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突破细菌包膜:吞噬细胞中穿孔素-2(MPEG1)的关键作用。

Breaching the Bacterial Envelope: The Pivotal Role of Perforin-2 (MPEG1) Within Phagocytes.

机构信息

Department of Microbiology and Immunology, Leonard M. Miller School of Medicine, University of Miami, Miami, FL, United States.

出版信息

Front Immunol. 2021 Feb 22;12:597951. doi: 10.3389/fimmu.2021.597951. eCollection 2021.

Abstract

The membrane attack complex (MAC) of the complement system and Perforin-1 are well characterized innate immune effectors. MAC is composed of C9 and other complement proteins that target the envelope of gram-negative bacteria. Perforin-1 is deployed when killer lymphocytes degranulate to destroy virally infected or cancerous cells. These molecules polymerize with MAC-perforin/cholesterol-dependent cytolysin (MACPF/CDC) domains of each monomer deploying amphipathic β-strands to form pores through target lipid bilayers. In this review we discuss one of the most recently discovered members of this family; Perforin-2, the product of the gene. Since their initial description more than 100 years ago, innumerable studies have made macrophages and other phagocytes some of the best understood cells of the immune system. Yet remarkably it was only recently revealed that Perforin-2 underpins a pivotal function of phagocytes; the destruction of phagocytosed microbes. Several studies have established that phagocytosed bacteria persist and in some cases flourish within phagocytes that lack Perforin-2. When challenged with either gram-negative or gram-positive pathogens knockout mice succumb to infectious doses that the majority of wild-type mice survive. As expected by their immunocompromised phenotype, bacterial pathogens replicate and disseminate to deeper tissues of knockout mice. Thus, this evolutionarily ancient gene endows phagocytes with potent bactericidal capability across taxa spanning sponges to humans. The recently elucidated structures of mammalian Perforin-2 reveal it to be a homopolymer that depends upon low pH, such as within phagosomes, to transition to its membrane-spanning pore conformation. Clinical manifestations of missense mutations further highlight the pivotal role of Perforin-2 within phagocytes. Controversies and gaps within the field of Perforin-2 research are also discussed as well as animal models that may be used to resolve the outstanding issues. Our review concludes with a discussion of bacterial counter measures against Perforin-2.

摘要

补体系统的膜攻击复合物(MAC)和穿孔素-1 是经过充分研究的先天免疫效应因子。MAC 由 C9 和其他补体蛋白组成,靶向革兰氏阴性菌的包膜。当杀伤性淋巴细胞脱颗粒时,穿孔素-1 会被部署以破坏病毒感染或癌变的细胞。这些分子与每个单体的 MAC-穿孔素/胆固醇依赖性细胞溶解物(MACPF/CDC)结构域聚合,通过靶脂质双层部署两亲性β-链来形成孔。在这篇综述中,我们讨论了该家族最近发现的成员之一;基因的产物穿孔素-2。自从 100 多年前首次描述以来,无数的研究使巨噬细胞和其他吞噬细胞成为免疫系统中研究最透彻的细胞之一。然而,令人惊讶的是,最近才发现穿孔素-2是吞噬细胞的一个关键功能的基础;吞噬的微生物的破坏。几项研究已经证实,缺乏穿孔素-2的吞噬细胞内吞噬的细菌会持续存在,在某些情况下甚至会繁殖。当受到革兰氏阴性或革兰氏阳性病原体的挑战时,敲除小鼠会屈服于感染剂量,而大多数野生型小鼠都能存活。由于其免疫功能受损的表型,细菌病原体在 敲除小鼠的深层组织中复制和传播。因此,这个进化古老的基因赋予了吞噬细胞在跨越海绵到人类的分类群中强大的杀菌能力。最近阐明的哺乳动物穿孔素-2结构揭示了它是一种同聚物,依赖于低 pH 值,如在吞噬体中,以转变为其跨膜孔构象。错义突变的临床表现进一步强调了穿孔素-2在吞噬细胞中的关键作用。我们还讨论了穿孔素-2研究领域的争议和差距,以及可能用于解决悬而未决问题的动物模型。我们的综述以讨论细菌对抗穿孔素-2的对策结束。

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