Department of Microbiology and Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia.
Department of Microbiology and Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia
Microbiol Mol Biol Rev. 2019 Feb 27;83(2). doi: 10.1128/MMBR.00058-18. Print 2019 May 15.
The entry of pathogens into nonphagocytic host cells has received much attention in the past three decades, revealing a vast array of strategies employed by bacteria and viruses. A method of internalization that has been extensively studied in the context of viral infections is the use of the clathrin-mediated pathway. More recently, a role for clathrin in the entry of some intracellular bacterial pathogens was discovered. Classically, clathrin-mediated endocytosis was thought to accommodate internalization only of particles smaller than 150 nm; however, this was challenged upon the discovery that requires clathrin to enter eukaryotic cells. Now, with discoveries that clathrin is required during other stages of some bacterial infections, another paradigm shift is occurring. There is a more diverse impact of clathrin during infection than previously thought. Much of the recent data describing clathrin utilization in processes such as bacterial attachment, cell-to-cell spread and intracellular growth may be due to newly discovered divergent roles of clathrin in the cell. Not only does clathrin act to facilitate endocytosis from the plasma membrane, but it also participates in budding from endosomes and the Golgi apparatus and in mitosis. Here, the manipulation of clathrin processes by bacterial pathogens, including its traditional role during invasion and alternative ways in which clathrin supports bacterial infection, is discussed. Researching clathrin in the context of bacterial infections will reveal new insights that inform our understanding of host-pathogen interactions and allow researchers to fully appreciate the diverse roles of clathrin in the eukaryotic cell.
病原体进入非吞噬宿主细胞一直是过去三十年的研究热点,揭示了细菌和病毒所采用的大量策略。在病毒感染的背景下,内化的一种方法就是网格蛋白介导的途径。最近,人们发现网格蛋白在一些胞内细菌病原体的入侵中也发挥了作用。经典的网格蛋白介导的内吞作用被认为只能容纳小于 150nm 的颗粒;然而,这一观点在发现 进入真核细胞需要网格蛋白时受到了挑战。现在,随着人们发现网格蛋白在一些细菌感染的其他阶段也需要网格蛋白,又出现了另一个范式转变。网格蛋白在感染过程中的影响比以前认为的要多样化。最近描述网格蛋白在细菌附着、细胞间传播和细胞内生长等过程中的利用的大量数据,可能是由于网格蛋白在细胞中的新发现的不同作用。网格蛋白不仅有助于从质膜进行内吞作用,还参与从内体和高尔基体出芽以及有丝分裂。本文讨论了细菌病原体对网格蛋白过程的操纵,包括其在入侵过程中的传统作用以及网格蛋白支持细菌感染的其他方式。在细菌感染的背景下研究网格蛋白,将揭示新的见解,从而增进我们对宿主-病原体相互作用的理解,并使研究人员充分认识到网格蛋白在真核细胞中的多种作用。