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镍离子和镉离子对微管滑动的抑制作用:牛精子轴丝中特定微管对差异反应的证据

Inhibition of microtubule sliding by Ni2+ and Cd2+: evidence for a differential response of certain microtubule pairs within the bovine sperm axoneme.

作者信息

Kanous K S, Casey C, Lindemann C B

机构信息

Department of Biological Sciences, Oakland University, Rochester, Michigan.

出版信息

Cell Motil Cytoskeleton. 1993;26(1):66-76. doi: 10.1002/cm.970260107.

Abstract

Bovine sperm, extracted with 0.1% Triton X-100, frozen at -20 degrees C for 48-120 hours, and thawed, disintegrated by microtubule sliding when 1 mM MgATP was added. Microtubules and outer dense fibers (ODFs) were usually extruded in groups or "bundles". A total of 44.5% of the cells extruded two distinct bundles, one from each side of the connecting piece, exhibiting opposite curvatures. Only one bundle was observed in 46.2% of the cells, and 9.2% showed no signs of sliding. Transmission electron microscopy (T.E.M.) showed one group consisting of the 4,5-6,7 elements, with the 9,1,2 elements on the other side of the axoneme making up the other bundle. T.E.M. revealed that when only one side of the axoneme had extruded elements, they were always from the 4,5-6,7 group. The remainder of the axoneme (8,9,1,2,3 and the central pair) was left relatively intact, suggesting a difference in the sliding response of the nine pairs of axonemal microtubules. These results indicate a predisposition for sliding between elements 7 and 8 over that between doublets 2 and 3, perhaps due to a disparity in activation thresholds. Also, both Ni2+ and Cd2+ appear to selectively block activation of 2-3 interdoublet sliding. Incubation with 0.25 mM Ni2+ prior to adding MgATP modified the percentages of sliding patterns: 8.6% demonstrated two-sided extrusion, 58.2% showed one-sided, and 33.2% had no extruded bundles. Again, when half the axoneme was missing, it was always the 4,5-6,7 group. Ten micromolar Cd2+ altered the sliding pattern similarly to Ni2+, with 28% two-sided extrusion, 55.9% one-sided extrusion and 16.1% with no extruded bundles. Either pretreatment regimen impeded extrusion of the 9,1,2 group in a high percentage of cells, compared to untreated cells. This specific inhibition of the 9,1,2 side by Ni2+ or Cd2+ is especially significant since Ni2+ also inhibits spontaneous wave initiation in bull sperm (Lindemann et al.: Journal of Cell Biology 87:420-426, 1980), and both Ni2+ and Cd2+ reportedly block the flagellar Ca(2+)-response in rat sperm (Lindemann and Goltz: Cell Motility and the Cytoskeleton 10:420-431, 1988; Lindemann et al.: Cell Motility and the Cytoskeleton 20:316-324, 1991).

摘要

用0.1%的曲拉通X-100提取的牛精子,在-20℃下冷冻48 - 120小时后解冻,当加入1 mM的MgATP时,会通过微管滑动而解体。微管和外周致密纤维(ODFs)通常成组或“束”状挤出。总共44.5%的细胞从连接段的两侧各挤出两个不同的束,呈现相反的曲率。在46.2%的细胞中仅观察到一个束,9.2%的细胞没有滑动迹象。透射电子显微镜(T.E.M.)显示一组由4、5 - 6、7号元件组成,轴丝另一侧的9、1、2号元件构成另一束。T.E.M.显示,当轴丝只有一侧有挤出元件时,它们总是来自4、5 - 6、7组。轴丝的其余部分(8、9、1、2、3号元件和中央微管对)相对保持完整,这表明九对轴丝微管的滑动反应存在差异。这些结果表明,7号和8号元件之间比2号和3号双联体之间更容易发生滑动,这可能是由于激活阈值的差异。此外,Ni2+和Cd2+似乎都能选择性地阻断2 - 3号双联体间滑动的激活。在加入MgATP之前用0.25 mM的Ni2+孵育会改变滑动模式的百分比:8.6%表现为双侧挤出,58.2%为单侧挤出,33.2%没有挤出束。同样,当轴丝的一半缺失时,总是4、5 - 6、7组。10微摩尔的Cd2+与Ni2+类似地改变了滑动模式,28%为双侧挤出,55.9%为单侧挤出,16.1%没有挤出束。与未处理的细胞相比,这两种预处理方案在高比例的细胞中都阻碍了9、1、2组的挤出。Ni2+或Cd2+对9、1、2侧的这种特异性抑制尤为显著,因为Ni2+还会抑制公牛精子中的自发波起始(Lindemann等人:《细胞生物学杂志》87:420 - 426,1980),并且据报道Ni2+和Cd2+都能阻断大鼠精子中的鞭毛Ca(2+)反应(Lindemann和Goltz:《细胞运动与细胞骨架》10:420 - 431,1988;Lindemann等人:《细胞运动与细胞骨架》20:316 - 324,1991)。

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