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阶段特异性合成超长链二氢神经酰胺赋予寄生虫休眠能力。

Stage-Specific Synthesis of Very-Long-Chain Dihydroceramides Confers Dormancy to Parasites.

机构信息

Division of Molecular and Cellular Immunoscience, Department of Biomolecular Sciences, Faculty of Medicine, Saga University, Saga, Japan

Laboratory for Metabolomics, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.

出版信息

mSphere. 2021 Mar 17;6(2):e00174-21. doi: 10.1128/mSphere.00174-21.

Abstract

Amoebiasis is a parasitic disease caused by infection and is a serious public health problem worldwide due to ill-prepared preventive measures as well as its high morbidity and mortality rates. Amoebiasis transmission is solely mediated by cysts. Cysts are produced by the differentiation of proliferative trophozoites in a process termed "encystation." encystation is a fundamental cell differentiation process and proceeds with substantial changes in cell metabolites, components, and morphology, which occur sequentially in an orchestrated manner. Lipids are plausibly among these metabolites that function as key factors for encystation. However, a comprehensive lipid analysis has not been reported, and the involved lipid metabolic pathways remain largely unknown. Here, we exploited the state-of-the-art untargeted lipidomics and characterized 339 molecules of 17 lipid subclasses. Of these, dihydroceramide (Cer-NDS) was found to be among the most induced lipid species during encystation. Notably, in encysting cells, amounts of Cer-NDS containing very long -acyl chains (≥26 carbon) were more than 30-fold induced as the terminal product of a metabolic pathway. We also identified three ceramide synthase genes responsible for producing the very-long-chain Cer-NDS molecules. These genes were upregulated during encystation. Furthermore, these ceramide species were shown to be indispensable for generating membrane impermeability, a prerequisite for becoming dormant cyst that shows resistance to environmental assault inside and outside the host for transmission. Hence, the lipid subclass of Cer-NDS plays a crucial role for cell differentiation and morphogenesis by alternating the membrane properties. is a protozoan parasite that thrives in its niche by alternating its two forms between a proliferative trophozoite and dormant cyst. Cysts are the only form able to transmit to a new host and are differentiated from trophozoites in a process termed "encystation." During encystation, cell metabolites, components, and morphology drastically change, which occur sequentially in an orchestrated manner. Lipids are plausibly among these metabolites. However, the involved lipid species and their metabolic pathways remain largely unknown. Here, we identified dihydroceramides (Cer-NDSs) containing very long -acyl chains (C to C) as a key metabolite for encystation by our state-of-the-art untargeted lipidomics. We also showed that these Cer-NDSs are critical to generate the membrane impermeability, a prerequisite for this parasite to show dormancy as a cyst that repels substances and prevents water loss. Hence, ceramide metabolism is essential for to maintain the parasitic lifestyle.

摘要

溶组织内阿米巴病是一种由 感染引起的寄生虫病,由于预防措施准备不足以及高发病率和死亡率,它是一个严重的全球公共卫生问题。溶组织内阿米巴病的传播仅通过囊包传播。囊包是由增殖滋养体分化产生的,这一过程被称为“囊化”。囊化是一种基本的细胞分化过程,伴随着细胞代谢物、成分和形态的实质性变化,这些变化以协调的方式依次发生。脂质可能是这些代谢物之一,作为囊化的关键因素发挥作用。然而,尚未进行全面的脂质分析,涉及的脂质代谢途径在很大程度上仍然未知。在这里,我们利用最先进的非靶向脂质组学技术,对 17 种脂质亚类的 339 种分子进行了表征。在这些脂质中,二氢神经酰胺(Cer-NDS)被发现是囊化过程中诱导程度最高的脂质之一。值得注意的是,在囊化细胞中,含有非常长酰基链(≥26 个碳原子)的 Cer-NDS 物质的含量增加了 30 多倍,成为代谢途径的终产物。我们还鉴定了三个负责产生非常长链 Cer-NDS 分子的神经酰胺合酶基因。这些基因在囊化过程中上调。此外,这些神经酰胺种类对于产生膜不可渗透性是必不可少的,膜不可渗透性是休眠囊形成的先决条件,休眠囊在宿主内外环境中具有抵抗环境攻击的能力,从而能够进行传播。因此,Cer-NDS 脂质亚类通过改变膜特性在 细胞分化和形态发生中起着至关重要的作用。是一种原生动物寄生虫,通过在增殖滋养体和休眠囊之间交替两种形式在其生态位中生存。囊是唯一能够传播到新宿主的形式,并且是在称为“囊化”的过程中从滋养体分化而来的。在 囊化过程中,细胞代谢物、成分和形态发生了巨大变化,这些变化以协调的方式依次发生。脂质可能是这些代谢物之一。然而,涉及的脂质种类及其代谢途径在很大程度上仍然未知。在这里,我们通过最先进的非靶向脂质组学技术,鉴定出含有非常长酰基链(C 至 C)的二氢神经酰胺(Cer-NDS)作为 囊化的关键代谢物。我们还表明,这些 Cer-NDS 对于产生膜不可渗透性至关重要,这是这种寄生虫作为休眠囊形成的先决条件,休眠囊排斥物质并防止水分流失。因此,神经酰胺代谢对于 维持寄生生活方式是必不可少的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7267/8546694/37827df124a4/msphere.00174-21_f001.jpg

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