首页> 美国卫生研究院文献>Springer Open Choice >Diversity of actin architecture in human osteoclasts: network of curved and branched actin supporting cell shape and intercellular micrometer-level tubes
【2h】

Diversity of actin architecture in human osteoclasts: network of curved and branched actin supporting cell shape and intercellular micrometer-level tubes

机译:人破骨细胞中肌动蛋白结构的多样性:弯曲和分支的肌动蛋白网络支持细胞形状和细胞间微米级管

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Osteoclasts are multinucleated bone-resorbing cells with a dynamic actin cytoskeleton. Osteoclasts are derived from circulating mononuclear precursors. Confocal and stimulated emission depletion (STED) super-resolution microscopy was used to investigate peripheral blood-derived human osteoclasts cultured on glass surfaces. STED and confocal microscopy demonstrated that the actin was curved and branched, for instance, in the vicinity of membrane ruffles. The overall architecture of the curved actin network extended from the podosomes to the top of the cell. The other novel finding was that a micrometer-level tube containing actin bridged the osteoclasts well above the level of the culture glass. The actin filaments of the tubes originated from the network of curved actin often surrounding a group of nuclei. Furthermore, nuclei were occasionally located inside the tubes. Our findings demonstrated the accumulation of c-Src, cortactin, cofilin, and actin around nuclei suggesting their role in nuclear processes such as the locomotion of nuclei. ARP2/3 labeling was abundant at the substratum level of osteoclasts and in the branched actin network, where it localized to the branching points. We speculate that the actin-containing tubes of osteoclasts may provide a means of transportation of nuclei, e.g., during the fusion of osteoclasts. These novel findings can pave the way for future studies aiming at the elucidation of the differentiation of multinucleated osteoclasts.Electronic supplementary materialThe online version of this article (doi:10.1007/s11010-017-3004-2) contains supplementary material, which is available to authorized users.
机译:破骨细胞是具有动态肌动蛋白细胞骨架的多核骨吸收细胞。破骨细胞衍生自循环的单核前体。共聚焦和激发发射耗尽(STED)超分辨率显微镜用于研究在玻璃表面培养的外周血来源的人类破骨细胞。 STED和共聚焦显微镜显示,肌动蛋白是弯曲的和分支的,例如在膜褶附近。弯曲肌动蛋白网络的整体结构从足小体延伸到细胞顶部。另一个新颖的发现是,含有肌动蛋白的微米级管桥接破骨细胞,远高于培养皿的水平。管的肌动蛋白丝起源于通常围绕一组核的弯曲肌动蛋白网络。此外,原子核偶尔位于试管内部。我们的发现表明,c-Src,cortactin,cofilin和肌动蛋白在核周围积聚,表明它们在核过程(例如核的运动)中的作用。 ARP2 / 3标记在破骨细胞的底层水平和分支的肌动蛋白网络中分布丰富,并位于分支点。我们推测破骨细胞的含肌动蛋白的管可以提供例如在破骨细胞融合期间细胞核的运输的方式。这些新颖的发现可以为以后阐明多核破骨细胞分化的研究铺平道路。电子补充材料本文的在线版本(doi:10.1007 / s11010-017-3004-2)包含补充材料,可用于授权用户。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号