决于束中旋转元素之间的密切接触,例如,通过肌动蛋白相关细丝或微管相关细丝(特征多边形,pysonympha轴柱)的相互缠绕和解绕。2)束的旋转元素形成超螺旋,它们的旋转导致微观的螺旋波(细菌鞭毛,螺旋丝状足,螺旋束的“螺旋”)。真核鞭毛通过最复杂的机械线圈-线圈相互作用,将其螺旋形双线微管和中心单线螺旋的潜在螺旋波转化为大的螺旋或单面弯曲波,并通过模型实验以简化的方式证明了这一点。