从原生动物到哺乳动物的酶家族:磷脂酶A2如何参与刚地弓形虫的入侵过程

Jorge Enrique Gomez-Marin, Annie Bonhomme, Jean-Michel Pinon
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引用次数: 1

摘要

刚地弓形虫是细胞内专性原生动物寄生虫。人类感染通常是亚临床的,但细胞免疫缺陷的宿主有严重疾病的危险。在许多国家,艾滋病毒感染者的先天性弓形虫病和弓形虫脑炎是发病率和死亡率的重要原因。本文综述了磷脂酶A2 (PLA2)家族成员在弓形虫侵染过程中的作用及其机制。在哺乳动物细胞中,PLA2被描述为一个由九组酶组成的家族,这些酶特异性地水解磷脂的sn-2键。每个PLA2组具有不同的底物偏好、定位和激活方式,表明不同的生理作用。我们在弓形虫中描述了三种PLA2亚型的存在。分泌PLA2亚型(sPLA2)和细胞质PLA2 (cPLA2)抑制剂表明,细胞和寄生虫sPLA2和寄生虫cPLA2,而不是细胞cPLA2,有利于弓形虫的入侵。将IFNγ添加到培养的受感染THP1细胞中,通过减少被寄生细胞数量的早期机制保护细胞免受弓形虫感染。通过IFN γ处理获得的被寄生细胞百分比的降低与寄生虫和细胞PLA2活性的降低有关。这是IFN γ抗弓形虫感染的一种新的作用机制。sPLA2 II型抑制剂具有抗弓形虫感染的药理学潜力,但仍有待体内试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Une famille d'enzymes présentes des protozoaires aux mammifères: comment les phospholipases A2 participent au processus d'invasion de Toxoplasma gondii

Toxoplasma gondii is an intracellular obligate protozoan parasite. Human infection is generally subclinical but hosts with defective cellular immunity are at risk of severe disease. In many countries, congenital toxoplasmosis and toxoplasmic encephalitis in HIV-infected individuals are significant causes of morbidity and mortality. We review here the role of the members of phospholipases A2 (PLA2) family and how they participate in the invasion process of T. gondii. PLA2 have been described in mammals cells as a family composed of nine groups of enzymes that specifically hydrolyse sn-2 bonds of phospholipids. Each PLA2 group have a distinctive substrate preference, localization and way of activation indicating different physiological roles. We describe the existence of three PLA2 isoforms in T. gondii. Inhibitors of secretory PLA2 isoforms (sPLA2) and cytosolic PLA2 (cPLA2), showed that cell and parasite sPLA2 and parasite cPLA2, but not cell cPLA2, favours T. gondii invasion. The addition of IFNγ to cultured infected THP1 cells protected against T. gondii infection by an early mechanism involving a reduction in the number of parasitized cells. The reduction in the percentage of parasitized cells obtained by treatment with IFN γ is linked with a decrease in parasite and cellular PLA2 activity. This is a new effector mechanism of IFN γ against T. gondii infection. The inhibitors of sPLA2 type II have a pharmacological potential against T. gondii infection that remain to be tested in vivo.

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