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一览式成像细胞器接触。

Imaging interorganelle contacts at a glance.

机构信息

Department of Cell Biology and Physiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.

出版信息

J Cell Sci. 2024 Oct 15;137(20). doi: 10.1242/jcs.262020. Epub 2024 Oct 23.

Abstract

Eukaryotic cells are compartmentalized into membrane-bound organelles that must coordinate their responses to stimuli. One way that organelles communicate is via membrane contact sites (MCSs), sites of close apposition between organelles used for the exchange of ions, lipids and information. In this Cell Science at a Glance article and the accompanying poster, we describe an explosion of new methods that have led to exciting progress in this area and discuss key examples of how these methods have advanced our understanding of MCSs. We discuss how diffraction-limited and super-resolution fluorescence imaging approaches have provided important insight into the biology of interorganelle communication. We also describe how the development of multiple proximity-based methods has enabled the detection of MCSs with high accuracy and precision. Finally, we assess how recent advances in electron microscopy (EM), considered the gold standard for detecting MCSs, have allowed the visualization of MCSs and associated proteins in 3D at ever greater resolution.

摘要

真核细胞被分隔成膜结合的细胞器,这些细胞器必须协调它们对刺激的反应。细胞器之间进行通讯的一种方式是通过膜接触位点(MCS),即细胞器之间紧密毗邻的位点,用于交换离子、脂质和信息。在本期《细胞科学一瞥》文章和配套海报中,我们描述了一系列新方法的爆发,这些方法在该领域取得了令人兴奋的进展,并讨论了这些方法如何促进我们对 MCS 的理解的关键实例。我们讨论了如何通过限制和超分辨率荧光成像方法为细胞器间通讯的生物学提供了重要的见解。我们还描述了多种基于邻近性的方法的发展如何能够以高精度和精密度检测 MCS。最后,我们评估了电子显微镜(EM)的最新进展(被认为是检测 MCS 的金标准)如何允许以更高的分辨率在 3D 中可视化 MCS 和相关蛋白质。

相似文献

1
Imaging interorganelle contacts at a glance.一览式成像细胞器接触。
J Cell Sci. 2024 Oct 15;137(20). doi: 10.1242/jcs.262020. Epub 2024 Oct 23.
2
Organization and function of membrane contact sites.膜接触位点的组织与功能。
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本文引用的文献

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In situ architecture of the ER-mitochondria encounter structure.内质网-线粒体接触结构的原位结构。
Nature. 2023 Jun;618(7963):188-192. doi: 10.1038/s41586-023-06050-3. Epub 2023 May 10.

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