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双色超分辨显微镜揭示了机械敏感足突的纳米级组织结构。

Dual-color superresolution microscopy reveals nanoscale organization of mechanosensory podosomes.

机构信息

Department of Tumor Immunology, Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen Medical Centre, 6500 HB Nijmegen, Netherlands.

出版信息

Mol Biol Cell. 2013 Jul;24(13):2112-23. doi: 10.1091/mbc.E12-12-0856. Epub 2013 May 1.

DOI:10.1091/mbc.E12-12-0856
PMID:23637461
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3694795/
Abstract

Podosomes are multimolecular mechanosensory assemblies that coordinate mesenchymal migration of tissue-resident dendritic cells. They have a protrusive actin core and an adhesive ring of integrins and adaptor proteins, such as talin and vinculin. We recently demonstrated that core actin oscillations correlate with intensity fluctuations of vinculin but not talin, suggesting different molecular rearrangements for these components. Detailed information on the mutual localization of core and ring components at the nanoscale is lacking. By dual-color direct stochastic optical reconstruction microscopy, we for the first time determined the nanoscale organization of individual podosomes and their spatial arrangement within large clusters formed at the cell-substrate interface. Superresolution imaging of three ring components with respect to actin revealed that the cores are interconnected and linked to the ventral membrane by radiating actin filaments. In core-free areas, αMβ2 integrin and talin islets are homogeneously distributed, whereas vinculin preferentially localizes proximal to the core and along the radiating actin filaments. Podosome clusters appear as self-organized contact areas, where mechanical cues might be efficiently transduced and redistributed. Our findings call for a reevaluation of the current "core-ring" model and provide a novel structural framework for further understanding the collective behavior of podosome clusters.

摘要

足突是多分子机械感觉组装体,协调组织驻留树突状细胞的间质迁移。它们具有突出的肌动蛋白核心和整合素及衔接蛋白(如 talin 和 vinculin)的黏附环。我们最近证明,核心肌动蛋白的振荡与 vinculin 而非 talin 的强度波动相关,表明这些成分存在不同的分子重排。关于核心和环成分在纳米尺度上的相互定位的详细信息尚不清楚。通过双色直接随机光学重建显微镜,我们首次确定了单个足突及其在细胞-基底界面上形成的大簇内的空间排列的纳米尺度组织。相对于肌动蛋白对三个环成分的超分辨率成像表明,核心相互连接,并通过辐射状肌动蛋白丝与腹膜相连。在无核心区域,αMβ2 整合素和 talin 岛均匀分布,而 vinculin 优先定位于核心附近和辐射状肌动蛋白丝上。足突簇呈现出自组织的接触区域,机械线索可能在此处被有效传递和再分布。我们的发现呼吁重新评估当前的“核心-环”模型,并为进一步理解足突簇的集体行为提供新的结构框架。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e17/3694795/52947516fd2f/2112fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e17/3694795/6bec6aeb5c28/2112fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e17/3694795/e80355efa1e3/2112fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e17/3694795/3863e7d16284/2112fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e17/3694795/5ebb858053d7/2112fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e17/3694795/e3523d32bf8b/2112fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e17/3694795/52947516fd2f/2112fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e17/3694795/6bec6aeb5c28/2112fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e17/3694795/e80355efa1e3/2112fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e17/3694795/3863e7d16284/2112fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e17/3694795/5ebb858053d7/2112fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e17/3694795/e3523d32bf8b/2112fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e17/3694795/52947516fd2f/2112fig6.jpg

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