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新兴巨吞噬体功能在宿主-病原体相互作用中的解密新方法。

New methods to decrypt emerging macropinosome functions during the host-pathogen crosstalk.

机构信息

Institut Pasteur, Dynamics of Host-Pathogen Interactions Unit and CNRS UMR 3691, Paris, France.

Division of Molecular and Cellular Biology, National Institute of Child Health and Human Development, NIH, Bethesda, Maryland, USA.

出版信息

Cell Microbiol. 2021 Jul;23(7):e13342. doi: 10.1111/cmi.13342. Epub 2021 May 6.

Abstract

Large volumes of liquid and other materials from the extracellular environment are internalised by eukaryotic cells via an endocytic process called macropinocytosis. It is now recognised that this fundamental and evolutionarily conserved pathway is hijacked by numerous intracellular pathogens as an entry portal to the host cell interior. Yet, an increasing number of additional cellular functions of macropinosomes in pathologic processes have been reported beyond this role for fluid internalisation. It emerges that the identity of macropinosomes can vary hugely and change rapidly during their lifetime. A deeper understanding of this important multi-faceted compartment is based on novel methods for their investigation. These methods are either imaging-based for the tracking of macropinosome dynamics, or they provide the means to extract macropinosomes at high purity for comprehensive proteomic analyses. Here, we portray these new approaches for the investigation of macropinosomes. We document how these method developments have provided insights for a new understanding of the intracellular lifestyle of the bacterial pathogens Shigella and Salmonella. We suggest that a systematic complete characterisation of macropinosome subversion with these approaches during other infection processes and pathologies will be highly beneficial for our understanding of the underlying cellular and molecular processes.

摘要

真核细胞通过一种称为巨胞饮的内吞作用过程将大量的液体和其他细胞外环境中的物质内化。现在人们认识到,这种基本的、进化上保守的途径被许多细胞内病原体劫持,成为进入宿主细胞内部的入口。然而,除了这种液体内化的作用之外,巨胞饮体在病理过程中的许多额外的细胞功能也被报道。巨胞饮体的身份在其生命周期中变化很大,而且变化很快。对这个重要的多方面隔室的更深入了解是基于对其进行研究的新方法。这些方法要么是基于成像的,用于跟踪巨胞饮体的动力学,要么是提供了以高纯度提取巨胞饮体进行全面蛋白质组分析的手段。在这里,我们描述了这些用于研究巨胞饮体的新方法。我们记录了这些方法的发展如何为理解细菌病原体志贺氏菌和沙门氏菌的细胞内生活方式提供了新的认识。我们认为,在其他感染过程和病理中,系统地用这些方法对巨胞饮体的颠覆进行全面描述,将非常有助于我们理解潜在的细胞和分子过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/715f/8365644/3797dcd529e7/CMI-23-e13342-g003.jpg

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