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吞噬体动力学与功能

Phagosome dynamics and function.

作者信息

Tjelle T E, Lovdal T, Berg T

机构信息

Norwegian Radium Hospital, Department of Biophysics, Institute for Cancer Research, Montebello, 0310 Oslo, Norway.

出版信息

Bioessays. 2000 Mar;22(3):255-63. doi: 10.1002/(SICI)1521-1878(200003)22:3<255::AID-BIES7>3.0.CO;2-R.

Abstract

Phagocytosis of microorganisms and other particles is mediated most efficiently by receptors such as Fc-receptors (FcR) and complement-receptors (C3R). Interaction between these receptors and ligands on the particle results in signal transduction events that lead to actin polymerisation and phagosome formation. The phagosome then undergoes a maturation process whereby it transforms into a phagolysosome. Phagosome maturation depends on interactions (fusion events) with early and late endosomes as well as with lysosomes. The fusion processes are regulated by small GTP-binding proteins and other proteins that are also involved in fusion processes in the endocytic pathway. Although most phagocytosed microorganisms are killed in the lysosome, some pathogens have developed survival strategies and are able to live in the harsh conditions in the phagolysosome or interfere with the maturation process and thereby evade destruction by acid hydrolases.

摘要

微生物和其他颗粒的吞噬作用最有效地由诸如Fc受体(FcR)和补体受体(C3R)等受体介导。这些受体与颗粒上的配体之间的相互作用导致信号转导事件,进而导致肌动蛋白聚合和吞噬体形成。吞噬体随后经历成熟过程,在此过程中它转变为吞噬溶酶体。吞噬体成熟取决于与早期和晚期内体以及溶酶体的相互作用(融合事件)。融合过程由小GTP结合蛋白和其他也参与内吞途径融合过程的蛋白质调节。尽管大多数被吞噬的微生物在溶酶体中被杀死,但一些病原体已经发展出生存策略,能够在吞噬溶酶体的恶劣条件下生存,或干扰成熟过程,从而逃避酸性水解酶的破坏。

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